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PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation

BACKGROUND: The gut microbiota play important roles in host adaptation and evolution, but are understudied in natural population of wild mammals. To address host adaptive evolution and improve conservation efforts of threatened mammals from a metagenomic perspective, we established a high-quality gu...

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Autores principales: Huang, Guangping, Shi, Wenyu, Wang, Le, Qu, Qingyue, Zuo, Zhenqiang, Wang, Jinfeng, Zhao, Fangqing, Wei, Fuwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559513/
https://www.ncbi.nlm.nih.gov/pubmed/37805557
http://dx.doi.org/10.1186/s40168-023-01657-0
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author Huang, Guangping
Shi, Wenyu
Wang, Le
Qu, Qingyue
Zuo, Zhenqiang
Wang, Jinfeng
Zhao, Fangqing
Wei, Fuwen
author_facet Huang, Guangping
Shi, Wenyu
Wang, Le
Qu, Qingyue
Zuo, Zhenqiang
Wang, Jinfeng
Zhao, Fangqing
Wei, Fuwen
author_sort Huang, Guangping
collection PubMed
description BACKGROUND: The gut microbiota play important roles in host adaptation and evolution, but are understudied in natural population of wild mammals. To address host adaptive evolution and improve conservation efforts of threatened mammals from a metagenomic perspective, we established a high-quality gut microbiome catalog of the giant panda (pandaGUT) to resolve the microbiome diversity, functional, and resistome landscapes using approximately 7 Tbp of long- and short-read sequencing data from 439 stool samples. RESULTS: The pandaGUT catalog comprises 820 metagenome-assembled genomes, including 40 complete closed genomes, and 64.5% of which belong to species that have not been previously reported, greatly expanding the coverage of most prokaryotic lineages. The catalog contains 2.37 million unique genes, with 74.8% possessing complete open read frames, facilitating future mining of microbial functional potential. We identified three microbial enterotypes across wild and captive panda populations characterized by Clostridium, Pseudomonas, and Escherichia, respectively. We found that wild pandas exhibited host genetic-specific microbial structures and functions, suggesting host-gut microbiota phylosymbiosis, while the captive cohorts encoded more multi-drug resistance genes. CONCLUSIONS: Our study provides largely untapped resources for biochemical and biotechnological applications as well as potential intervention avenues via the rational manipulation of microbial diversity and reducing antibiotic usage for future conservation management of wildlife. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01657-0.
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spelling pubmed-105595132023-10-08 PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation Huang, Guangping Shi, Wenyu Wang, Le Qu, Qingyue Zuo, Zhenqiang Wang, Jinfeng Zhao, Fangqing Wei, Fuwen Microbiome Research BACKGROUND: The gut microbiota play important roles in host adaptation and evolution, but are understudied in natural population of wild mammals. To address host adaptive evolution and improve conservation efforts of threatened mammals from a metagenomic perspective, we established a high-quality gut microbiome catalog of the giant panda (pandaGUT) to resolve the microbiome diversity, functional, and resistome landscapes using approximately 7 Tbp of long- and short-read sequencing data from 439 stool samples. RESULTS: The pandaGUT catalog comprises 820 metagenome-assembled genomes, including 40 complete closed genomes, and 64.5% of which belong to species that have not been previously reported, greatly expanding the coverage of most prokaryotic lineages. The catalog contains 2.37 million unique genes, with 74.8% possessing complete open read frames, facilitating future mining of microbial functional potential. We identified three microbial enterotypes across wild and captive panda populations characterized by Clostridium, Pseudomonas, and Escherichia, respectively. We found that wild pandas exhibited host genetic-specific microbial structures and functions, suggesting host-gut microbiota phylosymbiosis, while the captive cohorts encoded more multi-drug resistance genes. CONCLUSIONS: Our study provides largely untapped resources for biochemical and biotechnological applications as well as potential intervention avenues via the rational manipulation of microbial diversity and reducing antibiotic usage for future conservation management of wildlife. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01657-0. BioMed Central 2023-10-07 /pmc/articles/PMC10559513/ /pubmed/37805557 http://dx.doi.org/10.1186/s40168-023-01657-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Huang, Guangping
Shi, Wenyu
Wang, Le
Qu, Qingyue
Zuo, Zhenqiang
Wang, Jinfeng
Zhao, Fangqing
Wei, Fuwen
PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation
title PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation
title_full PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation
title_fullStr PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation
title_full_unstemmed PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation
title_short PandaGUT provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation
title_sort pandagut provides new insights into bacterial diversity, function, and resistome landscapes with implications for conservation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559513/
https://www.ncbi.nlm.nih.gov/pubmed/37805557
http://dx.doi.org/10.1186/s40168-023-01657-0
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