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Hybridization altered the gut microbiota of pigs

Mammalian gut microbiota plays an important role in the host’s nutrient metabolism, growth, and immune regulation. Hybridization can enable a progeny to acquire superior traits of the parents, resulting in the hybridization advantage. However, studies on the effects of hybridization on the pigs’ gut...

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Autores principales: Wei, Limin, Zeng, Bo, Zhang, Siyuan, Guo, Wei, Li, Feng, Zhao, Jiangchao, Li, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350513/
https://www.ncbi.nlm.nih.gov/pubmed/37465027
http://dx.doi.org/10.3389/fmicb.2023.1177947
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author Wei, Limin
Zeng, Bo
Zhang, Siyuan
Guo, Wei
Li, Feng
Zhao, Jiangchao
Li, Ying
author_facet Wei, Limin
Zeng, Bo
Zhang, Siyuan
Guo, Wei
Li, Feng
Zhao, Jiangchao
Li, Ying
author_sort Wei, Limin
collection PubMed
description Mammalian gut microbiota plays an important role in the host’s nutrient metabolism, growth, and immune regulation. Hybridization can enable a progeny to acquire superior traits of the parents, resulting in the hybridization advantage. However, studies on the effects of hybridization on the pigs’ gut microbiota are lacking. Therefore, this study used multi-omics technologies to compare and analyze the gut microbiota of the primary wild boar and its offspring. The 16S rRNA gene sequencing results revealed that the gut microbiota of F4 exhibited a host-like dominance phenomenon with a significant increase in the abundance of Lactobacillus and Bifidobacterium. The beta diversity of Duroc was significantly different from those of F0, F2, and F4; after the host hybridization, the similarity of the beta diversity in the progeny decreased with the decrease in the similarity of the F0 lineage. The metagenomic sequencing results showed that the significantly enriched metabolic pathways in F4, such as environmental, circulatory system, fatty acid degradation adaptation, and fatty acid biosynthesis, were similar to those in F0. Moreover, it also exhibited similar significantly enriched metabolic pathways as those in Duroc, such as carbohydrate metabolism, starch and sucrose metabolism, starch-degrading CAZymes, lactose-degrading CAZymes, and various amino acid metabolism pathways. However, the alpha-amylase-related KOs, lipid metabolism, and galactose metabolism in F4 were significantly higher than those in Duroc and F0. Non-targeted metabolome technology analysis found that several metabolites, such as docosahexaenoic acid, arachidonic acid, and citric acid were significantly enriched in the F4 pigs as compared to those in F0. Based on Spearman correlation analysis, Lactobacillus and Bifidobacterium were significantly positively correlated with these metabolites. Finally, the combined metagenomic and metabolomic analysis suggested that the metabolic pathways, such as valine, leucine, and isoleucine biosynthesis and alanine aspartate and glutamate metabolism were significantly enriched in F4 pigs. In conclusion, the gut microbiota of F4 showed a similar host “dominance” phenomenon, which provided reference data for the genetics and evolution of microbiota and the theory of microbial-assisted breeding.
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spelling pubmed-103505132023-07-18 Hybridization altered the gut microbiota of pigs Wei, Limin Zeng, Bo Zhang, Siyuan Guo, Wei Li, Feng Zhao, Jiangchao Li, Ying Front Microbiol Microbiology Mammalian gut microbiota plays an important role in the host’s nutrient metabolism, growth, and immune regulation. Hybridization can enable a progeny to acquire superior traits of the parents, resulting in the hybridization advantage. However, studies on the effects of hybridization on the pigs’ gut microbiota are lacking. Therefore, this study used multi-omics technologies to compare and analyze the gut microbiota of the primary wild boar and its offspring. The 16S rRNA gene sequencing results revealed that the gut microbiota of F4 exhibited a host-like dominance phenomenon with a significant increase in the abundance of Lactobacillus and Bifidobacterium. The beta diversity of Duroc was significantly different from those of F0, F2, and F4; after the host hybridization, the similarity of the beta diversity in the progeny decreased with the decrease in the similarity of the F0 lineage. The metagenomic sequencing results showed that the significantly enriched metabolic pathways in F4, such as environmental, circulatory system, fatty acid degradation adaptation, and fatty acid biosynthesis, were similar to those in F0. Moreover, it also exhibited similar significantly enriched metabolic pathways as those in Duroc, such as carbohydrate metabolism, starch and sucrose metabolism, starch-degrading CAZymes, lactose-degrading CAZymes, and various amino acid metabolism pathways. However, the alpha-amylase-related KOs, lipid metabolism, and galactose metabolism in F4 were significantly higher than those in Duroc and F0. Non-targeted metabolome technology analysis found that several metabolites, such as docosahexaenoic acid, arachidonic acid, and citric acid were significantly enriched in the F4 pigs as compared to those in F0. Based on Spearman correlation analysis, Lactobacillus and Bifidobacterium were significantly positively correlated with these metabolites. Finally, the combined metagenomic and metabolomic analysis suggested that the metabolic pathways, such as valine, leucine, and isoleucine biosynthesis and alanine aspartate and glutamate metabolism were significantly enriched in F4 pigs. In conclusion, the gut microbiota of F4 showed a similar host “dominance” phenomenon, which provided reference data for the genetics and evolution of microbiota and the theory of microbial-assisted breeding. Frontiers Media S.A. 2023-07-03 /pmc/articles/PMC10350513/ /pubmed/37465027 http://dx.doi.org/10.3389/fmicb.2023.1177947 Text en Copyright © 2023 Wei, Zeng, Zhang, Guo, Li, Zhao and Li. 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
Wei, Limin
Zeng, Bo
Zhang, Siyuan
Guo, Wei
Li, Feng
Zhao, Jiangchao
Li, Ying
Hybridization altered the gut microbiota of pigs
title Hybridization altered the gut microbiota of pigs
title_full Hybridization altered the gut microbiota of pigs
title_fullStr Hybridization altered the gut microbiota of pigs
title_full_unstemmed Hybridization altered the gut microbiota of pigs
title_short Hybridization altered the gut microbiota of pigs
title_sort hybridization altered the gut microbiota of pigs
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350513/
https://www.ncbi.nlm.nih.gov/pubmed/37465027
http://dx.doi.org/10.3389/fmicb.2023.1177947
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