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Diversity of gut microbiomes in marine fishes is shaped by host‐related factors

Microorganisms in the gastrointestinal tract of animals play vital roles in food digestion, homeostasis and immune response regulation. Globally, there are 33,700 fish species, representing almost half of all vertebrate diversity and a wide range of physiologies, ecologies and life histories. To inv...

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Detalles Bibliográficos
Autores principales: Huang, Qi, Sham, Ronia C., Deng, Yu, Mao, Yanping, Wang, Chunxiao, Zhang, Tong, Leung, Kenneth M. Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756402/
https://www.ncbi.nlm.nih.gov/pubmed/33084100
http://dx.doi.org/10.1111/mec.15699
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author Huang, Qi
Sham, Ronia C.
Deng, Yu
Mao, Yanping
Wang, Chunxiao
Zhang, Tong
Leung, Kenneth M. Y.
author_facet Huang, Qi
Sham, Ronia C.
Deng, Yu
Mao, Yanping
Wang, Chunxiao
Zhang, Tong
Leung, Kenneth M. Y.
author_sort Huang, Qi
collection PubMed
description Microorganisms in the gastrointestinal tract of animals play vital roles in food digestion, homeostasis and immune response regulation. Globally, there are 33,700 fish species, representing almost half of all vertebrate diversity and a wide range of physiologies, ecologies and life histories. To investigate gut microbiomes with high coverage, we performed 16S rRNA gene amplicon sequencing with 115 samples of 20 common marine fish species. The fish gut microbiome is a remarkably simple community with low microbial diversity (a maximum of 300 amplicon sequence variants only) and has up to 70% of unknown species in some fish species. The gut microbial community structure was significantly shaped by the combined influence of host‐associated factors, including the fish taxon (p < .001, R(2) = 0.16, ω (2) = 0.04), feeding habit (p < .001, R(2) = 0.06, ω (2) = 0.02) and trophic level (p < .01, R(2) = 0.04, ω (2) = 0.01), although the influence was subtle with a small effect size. The core gut microbiomes of different feeding habits were also previously discovered in animal‐associated and corresponding habitat samples. Certain energy metabolism pathways were enriched in herbivore/omnivore and zooplanktivore/zoobenthivore fishes, whereas lipid metabolism and glycan metabolism were enriched in zoobenthivore/piscivore fishes. Moreover, substantial taxonomic variability was found between the gut microbiomes of fish and animals, indicated by their low degree of shared microbiota. The data and observations reported herein pave the way for further investigations on the co‐evolution of fish gut microbiomes and their hosts, the physiological functions of gut microorganisms and the development of probiotics for improving the nutrition and health of aquaculture fish species.
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spelling pubmed-77564022020-12-28 Diversity of gut microbiomes in marine fishes is shaped by host‐related factors Huang, Qi Sham, Ronia C. Deng, Yu Mao, Yanping Wang, Chunxiao Zhang, Tong Leung, Kenneth M. Y. Mol Ecol ORIGINAL ARTICLES Microorganisms in the gastrointestinal tract of animals play vital roles in food digestion, homeostasis and immune response regulation. Globally, there are 33,700 fish species, representing almost half of all vertebrate diversity and a wide range of physiologies, ecologies and life histories. To investigate gut microbiomes with high coverage, we performed 16S rRNA gene amplicon sequencing with 115 samples of 20 common marine fish species. The fish gut microbiome is a remarkably simple community with low microbial diversity (a maximum of 300 amplicon sequence variants only) and has up to 70% of unknown species in some fish species. The gut microbial community structure was significantly shaped by the combined influence of host‐associated factors, including the fish taxon (p < .001, R(2) = 0.16, ω (2) = 0.04), feeding habit (p < .001, R(2) = 0.06, ω (2) = 0.02) and trophic level (p < .01, R(2) = 0.04, ω (2) = 0.01), although the influence was subtle with a small effect size. The core gut microbiomes of different feeding habits were also previously discovered in animal‐associated and corresponding habitat samples. Certain energy metabolism pathways were enriched in herbivore/omnivore and zooplanktivore/zoobenthivore fishes, whereas lipid metabolism and glycan metabolism were enriched in zoobenthivore/piscivore fishes. Moreover, substantial taxonomic variability was found between the gut microbiomes of fish and animals, indicated by their low degree of shared microbiota. The data and observations reported herein pave the way for further investigations on the co‐evolution of fish gut microbiomes and their hosts, the physiological functions of gut microorganisms and the development of probiotics for improving the nutrition and health of aquaculture fish species. John Wiley and Sons Inc. 2020-11-09 2020-12 /pmc/articles/PMC7756402/ /pubmed/33084100 http://dx.doi.org/10.1111/mec.15699 Text en © 2020 The Authors. Molecular Ecology published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle ORIGINAL ARTICLES
Huang, Qi
Sham, Ronia C.
Deng, Yu
Mao, Yanping
Wang, Chunxiao
Zhang, Tong
Leung, Kenneth M. Y.
Diversity of gut microbiomes in marine fishes is shaped by host‐related factors
title Diversity of gut microbiomes in marine fishes is shaped by host‐related factors
title_full Diversity of gut microbiomes in marine fishes is shaped by host‐related factors
title_fullStr Diversity of gut microbiomes in marine fishes is shaped by host‐related factors
title_full_unstemmed Diversity of gut microbiomes in marine fishes is shaped by host‐related factors
title_short Diversity of gut microbiomes in marine fishes is shaped by host‐related factors
title_sort diversity of gut microbiomes in marine fishes is shaped by host‐related factors
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756402/
https://www.ncbi.nlm.nih.gov/pubmed/33084100
http://dx.doi.org/10.1111/mec.15699
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