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Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet

Teleost omnivorous fish that coexist partially sharing resources are likely to modify their gut traits and microbiome as a feedback mechanism between ecological processes and evolution. However, we do not understand how the core gut microbiome supports the metabolic capacity of the host and regulate...

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Autores principales: Liu, Yaqiu, Li, Xinhui, Li, Yuefei, Li, Jie, Zhu, Shuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396210/
https://www.ncbi.nlm.nih.gov/pubmed/36016786
http://dx.doi.org/10.3389/fmicb.2022.936601
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author Liu, Yaqiu
Li, Xinhui
Li, Yuefei
Li, Jie
Zhu, Shuli
author_facet Liu, Yaqiu
Li, Xinhui
Li, Yuefei
Li, Jie
Zhu, Shuli
author_sort Liu, Yaqiu
collection PubMed
description Teleost omnivorous fish that coexist partially sharing resources are likely to modify their gut traits and microbiome as a feedback mechanism between ecological processes and evolution. However, we do not understand how the core gut microbiome supports the metabolic capacity of the host and regulates digestive functions in specialized omnivorous fish gut traits. Therefore, we evaluated the gut microbiome of eight omnivorous fish from a single family (i.e., Cyprinidae) in the current study. We examined the correlation between host phylogeny, diet composition, and intestinal morphological traits related to the intestinal microbiome. The results indicated that cyprinid fish with similar relative gut lengths had considerable gut microbiome similarity. Notably, the SL (short relative gut length) group, as zoobenthos and zooplankton specialists, was abundant in Proteobacteria and was less abundant in Firmicutes than in the ML (medium relative gut length) and LL (long relative gut length) groups. These fish could extract nutrients from aquatic plants and algae. Additionally, we found the relative abundance of Clostridium and Romboutsia to be positively correlated with host relative gut length but negatively correlated with the relative abundance of Cetobacterium, Plesiomonas, Bacteroides, and Lactobacillus, and host-relative gut length. We also show a positive linear relationship between host gut microbiome carbohydrate metabolism and relative gut length, while the amino acid and lipid metabolism of the gut microbiome was negatively correlated with host-relative gut length. In addition, omnivorous species competing for resources improve their ecological adaptability through the specialization of gut length, which is closely related to variation in the synergy of the gut microbiome. Above all, specialized gut microbiota and associated gut morphologies enable fish to variably tolerate resource fluctuation and improve the utilization efficiency of nutrient extraction from challenging food resources.
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spelling pubmed-93962102022-08-24 Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet Liu, Yaqiu Li, Xinhui Li, Yuefei Li, Jie Zhu, Shuli Front Microbiol Microbiology Teleost omnivorous fish that coexist partially sharing resources are likely to modify their gut traits and microbiome as a feedback mechanism between ecological processes and evolution. However, we do not understand how the core gut microbiome supports the metabolic capacity of the host and regulates digestive functions in specialized omnivorous fish gut traits. Therefore, we evaluated the gut microbiome of eight omnivorous fish from a single family (i.e., Cyprinidae) in the current study. We examined the correlation between host phylogeny, diet composition, and intestinal morphological traits related to the intestinal microbiome. The results indicated that cyprinid fish with similar relative gut lengths had considerable gut microbiome similarity. Notably, the SL (short relative gut length) group, as zoobenthos and zooplankton specialists, was abundant in Proteobacteria and was less abundant in Firmicutes than in the ML (medium relative gut length) and LL (long relative gut length) groups. These fish could extract nutrients from aquatic plants and algae. Additionally, we found the relative abundance of Clostridium and Romboutsia to be positively correlated with host relative gut length but negatively correlated with the relative abundance of Cetobacterium, Plesiomonas, Bacteroides, and Lactobacillus, and host-relative gut length. We also show a positive linear relationship between host gut microbiome carbohydrate metabolism and relative gut length, while the amino acid and lipid metabolism of the gut microbiome was negatively correlated with host-relative gut length. In addition, omnivorous species competing for resources improve their ecological adaptability through the specialization of gut length, which is closely related to variation in the synergy of the gut microbiome. Above all, specialized gut microbiota and associated gut morphologies enable fish to variably tolerate resource fluctuation and improve the utilization efficiency of nutrient extraction from challenging food resources. Frontiers Media S.A. 2022-08-09 /pmc/articles/PMC9396210/ /pubmed/36016786 http://dx.doi.org/10.3389/fmicb.2022.936601 Text en Copyright © 2022 Liu, Li, Li, Li and Zhu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Liu, Yaqiu
Li, Xinhui
Li, Yuefei
Li, Jie
Zhu, Shuli
Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet
title Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet
title_full Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet
title_fullStr Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet
title_full_unstemmed Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet
title_short Gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet
title_sort gut microbiomes of cyprinid fish exhibit host-species symbiosis along gut trait and diet
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396210/
https://www.ncbi.nlm.nih.gov/pubmed/36016786
http://dx.doi.org/10.3389/fmicb.2022.936601
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