Molecular trafficking between bacteria determines the shape of gut microbial community
Complex inter-bacterial interactions largely influence the structure and function of the gut microbial community. Though several host-associated phenomena have often been shown to be involved in the stability, structure, and function of the gut microbial community, the implication of contact-depende...
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Online Access: | http://dx.doi.org/10.1080/19490976.2021.1959841 |
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doaj-2a276e8cd47a41258c706d921cccf3212021-09-06T14:06:26ZengTaylor & Francis GroupGut Microbes1949-09761949-09842021-01-0113110.1080/19490976.2021.19598411959841Molecular trafficking between bacteria determines the shape of gut microbial communitySeenivasan Boopathi0Danrui Liu1Ai-Qun Jia2School of Life and Pharmaceutical Sciences, Key Laboratory of Tropical Biological Resources of Ministry Education, State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan UniversitySchool of Life and Pharmaceutical Sciences, Key Laboratory of Tropical Biological Resources of Ministry Education, State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan UniversitySchool of Life and Pharmaceutical Sciences, Key Laboratory of Tropical Biological Resources of Ministry Education, State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan UniversityComplex inter-bacterial interactions largely influence the structure and function of the gut microbial community. Though several host-associated phenomena have often been shown to be involved in the stability, structure, and function of the gut microbial community, the implication of contact-dependent and contact-independent inter-bacterial interactions has been overlooked. Such interactions are tightly governed at multiple layers through several extracellular organelles, including contact-dependent inhibition (CDI), nanotubes, type VI secretion system (T6SS), and membrane vesicles (MVs). Recent advancements in molecular techniques have revealed that such extracellular organelles function beyond exhibiting competitive behavior and are also involved in manifesting cooperative behaviors. Cooperation between bacteria occurs through the sharing of several beneficial molecules including nucleic acids, proteins, metabolites, and nutrients among the members of the community, while competition occurs by means of multiple toxins. Intrinsic coordination between contact-dependent and contact-independent mechanisms collectively provides a fitness advantage and increased colonization resistance to the gut microbiota, where molecular trafficking plays a key role. This review is intended to provide a comprehensive view of the salient features of the different bacterial interactions and to highlight how microbiota deploy multifaceted organelles, for exerting both cooperative and competitive behaviors. We discuss the current knowledge of bacterial molecular trafficking and its impact on shaping the gut microbial community.http://dx.doi.org/10.1080/19490976.2021.1959841microbiotacontact-dependent interactionnanotubesquorum sensingsocial behavior |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Seenivasan Boopathi Danrui Liu Ai-Qun Jia |
spellingShingle |
Seenivasan Boopathi Danrui Liu Ai-Qun Jia Molecular trafficking between bacteria determines the shape of gut microbial community Gut Microbes microbiota contact-dependent interaction nanotubes quorum sensing social behavior |
author_facet |
Seenivasan Boopathi Danrui Liu Ai-Qun Jia |
author_sort |
Seenivasan Boopathi |
title |
Molecular trafficking between bacteria determines the shape of gut microbial community |
title_short |
Molecular trafficking between bacteria determines the shape of gut microbial community |
title_full |
Molecular trafficking between bacteria determines the shape of gut microbial community |
title_fullStr |
Molecular trafficking between bacteria determines the shape of gut microbial community |
title_full_unstemmed |
Molecular trafficking between bacteria determines the shape of gut microbial community |
title_sort |
molecular trafficking between bacteria determines the shape of gut microbial community |
publisher |
Taylor & Francis Group |
series |
Gut Microbes |
issn |
1949-0976 1949-0984 |
publishDate |
2021-01-01 |
description |
Complex inter-bacterial interactions largely influence the structure and function of the gut microbial community. Though several host-associated phenomena have often been shown to be involved in the stability, structure, and function of the gut microbial community, the implication of contact-dependent and contact-independent inter-bacterial interactions has been overlooked. Such interactions are tightly governed at multiple layers through several extracellular organelles, including contact-dependent inhibition (CDI), nanotubes, type VI secretion system (T6SS), and membrane vesicles (MVs). Recent advancements in molecular techniques have revealed that such extracellular organelles function beyond exhibiting competitive behavior and are also involved in manifesting cooperative behaviors. Cooperation between bacteria occurs through the sharing of several beneficial molecules including nucleic acids, proteins, metabolites, and nutrients among the members of the community, while competition occurs by means of multiple toxins. Intrinsic coordination between contact-dependent and contact-independent mechanisms collectively provides a fitness advantage and increased colonization resistance to the gut microbiota, where molecular trafficking plays a key role. This review is intended to provide a comprehensive view of the salient features of the different bacterial interactions and to highlight how microbiota deploy multifaceted organelles, for exerting both cooperative and competitive behaviors. We discuss the current knowledge of bacterial molecular trafficking and its impact on shaping the gut microbial community. |
topic |
microbiota contact-dependent interaction nanotubes quorum sensing social behavior |
url |
http://dx.doi.org/10.1080/19490976.2021.1959841 |
work_keys_str_mv |
AT seenivasanboopathi moleculartraffickingbetweenbacteriadeterminestheshapeofgutmicrobialcommunity AT danruiliu moleculartraffickingbetweenbacteriadeterminestheshapeofgutmicrobialcommunity AT aiqunjia moleculartraffickingbetweenbacteriadeterminestheshapeofgutmicrobialcommunity |
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1717779253533081600 |