Understanding Horizontal Gene Transfer network in human gut microbiota

Abstract Background Horizontal Gene Transfer (HGT) is the process of transferring genetic materials between species. Through sharing genetic materials, microorganisms in the human microbiota form a network. The network can provide insights into understanding the microbiota. Here, we constructed the...

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Main Authors: Chen Li, Jiaxing Chen, Shuai Cheng Li
Format: Article
Language:English
Published: BMC 2020-07-01
Series:Gut Pathogens
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13099-020-00370-9
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spelling doaj-76c20adc5441427a8f489cf4dfc9c3d22020-11-25T03:02:39ZengBMCGut Pathogens1757-47492020-07-0112112010.1186/s13099-020-00370-9Understanding Horizontal Gene Transfer network in human gut microbiotaChen Li0Jiaxing Chen1Shuai Cheng Li2Department of Computer Science, City University of Hong KongDepartment of Computer Science, City University of Hong KongDepartment of Computer Science, City University of Hong KongAbstract Background Horizontal Gene Transfer (HGT) is the process of transferring genetic materials between species. Through sharing genetic materials, microorganisms in the human microbiota form a network. The network can provide insights into understanding the microbiota. Here, we constructed the HGT networks from the gut microbiota sequencing data and performed network analysis to characterize the HGT networks of gut microbiota. Results We constructed the HGT network and perform the network analysis to two typical gut microbiota datasets, a 283-sample dataset of Mother-to-Child and a 148-sample dataset of longitudinal inflammatory bowel disease (IBD) metagenome. The results indicated that (1) the HGT networks are scale-free. (2) The networks expand their complexities, sizes, and edge numbers, accompanying the early stage of lives; and microbiota established in children shared high similarity as their mother (p-value = 0.0138), supporting the transmission of microbiota from mother to child. (3) Groups harbor group-specific network edges, and network communities, which can potentially serve as biomarkers. For instances, IBD patient group harbors highly abundant communities of Proteobacteria (p-value = 0.0194) and Actinobacteria (p-value = 0.0316); children host highly abundant communities of Proteobacteria (p-value = 2.8785 $$e^{-5}$$ e - 5 ) and Actinobacteria (p-value = 0.0015), and the mothers host highly abundant communities of Firmicutes (p-value = 8.0091 $$e^{-7}$$ e - 7 ). IBD patient networks contain more HGT edges in pathogenic genus, including Mycobacterium, Sutterella, and Pseudomonas. Children’s networks contain more edges from Bifidobacterium and Escherichia. Conclusion Hence, we proposed the HGT network constructions from the gut microbiota sequencing data. The HGT networks capture the host state and the response of microbiota to the environmental and host changes, and they are essential to understand the human microbiota.http://link.springer.com/article/10.1186/s13099-020-00370-9HGT networkScale freeVon Newman entropyNetwork evolvingCommunity analysis
collection DOAJ
language English
format Article
sources DOAJ
author Chen Li
Jiaxing Chen
Shuai Cheng Li
spellingShingle Chen Li
Jiaxing Chen
Shuai Cheng Li
Understanding Horizontal Gene Transfer network in human gut microbiota
Gut Pathogens
HGT network
Scale free
Von Newman entropy
Network evolving
Community analysis
author_facet Chen Li
Jiaxing Chen
Shuai Cheng Li
author_sort Chen Li
title Understanding Horizontal Gene Transfer network in human gut microbiota
title_short Understanding Horizontal Gene Transfer network in human gut microbiota
title_full Understanding Horizontal Gene Transfer network in human gut microbiota
title_fullStr Understanding Horizontal Gene Transfer network in human gut microbiota
title_full_unstemmed Understanding Horizontal Gene Transfer network in human gut microbiota
title_sort understanding horizontal gene transfer network in human gut microbiota
publisher BMC
series Gut Pathogens
issn 1757-4749
publishDate 2020-07-01
description Abstract Background Horizontal Gene Transfer (HGT) is the process of transferring genetic materials between species. Through sharing genetic materials, microorganisms in the human microbiota form a network. The network can provide insights into understanding the microbiota. Here, we constructed the HGT networks from the gut microbiota sequencing data and performed network analysis to characterize the HGT networks of gut microbiota. Results We constructed the HGT network and perform the network analysis to two typical gut microbiota datasets, a 283-sample dataset of Mother-to-Child and a 148-sample dataset of longitudinal inflammatory bowel disease (IBD) metagenome. The results indicated that (1) the HGT networks are scale-free. (2) The networks expand their complexities, sizes, and edge numbers, accompanying the early stage of lives; and microbiota established in children shared high similarity as their mother (p-value = 0.0138), supporting the transmission of microbiota from mother to child. (3) Groups harbor group-specific network edges, and network communities, which can potentially serve as biomarkers. For instances, IBD patient group harbors highly abundant communities of Proteobacteria (p-value = 0.0194) and Actinobacteria (p-value = 0.0316); children host highly abundant communities of Proteobacteria (p-value = 2.8785 $$e^{-5}$$ e - 5 ) and Actinobacteria (p-value = 0.0015), and the mothers host highly abundant communities of Firmicutes (p-value = 8.0091 $$e^{-7}$$ e - 7 ). IBD patient networks contain more HGT edges in pathogenic genus, including Mycobacterium, Sutterella, and Pseudomonas. Children’s networks contain more edges from Bifidobacterium and Escherichia. Conclusion Hence, we proposed the HGT network constructions from the gut microbiota sequencing data. The HGT networks capture the host state and the response of microbiota to the environmental and host changes, and they are essential to understand the human microbiota.
topic HGT network
Scale free
Von Newman entropy
Network evolving
Community analysis
url http://link.springer.com/article/10.1186/s13099-020-00370-9
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