混合生物膜自然转化试验揭示了人类环境中葡萄球菌的存在,可以将SCCmec转移到金黄色葡萄球菌。

IF 3.1 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-09-22 DOI:10.1128/msphere.00442-25
Mais Maree, Yuri Ushijima, Annisa Krama, Maaya Sasaki, Terumi Miyata, Masato Higashide, Le Thuy Thi Nguyen, Kazuya Morikawa
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引用次数: 0

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)是引起卫生保健、社区和牲畜相关感染的重要病原体。甲氧西林耐药基因mecA嵌入被称为葡萄球菌盒染色体(SCCmec)的移动遗传元件中。SCCmec存在于人类和动物宿主的葡萄球菌中,在流行病学上被认为是SCCmec的遗传库。然而,多种耐甲氧西林葡萄球菌(MRS)作为金黄色葡萄球菌SCCmec供体的能力尚未得到实验测试。在这里,我们研究了157株来自宠物、肉类、牲畜和人类的MRS分离株将SCCmec转移到甲氧西林敏感的金黄色葡萄球菌菌株的能力,使用了最近开发的混合生物膜自然转化方案。我们发现157个分离株中有25个能够将SCCmec转移到金黄色葡萄球菌。最有效的供体种是表皮S.(33%)、猫S.(40%)和头S.(30%)。与来自日本的人类和宠物分离株(分别为35%和25%)相比,来自越南和泰国的肉类和牲畜分离株(分别为5%和3%)的SCCmec转移率较低(分别为25%和5%)。SCCmec转移依赖于由完整的attB位点介导的位点特异性整合/切除,这是由SCC重组酶Ccr识别的。我们的实验研究证明了SCCmec供体存在于我们的生活环境中,强调了特定葡萄球菌物种的重要性。重要性:半个多世纪以来,MRSA是如何出现的一直是关于抗菌素耐药性(AMR)问题日益严重的关键问题。在细菌学、流行病学、基因组生物学和医疗保健领域的广泛研究使人们普遍认识到SCCmec是在不同的葡萄球菌物种之间传播的。然而,全球为细胞间SCCmec传播提供经验证据的努力取得了有限的成果。我们最近建立了混合生物膜转化试验来评估细胞间和种间SCCmec传播。这种新颖的分析系统使我们能够深入了解“MRSA是如何出现的”这个问题,在这里,我们提供了关于潜在供体物种和栖息地的第一个实验结果。这是第一个显示不同来源的葡萄球菌将SCC转移到金黄色葡萄球菌的能力的报告。此外,新发现的S. felis是一种与人类不共生的有效供体,强化了“同一个健康”概念的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mixed-biofilm natural transformation assay reveals the presence of staphylococci in human environments that can transfer SCCmec to Staphylococcus aureus.

Methicillin-resistant Staphylococcus aureus (MRSA) is an important pathogen that causes healthcare-, community-, and livestock-associated infections. The methicillin resistance gene mecA is embedded in the mobile genetic element termed Staphylococcal Cassette Chromosome (SCCmec). SCCmec is shared among staphylococci inhabiting human and animal hosts, which are recognized epidemiologically as the genetic reservoir of SCCmec. However, the ability of diverse methicillin-resistant staphylococci (MRS) to serve as SCCmec donors for S. aureus has not been tested experimentally. Here, we investigated the ability of 157 MRS isolates from pets, meat, livestock, and humans to transfer SCCmec to methicillin-sensitive S. aureus strains using a recently developed natural transformation protocol in mixed biofilms. We found that 25 out of 157 isolates were able to transfer SCCmec to S. aureus. The most effective donor species were S. epidermidis (~33% of the tested isolates), S. felis (40%), and S. capitis (30%). Isolates from meat and livestock (collected in Vietnam and Thailand) had lower transfer rates of SCCmec (5% and 3%, respectively), compared to human and pet isolates from Japan (35% and 25%, respectively). The SCCmec transfer depended on site-specific integration/excision mediated by an intact attB site, which is recognized by the SCC recombinase Ccr. Our study experimentally demonstrates the presence of SCCmec donors in our living environments, highlighting the importance of specific staphylococcal species.IMPORTANCEHow MRSA emerges has long been the pivotal question regarding the ever-increasing burden of antimicrobial resistance (AMR) issues for over half a century. Extensive research efforts in bacteriology, epidemiology, genome biology, and healthcare fields have led to the common understanding that SCCmec is transmitted among distinct staphylococcal species. However, global efforts to provide empirical evidence for intercellular SCCmec transmission have yielded limited results. We recently established the mixed-biofilm transformation assay to evaluate intercellular and interspecies SCCmec transmission. This novel assay system allows us to gain insight into the question "How MRSA emerges," and here, we provide the first experimental results about the potential donor species and habitats. This is the first report to show the ability of staphylococci from distinct sources to transfer SCC to S. aureus. Moreover, the new finding of S. felis as an effective donor that is not commensal to humans reinforces the importance of the One Health concept.

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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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