野生啮齿动物肠道微生物群中抵抗组、病毒组和活动组的综合基因组目录分析。

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Kai-Meng Shang, He Ma, Hany M Elsheikha, Yong-Jie Wei, Ji-Xin Zhao, Ya Qin, Jian-Ming Li, Zi-Yu Zhao, Xiao-Xuan Zhang
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引用次数: 0

摘要

野生啮齿动物的肠道微生物群是抗生素耐药基因(ARGs)的重要储存库,其中抗菌素耐药细菌与移动遗传元件(MGEs)相互作用以促进水平基因转移。本研究分析了来自野生啮齿动物的12255个肠道细菌基因组,以表征ARGs和毒力因子基因(vfg)的分布,并鉴定其细菌宿主。共鉴定出8119个arg和7626个vfg。最普遍的ARGs产生了对埃famycin的耐药性,其次是与多类抗生素耐药性相关的ARGs。肠杆菌科,特别是大肠杆菌,含有最多数量的ARGs和vfg。观察到MGEs、ARGs和vfg之间存在很强的相关性,突出了抗性和毒力性状的共同选择和动员的潜力。这些发现强调了扩大监测的重要性,以监测和减轻野生啮齿动物向人类和动物种群传播耐药和潜在致病性细菌的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive genome catalog analysis of the resistome, virulome and mobilome in the wild rodent gut microbiota.

Wild rodent's gut microbiota serves as a crucial reservoir of antibiotic resistance genes (ARGs), where antimicrobial-resistant bacteria interact with mobile genetic elements (MGEs) to facilitate horizontal gene transfer. This study analyzed 12,255 gut-derived bacterial genomes from wild rodents to characterize the distribution of ARGs and virulence factor genes (VFGs), and to identify their bacterial hosts. A total of 8119 ARGs and 7626 VFGs were identified. The most prevalent ARGs conferred resistance to elfamycin, followed by those associated with multi-class antibiotic resistance. Enterobacteriaceae, particularly Escherichia coli, harbored the highest numbers of ARGs and VFGs. A strong correlation between the presence of MGEs, ARGs, and VFGs was observed, highlighting the potential for co-selection and mobilization of resistance and virulence traits. These findings underscore the importance of expanded surveillance to monitor and mitigate the risk of transmission of resistant and potentially pathogenic bacteria from wild rodents to human and animal populations.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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