新西兰金黄色葡萄球菌ST1的比较基因组学研究。

IF 3.1 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-09-23 DOI:10.1128/msphere.00376-25
Emma M Voss, Gregory M Cook, Christine Couldrey, Scott A Ferguson, Chad Harland, Ali Karkaba, Scott McDougall, Sergio E Morales, Jack Rolfe, James E Ussher, Rhys T White, Liam Williams, John Williamson
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引用次数: 0

摘要

金黄色葡萄球菌是一种主要的人畜共患性细菌病原体,可引起广泛的人类和动物疾病,包括皮肤感染、败血症、心内膜炎和牛乳腺炎。在地理上孤立的新西兰环境中,金黄色葡萄球菌的种群结构表现出独特的基因组图谱。在全球范围内,牛金黄色葡萄球菌分离株主要与序列类型(STs)、ST97和ST151相关,而在新西兰,ST1占主导地位,约占牛分离株的70%。ST1也是人类临床重要的序列类型。本研究采用One Health方法比较了从牛乳和人类临床样本中分离的520株金黄色葡萄球菌ST1的遗传差异。我们的目的是探索与宿主持久性和多样性相关的基因组特征,重点是抗菌素耐药性(AMR)、毒力和可移动遗传元件。比较基因组学显示,人类分离株携带AMR基因的负担明显更高,与临床选择压力一致。相比之下,83%的牛分离株含有与金黄色葡萄球菌φSaov3相似的噬菌体(φSabovST1)。这种噬菌体编码牛适应白细胞(LukMF),支持宿主特异性适应。系统发育分析显示分支较长,表明采样不足,强调需要更广泛的基因组监测来解决新西兰金黄色葡萄球菌ST1的进化关系和传播动力学。这些发现强调了宿主相互作用的复杂历史、历史传播事件和正在进行的细菌适应。扩大对人类、动物和环境水库的采样工作将提供对菌株多样性的更深入了解,阐明传播途径,并为减轻人畜共患病风险的策略提供信息。本研究对金黄色葡萄球菌ST1进行了全面的基因组分析,该谱系在新西兰的牛和人类种群中都具有不同寻常的优势。利用新西兰的地理隔离,我们对金黄色葡萄球菌的持久性、多样化和适应性提供了重要的见解,为促进公共和兽医卫生的疾病预防以及加强全球生物安全提供了宝贵的知识。第一个牛ST1参考基因组的开发为未来的研究提供了宝贵的资源,而携带牛特异性白细胞素的新噬菌体(φSabovST1)的鉴定强调了移动遗传元件在宿主特异性和毒力中的作用。人类分离株显示出较高的耐药基因流行率。系统发育分析进一步揭示了ST1的两个主要循环分支,它们具有分散的宿主起源,突出了综合的“同一个健康”方法的迫切需要,以便在农业和公共卫生系统中更有效地监测和管理人畜共患病原体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative genomics of endemic Staphylococcus aureus ST1 in New Zealand.

Staphylococcus aureus is a major zoonotic bacterial pathogen that causes a broad spectrum of human and animal diseases, including skin infections, sepsis, endocarditis, and bovine mastitis. In the geographically isolated setting of New Zealand, the population structure of S. aureus exhibits a distinct genomic profile. Globally, bovine S. aureus isolates are primarily associated with sequence types (STs), ST97 and ST151, whereas in New Zealand, ST1 predominates, accounting for approximately 70% of bovine isolates. ST1 is also a clinically significant sequence type in humans. This study employed a comparative One Health approach to investigate genetic differences in 520 S. aureus ST1 isolated from bovine milk and human clinical samples. We aimed to explore genomic features associated with persistence and diversification across hosts, focusing on antimicrobial resistance (AMR), virulence, and mobile genetic elements. Comparative genomics revealed that human isolates carried a significantly higher burden of AMR genes, consistent with clinical selective pressure. In contrast, 83% of bovine isolates harbored a prophage (φSabovST1) similar to S. aureus prophage φSaov3. This prophage encodes bovine-adapted leukocidins (LukMF'), supporting host-specific adaptation. Phylogenetic analysis revealed long branches, suggesting insufficient sampling, highlighting the need for broader genomic surveillance to resolve evolutionary relationships and transmission dynamics of S. aureus ST1 in New Zealand. These findings highlight the complex history of host interactions, historical transmission events, and ongoing bacterial adaptation. Expanding sampling efforts across human, animal, and environmental reservoirs will provide deeper insights into strain diversity, elucidate transmission pathways, and inform strategies to mitigate zoonotic risks.IMPORTANCEThis study presents a comprehensive genomic analysis of S. aureus ST1, a lineage that is unusually dominant in both bovine and human populations in New Zealand. Leveraging New Zealand's geographical isolation, we provide critical insights into the persistence, diversification, and adaptation of S. aureus, offering valuable knowledge to advance disease prevention in both public and veterinary health and strengthening global biosecurity. The development of the first bovine ST1 reference genome serves as a valuable resource for future research, while the identification of a novel prophage (φSabovST1) carrying bovine-specific leukocidins underscores the role of mobile genetic elements in host specificity and virulence. Human isolates exhibited a higher prevalence of antimicrobial resistance genes. Phylogenetic analysis further revealed two main circulating clades of ST1 with interspersed host origins, highlighting the critical need for integrated One Health approaches to more effectively monitor and manage zoonotic pathogens across agricultural and public health systems.

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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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