Genomic evidence for flies as carriers of zoonotic pathogens on dairy farms.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Andrew J Sommer, Joseph H Skarlupka, Serafino Teseo, Saria Otani, Garret Suen, Kerri L Coon, Panagiotis Sapountzis
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Abstract

Dairy farms are major reservoirs of zoonotic bacterial pathogens, which harbor antimicrobial resistance genes (ARGs), and raise critical questions about their dissemination on and off the farm environment. Here, we investigated the role of coprophagous muscid flies (Diptera: Muscidae) as carriers of zoonotic pathogens and antimicrobial resistance. We collected cow manure and flies on a dairy farm and used shotgun metagenomics to identify the presence of clinically relevant bacteria, virulence factors, and ARGs in both environments. Our results reveal that, although the fly microbiome is largely composed of manure-associated taxa, they also harbor specific insect-associated bacteria, which may be involved in nutrient provisioning to the host. Furthermore, we identifed shared ARGs, virulence factors, and zoonotic pathogens enriched within the fly gastrointestinal tract (GIT). Our study illustrates the potential flow of pathogenic microorganisms from manure to coprophagous flies, suggesting that flies may pose an important zoonotic threat on dairy farms.

苍蝇作为奶牛农场人畜共患病病原体携带者的基因组证据。
奶牛场是人畜共患病细菌病原体的主要储存库,其中含有抗微生物药物耐药性基因(ARGs),并对其在农场环境内外的传播提出了关键问题。本文研究了食蝇蝇(双翅目:蝇科)作为人畜共患病原体的载体及其耐药性的作用。我们在一个奶牛场收集了牛粪和苍蝇,并使用散弹枪宏基因组学来鉴定两种环境中临床相关细菌、毒力因子和ARGs的存在。我们的研究结果表明,虽然苍蝇的微生物群主要由粪便相关的分类群组成,但它们也含有特定的昆虫相关细菌,这些细菌可能参与向宿主提供营养。此外,我们还鉴定了果蝇胃肠道(GIT)中富集的共同ARGs、毒力因子和人畜共患病原体。我们的研究说明了病原微生物从粪便到食粪蝇的潜在流动,表明苍蝇可能对奶牛场构成重要的人畜共患病威胁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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