Updated on 2026/02/13

写真a

 
YAMADA TAKUJI
 
Organization
School of Life Science and Technology Professor
Title
Professor
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News & Topics
  • Personalized Gut Microbiome Analysis for Colorectal Cancer Classification with Explainable AI

    2023/04/14

    Languages: English

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    Explainable AI offers a promising solution for finding links between diseases and certain species of gut bacteria, finds a research team at Tokyo Tech. Using a concept borrowed from game theory,

  • Explainable AI(説明可能なAI)の活用による腸内細菌に基づく大腸がんの詳細な分類を実現 大腸がん診断とバイオマーカー同定のパーソナライズを促進

    2023/04/11

    Languages: Japanese

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    要点-「説明可能なAI」を利用して個人の腸内細菌パターンを特定し、大腸がん患者をより細かく層別化-ゲーム理論を応用した手法で、健常者と大腸がん患者を明確に判別できることを発見-今後さらにパーソナライズされた大腸がん診断とバイオマーカー同定の実現につながると

  • 焼酎黒麹の白色化によって起こる遺伝子変異

    2021/07/29

    Languages: Japanese

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    要点-実用黒麹、実用白麹、研究用白麹のゲノム比較を実施した。-研究用白麹と実用白麹には遺伝情報に明確な違いがあることを明らかにした。-実用白麹株では、白色化後の継代によって共通する変異が起きたと推測される。概要東京工業大学生命理工学院生命理工学系の山田拓司准教授らは、株式会社ぐるなびとの共同研究にお

  • 塩から始まる微生物群集のダイナミクス 地域を越えて働く野菜の塩漬けのメカニズム

    2021/04/13

    Languages: Japanese

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    要点-三大菜漬を用い、野菜の塩漬けメカニズムの微生物群集ダイナミクスと漬物成分の関係の一部を明らかに-低塩濃度で短期間漬け込む前処理工程では乳酸菌群優勢、高塩濃度で長期間漬け込む塩蔵工程では乳酸菌と好塩性細菌の割合が高い-塩蔵工程サンプルに分枝アミノ酸が多いのは、好塩性細菌が持つ分枝アミノ酸生合成経

  • ぬか漬けたくあんを作る発酵微生物とおいしさのひみつ 地域の気候を反映した製法の違いが与える多様性

    2021/01/27

    Languages: Japanese

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    要点-秋田と愛知のたくあんの独自の製法が発酵微生物や成分に与える影響を解析-製法の違いが発酵微生物の種類や多様性に影響-塩を好む微生物が漬け込み中にグルタミン酸を生成している可能性概要東京工業大学生命理工学院生命理工学系の山田拓司准教授らは、株式会社ぐるなびとの共同研究において、寒冷な豪雪地域である

  • 胃切除術による腸内環境の変化を解明 胃切除後の合併疾患の克服へ

    2020/01/17

    Languages: Japanese

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    要点-腸内細菌は、胃切除を含む様々な治療と関連する可能性があることが知られていますが、治療による腸内環境への影響は詳細には明らかになっていませんでした。-本研究では、便検体を用いたメタゲノム解析およびメタボローム解析により、健常者と胃切除術を受けた患者

  • 麹菌A. oryzaeの進化と家畜化の関係 大規模比較ゲノム解析で新たな仮説を提唱

    2019/12/02

    Languages: Japanese

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    要点-日本全国から収集した麹菌82株の全ゲノムレベルの多様性を解読-祖先株間で複数の有性生殖が起こっていたことが明らかに-人間による家畜化が麹菌のゲノム進化に及ぼす影響を提唱概要東京工業大学生命理工学院生命理工学系の山田拓司准教授、渡来直生

  • メタゲノム・メタボローム解析により大腸がん発症関連細菌を特定 便から大腸がんを早期に診断する新技術

    2019/06/07

    Languages: Japanese

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    大腸がんの発がんに関連する細菌を発見 健常者、多発ポリープ(腺腫)、粘膜内がん、早期がん、進行がんを対象(616例)に、便を用いてメタゲノム解析とメタボローム解析 行うことにより、健常者と比較してがんの進行段階で増減している細菌や代謝物質を同定 大腸がんの早期診断や予防、大腸がんになる前に治療を行う(先制医療)への応用に期待

  • New simple storage method for faecal samples offers improvements in the metagenomic analysis and the study of disease

    2016/08/17

    Languages: English

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    Associate Professor Takuji Yamada of Tokyo Institute of Technology, Laboratory Head Shinichi Yachida of National Cancer Center and colleagues developed a new faecal microbiome preservation method to support metagenomic analysis of intestinal flora, bacteria in the intestines. Recent developments in gene-sequencing technology have enabled researchers to identify the genomes of natural bacteria in the intestines. Reports have shown that these bacteria are strongly associated with obesity, diabetes, inflammatory bowel disease and allergies. They also show potential as disease markers to identify cancer risks.

  • Oligosaccharides in breast milk are key

    2016/07/14

    Languages: English

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    Tokyo Institute of Technology, Yakult Central Institute, and Teikyo University have jointly unraveled the mechanism which shapes intestinal flora (microbial communities in the intestines) of infants in its transition towards dominance of bifidobacteria.

  • 腸内細菌叢(腸内フローラ)のメタゲノム解析による発がん研究の加速に期待

    2016/07/13

    Languages: Japanese

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    本研究成果のポイント 腸内細菌叢(腸内フローラ)のメタゲノム解析に欠かせない研究試料である糞便の収集方法について、標準方法とされる冷凍保存よりも簡便な収集方法を確立 既存溶液を活用した室温保存について、冷凍保存と同レベルの解析結果が得られることを実証した。 大腸内視鏡検査により腸内細菌叢は変動しないことを確認 大腸内視鏡検査とその前処置(腸管洗浄剤内服による洗浄)に伴う腸内細菌叢への影響を検討し、大腸内視鏡検査の前後で腸内細菌叢の組成の変動はみられないことが明らかになった。

  • ビフィズス菌が優勢になる乳児の腸内フローラ形成機構を解明―母乳に含まれるオリゴ糖の主要成分の利用がカギ―

    2016/06/30

    Languages: Japanese

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    要点 ビフィズス菌は、乳児期の腸内フローラにおいて優勢になることが知られていたがメカニズムが分かっていなかった。本研究では、生後1か月の間に乳児の腸内フローラが大きく変化し、腸内細菌科およびスタフィロコッカス科に属する細菌群が優勢のフローラ構成から、ビフィズス菌が優勢のフローラ構成に変動することを明らかにした。ビフィズス菌が優勢になるためには、母乳に含まれるオリゴ糖の主要構成成分「フコシルラクトース」が重要な役割を果たしていることをゲノム解析により解明した。

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Research Interests

  • 代謝ネットワーク

  • 腸内細菌

  • バイオインフォマティクス

  • 応用微生物

  • 酵素

Research Areas

  • Life Science / Genome biology

Research History

  • Institute of Science Tokyo   Department of Life Science and Technology   Professor

    2025.12

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    Country:Japan

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  • Tokyo Institute of Technology   School of Life Science and Technology   Associate Professor

    2016.4

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  • Tokyo Institute of Technology   Lecturer

    2013.4 - 2016.3

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  • EMBL   Senior Technical Officer

    2010.4 - 2012.3

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  • EMBL   Structural and Computational Biology Unit   Postdoctoral Fellow

    2007.4 - 2010.3

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  • Kyoto University   Institute for Chemical Research

    2006.4 - 2007.3

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    Country:Japan

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Papers

  • Dynamics of the gut microbiome in FAP patients undergoing intensive endoscopic reduction of polyp burden Reviewed

    Sayaka Mizutani, Ayako Tamaki, Satoshi Shiba, Felix Salim, Masayoshi Yamada, Hiroyuki Takamaru, Takeshi Nakajima, Naohisa Yoshida, Shoko Ikuta, Tatsuo Yachida, Tatsuhiro Shibata, Tomoyoshi Soga, Yutaka Saito, Shinji Fukuda, Hideki Ishikawa, Takuji Yamada, Shinichi Yachida

    Gut   gutjnl - 2024   2024.8

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    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:BMJ  

    DOI: 10.1136/gutjnl-2024-332381

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  • Enteropathway: the metabolic pathway database for the human gut microbiota. Reviewed International journal

    Hirotsugu Shiroma, Youssef Darzi, Etsuko Terajima, Zenichi Nakagawa, Hirotaka Tsuchikura, Naoki Tsukuda, Yuki Moriya, Shujiro Okuda, Susumu Goto, Takuji Yamada

    Briefings in bioinformatics   25 ( 5 )   2024.7

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    Authorship:Last author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    The human gut microbiota produces diverse, extensive metabolites that have the potential to affect host physiology. Despite significant efforts to identify metabolic pathways for producing these microbial metabolites, a comprehensive metabolic pathway database for the human gut microbiota is still lacking. Here, we present Enteropathway, a metabolic pathway database that integrates 3269 compounds, 3677 reactions, and 876 modules that were obtained from 1012 manually curated scientific literature. Notably, 698 modules of these modules are new entries and cannot be found in any other databases. The database is accessible from a web application (https://enteropathway.org) that offers a metabolic diagram for graphical visualization of metabolic pathways, a customization interface, and an enrichment analysis feature for highlighting enriched modules on the metabolic diagram. Overall, Enteropathway is a comprehensive reference database that can complement widely used databases, and a tool for visual and statistical analysis in human gut microbiota studies and was designed to help researchers pinpoint new insights into the complex interplay between microbiota and host metabolism.

    DOI: 10.1093/bib/bbae419

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  • Leveraging explainable AI for gut microbiome-based colorectal cancer classification. Reviewed International journal

    Ryza Rynazal, Kota Fujisawa, Hirotsugu Shiroma, Felix Salim, Sayaka Mizutani, Satoshi Shiba, Shinichi Yachida, Takuji Yamada

    Genome biology   24 ( 1 )   21 - 21   2023.2

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    Authorship:Last author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    Studies have shown a link between colorectal cancer (CRC) and gut microbiome compositions. In these studies, machine learning is used to infer CRC biomarkers using global explanation methods. While these methods allow the identification of bacteria generally correlated with CRC, they fail to recognize species that are only influential for some individuals. In this study, we investigate the potential of Shapley Additive Explanations (SHAP) for a more personalized CRC biomarker identification. Analyses of five independent datasets show that this method can even separate CRC subjects into subgroups with distinct CRC probabilities and bacterial biomarkers.

    DOI: 10.1186/s13059-023-02858-4

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  • Metagenomic Analysis of Gut Microbiota for Abdominal Aortic Aneurysm.

    Eisaku Ito, Takao Ohki, Naoki Toya, Takuo Emoto, Tomoya Yamashita, Tomomi Sugiyama, Takuji Yamada, Hiroshi Mori, Atsushi Toyoda, Ken-Ichi Hirata

    Annals of vascular diseases   18 ( 1 )   2025

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    Language:English   Publishing type:Research paper (scientific journal)  

    Objectives: The pathophysiological mechanism of abdominal aortic aneurysm (AAA) remains unclear. We previously reported that Bifidobacterium adolescentis levels were reduced in the feces of patients with AAA by 16S ribosomal ribonucleic acid (RNA) gene sequencing. In this study, we increased the number of cases and conducted metagenomic analyses to examine bacterial genes associated with the pathophysiology of AAA. Methods: For gut microbiota data, feces from 55 patients with AAA and 52 patients with no history of AAA, lower extremity artery disease, or coronary artery disease (control group) were collected. Metagenomic analysis was performed by collecting raw stool samples from patients. For intestinal microbiota analysis, metagenomic analysis of the fecal samples was performed. Results: Oral bacteria, including Actinomyces oris (p <0.0001), Streptococcus salivarius (p <0.001), Lactobacillus salivarius (p <0.001), and Streptococcus sp. (p <0.001), were increased in the feces of patients with AAA. In addition, bacterial genes related to alpha lipoic acid (ALA) biosynthesis (M00882, M00883, and M00884, p <0.0001) were decreased in patients with AAA. Conclusions: In the feces of patients with AAA, there was an increase in oral bacteria, and the expression of bacterial genes related to ALA biosynthesis was reduced. The results suggest the possibility of developing gut microbial drug treatments for AAA.

    DOI: 10.3400/avd.oa.24-00105

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  • Automated Harmonization and Large-Scale Integration of Heterogeneous Biomedical Sample Metadata Using Large Language Models

    Koichi Higashi, Zenichi Nakagawa, Takuji Yamada, Hiroshi Mori

    2024.10

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    Publisher:Cold Spring Harbor Laboratory  

    The exponential growth of biomedical data has created an urgent need for efficient integration and analysis of heterogeneous sample metadata across studies. However, current methods for harmonizing and standardizing these metadata are largely manual, time-consuming, and prone to inconsistencies. Here, we present a novel computational framework that leverages large language models (LLMs) to automate the harmonization and large-scale integration of diverse biomedical sample metadata. Our approach combines semantic clustering techniques with LLM-driven natural language processing to extract, interpret, and standardize metadata from various sources, including research papers, supplementary tables, and text data from public databases. We demonstrate the efficacy of our framework by applying it to thousands of human gut microbiome papers, successfully extracting and integrating metadata from over 400,000 samples. Our method achieved a 50% recovery rate of manually curated metadata, significantly outperforming traditional rule-based methods. Furthermore, our framework enabled the creation of a unified, searchable database of standardized metadata, facilitating cross-study analyses and revealing previously obscured patterns in microbiome composition across diverse populations and conditions. The scalability and adaptability of our approach suggest its potential applicability to a wide range of biomedical fields, potentially accelerating meta-analyses and fostering new insights from existing data. This work represents a significant advancement in biomedical data integration, offering a powerful tool for researchers to unlock the full potential of accumulated scientific knowledge.

    DOI: 10.1101/2024.10.26.620145

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  • Fusobacterium species are distinctly associated with patients with Lynch Syndrome colorectal cancer Reviewed

    Felix Salim, Sayaka Mizutani, Satoshi Shiba, Hiroyuki Takamaru, Masayoshi Yamada, Takeshi Nakajima, Tatsuo Yachida, Tomoyoshi Soga, Yutaka Saito, Shinji Fukuda, Shinichi Yachida, Takuji Yamada

    iScience   110181 - 110181   2024.6

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    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:Elsevier BV  

    DOI: 10.1016/j.isci.2024.110181

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  • Intestinal Bacteria Fluctuating in Early-Stage Colorectal Cancer Carcinogenesis are Associated with Diet in Healthy Adults. International journal

    Nobuhiro Narii, Ling Zha, Tomotaka Sobue, Tetsuhisa Kitamura, Masayo Komatsu, Yoshimitsu Shimomura, Satoshi Shiba, Sayaka Mizutani, Takuji Yamada, Shinichi Yachida

    Nutrition and cancer   1 - 8   2024.4

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    Language:English   Publishing type:Research paper (scientific journal)  

    This hospital-based, cross-sectional study aimed to explore the association between diet and fluctuating intestinal bacteria in early-stage colorectal cancer (CRC) (Atopobium parvulum, Actinomyces odontolyticus, Solobacterium moorei, and Bifidobacterium longum). Healthy participants (n = 212) who underwent total colonoscopy at National Cancer Center Hospital (Tokyo, Japan) were divided into two groups according to the relative abundance of bacteria in their feces: those in the top 25% of relative bacterial abundance as cases and the bottom 25% as controls. The participants were divided into three groups (low, medium, and high) according to their intake of food groups associated with CRC. Multivariable logistic regression analysis was conducted to estimate the association between dietary intake and higher relative abundance of bacteria. Dairy products were inversely associated with a higher relative abundance of A. parvulum, A. odontolyticus, and S. moorei, with odds ratios (high vs. low) and 95% confidence interval as follows: 0.16 (0.06-0.44), 0.25 (0.08-0.82), and 0.29 (0.11-0.78), respectively. Additionally, dietary fiber was inversely associated with a higher relative abundance of S.moorei (0.29 [0.11-0.78]). No association was observed between diet and B.longum. In conclusion, healthy adults with a higher intake of dairy products and fiber had lower odds of having a higher relative abundance of CRC-associated microbiota.

    DOI: 10.1080/01635581.2024.2344257

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  • High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection

    Minami Nagai, Miyu Moriyama, Chiharu Ishii, Hirotake Mori, Hikaru Watanabe, Taku Nakahara, Takuji Yamada, Dai Ishikawa, Takamasa Ishikawa, Akiyoshi Hirayama, Ikuo Kimura, Akihito Nagahara, Toshio Naito, Shinji Fukuda, Takeshi Ichinohe

    Nature Communications   14 ( 1 )   2023.6

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    Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    Abstract

    Fever is a common symptom of influenza and coronavirus disease 2019 (COVID-19), yet its physiological role in host resistance to viral infection remains less clear. Here, we demonstrate that exposure of mice to the high ambient temperature of 36 °C increases host resistance to viral pathogens including influenza virus and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). High heat-exposed mice increase basal body temperature over 38 °C to enable more bile acids production in a gut microbiota-dependent manner. The gut microbiota-derived deoxycholic acid (DCA) and its plasma membrane-bound receptor Takeda G-protein-coupled receptor 5 (TGR5) signaling increase host resistance to influenza virus infection by suppressing virus replication and neutrophil-dependent tissue damage. Furthermore, the DCA and its nuclear farnesoid X receptor (FXR) agonist protect Syrian hamsters from lethal SARS-CoV-2 infection. Moreover, we demonstrate that certain bile acids are reduced in the plasma of COVID-19 patients who develop moderate I/II disease compared with the minor severity of illness group. These findings implicate a mechanism by which virus-induced high fever increases host resistance to influenza virus and SARS-CoV-2 in a gut microbiota-dependent manner.

    DOI: 10.1038/s41467-023-39569-0

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    Other Link: https://www.nature.com/articles/s41467-023-39569-0

  • The fecal microbiomes analysis of Marabou storks (Leptoptilos crumenifer) reveals their acclimatization to the feeding environment in the Kampala urban areas, Uganda. Reviewed

    Sayaka Tsuchida, Atsushi Ueda, Steven Kakooza, Torahiko Okubo, Eddie M Wampande, Takuji Yamada, Kazunari Ushida

    The Journal of veterinary medical science   85 ( 4 )   450 - 458   2023.3

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    The Marabou stork (Leptoptilos crumenifer) is a typical scavenging bird and adapted to the Savannah environment, where they show a carnivorous feeding style. However, Marabou stork recently penetrated into the city areas and acclimatized to the urban environment, where they modified their feeding habits to an omnivorous type toward more carbohydrate. To reveal their adaptation to the variable feeding customs, this study compared the gut microbiomes and chemical compositions of feces of Marabou storks inhabiting two different locations in peri urban Kampala: one is a slaughter house floc that predicted their original carnivorous feeding, and the other is a landfill floc that adapted more to the omnivorous feeding. 16S rRNA gene sequencing analysis revealed more diverse gut microbiome, more enriched Lactobacilli, and less abundant Peptostreptococci in the landfill flock comparing to the slaughter house flock. Isolation work and predicted metagenome analysis confirmed more diverse Lactobacilli and more enriched functions for carbohydrate metabolism in the landfill flock. In addition, chemical composition of feces revealed higher ammonia in the former, which is consisting with higher Peptostreptococci and their practice of carnivorous feeding. These results highlighted their adaptation to the variable feeding environment, which presumably protects their health and ensure survival of species.

    DOI: 10.1292/jvms.22-0580

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  • 微生物バイオインフォマティクスの最前線 マイクロバイオーム研究を先導するハブを目指したMicrobiome Datahubの開発

    森 宙史, 藤澤 貴智, 東 光一, 中村 保一, 山田 拓司, 松井 求, 内山 郁夫

    日本細菌学雑誌   78 ( 1 )   30 - 30   2023.2

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    Language:Japanese   Publisher:日本細菌学会  

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  • Recent advances of machine learning applications in human gut microbiota study: from observational analysis toward causal inference and clinical intervention. Reviewed International journal

    Felix Salim, Sayaka Mizutani, Moreno Zolfo, Takuji Yamada

    Current opinion in biotechnology   79   102884 - 102884   2023.2

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    Authorship:Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    Statistical methods, especially machine learning, learning(ML), are pivotal for the analyses of large data generated by multiomics human gut microbiota study. These analyses lead to the discovery of microbe-disease associations. Furthermore, recent efforts for more data transparency and accessible analytical tools improved data availability and study reproducibility. Our recent accumulated knowledge on microbe-disease associations brings light to the next questions: what is the role of microbes in disease progression and how can we apply our knowledge of microbiome in clinical settings? Here, we introduce recent studies that implemented ML to answer the questions of causal inference and clinical translation.

    DOI: 10.1016/j.copbio.2022.102884

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  • Association Between Diet and Fusobacterium nucleatum in the Feces of Healthy Adults: A Hospital-based Cross-sectional Study. International journal

    Nobuhiro Narii, Ling Zha, Tomotaka Sobue, Tetsuhisa Kitamura, Satoshi Shiba, Sayaka Mizutani, Takuji Yamada, Shinichi Yachida

    Cancer prevention research (Philadelphia, Pa.)   OF1-OF8   2023.1

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    UNLABELLED: Fusobacterium nucleatum is involved in the development and progression of colorectal cancer. Although the gut microbiota is influenced by diet, studies on the association between diet and F. nucleatum are limited. We aimed to evaluate the association between various dietary factors and fecal F. nucleatum in healthy adults without a history of colorectal cancer or precancerous lesions. This was a cross-sectional study. Subjects who underwent total colonoscopy at the National Cancer Center Hospital (Tokyo, Japan) were included. Healthy subjects (n = 212) were divided into two groups according to the presence or absence of F. nucleatum in their feces which was calculated from data of whole-genome shotgun sequencing, with the group with F. nucleatum serving as cases and the group without F. nucleatum serving as controls. Multivariable logistic regression analysis adjusted potential confounders was conducted to estimate the associations between dietary intake and nutrients estimated by a validated food frequency questionnaire and the presence of F. nucleatum in the feces. There was a significant inverse association between dairy products and the presence of fecal F. nucleatum [high vs. low; OR, 0.41; 95% confidence interval, 0.17-0.95; Ptrend, 0.039]. These results may have important implications for colorectal cancer prevention through nutritional intervention. PREVENTION RELEVANCE: F. nucleatum is well known as a colorectal cancer-associated bacterium. Dietary habits alter the composition and function of the intestinal microbiota. A high intake of dairy products in healthy adults may reduce F. nucleatum and prevent colorectal cancer.

    DOI: 10.1158/1940-6207.CAPR-22-0399

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  • Modeling and analysis of the dynamics of communities of microbial DNA sequences in environments Reviewed International journal

    Hitoshi Koyano, Kazunori Sawada, Nozomi Yamamoto, Takuji Yamada

    Nonlinear Dynamics   111 ( 6 )   5767 - 5797   2023

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    DOI: 10.1007/s11071-022-08105-y

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  • Mediation effect of intestinal microbiota on the relationship between fiber intake and colorectal cancer. Reviewed International journal

    Yoshimitsu Shimomura, Ling Zha, Sho Komukai, Nobuhiro Narii, Tomotaka Sobue, Tetsuhisa Kitamura, Satoshi Shiba, Sayaka Mizutani, Takuji Yamada, Norie Sawada, Shinichi Yachida

    International journal of cancer   152 ( 9 )   1752 - 1762   2022.12

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    Higher fiber intake has been associated with a lower risk of colorectal cancer (CRC) and has been shown to protect against CRC based on probable evidence. Recent studies revealed a possible mechanism whereby the interaction between intestinal microbiota and fiber intake mediates CRC risk. However, the specific intestinal bacteria and the amount of these bacteria involved in this mechanism are not fully known. Therefore, this single-center study aimed to determine whether specific intestinal bacteria mediated the relationship between fiber intake and CRC risk. We enrolled patients who received colonoscopy at National Cancer Center Hospital. This cross-sectional study included 180 patients with clinically diagnosed CRC and 242 controls. We conducted a causal mediation analysis to assess the natural indirect effect and natural direct effect of specific intestinal bacteria on association between fiber intake and CRC risk. The median age was 64 (interquartile range, 54-70) years, and 58% of the participants were males. We used metagenomics for profiling gut microbiomes. The relative abundance of each species in each sample was calculated. Among the candidate, Fusobacterium nucleatum and Gemella morbillorum had a significant natural indirect effect based on their highest fiber intake compared to the lowest fiber intake, with a risk difference (95% confidence interval, proportion of mediation effect) of -0.06 [-0.09 to -0.03, 23%] and -0.03 [-0.06 to -0.01, 10.5%], respectively. Other bacteria did not display natural indirect effects. In conclusion, Fusobacterium nucleatum and Gemella morbillorum were found to mediate the relationship between fiber intake and CRC risk.

    DOI: 10.1002/ijc.34398

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  • Association between Diet and Fusobacterium nucleatum in the Feces of Healthy Adults: A hospital-based cross-sectional study. International journal

    Nobuhiro Narii, Ling Zha, Tomotaka Sobue, Tetsuhisa Kitamura, Satoshi Shiba, Sayaka Mizutani, Takuji Yamada, Shinichi Yachida

    Cancer prevention research (Philadelphia, Pa.)   2022.12

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    Fusobacterium nucleatum is involved in the development and progression of colorectal cancer. Although the gut microbiota is influenced by diet, studies on the association between diet and F. nucleatum are limited. We aimed to evaluate the association between various dietary factors and fecal F. nucleatum in healthy adults without a history of colorectal cancer or precancerous lesions. This was a cross-sectional study. Subjects who underwent total colonoscopy at the National Cancer Center Hospital (Tokyo, Japan) were included. Healthy subjects (n = 212) were divided into two groups according to the presence or absence of F. nucleatum in their feces which was calculated from data of whole-genome shotgun sequencing, with the group with F. nucleatum serving as cases and the group without F. nucleatum serving as controls. Multivariable logistic regression analysis adjusted potential confounders was conducted to estimate the associations between dietary intake and nutrients estimated by a validated food frequency questionnaire and the presence of F. nucleatum in the feces. There was a significant inverse association between dairy products and the presence of fecal F. nucleatum (High vs. Low, OR 0.41, 95% CI 0.17-0.95, P for trend 0.039). These results may have important implications for colorectal cancer prevention through nutritional intervention.

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  • Surgical Treatment for Colorectal Cancer Partially Restores Gut Microbiome and Metabolome Traits Reviewed International journal

    Shiroma, H, Shiba, S, Erawijantari, P.P, Takamaru, H, Yamada, M, Sakamoto, T, Kanemitsu, Y, Mizutani, S, Soga, T, Saito, Y, Shibata, T, Fukuda, S, Yachida, S, Yamada, T

    mSystems   7 ( 2 )   e0001822   2022.4

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    Accumulating evidence indicates that the gut microbiome and metabolites are associated with colorectal cancer (CRC). However, the influence of surgery for CRC treatment on the gut microbiome and metabolites and how it relates to CRC risk in postoperative CRC patients remain partially understood. Here, we collected 170 fecal samples from 85 CRC patients pre- and approximately 1 year postsurgery and performed shotgun metagenomic sequencing and capillary electrophoresis-time of flight mass spectrometry-based metabolomics analyses to characterize alterations between pre- and postsurgery. We determined that the relative abundance of 114 species was altered postsurgery (P < 0.005). CRC-associated species, such as Fusobacterium nucleatum, were decreased postsurgery. On the other hand, Clostridium scindens, carcinogenesis-associated deoxycholate (DCA)-producing species, and its biotransformed genes (bai operon) were increased postsurgery. The concentration of 60 fecal metabolites was also altered postsurgery (P < 0.005). Two bile acids, cholate and DCA, were increased postsurgery. We developed methods to estimate postoperative CRC risk based on the gut microbiome and metabolomic compositions using a random forest machine-learning algorithm that classifies large adenoma or early-stage CRC and healthy controls from publicly available data sets. We applied methods to preoperative samples and then compared the estimated CRC risk between the two groups according to the presence of large adenoma or tumors 5 years postsurgery (P < 0.05). Overall, our results show that the gut microbiome and metabolites dynamically change from pre- to postsurgery. In postoperative CRC patients, potential CRC risk derived from gut microbiome and metabolites still remains, which indicates the importance of follow-up assessments. IMPORTANCE The gut microbiome and metabolites are associated with CRC progression and carcinogenesis. Postoperative CRC patients are reported to be at an increased CRC risk; however, how gut microbiome and metabolites are related to CRC risk in postoperative patients remains only partially understood. In this study, we investigated the influence of surgical CRC treatment on the gut microbiome and metabolites. We found that the CRC-associated species Fusobacterium nucleatum was decreased postsurgery, whereas carcinogenesis-associated DCA and its producing species and genes were increased postsurgery. We developed methods to estimate postoperative CRC risk based on the gut microbiome and metabolomic compositions. We applied methods to compare the estimated CRC risk between two groups according to the presence of large adenoma or tumors after 5 years postsurgery. To our knowledge, this study is the first report on differences between pre- and postsurgery using metagenomics and metabolomics data analysis. Our methods might be used for CRC risk assessment in postoperative patients.

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  • Integrated gut microbiome and metabolome analyses identified fecal biomarkers for bowel movement regulation by Bifidobacterium longum BB536 supplementation: A RCT

    Yuya Nakamura, Shinya Suzuki, Shinnosuke Murakami, Yuichiro Nishimoto, Koichi Higashi, Naoki Watarai, Junpei Umetsu, Chiharu Ishii, Yutaro Ito, Yuka Mori, Mamiko Kohno, Takuji Yamada, Shinji Fukuda

    Computational and Structural Biotechnology Journal   20   5847 - 5858   2022

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  • Bacteroides spp. promotes branched-chain amino acid catabolism in brown fat and inhibits obesity

    Naofumi Yoshida, Tomoya Yamashita, Tatsunori Osone, Tetsuya Hosooka, Masakazu Shinohara, Seiichi Kitahama, Kengo Sasaki, Daisuke Sasaki, Takeshi Yoneshiro, Tomohiro Suzuki, Takuo Emoto, Yoshihiro Saito, Genki Ozawa, Yushi Hirota, Yasuyuki Kitaura, Yoshiharu Shimomura, Yuko Okamatsu-Ogura, Masayuki Saito, Akihiko Kondo, Shingo Kajimura, Takeshi Inagaki, Wataru Ogawa, Takuji Yamada, Ken-ichi Hirata

    iScience   24 ( 11 )   103342 - 103342   2021.11

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  • Analysis of genomic characteristics and their influence on metabolism in Aspergillus luchuensis albino mutants using genome sequencing. International journal

    Nozomi Yamamoto, Naoki Watarai, Hitoshi Koyano, Kazunori Sawada, Atsushi Toyoda, Ken Kurokawa, Takuji Yamada

    Fungal genetics and biology : FG & B   155   103601 - 103601   2021.10

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    Black Aspergillus luchuensis and its white albino mutant are essential fungi for making alcoholic beverages in Japan. A large number of industrial strains have been created using novel isolation or gene/genome mutation techniques. Such mutations influence metabolic and phenotypic characteristics in industrial strains, but few comparative studies of inter-strain mutation have been conducted. We carried out comparative genome analyses of 8 industrial strains of A. luchuensis and A. kawachii IFO 4308, the latter being the first albino strain to be isolated. Phylogenetic analysis based on 8938 concatenated genes exposed the diversity of black koji strains and uniformity among albino industrial strains, suggesting that passaged industrial albino strains have more genetic mutations compared with strain IFO 4308 and black koji strains. Comparative analysis showed that the albino strains had mutations in genes not only for conidial pigmentation but also in those that encode N-terminal acetyltransferase A and annexin XIV-like protein. The results also suggest that some mutations may have emerged through subculturing of albino strains. For example, mutations in the genes for isocitrate lyase and sugar transporters were observed only in industrial albino strains. This implies that selective pressure for increasing enzyme activity or secondary metabolites may have influenced the mutation of genes associated with environmental stress responses in A. luchuensis albino strains. Our study clarifies hitherto unknown genetic and metabolic characteristics of A. luchuensis industrial strains and provides potential applications for comparative genome analysis for breeding koji strains.

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  • Identification of Faecalibacterium prausnitzii strains for gut microbiome-based intervention in Alzheimer's-type dementia. International journal

    Atsushi Ueda, Shoji Shinkai, Hirotsugu Shiroma, Yu Taniguchi, Sayaka Tsuchida, Takahiro Kariya, Tomohiro Kawahara, Yodai Kobayashi, Noriyuki Kohda, Kazunari Ushida, Akihiko Kitamura, Takuji Yamada

    Cell reports. Medicine   2 ( 9 )   100398 - 100398   2021.9

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    Evidence linking the gut-brain axis to Alzheimer's disease (AD) is accumulating, but the characteristics of causally important microbes are poorly understood. We perform a fecal microbiome analysis in healthy subjects and those with mild cognitive impairment (MCI) and AD. We find that Faecalibacterium prausnitzii (F. prausnitzii) correlates with cognitive scores and decreases in the MCI group compared with the healthy group. Two isolated strains from the healthy group, live Fp360 and pasteurized Fp14, improve cognitive impairment in an AD mouse model. Whole-genome comparison of isolated strains reveals specific orthologs that are found only in the effective strains and are more abundant in the healthy group compared with the MCI group. Metabolome and RNA sequencing analyses of mouse brains provides mechanistic insights into the relationship between the efficacy of pasteurized Fp14, oxidative stress, and mitochondrial function. We conclude that F. prausnitzii strains with these specific orthologs are candidates for gut microbiome-based intervention in Alzheimer's-type dementia.

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  • Metagenomic analysis of gut microbiota reveals its role in trimethylamine metabolism in heart failure. International journal

    Takuo Emoto, Tomohiro Hayashi, Tokiko Tabata, Tomoya Yamashita, Hikaru Watanabe, Tomoya Takahashi, Yasuhiro Gotoh, Kenjiro Kami, Naofumi Yoshida, Yoshihiro Saito, Hidekazu Tanaka, Kensuke Matsumoto, Tetsuya Hayashi, Takuji Yamada, Ken-Ichi Hirata

    International journal of cardiology   338   138 - 142   2021.9

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    BACKGROUND: We had previously reported an increase in trimethylamine N-oxide (TMAO) levels in patients with both compensated and decompensated heart failure (HF) and alteration in gut microbiota composition using 16S rRNA gene amplicon analysis. Although a metagenome-wide analysis showed that choline-TMA lyase levels increased in HF patients, which TMA generation pathway from choline, carnitine, or betaine contributes to the increase in TMAO levels in HF needs to be elucidated. METHODS: We conducted a metagenome-wide shotgun sequencing analysis of gut microbiota and measured the TMAO levels in plasma of 22 HF patients during the compensated phase and 11 age-, sex-, and comorbidity-matched control subjects, whose gut microbiota compositions were reported in a previous 16S rRNA-based analysis. RESULTS: The abundance of cntA/B was positively correlated with TMAO, especially in HF patients, whereas that of cutC/D or betaine reductase was not correlated either in controls or HF patients. The abundance of cntA/B was mainly derived from the genera Escherichia and Klebsiella either in controls or HF patients. CONCLUSION: TMAO levels in plasma depend on the abundance of cntA/B in HF. Although it is difficult to exclude the involvement of confounding factors, microbial dysbiosis connecting the abundance of cntA/B in the gut and the increase of TMAO in plasma can be a therapeutic target for HF.

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  • The effects of vegetable pickling conditions on the dynamics of microbiota and metabolites

    Kazunori Sawada, Hitoshi Koyano, Nozomi Yamamoto, Takuji Yamada

    PeerJ   9   2021.4

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    DOI: 10.7717/peerj.11123

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  • Uncovering the Role of Gut Microbiota in Amino Acid Metabolic Disturbances in Heart Failure Through Metagenomic Analysis. International journal

    Tomohiro Hayashi, Tomoya Yamashita, Tomoya Takahashi, Tokiko Tabata, Hikaru Watanabe, Yasuhiro Gotoh, Masakazu Shinohara, Kenjiro Kami, Hidekazu Tanaka, Kensuke Matsumoto, Tetsuya Hayashi, Takuji Yamada, Ken-Ichi Hirata

    Frontiers in cardiovascular medicine   8   789325 - 789325   2021

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    Aims: Circulating amino acid (AA) abnormalities serve as predictors of adverse outcomes in patients with heart failure (HF). However, the role of the gut microbiota in AA disturbances remains unknown. Thus, we investigated gut microbial functions and their associations with AA metabolic alterations in patients with HF. Methods and Results: We performed whole-genome shotgun sequencing of fecal samples and mass spectrometry-based profiling of AAs in patients with compensated HF. Plasma levels of total essential AAs (EAAs) and histidine were significantly lower in patients with HF than in control subjects. HF patients also displayed increased and decreased abundance of gut microbial genes involved in the degradation and biosynthesis, respectively, of EAAs, including branched-chain AAs (BCAAs) and histidine. Importantly, a significant positive correlation was observed between the abundance of microbial genes involved in BCAA biosynthesis and plasma BCAA levels in patients with HF, but not in controls. Moreover, network analysis revealed that the depletion of Eubacterium and Prevotella, which harbor genes for BCAA and histidine biosynthesis, contributed to decreased abundance of microbial genes involved in the biosynthesis of those EAAs in patients with HF. Conclusions: The present study demonstrated the relationship between gut microbiota and AA metabolic disturbances in patients with HF.

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  • The Nutritional Efficacy of Chlorella Supplementation Depends on the Individual Gut Environment: A Randomised Control Study. International journal

    Yuichiro Nishimoto, Tatsuhiro Nomaguchi, Yuka Mori, Masaki Ito, Yuya Nakamura, Masaki Fujishima, Shinnosuke Murakami, Takuji Yamada, Shinji Fukuda

    Frontiers in nutrition   8   648073 - 648073   2021

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    Recent studies have accumulated evidence that the intestinal environment is strongly correlated with host diet, which influences host health. A number of dietary products whose mechanisms of influence operate via the gut microbiota have been revealed, but they are still limited. Here, we investigated the dietary influence of Chlorella, a green alga commercially available as a dietary supplement. A randomised, double-blind, placebo-controlled crossover trial including 40 Japanese participants with constipation was performed. In this study, the primary outcome and secondary outcome were set as defecation frequency and blood folate level, respectively. In both outcomes, no significant differences were detected compared to the control intake. Therefore, we analysed the gut microbiome, gut metabolome, and blood parameters in an integrated manner as an exploratory analysis. We revealed that the consumption of Chlorella increased the level of several dicarboxylic acids in faeces. Furthermore, the analysis showed that individuals with low concentrations of faecal propionate showed an increase in propionate concentration upon Chlorella intake. In addition, increasing blood folate levels were negatively correlated with defecation frequency at baseline. Our study suggested that the effect of Chlorella consumption varies among individuals depending on their intestinal environment, which illustrates the importance of stratified dietary management based on the intestinal environment in individuals.

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  • A possible beneficial effect of Bacteroides on faecal lipopolysaccharide activity and cardiovascular diseases Reviewed

    Naofumi Yoshida, Tomoya Yamashita, Shigenobu Kishino, Hikaru Watanabe, Kengo Sasaki, Daisuke Sasaki, Tokiko Tabata, Yuta Sugiyama, Nahoko Kitamura, Yoshihiro Saito, Takuo Emoto, Tomohiro Hayashi, Tomoya Takahashi, Masakazu Shinohara, Ro Osawa, Akihiko Kondo, Takuji Yamada, Jun Ogawa, Ken-ichi Hirata

    Scientific Reports   10 ( 1 )   2020.12

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  • マイクロバイオームとがん発症・進展、がん免疫研究の最前線 メタゲノムおよびメタボローム解析を用いた大腸がんの多段階発がんに伴う腸内環境の変化

    山田 拓司, 水谷 紗弥佳, 谷内田 真一, 城間 博紹, 柴 知史

    日本癌学会総会記事   79回   S6 - 1   2020.10

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  • Metabolomic LC-MS/MS analyses and meta 16S rRNA gene analyses on cecal feces of Japanese rock ptarmigans reveal fundamental differences between semi-wild and captive raised individuals.

    Atsushi Kobayashi, Sayaka Tsuchida, Takanari Hattori, Koretsugu Ogata, Atsushi Ueda, Takuji Yamada, Koichi Murata, Hiroshi Nakamura, Kazunari Ushida

    The Journal of veterinary medical science   82 ( 8 )   1165 - 1172   2020.8

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    Ex situ conservation of Japanese rock ptarmigans began in 2015 with the aim of reintroducing artificially raised birds into their original habitat. However, the current raising method in captivity seems insufficient in terms of the survivability of artificially raised birds in natural conditions. Feeding management is one potential reason for such insufficiency. In this study, we performed a comprehensive analysis of the hydrophilic metabolites by LC-MS/MS for the cecal feces of Japanese rock ptarmigans under in situ and ex situ conservation to reveal their gut chemical environment. We also analyzed the developmental processes of cecal microbiomes both in situ semi-wild and ex situ captive individuals. Metabolites of nucleic acid were rich in the in situ individuals, and free amino acids were rich in the ex situ individuals. The differences in the microbiome composition between in situ and ex situ individuals were also pronounced; major genera of in situ individuals were not detected or few in ex situ individuals. The alpha diversity of the cecal microbiome of semi-wild chicks at 1 week of age was almost the same as that of their hens, while it was very low in captive individuals. Sub-therapeutic use of oxytetracycline, a diet rich in protein and energy, and isolation from adult birds are considered to be causes for these great differences in gut chemical and microbiological environment between in situ and ex situ individuals.

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  • Influence of gastrectomy for gastric cancer treatment on faecal microbiome and metabolome profiles. Reviewed International journal

    Pande Putu Erawijantari, Sayaka Mizutani, Hirotsugu Shiroma, Satoshi Shiba, Takeshi Nakajima, Taku Sakamoto, Yutaka Saito, Shinji Fukuda, Shinichi Yachida, Takuji Yamada

    Gut   69 ( 8 )   1404 - 1415   2020.8

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    OBJECTIVE: Recent evidence points to the gut microbiome's involvement in postoperative outcomes, including after gastrectomy. Here, we investigated the influence of gastrectomy for gastric cancer on the gut microbiome and metabolome, and how it related to postgastrectomy conditions. DESIGN: We performed shotgun metagenomics sequencing and capillary electrophoresis time-of-flight mass spectrometry-based metabolomics analyses on faecal samples collected from participants with a history of gastrectomy for gastric cancer (n=50) and compared them with control participants (n=56). RESULTS: The gut microbiota in the gastrectomy group showed higher species diversity and richness (p<0.05), together with greater abundance of aerobes, facultative anaerobes and oral microbes. Moreover, bile acids such as genotoxic deoxycholic acid and branched-chain amino acids were differentially abundant between the two groups (linear discriminant analysis (LDA) effect size (LEfSe): p<0.05, q<0.1, LDA>2.0), as were also Kyoto Encyclopedia of Genes and Genomes modules involved in nutrient transport and organic compounds biosynthesis (LEfSe: p<0.05, q<0.1, LDA>2.0). CONCLUSION: Our results reveal alterations of gut microbiota after gastrectomy, suggesting its association with postoperative comorbidities. The multi-omic approach applied in this study could complement the follow-up of patients after gastrectomy.

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  • Significance of the gut microbiome in multistep colorectal carcinogenesis. International journal

    Sayaka Mizutani, Takuji Yamada, Shinichi Yachida

    Cancer science   111 ( 3 )   766 - 773   2020.3

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    Colorectal cancer (CRC) is highly prevalent worldwide. In 2018, there were over 1.8 million new cases. Most sporadic CRC develop from polypoid adenomas and are preceded by intramucosal carcinoma (stage 0), which can progress into more malignant forms. This developmental process is known as the adenoma-carcinoma sequence. Early detection and endoscopic removal are crucial for CRC management. Accumulating evidence suggests that the gut microbiota is associated with CRC development in humans. Comprehensive characterization of this microbiota is of great importance to assess its potential as a diagnostic marker in the very early stages of CRC. In this review, we summarized recent studies on CRC-associated bacteria and their carcinogenic mechanisms in animal models, human cell lines and human cohorts. High-throughput technologies have facilitated the identification of CRC-associated bacteria in human samples. We have presented our metagenome and metabolome studies on fecal samples collected from a large Japanese cohort that revealed stage-specific phenotypes of the microbiota in CRC. Furthermore, we have discussed the potential carcinogenic mechanisms of the gut microbiota, from which we can infer whether changes in the gut microbiota are a cause or effect in the multi-step process of CRC carcinogenesis.

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  • Essential role of the Crk family-dosage in DiGeorge-like anomaly and metabolic homeostasis. Reviewed International journal

    Akira Imamoto, Sewon Ki, Leiming Li, Kazunari Iwamoto, Venkat Maruthamuthu, John Devany, Ocean Lu, Tomomi Kanazawa, Suxiang Zhang, Takuji Yamada, Akiyoshi Hirayama, Shinji Fukuda, Yutaka Suzuki, Mariko Okada

    Life science alliance   3 ( 2 )   2020.2

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    CRK and CRKL (CRK-like) encode adapter proteins with similar biochemical properties. Here, we show that a 50% reduction of the family-combined dosage generates developmental defects, including aspects of DiGeorge/del22q11 syndrome in mice. Like the mouse homologs of two 22q11.21 genes CRKL and TBX1, Crk and Tbx1 also genetically interact, thus suggesting that pathways shared by the three genes participate in organogenesis affected in the syndrome. We also show that Crk and Crkl are required during mesoderm development, and Crk/Crkl deficiency results in small cell size and abnormal mesenchyme behavior in primary embryonic fibroblasts. Our systems-wide analyses reveal impaired glycolysis, associated with low Hif1a protein levels as well as reduced histone H3K27 acetylation in several key glycolysis genes. Furthermore, Crk/Crkl deficiency sensitizes MEFs to 2-deoxy-D-glucose, a competitive inhibitor of glycolysis, to induce cell blebbing. Activated Rapgef1, a Crk/Crkl-downstream effector, rescues several aspects of the cell phenotype, including proliferation, cell size, focal adhesions, and phosphorylation of p70 S6k1 and ribosomal protein S6. Our investigations demonstrate that Crk/Crkl-shared pathways orchestrate metabolic homeostasis and cell behavior through widespread epigenetic controls.

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  • Probabilistic model based on circular statistics for quantifying coverage depth dynamics originating from DNA replication

    Shinya Suzuki, Takuji Yamada

    PeerJ   2020 ( 3 )   2020

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    DOI: 10.7717/peerj.8722

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  • Evolution of aspergillus oryzae before and after domestication inferred by large-scale comparative genomic analysis

    Naoki Watarai, Nozomi Yamamoto, Kazunori Sawada, Takuji Yamada

    DNA Research   26 ( 6 )   465 - 472   2019.12

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    DOI: 10.1093/dnares/dsz024

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  • Comparison of oral microbiome profiles in stimulated and unstimulated saliva, tongue, and mouth-rinsed water

    Ryutaro Jo, Yuichiro Nishimoto, Kouta Umezawa, Kazuma Yama, Yuto Aita, Yuko Ichiba, Shinnosuke Murakami, Yasushi Kakizawa, Takashi Kumagai, Takuji Yamada, Shinji Fukuda

    Scientific Reports   9 ( 1 )   2019.12

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    DOI: 10.1038/s41598-019-52445-6

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  • Role of coprophagy in the cecal microbiome development of an herbivorous bird Japanese rock ptarmigan.

    Atsushi Kobayashi, Sayaka Tsuchida, Atsushi Ueda, Takuji Yamada, Koichi Murata, Hiroshi Nakamura, Kazunari Ushida

    The Journal of veterinary medical science   81 ( 9 )   1389 - 1399   2019.10

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    The transgenerational maintenance of symbiotic microbes that benefit host nutrition and health is evolutionarily advantageous. In some vertebrate lineages, coprophagy is used as a strategy for effectively transmitting microbes across generations. However, this strategy has still not been studied in birds. Accordingly, the aim of the present study was to evaluate the role of maternal cecal feces consumption by Japanese rock ptarmigan (Lagopus muta japonica) chicks as a strategy for acquiring essential gut microbes. Both the duration of coprophagy behavior by the chicks and the development process of the chick cecal microbiome (n=20 one- to three-week-old chicks, from three broods) were investigated. In all three broods, coprophagy behavior was only observed from 3 to 18 days of age. Furthermore, there was no significant difference in the number of bacterial operational taxonomic units (OTUs) in 1-week-old chicks (n=651) and adults (n=609), and most of the main OTUs observed in the adults were already present in the 1-week-old chicks. These results indicate that, in this precocial bird species, coprophagy may contribute to the early establishment of cecal bacteria that are essential for food digestion and, thus, chick survival. In fact, Japanese rock ptarmigan chicks consume the same food as their hens from the time of hatching. This behavior may have applications to ex-situ conservation.

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  • Author Correction: Metagenomic analysis of colorectal cancer datasets identifies cross-cohort microbial diagnostic signatures and a link with choline degradation. Reviewed International journal

    Thomas AM, Manghi P, Asnicar F, Pasolli E, Armanini F, Zolfo M, Beghini F, Manara S, Karcher N, Pozzi C, Gandini S, Serrano D, Tarallo S, Francavilla A, Gallo G, Trompetto M, Ferrero G, Mizutani S, Shiroma H, Shiba S, Shibata T, Yachida S, Yamada T, Wirbel J, Schrotz-King P, Ulrich CM, Brenner H, Arumugam M, Bork P, Zeller G, Cordero F, Dias-Neto E, Setubal JC, Tett A, Pardini B, Rescigno M, Waldron L, Naccarati A, Segata N

    Nature medicine   25 ( 12 )   1948 - 1948   2019.10

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    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

    DOI: 10.1038/s41591-019-0663-4

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  • Role of coprophagy in the cecal microbiome development of an herbivorous bird Japanese rock ptarmigan

    Atsushi Kobayashi, Sayaka Tsuchida, Atsushi Ueda, Takuji Yamada, Koichi Murata, Hiroshi Nakamura, Kazunari Ushida

    JOURNAL OF VETERINARY MEDICAL SCIENCE   81 ( 9 )   1389 - 1399   2019.9

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  • 糞便メタゲノムおよびメタボローム解析を用いた大腸がんの多段階発がんに伴う腸内環境の変化

    水谷 紗弥佳, 谷内田 真一, 城間 博紹, 柴 知史, 山田 拓司

    日本生化学会大会プログラム・講演要旨集   92回   [1T09a - 05]   2019.9

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  • Bacteroides vulgatusとBacteroides doreiは腸内細菌のLPS産生を減少させ動脈硬化を抑制する Reviewed

    吉田 尚史, 山下 智也, 江本 拓央, 渡邊 日佳流, 林 友鴻, 田畑 論子, 山田 拓司, 平田 健一

    日本動脈硬化学会総会プログラム・抄録集   51回   YIA - 1   2019.7

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  • Metagenomic and metabolomic analyses reveal distinct stage-specific phenotypes of the gut microbiota in colorectal cancer. Reviewed

    Yachida S, Mizutani S, Shiroma H, Shiba S, Nakajima T, Sakamoto T, Watanabe H, Masuda K, Nishimoto Y, Kubo M, Hosoda F, Rokutan H, Matsumoto M, Takamaru H, Yamada M, Matsuda T, Iwasaki M, Yamaji T, Yachida T, Soga T, Kurokawa K, Toyoda A, Ogura Y, Hayashi T, Hatakeyama M, Nakagama H, Saito Y, Fukuda S, Shibata T, Yamada T

    Nature medicine   25 ( 6 )   968 - 976   2019.6

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  • Meta-analysis of fecal metagenomes reveals global microbial signatures that are specific for colorectal cancer. Reviewed International journal

    Wirbel J, Pyl PT, Kartal E, Zych K, Kashani A, Milanese A, Fleck JS, Voigt AY, Palleja A, Ponnudurai R, Sunagawa S, Coelho LP, Schrotz-King P, Vogtmann E, Habermann N, Niméus E, Thomas AM, Manghi P, Gandini S, Serrano D, Mizutani S, Shiroma H, Shiba S, Shibata T, Yachida S, Yamada T, Waldron L, Naccarati A, Segata N, Sinha R, Ulrich CM, Brenner H, Arumugam M, Bork P, Zeller G

    Nature medicine   25 ( 4 )   679 - 689   2019.4

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    Association studies have linked microbiome alterations with many human diseases. However, they have not always reported consistent results, thereby necessitating cross-study comparisons. Here, a meta-analysis of eight geographically and technically diverse fecal shotgun metagenomic studies of colorectal cancer (CRC, n = 768), which was controlled for several confounders, identified a core set of 29 species significantly enriched in CRC metagenomes (false discovery rate (FDR) < 1 × 10-5). CRC signatures derived from single studies maintained their accuracy in other studies. By training on multiple studies, we improved detection accuracy and disease specificity for CRC. Functional analysis of CRC metagenomes revealed enriched protein and mucin catabolism genes and depleted carbohydrate degradation genes. Moreover, we inferred elevated production of secondary bile acids from CRC metagenomes, suggesting a metabolic link between cancer-associated gut microbes and a fat- and meat-rich diet. Through extensive validations, this meta-analysis firmly establishes globally generalizable, predictive taxonomic and functional microbiome CRC signatures as a basis for future diagnostics.

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  • Metagenomic analysis of colorectal cancer datasets identifies cross-cohort microbial diagnostic signatures and a link with choline degradation. Reviewed International journal

    Thomas AM, Manghi P, Asnicar F, Pasolli E, Armanini F, Zolfo M, Beghini F, Manara S, Karcher N, Pozzi C, Gandini S, Serrano D, Tarallo S, Francavilla A, Gallo G, Trompetto M, Ferrero G, Mizutani S, Shiroma H, Shiba S, Shibata T, Yachida S, Yamada T, Wirbel J, Schrotz-King P, Ulrich CM, Brenner H, Arumugam M, Bork P, Zeller G, Cordero F, Dias-Neto E, Setubal JC, Tett A, Pardini B, Rescigno M, Waldron L, Naccarati A, Segata N

    Nature medicine   25 ( 4 )   667 - 678   2019.4

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    Several studies have investigated links between the gut microbiome and colorectal cancer (CRC), but questions remain about the replicability of biomarkers across cohorts and populations. We performed a meta-analysis of five publicly available datasets and two new cohorts and validated the findings on two additional cohorts, considering in total 969 fecal metagenomes. Unlike microbiome shifts associated with gastrointestinal syndromes, the gut microbiome in CRC showed reproducibly higher richness than controls (P < 0.01), partially due to expansions of species typically derived from the oral cavity. Meta-analysis of the microbiome functional potential identified gluconeogenesis and the putrefaction and fermentation pathways as being associated with CRC, whereas the stachyose and starch degradation pathways were associated with controls. Predictive microbiome signatures for CRC trained on multiple datasets showed consistently high accuracy in datasets not considered for model training and independent validation cohorts (average area under the curve, 0.84). Pooled analysis of raw metagenomes showed that the choline trimethylamine-lyase gene was overabundant in CRC (P = 0.001), identifying a relationship between microbiome choline metabolism and CRC. The combined analysis of heterogeneous CRC cohorts thus identified reproducible microbiome biomarkers and accurate disease-predictive models that can form the basis for clinical prognostic tests and hypothesis-driven mechanistic studies.

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  • FuncTree2: an interactive radial tree for functional hierarchies and omics data visualization. Reviewed

    Darzi Y, Yamate Y, Yamada T

    Bioinformatics (Oxford, England)   2019.4

  • Gut Microbiome and Plasma Microbiome-Related Metabolites in Patients With Decompensated and Compensated Heart Failure. Reviewed

    Tomohiro Hayashi, Tomoya Yamashita, Hikaru Watanabe, Kenjiro Kami, Naofumi Yoshida, Tokiko Tabata, Takuo Emoto, Naoto Sasaki, Taiji Mizoguchi, Yasuhiro Irino, Ryuji Toh, Masakazu Shinohara, Yuko Okada, Wataru Ogawa, Takuji Yamada, Ken-Ichi Hirata

    Circulation journal : official journal of the Japanese Circulation Society   83 ( 1 )   182 - 192   2018.12

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    BACKGROUND: Gut microbiome composition or circulating microbiome-related metabolites in patients with heart failure (HF) have not been investigated at different time points (i.e., in the decompensated (Decomp) and compensated (Comp) phases). Methods and Results: We prospectively enrolled 22 patients admitted for HF and 11 age-, sex-, and comorbidity-matched hospitalized control subjects without a history of HF. Gut flora and plasma microbiome-related metabolites were evaluated by amplicon sequencing of the bacterial 16S ribosomal RNA gene and capillary electrophoresis time-of-flight mass spectrometry, respectively. HF patients were evaluated in both the Decomp and Comp phases during hospitalization. The phylum Actinobacteria was enriched in HF patients compared with control subjects. At the genus level, Bifiodobacterium was abundant while Megamonas was depleted in HF patients. Meanwhile, plasma concentration of trimethylamine N-oxide (TMAO), a gut microbiome-derived metabolite, was increased in HF patients (Decomp HF vs. control, P=0.003; Comp HF vs. control, P=0.004). A correlation analysis revealed positive correlations between the abundance of the genus Escherichia/Shigella and levels of TMAO and indoxyl sulfate (IS, a microbe-dependent uremic toxin) in Comp HF (TMAO: r=0.62, P=0.002; IS: r=0.63, P=0.002). Escherichia/Shigella was more abundant in Decomp than in Comp HF (P=0.030). CONCLUSIONS: Our results suggest that gut microbiome composition and microbiome-related metabolites are altered in HF patients.

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  • Bacteroides vulgatus and Bacteroides dorei Reduce Gut Microbial Lipopolysaccharide Production and Inhibit Atherosclerosis. Reviewed International journal

    Naofumi Yoshida, Takuo Emoto, Tomoya Yamashita, Hikaru Watanabe, Tomohiro Hayashi, Tokiko Tabata, Namiko Hoshi, Naoya Hatano, Genki Ozawa, Naoto Sasaki, Taiji Mizoguchi, Hilman Zulkifli Amin, Yushi Hirota, Wataru Ogawa, Takuji Yamada, Ken-Ichi Hirata

    Circulation   138 ( 22 )   2486 - 2498   2018.11

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    BACKGROUND: It is increasingly recognized that gut microbiota play a pivotal role in the development of atherosclerotic cardiovascular disease. Previously, we have reported that the abundance of genus Bacteroides is lower in patients with coronary artery disease (CAD) than in patients without CAD with coronary risk factors or in healthy volunteers. However, it remains unclear which and how specific gut bacteria contribute to the progression of atherosclerosis. METHODS: We recruited patients with CAD patients and controls without CAD with coronary risk factors. We then compared gut microbial composition using 16S ribosomal RNA gene sequencing in fecal samples to detect species with differential abundance between 2 groups. Subsequently, we used atherosclerosis-prone mice to study the mechanisms underlying the relationship between such species and atherosclerosis. RESULTS: Human fecal 16S ribosomal RNA gene sequencing revealed a significantly lower abundance of Bacteroides vulgatus and Bacteroides dorei in patients with CAD. This significant differential abundance was confirmed by quantitative polymerase chain reaction. Gavage with live B. vulgatus and B. dorei attenuated atherosclerotic lesion formation in atherosclerosis-prone mice, markedly ameliorating endotoxemia followed by decreasing gut microbial lipopolysaccharide production, effectively suppressing proinflammatory immune responses. Furthermore, fecal lipopolysaccharide levels in patients with CAD were significantly higher and negatively correlated with the abundance of B. vulgatus and B. dorei. CONCLUSIONS: Our translational research findings identify a previously unknown link between specific gut bacteria and atherosclerosis. Treatment with live B. vulgatus and B. dorei may help prevent CAD. CLINICAL TRIAL REGISTRATION: URL: https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018051 . Unique identifier: UMIN000015703.

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  • Cecal Microbiome Analyses on Wild Japanese Rock Ptarmigans (Lagopus muta japonica) Reveals High Level of Coexistence of Lactic Acid Bacteria and Lactate-Utilizing Bacteria Reviewed

    Atsushi Ueda, Atsushi Kobayashi, Sayaka Tsuchida, Takuji Yamada, Koichi Murata, Hiroshi Nakamura, Kazunari Ushida

    Microorganisms   6 ( 3 )   77 - 77   2018.7

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    Preservation of indigenous gastrointestinal microbiota is critical for successful captive breeding of endangered wild animals, yet its biology is poorly understood. Here, we compared the cecal microbial composition of wild living Japanese rock ptarmigans (Lagopus muta japonica) in different locations of Japanese mountains, and the dominant cecal microbial structure of wild Japanese rock ptarmigans is elucidated. Coriobacteraceae and Lachnospraceae were the two dominant bacterial families in all samples analyzed. At the genus level, 10 genera Olsenella, Actinomyces, Megasphaera, Slackia, Cloacibacillus, Bifidobacterium,Escherichia,Dialister, Megamonas, and Bilophila were dominant. These results reveal the high level of coexistence of lactic acid bacteria (Olsenella and Bifidobacterium) and lactate-utilizing bacteria (Megasphaera). This coexistence should be taken into account for the successful breeding of captive Japanese rock ptarmigans in the national conservation program.

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  • iPath3.0: interactive pathways explorer v3. Reviewed

    Darzi Y, Letunic I, Bork P, Yamada T

    Nucleic acids research   46 ( W1 )   W510 - W513   2018.7

  • Bacteroidesは糞便LPS値を低下させる事で動脈硬化を抑制する Reviewed

    吉田 尚史, 山下 智也, 江本 拓央, 渡邊 日佳流, 林 友鴻, 田畑 論子, 小澤 元希, 佐々木 直人, 山田 拓司, 平田 健一

    日本動脈硬化学会総会プログラム・抄録集   50回   287 - 287   2018.6

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  • Bacteroidesは腸内細菌のLPS産生を制御し動脈硬化を抑制する Reviewed

    吉田 尚史, 山下 智也, 江本 拓央, 渡邊 日佳流, 林 友鴻, 田畑 論子, 小澤 元希, 山田 拓司, 平田 健一

    腸内細菌学雑誌   32 ( 2 )   96 - 96   2018.4

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  • VITCOMIC2: visualization tool for the phylogenetic composition of microbial communities based on 16S rRNA gene amplicons and metagenomic shotgun sequencing. Reviewed International journal

    Hiroshi Mori, Takayuki Maruyama, Masahiro Yano, Takuji Yamada, Ken Kurokawa

    BMC systems biology   12 ( Suppl 2 )   30 - 30   2018.3

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    BACKGROUND: The 16S rRNA gene-based amplicon sequencing analysis is widely used to determine the taxonomic composition of microbial communities. Once the taxonomic composition of each community is obtained, evolutionary relationships among taxa are inferred by a phylogenetic tree. Thus, the combined representation of taxonomic composition and phylogenetic relationships among taxa is a powerful method for understanding microbial community structure; however, applying phylogenetic tree-based representation with information on the abundance of thousands or more taxa in each community is a difficult task. For this purpose, we previously developed the tool VITCOMIC (VIsualization tool for Taxonomic COmpositions of MIcrobial Community), which is based on the genome-sequenced microbes' phylogenetic information. Here, we introduce VITCOMIC2, which incorporates substantive improvements over VITCOMIC that were necessary to address several issues associated with 16S rRNA gene-based analysis of microbial communities. RESULTS: We developed VITCOMIC2 to provide (i) sequence identity searches against broad reference taxa including uncultured taxa; (ii) normalization of 16S rRNA gene copy number differences among taxa; (iii) rapid sequence identity searches by applying the graphics processing unit-based sequence identity search tool CLAST; (iv) accurate taxonomic composition inference and nearly full-length 16S rRNA gene sequence reconstructions for metagenomic shotgun sequencing; and (v) an interactive user interface for simultaneous representation of the taxonomic composition of microbial communities and phylogenetic relationships among taxa. We validated the accuracy of processes (ii) and (iv) by using metagenomic shotgun sequencing data from a mock microbial community. CONCLUSIONS: The improvements incorporated into VITCOMIC2 enable users to acquire an intuitive understanding of microbial community composition based on the 16S rRNA gene sequence data obtained from both metagenomic shotgun and amplicon sequencing.

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  • Minor taxa in human skin microbiome contribute to the personal identification. Reviewed International journal

    Hikaru Watanabe, Issei Nakamura, Sayaka Mizutani, Yumiko Kurokawa, Hiroshi Mori, Ken Kurokawa, Takuji Yamada

    PloS one   13 ( 7 )   e0199947   2018

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    The human skin microbiome can vary over time, and inter-individual variability of the microbiome is greater than the temporal variability within an individual. The skin microbiome has become a useful tool to identify individuals, and one type of personal identification using the skin microbiome has been reported in a community of less than 20 individuals. However, identification of individuals based on the skin microbiome has shown low accuracy in communities larger than 80 individuals. Here, we developed a new approach for personal identification, which considers that minor taxa are one of the important factors for distinguishing between individuals. We originally established a human skin microbiome for 66 samples from 11 individuals over two years (33 samples each year). Our method could classify individuals with 85% accuracy beyond a one-year sampling period. Moreover, we applied our method to 837 publicly available skin microbiome samples from 89 individuals and succeeded in identifying individuals with 78% accuracy. In short, our results investigate that (i) our new personal identification method worked well with two different communities (our data: 11 individuals; public data: 89 individuals) using the skin microbiome, (ii) defining the personal skin microbiome requires samples from several time points, (iii) inclusion of minor skin taxa strongly contributes to the effectiveness of personal identification.

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  • Comprehensive microbiome analysis of tonsillar crypts in IgA nephropathy. Reviewed International journal

    Hirofumi Watanabe, Shin Goto, Hiroshi Mori, Koichi Higashi, Kazuyoshi Hosomichi, Naotaka Aizawa, Nao Takahashi, Masafumi Tsuchida, Yusuke Suzuki, Takuji Yamada, Arata Horii, Ituro Inoue, Ken Kurokawa, Ichiei Narita

    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association   32 ( 12 )   2072 - 2079   2017.12

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    Background: Immunoglobulin A nephropathy (IgAN) is the most prevalent primary chronic glomerular disease, in which the mucosal immune response elicited particularly in the tonsils or intestine has been estimated to be involved in the development of the disease. To explore the relationship between IgAN and bacterial flora in the tonsils, we conducted a comprehensive microbiome analysis. Methods: We enrolled 48 IgAN patients, 21 recurrent tonsillitis (RT) patients without urine abnormalities and 30 children with tonsillar hyperplasia (TH) who had undergone tonsillectomy previously. Genomic DNA from tonsillar crypts of each patient was extracted, and V4 regions of the 16S ribosomal RNA gene were amplified and analysed using a high-throughput multiplexed sequencing approach. Differences in genus composition among the three study groups were statistically analysed by permutational multivariate analysis of variance and visualized by principal component analysis (PCA). Results: Substantial diversity in bacterial composition was detected in each sample. Prevotella spp., Fusobacterium spp., Sphingomonas spp. and Treponema spp. were predominant in IgAN patients. The percentage of abundance of Prevotella spp., Haemophilus spp., Porphyromonas spp. and Treponema spp. in IgAN patients was significantly different from that in TH patients. However, there was no significant difference in the percentage of abundance of any bacterial genus between IgAN and RT patients. PCA did not distinguish IgAN from RT, although it discriminated TH. No significant differences in microbiome composition among the groups of IgAN patients according to clinicopathological parameters were observed. Conclusions: Similar patterns of bacteria are present in tonsillar crypts of both IgAN and RT patients, suggesting that the host response to these bacteria might be important in the development of IgAN.

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  • メタゲノム解析を用いた大腸がん疾病マーカー遺伝子の探索

    城間 博紹, 水谷 紗弥佳, 谷内田 真一, 山田 拓司

    生命科学系学会合同年次大会   2017年度   [2PT26 - 1145)]   2017.12

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  • The true distribution volume and bioavailability of mizoribine in children with chronic kidney disease Reviewed

    Takuhito Nagai, Osamu Uemura, Hisashi Kaneda, Katsumi Ushijima, Kazuhide Ohta, Yoshimitsu Gotoh, Kenichi Satomura, Masaki Shimizu, Mikiya Fujieda, Masashi Morooka, Takuji Yamada, Masayoshi Yamada, Naohiro Wada, Yukiya Hashimoto

    CLINICAL AND EXPERIMENTAL NEPHROLOGY   21 ( 5 )   884 - 888   2017.10

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  • High stability of faecal microbiome composition in guanidine thiocyanate solution at room temperature and robustness during colonoscopy Reviewed

    Yuichiro Nishimoto, Sayaka Mizutani, Takeshi Nakajima, Fumie Hosoda, Hikaru Watanabe, Yutaka Saito, Tatsuhiro Shibata, Shinichi Yachida, Takuji Yamada

    GUT   65 ( 9 )   1574 - +   2016.9

  • High-affinity monoclonal IgA regulates gut microbiota and prevents colitis in mice Reviewed

    Shinsaku Okai, Fumihito Usui, Shuhei Yokota, Yusaku Hori-i, Makoto Hasegawa, Toshinobu Nakamura, Manabu Kurosawa, Seiji Okada, Kazuya Yamamoto, Eri Nishiyama, Hiroshi Mori, Takuji Yamada, Ken Kurokawa, Satoshi Matsumoto, Masanobu Nanno, Tomoaki Naito, Yohei Watanabe, Tamotsu Kato, Eiji Miyauchi, Hiroshi Ohno, Reiko Shinkura

    NATURE MICROBIOLOGY   1 ( 9 )   16103   2016.9

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  • A key genetic factor for fucosyllactose utilization affects infant gut microbiota development Reviewed

    Takahiro Matsuki, Kana Yahagi, Hiroshi Mori, Hoshitaka Matsumoto, Taeko Hara, Saya Tajima, Eishin Ogawa, Hiroko Kodama, Kazuya Yamamoto, Takuji Yamada, Satoshi Matsumoto, Ken Kurokawa

    NATURE COMMUNICATIONS   7   11939   2016.6

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  • Identification of Enzyme Genes Using Chemical Structure Alignments of Substrate-Product Pairs Reviewed

    Yuki Moriya, Takuji Yamada, Shujiro Okuda, Zenichi Nakagawa, Masaaki Kotera, Toshiaki Tokimatsu, Minoru Kanehisa, Susumu Goto

    JOURNAL OF CHEMICAL INFORMATION AND MODELING   56 ( 3 )   510 - 516   2016.3

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  • The transcription factor ATF7 mediates lipopolysaccharide-induced epigenetic changes in macrophages involved in innate immunological memory Reviewed

    Keisuke Yoshida, Toshio Maekawa, Yujuan Zhu, Claire Renard-Guillet, Bruno Chatton, Kentaro Inoue, Takeru Uchiyama, Ken-ichi Ishibashi, Takuji Yamada, Naohito Ohno, Katsuhiko Shirahige, Mariko Okada-Hatakeyama, Shunsuke Ishii

    NATURE IMMUNOLOGY   16 ( 10 )   1034 - +   2015.10

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  • Inter-Individual Differences in the Oral Bacteriome Are Greater than Intra-Day Fluctuations in Individuals Reviewed

    Yukuto Sato, Junya Yamagishi, Riu Yamashita, Natsuko Shinozaki, Bin Ye, Takuji Yamada, Masayuki Yamamoto, Masao Nagasaki, Akito Tsuboi

    PLOS ONE   10 ( 6 )   e0131607   2015.6

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  • FuncTree: Functional Analysis and Visualization for Large-Scale Omics Data Reviewed

    Takeru Uchiyama, Mitsuru Irie, Hiroshi Mori, Ken Kurokawa, Takuji Yamada

    PLOS ONE   10 ( 5 )   e0126967   2015.5

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  • DomSign: a top-down annotation pipeline to enlarge enzyme space in the protein universe Reviewed

    Tianmin Wang, Hiroshi Mori, Chong Zhang, Ken Kurokawa, Xin-Hui Xing, Takuji Yamada

    BMC BIOINFORMATICS   16   96   2015.3

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    DOI: 10.1186/s12859-015-0499-y

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  • CLAST: CUDA implemented large-scale alignment search tool Reviewed

    Masahiro Yano, Hiroshi Mori, Yutaka Akiyama, Takuji Yamada, Ken Kurokawa

    BMC BIOINFORMATICS   15   406   2014.12

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  • Potential of fecal microbiota for early-stage detection of colorectal cancer Reviewed

    Georg Zeller, Julien Tap, Anita Y. Voigt, Shinichi Sunagawa, Jens Roat Kultima, Paul I. Costea, Aurelien Amiot, Jurgen Bohm, Francesco Brunetti, Nina Habermann, Rajna Hercog, Moritz Koch, Alain Luciani, Daniel R. Mende, Martin A. Schneider, Petra Schrotz-King, Christophe Tournigand, Jeanne Tran Van Nhieu, Takuji Yamada, Jurgen Zimmermann, Vladimir Benes, Matthias Kloor, Cornelia M. Ulrich, Magnus Von Knebel Doeberitz, Iradj Sobhani, Peer Bork

    MOLECULAR SYSTEMS BIOLOGY   10 ( 11 )   766   2014.11

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  • Identification and assembly of genomes and genetic elements in complex metagenomic samples without using reference genomes Reviewed

    H. Bjorn Nielsen, Mathieu Almeida, Agnieszka Sierakowska Juncker, Simon Rasmussen, Junhua Li, Shinichi Sunagawa, Damian R. Plichta, Laurent Gautier, Anders G. Pedersen, Emmanuelle Le Chatelier, Eric Pelletier, Ida Bonde, Trine Nielsen, Chaysavanh Manichanh, Manimozhiyan Arumugam, Jean-Michel Batto, Marcelo B. Quintanilha dos Santos, Nikolaj Blom, Natalia Borruel, Kristoffer S. Burgdorf, Fouad Boumezbeur, Francesc Casellas, Joel Dore, Piotr Dworzynski, Francisco Guarner, Torben Hansen, Falk Hildebrand, Rolf S. Kaas, Sean Kennedy, Karsten Kristiansen, Jens Roat Kultima, Pierre Leonard, Florence Levenez, Ole Lund, Bouziane Moumen, Denis Le Paslier, Nicolas Pons, Oluf Pedersen, Edi Prifti, Junjie Qin, Jeroen Raes, Soren Sorensen, Julien Tap, Sebastian Tims, David W. Ussery, Takuji Yamada, Pierre Renault, Thomas Sicheritz-Ponten, Peer Bork, Jun Wang, Soren Brunak, S. Dusko Ehrlich

    NATURE BIOTECHNOLOGY   32 ( 8 )   822 - 828   2014.8

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  • Classification and quantification of bacteriophage taxa in human gut metagenomes Reviewed

    Alison S. Waller, Takuji Yamada, David M. Kristensen, Jens Roat Kultima, Shinichi Sunagawa, Eugene V. Koonin, Peer Bork

    ISME JOURNAL   8 ( 7 )   1391 - 1402   2014.7

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  • Klebsormidium flaccidum genome reveals primary factors for plant terrestrial adaptation. Reviewed International journal

    Koichi Hori, Fumito Maruyama, Takatomo Fujisawa, Tomoaki Togashi, Nozomi Yamamoto, Mitsunori Seo, Syusei Sato, Takuji Yamada, Hiroshi Mori, Naoyuki Tajima, Takashi Moriyama, Masahiko Ikeuchi, Mai Watanabe, Hajime Wada, Koichi Kobayashi, Masakazu Saito, Tatsuru Masuda, Yuko Sasaki-Sekimoto, Kiyoshi Mashiguchi, Koichiro Awai, Mie Shimojima, Shinji Masuda, Masako Iwai, Takashi Nobusawa, Takafumi Narise, Satoshi Kondo, Hikaru Saito, Ryoichi Sato, Masato Murakawa, Yuta Ihara, Yui Oshima-Yamada, Kinuka Ohtaka, Masanori Satoh, Kohei Sonobe, Midori Ishii, Ryosuke Ohtani, Miyu Kanamori-Sato, Rina Honoki, Daichi Miyazaki, Hitoshi Mochizuki, Jumpei Umetsu, Kouichi Higashi, Daisuke Shibata, Yuji Kamiya, Naoki Sato, Yasukazu Nakamura, Satoshi Tabata, Shigeru Ida, Ken Kurokawa, Hiroyuki Ohta

    Nature communications   5   3978 - 3978   2014.5

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    The colonization of land by plants was a key event in the evolution of life. Here we report the draft genome sequence of the filamentous terrestrial alga Klebsormidium flaccidum (Division Charophyta, Order Klebsormidiales) to elucidate the early transition step from aquatic algae to land plants. Comparison of the genome sequence with that of other algae and land plants demonstrate that K. flaccidum acquired many genes specific to land plants. We demonstrate that K. flaccidum indeed produces several plant hormones and homologues of some of the signalling intermediates required for hormone actions in higher plants. The K. flaccidum genome also encodes a primitive system to protect against the harmful effects of high-intensity light. The presence of these plant-related systems in K. flaccidum suggests that, during evolution, this alga acquired the fundamental machinery required for adaptation to terrestrial environments.

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  • Orthologous Gene Clusters and Taxon Signature Genes for Viruses of Prokaryotes Reviewed

    David M. Kristensen, Alison S. Waller, Takuji Yamada, Peer Bork, Arcady R. Mushegian, Eugene V. Koonin

    JOURNAL OF BACTERIOLOGY   195 ( 5 )   941 - 950   2013.3

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  • Whole-genome sequence of the purple photosynthetic bacterium Rhodovulum sulfidophilum strain W4 Reviewed

    Shinji Masuda, Koichi Hori, Fumito Maruyama, Shukun Ren, Saori Sugimoto, Nozomi Yamamoto, Hiroshi Mori, Takuji Yamada, Shusei Sato, Satoshi Tabata, Hiroyuki Ohta, Ken Kurokawa

    Genome Announcements   1 ( 4 )   2013

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  • Prediction and identification of sequences coding for orphan enzymes using genomic and metagenomic neighbours Reviewed

    Takuji Yamada, Alison S. Waller, Jeroen Raes, Aleksej Zelezniak, Nadia Perchat, Alain Perret, Marcel Salanoubat, Kiran R. Patil, Jean Weissenbach, Peer Bork

    MOLECULAR SYSTEMS BIOLOGY   8   581   2012.5

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  • iPath2.0: interactive pathway explorer Reviewed

    Takuji Yamada, Ivica Letunic, Shujiro Okuda, Minoru Kanehisa, Peer Bork

    NUCLEIC ACIDS RESEARCH   39 ( Web Server issue )   W412 - W415   2011.7

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    DOI: 10.1093/nar/gkr313

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  • Enterotypes of the human gut microbiome Reviewed

    Manimozhiyan Arumugam, Jeroen Raes, Eric Pelletier, Denis Le Paslier, Takuji Yamada, Daniel R. Mende, Gabriel R. Fernandes, Julien Tap, Thomas Bruls, Jean-Michel Batto, Marcelo Bertalan, Natalia Borruel, Francesc Casellas, Leyden Fernandez, Laurent Gautier, Torben Hansen, Masahira Hattori, Tetsuya Hayashi, Michiel Kleerebezem, Ken Kurokawa, Marion Leclerc, Florence Levenez, Chaysavanh Manichanh, H. Bjorn Nielsen, Trine Nielsen, Nicolas Pons, Julie Poulain, Junjie Qin, Thomas Sicheritz-Ponten, Sebastian Tims, David Torrents, Edgardo Ugarte, Erwin G. Zoetendal, Jun Wang, Francisco Guarner, Oluf Pedersen, Willem M. de Vos, Soren Brunak, Joel Dore, Jean Weissenbach, S. Dusko Ehrlich, Peer Bork

    NATURE   473 ( 7346 )   174 - 180   2011.5

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    DOI: 10.1038/nature09944

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  • Toward molecular trait-based ecology through integration of biogeochemical, geographical and metagenomic data Reviewed

    Jeroen Raes, Ivica Letunic, Takuji Yamada, Lars Juhl Jensen, Peer Bork

    MOLECULAR SYSTEMS BIOLOGY   7   473   2011.3

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    DOI: 10.1038/msb.2011.6

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  • The Ecoresponsive Genome of Daphnia pulex Reviewed

    John K. Colbourne, Michael E. Pfrender, Donald Gilbert, W. Kelley Thomas, Abraham Tucker, Todd H. Oakley, Shinichi Tokishita, Andrea Aerts, Georg J. Arnold, Malay Kumar Basu, Darren J. Bauer, Carla E. Caceres, Liran Carmel, Claudio Casola, Jeong-Hyeon Choi, John C. Detter, Qunfeng Dong, Serge Dusheyko, Brian D. Eads, Thomas Froehlich, Kerry A. Geiler-Samerotte, Daniel Gerlach, Phil Hatcher, Sanjuro Jogdeo, Jeroen Krijgsveld, Evgenia V. Kriventseva, Dietmar Kueltz, Christian Laforsch, Erika Lindquist, Jacqueline Lopez, J. Robert Manak, Jean Muller, Jasmyn Pangilinan, Rupali P. Patwardhan, Samuel Pitluck, Ellen J. Pritham, Andreas Rechtsteiner, Mina Rho, Igor B. Rogozin, Onur Sakarya, Asaf Salamov, Sarah Schaack, Harris Shapiro, Yasuhiro Shiga, Courtney Skalitzky, Zachary Smith, Alexander Souvorov, Way Sung, Zuojian Tang, Dai Tsuchiya, Hank Tu, Harmjan Vos, Mei Wang, Yuri I. Wolf, Hideo Yamagata, Takuji Yamada, Yuzhen Ye, Joseph R. Shaw, Justen Andrews, Teresa J. Crease, Haixu Tang, Susan M. Lucas, Hugh M. Robertson, Peer Bork, Eugene V. Koonin, Evgeny M. Zdobnov, Igor V. Grigoriev, Michael Lynch, Jeffrey L. Boore

    SCIENCE   331 ( 6017 )   555 - 561   2011.2

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    DOI: 10.1126/science.1197761

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  • A human gut microbial gene catalogue established by metagenomic sequencing Reviewed

    Junjie Qin, Ruiqiang Li, Jeroen Raes, Manimozhiyan Arumugam, Kristoffer Solvsten Burgdorf, Chaysavanh Manichanh, Trine Nielsen, Nicolas Pons, Florence Levenez, Takuji Yamada, Daniel R. Mende, Junhua Li, Junming Xu, Shaochuan Li, Dongfang Li, Jianjun Cao, Bo Wang, Huiqing Liang, Huisong Zheng, Yinlong Xie, Julien Tap, Patricia Lepage, Marcelo Bertalan, Jean-Michel Batto, Torben Hansen, Denis Le Paslier, Allan Linneberg, H. Bjorn Nielsen, Eric Pelletier, Pierre Renault, Thomas Sicheritz-Ponten, Keith Turner, Hongmei Zhu, Chang Yu, Shengting Li, Min Jian, Yan Zhou, Yingrui Li, Xiuqing Zhang, Songgang Li, Nan Qin, Huanming Yang, Jian Wang, Soren Brunak, Joel Dore, Francisco Guarner, Karsten Kristiansen, Oluf Pedersen, Julian Parkhill, Jean Weissenbach, Peer Bork, S. Dusko Ehrlich, Jun Wang

    NATURE   464 ( 7285 )   59 - U70   2010.3

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    DOI: 10.1038/nature08821

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  • Functional and Evolutionary Insights from the Genomes of Three Parasitoid Nasonia Species Reviewed

    John H. Werren, Stephen Richards, Christopher A. Desjardins, Oliver Niehuis, Juergen Gadau, John K. Colbourne, Leo W. Beukeboom, Claude Desplan, Christine G. Elsik, Cornelis J. P. Grimmelikhuijzen, Paul Kitts, Jeremy A. Lynch, Terence Murphy, Deodoro C. S. G. Oliveira, Christopher D. Smith, Louis van de Zande, Kim C. Worley, Evgeny M. Zdobnov, Maarten Aerts, Stefan Albert, Victor H. Anaya, Juan M. Anzola, Angel R. Barchuk, Susanta K. Behura, Agata N. Bera, May R. Berenbaum, Rinaldo C. Bertossa, Marcia M. G. Bitondi, Seth R. Bordenstein, Peer Bork, Erich Bornberg-Bauer, Marleen Brunain, Giuseppe Cazzamali, Lesley Chaboub, Joseph Chacko, Dean Chavez, Christopher P. Childers, Jeong-Hyeon Choi, Michael E. Clark, Charles Claudianos, Rochelle A. Clinton, Andrew G. Cree, Alexandre S. Cristino, Phat M. Dang, Alistair C. Darby, Dirk C. de Graaf, Bart Devreese, Huyen H. Dinh, Rachel Edwards, Navin Elango, Eran Elhaik, Olga Ermolaeva, Jay D. Evans, Sylvain Foret, Gerald R. Fowler, Daniel Gerlach, Joshua D. Gibson, Donald G. Gilbert, Dan Graur, Stefan Grunder, Darren E. Hagen, Yi Han, Frank Hauser, Dan Hultmark, Henry C. Hunter, Shalini N. Jhangian, Huaiyang Jiang, Reed M. Johnson, Andrew K. Jones, Thomas Junier, Tatsuhiko Kadowaki, Albert Kamping, Yuri Kapustin, Bobak Kechavarzi, Jaebum Kim, Jay Kim, Boris Kiryutin, Tosca Koevoets, Christie L. Kovar, Evgenia V. Kriventseva, Robert Kucharski, Heewook Lee, Sandra L. Lee, Kristin Lees, Lora R. Lewis, David W. Loehlin, John M. Logsdon, Jacqueline A. Lopez, Ryan J. Lozado, Donna Maglott, Ryszard Maleszka, Anoop Mayampurath, Danielle J. Mazur, Marcella A. McClure, Andrew D. Moore, Margaret B. Morgan, Jean Muller, Monica C. Munoz-Torres, Donna M. Muzny, Lynne V. Nazareth, Susanne Neupert, Ngoc B. Nguyen, Francis M. F. Nunes, John G. Oakeshott, Geoffrey O. Okwuonu, Bart A. Pannebakker, Vikas R. Pejaver, Zuogang Peng, Stephen C. Pratt, Reinhard Predel, Ling-Ling Pu, Hilary Ranson, Rhitoban Raychoudhury, Andreas Rechtsteiner, Justin T. Reese, Jeffrey G. Reid, Megan Riddle, Il High M. Robertson, Jeanne Romero-Severson, Miriam Rosenberg, Timothy B. Sackton, David B. Sattelle, Helge Schluens, Thomas Schmitt, Martina Schneider, Andreas Schueler, Andrew M. Schurko, David M. Shuker, Zila L. P. Simoes, Saurabh Sinha, Zachary Smith, Victor Solovyev, Alexandre Souvorov, Andreas Springauf, Elisabeth Stafflinger, Deborah E. Stage, Mario Stanke, Yoshiaki Tanaka, Arndt Telschow, Carol Trent, Selina Vattathil, Eveline C. Verhulst, Lumi Viljakainen, Kevin W. Wanner, Robert M. Waterhouse, James B. Whitfield, Timothy E. Wilkes, Michael Williamson, Judith H. Willis, Florian Wolschin, Stefan Wyder, Takuji Yamada, Soojin V. Yi, Courtney N. Zecher, Lan Zhang, Richard A. Gibbs

    SCIENCE   327 ( 5963 )   343 - 348   2010.1

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    DOI: 10.1126/science.1178028

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  • Evolution of biomolecular networks - lessons from metabolic and protein interactions Reviewed

    Takuji Yamada, Peer Bork

    NATURE REVIEWS MOLECULAR CELL BIOLOGY   10 ( 11 )   791 - 803   2009.11

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  • Transcriptome Complexity in a Genome-Reduced Bacterium Reviewed

    Marc Gueell, Vera van Noort, Eva Yus, Wei-Hua Chen, Justine Leigh-Bell, Konstantinos Michalodimitrakis, Takuji Yamada, Manimozhiyan Arumugam, Tobias Doerks, Sebastian Kuehner, Michaela Rode, Mikita Suyama, Sabine Schmidt, Anne-Claude Gavin, Peer Bork, Luis Serrano

    SCIENCE   326 ( 5957 )   1268 - 1271   2009.11

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    DOI: 10.1126/science.1176951

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  • Impact of Genome Reduction on Bacterial Metabolism and Its Regulation Reviewed

    Eva Yus, Tobias Maier, Konstantinos Michalodimitrakis, Vera van Noort, Takuji Yamada, Wei-Hua Chen, Judith A. H. Wodke, Marc Gueell, Sira Martinez, Ronan Bourgeois, Sebastian Kuehner, Emanuele Raineri, Ivica Letunic, Olga V. Kalinina, Michaela Rode, Richard Herrmann, Ricardo Gutierrez-Gallego, Robert B. Russell, Anne-Claude Gavin, Peer Bork, Luis Serrano

    SCIENCE   326 ( 5957 )   1263 - 1268   2009.11

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    DOI: 10.1126/science.1177263

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  • Proteome Organization in a Genome-Reduced Bacterium Reviewed

    Sebastian Kuehner, Vera van Noort, Matthew J. Betts, Alejandra Leo-Macias, Claire Batisse, Michaela Rode, Takuji Yamada, Tobias Maier, Samuel Bader, Pedro Beltran-Alvarez, Daniel Castano-Diez, Wei-Hua Chen, Damien Devos, Marc Gueell, Tomas Norambuena, Ines Racke, Vladimir Rybin, Alexander Schmidt, Eva Yus, Ruedi Aebersold, Richard Herrmann, Bettina Boettcher, Achilleas S. Frangakis, Robert B. Russell, Luis Serrano, Peer Bork, Anne-Claude Gavin

    SCIENCE   326 ( 5957 )   1235 - 1240   2009.11

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    DOI: 10.1126/science.1176343

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  • Quantifying environmental adaptation of metabolic pathways in metagenomics Reviewed

    Tara A. Gianoulis, Jeroen Raes, Prianka V. Patel, Robert Bjornson, Jan O. Korbel, Ivica Letunic, Takuji Yamada, Alberto Paccanaro, Lars J. Jensen, Michael Snyder, Peer Bork, Mark B. Gerstein

    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA   106 ( 5 )   1374 - 1379   2009.2

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    DOI: 10.1073/pnas.0808022106

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  • KEGG Atlas mapping for global analysis of metabolic pathways Reviewed

    Shujiro Okuda, Takuji Yamada, Masami Hamajima, Masumi Itoh, Toshiaki Katayama, Peer Bork, Susumu Goto, Minoru Kanehisa

    NUCLEIC ACIDS RESEARCH   36 ( Web Server issue )   W423 - W426   2008.7

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    DOI: 10.1093/nar/gkn282

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  • iPath: interactive exploration of biochemical pathways and networks Reviewed

    Ivica Letunic, Takuji Yamada, Minoru Kanehisa, Peer Bork

    TRENDS IN BIOCHEMICAL SCIENCES   33 ( 3 )   101 - 103   2008.3

  • VisANT 3.0: new modules for pathway visualization, editing, prediction and construction Reviewed

    Zhenjun Hu, David M. Ng, Takuji Yamada, Chunnuan Chen, Shuichi Kawashima, Joe Mellor, Bolan Linghu, Minoru Kanehisa, Joshua M. Stuart, Charles DeLisi

    NUCLEIC ACIDS RESEARCH   35 ( Web Server issue )   W625 - W632   2007.7

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    DOI: 10.1093/nar/gkm295

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  • Systematic analysis of enzyme-catalyzed reaction patterns and prediction of microbial biodegradation pathways Reviewed

    Mina Oh, Takuji Yamada, Masahiro Hattori, Susumu Goto, Minoru Kanehisa

    JOURNAL OF CHEMICAL INFORMATION AND MODELING   47 ( 4 )   1702 - 1712   2007.7

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    DOI: 10.1021/ci700006f

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  • Extraction of phylogenetic network modules from the metabolic network Reviewed

    Takuji Yamada, Minoru Kanehisa, Susumu Goto

    BMC BIOINFORMATICS   7   130   2006.3

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    DOI: 10.1186/1471-2105/7/130

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  • The role of log-normal dynamics in the evolution of biochemical pathways Reviewed

    J. C. Nacher, T. Ochiai, T. Yamada, M. Kanehisa, T. Akutsu

    BioSystems   83 ( 1 )   26 - 37   2006.1

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    DOI: 10.1016/j.biosystems.2005.09.003

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  • The repertoire of desaturases for unsaturated fatty acid synthesis in 397 genomes. Reviewed

    Hashimoto K, Yoshizawa AC, Saito K, Yamada T, Kanehisa M

    Genome informatics. International Conference on Genome Informatics   17 ( 1 )   173 - 183   2006

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    Fatty acids are the major components of membrane molecules. The fact that unsaturated fattyacids play multiple important roles, physically and biologically, means that the ratio of unsaturatedto saturated fatty acids in the membrane needs to be strictly regulated to maintain cellular homeostasis.The most ubiquitous and widespread modification to fatty acids, which results in a greatdiversity of different structures, is the insertion of double bonds. Fatty acid desaturases directlyintroduce regioselective double bonds into fatty acids. A phylogenetic analysis of desaturases suggeststhat the sequences of these proteins include a highly conserved domain, which determines thedifferences in specificity and regioselectivity found in these enzymes. In this study, we performeda systematic analysis of fatty acid desaturases found in the genomic data of 397 organisms. Weobtained a set of desaturases clustered by regioselectivity using a hierarchal clustering analysis.

    DOI: 10.11234/gi1990.17.173

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  • Analysis of the differences in metabolic network expansion between prokaryotes and eukaryotes. Reviewed

    Tanaka M, Yamada T, Itoh M, Okuda S, Goto S, Kanehisa M

    Genome informatics. International Conference on Genome Informatics   17 ( 1 )   230 - 239   2006

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    Recent evidence points to the existence of scale-free properties in many biological networks. By topological analysis, several models including preferential attachment and hierarchical modules have been proposed to explain how these networks are organized. On the other hand, analyses using dynamics have suggested that gene expression and metabolic networks have been organized with the scale-free property by the other models such as "rich-travel-more" and "log-normal dynamics." Because most of these approaches are based on comparative genomics of extant species, and did not consider evolutionary events such as horizontal gene transfer, gene loss and gene gain, we have analyzed transition of metabolic networks from the vertical point of view of evolution. First, to identify metabolic networks of common ancestors, we applied a parsimony algorithm for the enzymatic reaction set. Then by comparing the estimated metabolic networks among common ancestors, we investigated the transition of metabolic networks along the evolutionary process. As a result, we estimated enzymatic reaction contents of 227 common ancestors from 228 extant species, and found that links of several specific metabolites have frequently changed during the course of evolution.

    DOI: 10.11234/gi1990.17.230

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  • An odorant-binding protein facilitates odorant transfer from air to hydrophilic surroundings in the blowfly Reviewed

    K Tsuchihara, K Fujikawa, M Ishiguro, T Yamada, C Tada, K Ozaki, M Ozaki

    CHEMICAL SENSES   30 ( 7 )   559 - 564   2005.9

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    DOI: 10.1093/chemse/bji049

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  • VisANT: data-integrating visual framework for biological networks and modules Reviewed

    ZJ Hu, J Mellor, J Wu, T Yamada, D Holloway, C DeLisi

    NUCLEIC ACIDS RESEARCH   33 ( Web Server Issue )   W352 - W357   2005.7

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    DOI: 10.1093/nar/gki431

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  • Two complementary representations of a scale-free network Reviewed

    J. C. Nacher, T. Yamada, S. Goto, M. Kanehisa, T. Akutsu

    Physica A: Statistical Mechanics and its Applications   349 ( 1-2 )   349 - 363   2005.4

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    DOI: 10.1016/j.physa.2004.09.013

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  • Comprehensive analysis and prediction of synthetic lethality using subcellular locations. Reviewed

    Takuji Yamada, Shuichi Kawashima, Hiroshi Mamitsuka, Susumu Goto, Minoru Kanehisa

    Genome informatics. International Conference on Genome Informatics   16 ( 1 )   150 - 8   2005

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    The lethality of a gene is a fundamental and representative measure for understanding the function of a gene and its associated bio-systems. Recently, many research groups have started focusing on the concept of synthetic lethality. The synthetic lethality between genes is defined by the combination of mutations in two genes causing cell death. Here, we confirm that synthetic lethality and cellular location have close relationships among the Saccharomyces cerevisiae genes. Furthermore, we attempt the prediction of candidate gene pairs with synthetic lethality. The prediction is based on the hierarchical aspect model (HAM) which learns from a data set of cellular location to estimate a likelihood value indicating the synthetic lethality between genes.

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  • Clustering under the line graph transformation: application to reaction network Reviewed

    JC Nacher, N Ueda, T Yamada, M Kanehisa, T Akutsu

    BMC BIOINFORMATICS   5   207   2004.12

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    DOI: 10.1186/1471-2105-5-207

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  • Extraction of phylogenetic network modules from prokayrote metabolic pathways. Reviewed

    Yamada T, Goto S, Kanehisa M

    Genome informatics. International Conference on Genome Informatics   15 ( 1 )   249 - 258   2004

  • Extraction of Modules from the Metabolic Pathways with Phylogenetic Profile

    Yamada Takuji, Yamanishi Yoshihiro, Goto Susumu, Kanehisa Minoru

    GI   13   353 - 354   2002

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    DOI: 10.11234/gi1990.13.353

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MISC

  • Functional annotation atlas for human gut microbiome

    城間博紹, 山田拓司

    生化学   95 ( 4 )   2023

  • Development of an integrated microbiome database: Microbiome Datahub

    森宙史, 藤澤貴智, 東光一, 中村保一, 山田拓司, 松井求, 内山郁夫

    日本細菌学雑誌(Web)   78 ( 1 )   2023

  • MicrobeDB.jpからMicrobiome Datahubへ: 微生物・植物・メタボロームのデータ統合と統合微生物データベースの再構築

    藤澤 貴智, 平川 英樹, 守屋 勇樹, 信定 知江, 金谷 重彦, 有田 正規, 田畑 哲之, 磯部 祥子, 東 光一, 中村 保一, 松井 求, 山田 拓司, 内山 郁夫, 黒川 顕, 森 宙史

    トーゴーの日2022   1   2022.10

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    DOI: 10.18908/togo2022.p010

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  • 微生物統合データベースMicrobeDB.jpを用いたマイクロバイオーム研究への応用

    森宙史, 藤澤貴智, 西出浩世, 矢口貴志, 高橋弘喜, 中川善一, 山田拓司, 内山郁夫, 中村保一, 黒川顕

    日本ゲノム微生物学会年会要旨集   16th (Web)   2022

  • 微生物統合データベースMicrobeDB.jpと微生物群集解析

    森 宙史, 藤澤 貴智, 西出 浩世, 矢口 貴志, 高橋 弘喜, 中川 善一, 山田 拓司, 内山 郁夫, 中村 保一, 黒川 顕

    トーゴーの日2021   1   2021.10

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    DOI: 10.18908/togo2021.p046

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  • MicrobeDB.jp and related microbiome analysis tools

    黒川顕, 森宙史, 藤澤貴智, 西出浩世, 矢口貴志, 高橋弘喜, 中川善一, 山田拓司, 内山郁夫, 中村保一

    日本分子生物学会年会プログラム・要旨集(Web)   44th   2021

  • Oral microbiota in colorectal cancer progression model

    水谷紗弥佳, 水谷紗弥佳, 山田拓司, 山田拓司, 山田拓司, 山田拓司

    実験医学   39 ( 16 )   2527 - 2531   2021

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    J-GLOBAL

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  • 微生物統合データベースMicrobeDB.jp version3とマイクロバイオーム解析

    森宙史, 藤澤貴智, 西出浩世, 矢口貴志, 高橋弘喜, 中川善一, 山田拓司, 内山郁夫, 中村保一, 黒川顕

    日本ゲノム微生物学会年会要旨集   15th (Web)   2021

  • 近未来の臨床応用に向けたゲノム解析 胃がん治療のための胃切除による腸内細菌や代謝産物への影響

    山田 拓司, Erawijantari Pande, 水谷 紗弥佳, 城間 博紹

    日本癌学会総会記事   80th   [S11 - 4]   2021

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    J-GLOBAL

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  • 腸内細菌叢 11 大腸がんと腸内環境のダイナミクス

    水谷紗弥佳, 水谷紗弥佳, 山田拓司

    モダンメディア   66 ( 2 )   37 - 42   2020

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  • Gut microbiome and metabolome alteration after treatment for colorectal cancer

    城間博紹, 水谷紗弥佳, 谷内田真一, 山田拓司

    腸内細菌学雑誌   34 ( 2 )   2020

  • 微生物統合データベースMicrobeDB.jp version 3

    森宙史, 藤澤貴智, 西出浩世, 矢口貴志, 高橋弘喜, 中川善一, 山田拓司, 内山郁夫, 中村保一, 黒川顕

    日本ゲノム微生物学会年会要旨集   14th   2020

  • 統合微生物データベースMicrobeDB.jpポータルサイト拡張

    藤澤 貴智, 森 宙史, 谷澤 靖洋, 児玉 悠一, 内山 郁夫, 中川 善一, 山田 拓司, 高橋 弘喜, 中村 保一, 黒川 顕

    トーゴーの日2019   1   2019.10

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    DOI: 10.18908/togo2019.p043

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  • 大腸がんを切除したヒトの腸内細菌叢メタゲノム解析

    城間 博紹, 水谷 紗弥佳, 谷内田 真一, 山田 拓司

    日本細菌学雑誌   74 ( 1 )   70 - 70   2019.3

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  • 糞便メタゲノムおよびメタボローム解析を用いた大腸がんの多段階発がんに伴う腸内環境の変化

    水谷紗弥佳, 水谷紗弥佳, 谷内田真一, 谷内田真一, 城間博紹, 柴知史, 山田拓司, 山田拓司

    日本生化学会大会(Web)   92nd ( 1 )   143 - 143   2019

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  • Metagenomic analysis of human gut microbiome in post-operative status of colorectal cancer

    城間博紹, 水谷紗弥佳, 谷内田真一, 山田拓司

    日本細菌学雑誌(Web)   74 ( 1 )   2019

  • アジア各国の腸内細菌叢の有する遺伝子機能に関する研究

    堀野美里, 田中優, 内川彩夏, 百田理恵, 園元謙二, 小椋義俊, 豊田敦, 山田拓司, 黒川顕, 林哲也, 中山二郎

    日本乳酸菌学会誌   29 ( 2 )   114 - 114   2018.7

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  • MicrobeDB.jpポータル:統合微生物データベースのポータルサイト構築

    藤澤貴智, 森宙史, 谷沢靖洋, 神沼英里, 内山郁夫, 山田拓司, 高橋弘喜, 中村保一, 黒川顕

    日本ゲノム微生物学会年会要旨集   12th   79   2018.3

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  • 野生ニホンライチョウ腸内細菌叢の特徴と地域差

    牛田一成, 牛田一成, 土田さやか, 小林篤, 長谷川雅美, 上田敦史, 山田拓司, 村田浩一, 中村浩志

    日本生態学会大会講演要旨(Web)   65th   2018

  • ライチョウの雛はなぜ母親の盲腸糞を食べるのか-その適応的意義と保全への応用-

    小林篤, 土田さやか, 上田敦史, 山田拓司, 長谷川雅美, 村田浩一, 中村浩志, 牛田一成

    日本生態学会大会講演要旨(Web)   65th   2018

  • メタゲノム解析を用いた大腸がん疾病マーカーの探索

    城間博紹, 水谷紗弥佳, 谷内田真一, 山田拓司

    日本ゲノム微生物学会年会要旨集   12th   2018

  • ライチョウの雛は母親のうんちを食べて腸内細菌を手に入れる

    小林篤, 土田さやか, 上田敦史, 山田拓司, 村田浩一, 中村浩志, 牛田一成

    日本鳥学会大会講演要旨集   2018   2018

  • メタゲノム解析を用いた大腸がん疾病マーカー遺伝子の探索

    城間博紹, 水谷紗弥佳, 谷内田真一, 山田拓司

    日本生化学会大会(Web)   90th   2017

  • メタゲノム解析を用いた大腸がん疾病マーカー遺伝子の探索

    城間博紹, 西本悠一郎, 水谷紗弥佳, 谷内田真一, 山田拓司

    日本ゲノム微生物学会年会要旨集   11th   2017

  • 腸内メタゲノム・メタボロームデータを用いた大腸がんの腸内細菌叢の解析

    水谷紗弥佳, 城間博紹, 谷内田真一, 谷内田真一, 山田拓司

    日本生化学会大会(Web)   90th   [1LBA - 042]   2017

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  • ITS配列解析によるP.acnes株群集構造解析

    渡邊日佳流, 森宙史, 黒川顕, 黒川顕, 山田拓司

    日本ゲノム微生物学会年会要旨集   10th   60   2016

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  • ヒト腸内細菌オミックスデータを用いた超早期大腸がんマーカーの探索

    西本悠一郎, 水谷紗弥佳, 伊東泰雄, 谷内田真一, 山田拓司

    日本ゲノム微生物学会年会要旨集   10th   2016

  • 河川細菌群集構造変化の普遍的ダイナミクス

    黒澤晋, 黒川顕, 中島信孝, 山田拓司, 森宙史, 東光一, 鈴木真也

    日本ゲノム微生物学会年会要旨集   10th   91   2016

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  • ヒト腸内細菌の代謝反応データベース構築

    佃直紀, 山本希, 東光一, 入江満, 五斗進, 奥田修二郎, 守屋勇樹, 森宙史, 黒川顕, 山田拓司

    日本ゲノム微生物学会年会要旨集   10th   88   2016

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  • 大規模オミックスデータの可視化・解析ツール「FuncTree」の開発

    山手雄太, 森宙史, 黒川顕, 山田拓司

    日本ゲノム微生物学会年会要旨集   10th   90   2016

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  • クローズアップ実験法 Series262 次世代シークエンサーによる腸内細菌メタゲノム解析

    YAMADA TAKUJI

    実験医学   33 ( 8 )   1323 - 1327   2015.5

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  • ヒト腸内細菌叢代謝経路データベースの構築

    YAMADA TAKUJI

    日本細菌学雑誌   70 ( 1 )   100   2015.2

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  • 3S-Dp01 Metabolic pathway database for Human gut microbiome :

    Yamada Takuji, Tsukuda Naoki, Mizutani Sayaka, Mori Hiroshi, Kurokawa Ken, Moriya Yuki, Okuda Shujiro, Goto Susumu

    67   357 - 357   2015

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  • IgA腎症の口蓋扁桃陰窩のマイクロバイオーム解析

    渡辺博文, 後藤眞, 土田雅史, 森宙史, 東光一, 近藤大介, 山崎肇, 青柳竜治, 高田琢磨, 細道一善, 山田拓司, 井ノ上逸朗, 黒川顕, 成田一衛

    IgA腎症研究会抄録   38th   2015

  • 菌叢情報と疫学データの統合解析に向けた疫学データ解析のデータ整備と統計手法の開発

    伊東泰雄, 水谷紗弥佳, 西本悠一郎, 谷内田真一, 山田拓司

    日本微生物生態学会大会(Web)   30th   2015

  • ヒト腸内細菌代謝機能データベースの構築

    YAMADA TAKUJI

    日本抗加齢医学会総会プログラム・抄録集   15th   141   2015

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  • Metagenomics for Human Gut Microbiome

    YAMADA TAKUJI

    腸内細菌学雑誌   29 ( 1 )   19-22 (J-STAGE)   2015

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  • ヒト腸内細菌叢メタゲノムデータを用いた腸内環境代謝機構の解明

    YAMADA TAKUJI

    上原記念生命科学財団研究報告集(CD-ROM)   28   ROMBUNNO.164 - 4   2014.12

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  • ヒト腸内細菌叢からヒトの特徴

    YAMADA TAKUJI

    日本土壌微生物学会講演要旨集   2014   61 - 61   2014.10

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  • 腸内細菌代謝経路データベースの構築(メタゲノムから見える環境と(微)生物の生き様-ここまでわかるメタゲノム解析,シンポジウム(1),環境微生物系学会合同大会2014講演要旨)

    山田 拓司

    土と微生物   68 ( 2 )   95 - 96   2014.10

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  • 腸内細菌代謝反応データベースの構築

    YAMADA TAKUJI

    日本動脈硬化学会総会・学術集会プログラム・抄録集(Web)   46th   SHIMPOJIUMU6,5 (WEB ONLY)   2014.6

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  • ヒト腸内細菌叢代謝経路データベース

    YAMADA TAKUJI, TSUKUDA NAOKI, TAKAHASHI TOMONORI, MORI HIROSHI, KUROKAWA KEN, MORIYA YUKI, OKUDA SHUJIRO, GOTO SUSUMU

    腸内細菌学雑誌   28 ( 2 )   (JA)59,(EN)60   2014.4

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  • 常在細菌叢が操るヒトの健康と疾患 第1章 常在細菌叢をいかに読み解くのか 2.ヒト常在細菌叢の解析手法

    YAMADA TAKUJI

    実験医学   32 ( 5 )   688 - 692   2014.3

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  • 車軸藻植物門クレブソルミディウムのゲノム解読と他植物との比較解析

    HORI KOICHI, YAMAMOTO MARE, UMEZU JUMPEI, TOGASHI TOMOAKI, MADOKA YUKA, SHIMOJIMA MIE, SEO MITSUNORI, KONDO SATOSHI, OTAKA KINUKA, TOUSHI NORIAKI, WATANABE MIGIWA, AZUMA KOICHI, MORI HIROSHI, YAMADA TAKUJI, MASUDA SHINJI, KUROKAWA AKIRA, OTA HIROYUKI

    日本植物生理学会年会要旨集   55th   388   2014.3

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  • Enterotypes of the human gut microbiome (vol 473, pg 174, 2011)

    Manimozhiyan Arumugam, Jeroen Raes, Eric Pelletier, Denis Le Paslier, Takuji Yamada, Daniel R. Mende, Gabriel R. Fernandes, Julien Tap, Thomas Bruls, Jean-Michel Batto, Marcelo Bertalan, Natalia Borruel, Francesc Casellas, Leyden Fernandez, Laurent Gautier, Torben Hansen, Masahira Hattori, Tetsuya Hayashi, Michiel Kleerebezem, Ken Kurokawa, Marion Leclerc, Florence Levenez, Chaysavanh Manichanh, H. Bjorn Nielsen, Trine Nielsen, Nicolas Pons, Julie Poulain, Junjie Qin, Thomas Sicheritz-Ponten, Sebastian Tims, David Torrents, Edgardo Ugarte, Erwin G. Zoetendal, Jun Wang, Francisco Guarner, Oluf Pedersen, Willem M. de Vos, Soren Brunak, Joel Dore, Jean Weissenbach, S. Dusko Ehrlich, Peer Bork

    NATURE   506 ( 7489 )   2014.2

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  • 腸炎モデルマウスに対する腸管IgA抗体の作用機序の解明

    岡井晋作, 臼井文人, 野村慎太郎, 中村肇伸, 山本和也, 西山依里, 森宙史, 山田拓司, 黒川顕, 加藤保, 大野博司, 新蔵礼子, 新蔵礼子

    日本分子生物学会年会プログラム・要旨集(Web)   37th   2014

  • k‐mer使用頻度を用いた類似メタゲノムサンプル予測法

    YANO MASAHIRO, MORI HIROSHI, YAMADA TAKUJI, KUROKAWA AKIRA

    日本ゲノム微生物学会年会要旨集   8th   79   2014

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  • 歯垢検体の保存温度および保存期間による細菌叢への影響

    SHINOZAKI NATSUKO, YAMAGISHI JUN'YA, SATO YUKUTO, YAMASHITA RIU, YAMADA TAKUJI, NAGASAKI MASAO, TSUBOI AKITO

    日本ゲノム微生物学会年会要旨集   8th   66   2014

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  • ヒト皮膚細菌叢の網羅的解析

    YAMADA TAKUJI, NAKAMURA KAZUNARI, WATANABE HIKARU, MORI HIROSHI, KUROKAWA AKIRA

    日本分子生物学会年会プログラム・要旨集(Web)   37th   2W5-10(2P-0963) (WEB ONLY)   2014

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  • 腸管IgA抗体は多種類の腸内細菌の同一タンパク質を認識し制御している

    USUI FUMITO, OKAI SHINSAKU, HASEGAWA MAKOTO, YAMAMOTO KAZUYA, NISHIYAMA ERI, MORI HIROSHI, YAMADA TAKUJI, KUROKAWA AKIRA, SHINKURA REIKO

    日本分子生物学会年会プログラム・要旨集(Web)   37th   3P-0701 (WEB ONLY)   2014

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  • ヒト腸内細菌代謝経路データベースの構築

    YAMADA TAKUJI, TSUKUDA NAOKI, MORI HIROSHI, KUROKAWA AKIRA, KUROKAWA AKIRA, MORIYA YUKI, OKUDA SHUJIRO, GOTO SUSUMU

    日本臨床腸内微生物学会誌   17 ( 1 )   18   2014

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  • 大規模なヒト腸内フローラのメタゲノム解析による大腸がんの病因解明と先制医療の可能性

    YACHIDA SHIN'ICHI, NAKAJIMA KEN, YAMADA TAKUJI

    日本分子生物学会年会プログラム・要旨集(Web)   37th   WEB ONLY 3W18-1(3P-0941)   2014

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  • ヒト腸内細菌叢解析のためのパスウェイデータベース構築

    OKUDA SHUJIRO, TSUKUDA NAOKI, YAMAMOTO MARE, NISHIMOTO YUICHIRO, TAKAHASHI TOMONORI, MORI HIROSHI, KUROKAWA AKIRA, MORIYA YUKI, GOTO SUSUMU, YAMADA TAKUJI

    日本分子生物学会年会プログラム・要旨集(Web)   37th   WEB ONLY 3W18-5(3P-0945)   2014

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  • IgA腎症の口蓋扁桃細菌叢の網羅的解析

    WATANABE HIROFUMI, GOTO MAKOTO, MORI HIROSHI, HIGASHI KOICHI, HOSOMICHI KAZUYOSHI, YAMADA TAKUJI, INOUE ITSURO, KUROKAWA AKIRA, NARITA ICHIEI

    日本遺伝子診療学会大会プログラム・抄録集   21st   345   2014

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  • ヒト腸内メタゲノム解析が広げる医療展開

    YAMADA TAKUJI

    化学と生物   51 ( 12 )   802 - 808   2013.12

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    DOI: 10.1271/kagakutoseibutsu.51.802

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  • 車軸藻植物門クレブソルミディウムのゲノム解析と脂質代謝系の進化過程の解析

    HORI KOICHI, MARUYAMA FUMITO, FUJISAWA TAKANORI, TOGASHI TOMOAKI, YAMAMOTO MARE, MADOKA YUKA, SHIMOJIMA MIE, SEO MITSUNORI, SATO SHUSEI, YAMADA TAKUJI, MORI HIROSHI, TAJIMA NAOYUKI, MORIYAMA SO, IKEUCHI MASAHIKO, WATANABE MAI, WADA MOTOI, KOBAYASHI KOICHI, SAITO MASAKAZU, MASUDA TATSURU, SEKIMOTO(SASAKI) YUIKO, MASUGUCHI KIYOSHI, AWAI KOICHIRO, MASUDA SHINJI, IWAI MASAKO, NOBUSAWA TAKESHI, NARUSE TAKASHI, KONDO SATOSHI, SAITO TAKESHI, SATO RYOICHI, MURAKAWA MASATO, IHARA YUTA, OSHIMA(YAMADA) YUI, OTAKA KINUKA, SATO MASANORI

    日本植物学会大会研究発表記録   77th   126   2013.8

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  • 車軸藻綱クレブソルミディウムのゲノム解析と植物の陸上化要因の予測

    HORI KOICHI, MARUYAMA FUMITO, FUJISAWA TAKANORI, TOGASHI TOMOAKI, YAMAMOTO MARE, SEO MITSUNORI, SATO SHUSEI, YAMADA TAKUJI, MORI HIROSHI, TAJIMA NAOYUKI, MORIYAMA SO, IKEUCHI MASAHIKO, WATANABE MAI, WADA MOTOI, KOBAYASHI KOICHI, SAITO MASAKAZU, MASUDA TATSURU, SEKIMOTO(SASAKI) YUKO, MASUGUCHI KIYOSHI, AWAI KOICHIRO, SHIMOJIMA MIE, MASUDA SHINJI, IWAI MASAKO, NOBUSAWA TAKESHI, NARUSE TAKASHI, KONDO SATOSHI, SAITO TAKESHI, SATO RYOICHI, MURAKAWA MASATO, IHARA YUTA, OSHIMA YUI, OTAKA KINUKA, SATO MASANORI, SONOBE KOHEI, ISHII MIDORI, OTANI RYOSUKE, KANAMORI MIYU, HOOGI RINA, MIYAZAKI DAICHI

    日本植物生理学会年会要旨集   54th   220   2013.3

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  • Oral administration of poly-reactive high-affinity IgA monoclonal antibody against intestinal microbiota improved inflammatory colitis in mice.

    OKAI Shinsaku, HORII Yusaku, SHIRAKI Yoshitaka, NAITO Tomoaki, MATSUMOTO Satoshi, NANNO Masanobu, YAMAMOTO Kazuya, MORI Hiroshi, YAMADA Takuji, KUROKAWA Ken, NOMURA Shintaro, SHINKURA Reiko, SHINKURA Reiko

    日本免疫学会総会・学術集会記録   42 ( Proceedings )   2013

  • ヒト腸内細菌叢の3タイプ

    YAMADA TAKUJI

    日本ゲノム微生物学会年会要旨集   7th   48   2013

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  • 環境メタデータと系統組成の統合解析

    YOSHINO KOJI, NISHIYAMA IRI, SUDA KONOMI, TAKEHARA JUN'ICHI, YAMAMOTO MARE, MORI HIROSHI, YAMADA TAKUJI, MARUYAMA FUMITO, UENO YUICHIRO, MARUYAMA SHIGENORI, KUROKAWA AKIRA

    日本ゲノム微生物学会年会要旨集   7th   89   2013

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  • 環境メタITS解析を目指したバクテリアITSデータベースの構築

    MISAKI MASATO, YOSHINO KOJI, MORI HIROSHI, YAMADA TAKUJI, KUROKAWA AKIRA

    日本ゲノム微生物学会年会要旨集   7th   88   2013

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  • Current and future trends in metagenomics : Development of knowledge bases

    MORI Hiroshi, YAMADA Takuji, KUROKAWA Ken

    Journal of Information Processing and Management   55 ( 3 )   167 - 175   2012

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    Microbes are essential for every part of life on Earth. Numerous microbes inhabit the biosphere, many of which are uncharacterized or uncultivable. They form a complex microbial community that deeply affects against surrounding environments. Metagenome analysis provides a radically new way of examining such complex microbial community without isolation or cultivation of individual bacterial community members. In this article, we present a brief discussion about a metagenomics and the development of knowledge bases, and also discuss about the future trends in metagenomics.

    DOI: 10.1241/johokanri.55.167

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  • Enterotypes of the human gut microbiome (vol 473, pg 174, 2011)

    Manimozhiyan Arumugam, Jeroen Raes, Eric Pelletier, Denis Le Paslier, Takuji Yamada, Daniel R. Mende, Gabriel R. Fernandes, Julien Tap, Thomas Bruls, Jean-Michel Batto, Marcelo Bertalan, Natalia Borruel, Francesc Casellas, Leyden Fernandez, Laurent Gautier, Torben Hansen, Masahira Hattori, Tetsuya Hayashi, Michiel Kleerebezem, Ken Kurokawa, Marion Leclerc, Florence Levenez, Chaysavanh Manichanh, H. Bjorn Nielsen, Trine Nielsen, Nicolas Pons, Julie Poulain, Junjie Qin, Thomas Sicheritz-Ponten, Sebastian Tims, David Torrents, Edgardo Ugarte, Erwin G. Zoetendal, JunWang, Francisco Guarner, Oluf Pedersen, Willem M. de Vos, Soren Brunak, Joel Dore, Jean Weissenbach, S. Dusko Ehrlich, Peer Bork, Karsten Kristiansen

    NATURE   474 ( 7353 )   2011.6

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  • Analysis of atom transformation patterns in enzymatic reactions based on the comparison of chemical compound structures

    HATTORI Masahiro, YAMADA Takuji, OH Min-A, GOTO Susumu, KANEHISA Minoru

    IPSJ SIG technical reports   2005 ( 128 )   21 - 25   2005.12

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    After calculating the atom alignment between two chemical compounds, we can elucidate three types of informative atoms through enzymatic reactions, (i) atoms which don't change their physicochemical properties, (ii) atoms which can be changed by addition or deletion, and (iii) atoms which locate between two former parts and seem to be the reaction centers. We have annotated those atom transformation patterns for each enzymatic reaction and developed the RPAIR database in KEGG Based on these data, here, we analyzed the continuous chemical reaction module along metabolic pathways and demonstrated the distribution of such atom transformation patters found in degradation pathways.

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    Other Link: http://id.nii.ac.jp/1001/00059079/

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  • 運動と食生活による前立腺癌の増殖制御の解明と革新的ながん予防への展開

    Grant number:25K02772  2025.4 - 2028.3

    日本学術振興会  科学研究費助成事業  基盤研究(B)

    波多野 浩士, 森井 英一, 山田 拓司, 谷内田 真一, 野々村 祝夫, 松下 慎, 藤田 和利, 林 拓自, 岡 利樹, 岡田 随象, 中村 昇太, 谷 優

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    Grant amount:\18850000 ( Direct Cost: \14500000 、 Indirect Cost:\4350000 )

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  • Platform for Advanced Genome Science

    Grant number:22H04925  2022.4 - 2028.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Transformative Research Areas (platforms for Advanced Technologies and Research Resources)

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    Grant amount:\7732140000 ( Direct Cost: \5947800000 、 Indirect Cost:\1784340000 )

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  • 遺伝的素因、生活習慣、腸内細菌叢の多面的解析に基づく前立腺癌の早期診断戦略の構築

    Grant number:22H03212  2022.4 - 2026.3

    日本学術振興会  科学研究費助成事業  基盤研究(B)

    野々村 祝夫, 柴 知史, 山田 拓司, 谷内田 真一, 松下 慎, 藤田 和利, 波多野 浩士, 岡田 随象, 中村 昇太

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    Grant amount:\17290000 ( Direct Cost: \13300000 、 Indirect Cost:\3990000 )

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  • Diagnostic strategy for prostate cancer based on multifaceted analyses of genetic background, life style and gut microbiome

    Grant number:23K24471  2022.4 - 2026.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (B)

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    Grant amount:\17290000 ( Direct Cost: \13300000 、 Indirect Cost:\3990000 )

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  • 先進ゲノム解析研究推進プラットフォーム

    Grant number:16H06279  2016 - 2021

    日本学術振興会  科学研究費助成事業  新学術領域研究(研究領域提案型)『学術研究支援基盤形成』

    小原 雄治, 加藤 和人, 川嶋 実苗, 豊田 敦, 鈴木 穣, 三井 純, 林 哲也, 時野 隆至, 黒川 顕, 中村 保一, 野口 英樹, 高木 利久, 岩崎 渉, 森下 真一, 浅井 潔, 笠原 雅弘, 伊藤 武彦, 山田 拓司, 小椋 義俊, 久原 哲, 高橋 弘喜, 瀬々 潤, 榊原 康文

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    Grant amount:\7698340000 ( Direct Cost: \5921800000 、 Indirect Cost:\1776540000 )

    ①総括支援活動では、応募の機会増加の要望に応えるため今年度から年2回の公募とした。その結果、合計466の応募課題があり、207課題(44%)を採択した。コロナ禍の影響の中、昨年度より応募数は100件近く増加したが、支援内容の精査や支援経費の限度額設定等により、40%超の採択率を維持した。審査委員はすべてプラットフォーム外の専門家とし、評価が同程度の場合は若手、女性、少額科研費からの課題、初めての応募課題を優先した。支援課題は科研費生物系のほぼすべての分野に渡っており、支援の成果を含む論文として2020年度に161報が発表された。この中には「単核貪食細胞系の分化における遺伝子発現制御機構の包括的解明」(Nature Immunol.)、「キンギョの変異体の表現型多様性を作り上げる分子機構の理解」(Current Biol.)、「植物二次代謝経路のゲノム進化に学ぶ生合成デザイン」(Nature Comm.)など広い分野でのレベルの高い成果が含まれている。拡大班会議や情報解析講習会はオンサイト開催が必要なためにコロナ禍の中で見送ったが、WEB開催としたヒトゲノム研究倫理を考える会は5回開催し、各回約500名が参加した。
    ②大規模配列解析拠点ネットワーク支援活動においては、最先端技術を支援に提供するとともに、染色体レベルの高精度ゲノム配列決定、シングルセル・空間遺伝子発現解析等の支援技術高度化を進めた。
    ③高度情報解析支援ネットワーク活動では、支援から浮かび上がった課題を解決するソフトウェアの開発を進め、実際の課題への適用を進めた。2020年度には、超高速相同性検索ソフトウェアPZLASTの開発、Hi-Cデータを使ったゲノムアセンブリソフトウエア、ロングリードシミュレータPBSIM2の開発などを進め、②と合わせて24報の論文を発表した。

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  • Changes of intestinal microbiome of preterm labor cases and endometriosis cases by metagenome analysis.

    Grant number:26670717  2014.4 - 2017.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Challenging Exploratory Research

    SAITO Shigeru

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    Grant amount:\3640000 ( Direct Cost: \2800000 、 Indirect Cost:\840000 )

    Preterm delivery and endometriosis are classified to inflammatory diseases. Recent data demonstrate that the changes of intestinal flora are correlated with inflammatory diseases by affecting immune system. Therefore, we have studied the metagenome profile in preterm labor cases and endometriosis cases. We have not found significant changes in intestinal flora, but abundance of Escherichia/Shigella was found in some preterm labor cases, and abundance of Meganonas and decreased Parabacteroides were found in some endometriosis cases. We should clarified the relationship between patients conditions and abnormality of intestinal flora.

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  • Understanding metabolic systems for human gut microbiome

    Grant number:25710016  2013.4 - 2016.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Young Scientists (A)

    Yamada Takuji

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    Grant amount:\25870000 ( Direct Cost: \19900000 、 Indirect Cost:\5970000 )

    Human gut harbors millions of microbiome, and their functional ability have wide diversity. Most of related works are based on KEGG database for their functional annotation, however, most of functional modules are not well known.
    Here we developed the database for gut microbiome, called as “enteropathway”, allows researchers uncover functionality of gut microbiome more clearly. For example, we suggested few modules have high diversity across 1000 individuals, showing the diverse metabolic potential. In addition, these novel defined modules are under represented in Obesity patients comparing with healthy individuals.

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  • 真菌類ゲノムからの新規酵素遺伝子発見

    Grant number:25108708  2013.4 - 2015.3

    日本学術振興会  科学研究費助成事業  新学術領域研究(研究領域提案型)

    山田 拓司

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    Grant amount:\7020000 ( Direct Cost: \5400000 、 Indirect Cost:\1620000 )

    本研究では真菌類ゲノムを用いて、遺伝子が未定義の酵素反応に対する遺伝子配列を明らかにしていくことを目的としている。代表者らは先行研究において、微生物ゲノムを用い100種類以上の遺伝子未知酵素反応について対応する遺伝子を計算機的に予測し、2例については実験的にその酵素活性を実証している。真核生物に関しては遺伝子未知の代謝反応が数多く報告されているにもかかわらず、遺伝子のゲノム上の位置関係とそれらの遺伝子機能類似性に相関がないために上記の手法を利用することができなかった。本研究計画の目的はオーファン酵素の遺伝子配列を真菌ゲノムを利用して発見することである。本研究でこれらの遺伝子が明らかになれば、これまで機能の存在すらわからなかった酵素反応機構を大規模な配列類似性検索で予測することが可能になり、昨今のデータ解析の時代において、非常に大きな前進になることは間違いない。本研究ではそこで開発した解析パイプラインを活用し、真菌類に用いるために改良した。
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    真菌類においては遺伝子がオペロン構造を取る例がほとんどないため、遺伝子のゲノム上の隣接関係を利用することが困難である。しかしながら遺伝子系統プロファイル類似度などのパラメーターを利用することで原核生物種にたいする予測パイプラインと同様に、真菌類に対しても80%以上の正答率でオーファン酵素に対する遺伝子配列を予測することが可能となり、現在報告論文を準備中である。また、本遺伝子予測パイプラインの一部であるドメインを利用した機能アノテーションについては論文として報告している。ここでは特定の酵素反応に特的に現れるドメイン構造をデータベース化しており、そのドメイン構造から遺伝子予測を行うパイプラインである。

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