Phylogenetic intermixing reveals stable fly-mediated circulation of mastitis-associated bacteria in dairy settings.

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-23 Epub Date: 2025-08-01 DOI:10.1128/msystems.00215-25
Andrew J Sommer, Travis K Worley, Panagiotis Sapountzis, Kerri L Coon
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引用次数: 0

Abstract

Stomoxys flies are common blood-feeding pests on dairy farms and are suspected carriers of pathogenic bacteria due to their close association with manure and cattle hosts. While prior studies have used amplicon sequencing and culture-dependent methodologies to characterize the composition of the Stomoxys microbiota, little is known about strain-level acquisition of mastitis-causing bacteria from manure by Stomoxys or the functional diversity of Stomoxys-associated taxa. In this study, we address these key knowledge gaps by using whole genome sequencing to provide the first comparative genomic analysis of Stomoxys-derived Escherichia coli, Klebsiella pneumoniae, and Staphylococcaceae isolates. Our results show that fly and manure isolates collected from the same farm system are phylogenetically interspersed, with subsequent pairwise genome alignments revealing near-identical strains and plasmids shared between the two sources. We further identify a phylogenetic clade of Mammaliicoccus sciuri containing known mastitis agents associated with both flies and manure. Functional analysis reveals that this clade is highly enriched in xylose metabolism genes that are rare across other M. sciuri lineages, suggesting potential niche differentiation within the genus. Collectively, our results provide strong evidence for the acquisition of fecal-associated bacteria by adult Stomoxys flies, confirming the link between biting muscid flies and manure habitats. The intermixing of fly and manure isolates in clinically relevant taxonomic groups strongly suggests that flies serve as carriers of opportunistic mastitis-causing or other fecal-borne pathogens and may serve as important vehicles of pathogen dissemination across the dairy farm environment.IMPORTANCEBovine mastitis causes up to $32 billion dollars in losses annually in the global dairy industry. Opportunistic intramammary pathogens can be transmitted through incidental contact with bacteria in environmental reservoirs like manure. However, factors affecting the abundance, persistence, and spread of these bacteria are not well understood. Our research shows that mastitis pathogens are present in the guts of blood-feeding Stomoxys (stable) flies, which develop in cow feces and bite cows. Genomic analysis of isolates from flies, manure, and mastitis cases reveals that strains and antimicrobial resistance genes are shared between these sources. Further analysis of fly gut isolates shows virulence factors and possible niche specialization, identifying fly-associated clades with known mastitis agents from mastitic cows. This strongly suggests that Stomoxys flies play a role in the carriage and circulation of bovine mastitis pathogens from manure in dairy settings.

系统发育混合揭示了奶牛环境中乳腺炎相关细菌的稳定的苍蝇介导循环。
口蝇是奶牛场常见的吸血害虫,由于它们与粪便和牛宿主密切相关,因此被怀疑是致病菌的携带者。虽然先前的研究已经使用扩增子测序和培养依赖的方法来表征Stomoxys微生物群的组成,但对于Stomoxys从粪便中获得乳腺炎引起的细菌的菌株水平或Stomoxys相关分类群的功能多样性知之甚少。在这项研究中,我们通过使用全基因组测序来解决这些关键的知识空白,提供了stomoxys衍生的大肠杆菌,肺炎克雷伯菌和葡萄球菌科分离物的首次比较基因组分析。我们的研究结果表明,从同一农场系统收集的苍蝇和粪便分离株在系统发育上是穿插的,随后的成对基因组比对显示两个来源之间共享的几乎相同的菌株和质粒。我们进一步确定了一个哺乳球菌的系统发育分支,该分支含有与苍蝇和粪便相关的已知乳腺炎因子。功能分析表明,该分支高度富含木糖代谢基因,这在其他分枝中是罕见的,表明该属内存在潜在的生态位分化。总的来说,我们的研究结果为成年Stomoxys蝇获得粪便相关细菌提供了强有力的证据,证实了叮咬蝇与粪便栖息地之间的联系。在临床相关的分类群中,苍蝇和粪便分离物的混合强烈表明,苍蝇是机会性乳腺炎或其他粪便传播病原体的携带者,可能是病原体在奶牛场环境中传播的重要载体。牛乳腺炎每年在全球乳制品行业造成高达320亿美元的损失。机会性乳腺内病原体可通过偶然接触粪便等环境宿主中的细菌而传播。然而,影响这些细菌的丰度、持久性和传播的因素尚不清楚。我们的研究表明,乳腺炎病原体存在于喂血的Stomoxys(稳定的)苍蝇的肠道中,这种苍蝇在牛的粪便中发育并叮咬牛。对来自苍蝇、粪便和乳腺炎病例的分离株的基因组分析显示,菌株和抗微生物药物耐药性基因在这些来源之间是共享的。进一步分析苍蝇肠道分离物显示了毒力因素和可能的生态位特化,从乳腺炎奶牛中鉴定出具有已知乳腺炎病原体的苍蝇相关分支。这强烈表明,口蝇在奶牛粪便中的牛乳腺炎病原体的运输和循环中起作用。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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