4.8 Article

Insights into the roles of fungi and protist in the giant panda gut microbiome and antibiotic resistome

期刊

ENVIRONMENT INTERNATIONAL
卷 155, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.envint.2021.106703

关键词

Fungi; Protist; Antibiotic resistance genes; Network analysis; Multitrophic communities; Neutral model

资金

  1. National Natural Science Foundation of China [42077216, 42090063, 42071279]
  2. Innovative Team Foundation of China West Normal University [CXTD20202]

向作者/读者索取更多资源

This study reveals the presence of diverse protists in the giant panda gut microbiome, with their population abundance closely related to the age and diet of the pandas. Diet plays a key role in driving variation in antibiotic resistance genes in the giant panda gut microbiome.
The mammal gut is a rich reservoir of antibiotic resistance genes (ARGs), and the relationship between bacterial communities and ARGs has been widely studied. Despite ecological significance of microeukaryotes (fungi and protists), our understanding of their roles in the mammal gut microbiome and antibiotic resistome is still limited. Here, we used amplicon sequencing, metagenomic sequencing and high-throughput quantitative PCR to examine microbiomes and antibiotic resistomes of 41 giant panda fecal samples from individuals with different genders, ages, sampling sites and diet. Our results show that diverse protists inhabit in the giant panda gut ecosystem, dominated by consumers. Higher abundance of protistan consumers was detected in the elder compared to subadult and adult giant pandas. Diet is the main driving factor of variation in ARGs in the giant panda gut microbiome. Weighted correlation network analysis identified two key microbial modules from multitrophic communities, which all contributed to the variation in ARGs in the giant panda gut. Protists occupied an important position in the two modules which were dominated by fungal taxa. Deterministic processes made a more important contribution to microbial community assembly of the two modules than to bacterial, fungal and protistan communities. This study sheds new light on how key microbial modules contribute to the variation in ARGs, which is crucial in understanding dynamics of antibiotic resistome in the mammal gut, particularly endangered species.

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