TY - JOUR
T1 - Modeling spatial interaction networks of the gut microbiota
AU - Cao, Xiaocang
AU - Dong, Ang
AU - Kang, Guangbo
AU - Wang, Xiaoli
AU - Duan, Liyun
AU - Hou, Huixing
AU - Zhao, Tianming
AU - Wu, Shuang
AU - Liu, Xinjuan
AU - Huang, He
AU - Wu, Rongling
N1 - Funding Information:
This work was supported by grants from National Key Research and Development Project (No. 2019YFA0905600), Science and Technology Program of Tianjin, China (No. 19YFSLQY00110), and the National Natural Science Foundation of China (82070559). We specially thank our colleague Jing Feng from the Department of Respiratory and Critical Care Medicine for his important advice. We appreciate Jun He from Jiangsu Vedkang Medical Science & Technology Co., Ltd for technology support. We are grateful to our colleagues Li Liang, Lin Fang, Fengying Tian, Lu Xiao, Ying Li, Yan Wang, Ting Li, Xuele Lu, Qi Zhang, Xinyao Zhao (Department of Gastroenterology and Hepatology Endoscopy Center) and Wenjing Song (Department of Pathology), Xin Zhao (Department of Radiology) for their professional help. We sincerely thank the patients and their family for their support and dedication.
Publisher Copyright:
© 2022 The Author(s). Published with license by Taylor & Francis Group, LLC.
PY - 2022
Y1 - 2022
N2 - How the gut microbiota is organized across space is postulated to influence microbial succession and its mutualistic relationships with the host. The lack of dynamic or perturbed abundance data poses considerable challenges for characterizing the spatial pattern of microbial interactions. We integrate allometric scaling theory, evolutionary game theory, and prey-predator theory into a unified framework under which quasi-dynamic microbial networks can be inferred from static abundance data. We illustrate that such networks can capture the full properties of microbial interactions, including causality, the sign of the causality, strength, and feedback loop, and are dynamically adaptive along spatial gradients, and context-specific, characterizing variability between individuals and within the same individual across time and space. We design and conduct a gut microbiota study to validate the model, characterizing key spatial determinants of the microbial differences between ulcerative colitis and healthy controls. Our model provides a sophisticated means of unraveling a complete atlas of how microbial interactions vary across space and quantifying causal relationships between such spatial variability and change in health state.
AB - How the gut microbiota is organized across space is postulated to influence microbial succession and its mutualistic relationships with the host. The lack of dynamic or perturbed abundance data poses considerable challenges for characterizing the spatial pattern of microbial interactions. We integrate allometric scaling theory, evolutionary game theory, and prey-predator theory into a unified framework under which quasi-dynamic microbial networks can be inferred from static abundance data. We illustrate that such networks can capture the full properties of microbial interactions, including causality, the sign of the causality, strength, and feedback loop, and are dynamically adaptive along spatial gradients, and context-specific, characterizing variability between individuals and within the same individual across time and space. We design and conduct a gut microbiota study to validate the model, characterizing key spatial determinants of the microbial differences between ulcerative colitis and healthy controls. Our model provides a sophisticated means of unraveling a complete atlas of how microbial interactions vary across space and quantifying causal relationships between such spatial variability and change in health state.
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U2 - 10.1080/19490976.2022.2106103
DO - 10.1080/19490976.2022.2106103
M3 - Article
C2 - 35921525
AN - SCOPUS:85135501128
SN - 1949-0976
VL - 14
JO - Gut Microbes
JF - Gut Microbes
IS - 1
M1 - 2106103
ER -