Plasmid-driven clonal expansion of multidrug-resistant monophasic Salmonella Typhimurium in a Global Food Trade Hub.

IF 7.5 2区 医学 Q1 IMMUNOLOGY
Dingjie Huang,Ziqi Wu,Yixiang Jiang,Lulu Hu,Rui Cai,Xi Yang,Chen Du,Shiting Chen,Panpan Yang,Bingchan Guo,Xiaolu Shi,Shuang Wu,Yinghui Li,Zhemin Zhou,Qinghua Hu
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Abstract

Shenzhen, a major port city with a heavily imported food supply, offers a critical setting to examine the spread and adaptation of multidrug-resistant Salmonella 1,4,[5],12:i: - (S. 1,4,[5],12:i:-). This study integrates 17 years of genomic, epidemiological, and food safety data. We explored the serovar's population structure, antibiotic resistance gene (ARG) patterns, and transmission dynamics locally and globally. Our analyses revealed substantial rise in S. 1,4,[5],12:i: - prevalence among non-typhoidal Salmonella isolates over the past 17 years, from 2.27% in 2007 to 24.79% in 2023. S. 1,4,[5],12:i: - was predominated by ST34 (97.9%), with high genotypic resistance to aminoglycosides (100%), tetracyclines (96.6%), β-lactams (89.3%), and sulphonamides (88.5%). Phylogenetic analysis separated S. 1,4,[5],12:i: - into four clades. Clade 4, first detected in Shenzhen in 2013, emerged as the predominant lineage by 2023 (56.9%). This clade exhibited minimal genetic diversity (≤ 38 core SNPs), with adaptive traits linked to the acquisition of resistance-associated plasmids. Notably, plasmid-driven ARGs, including carbapenem resistance genes, have emerged as a growing concern. Transmission analysis identified two key transmission dynamics: transient outbreaks primarily involving food handlers and persistent lineages sustained through local and international spread, often facilitated by the food supply chain. These findings underscore the role of occupational carriers and imported food products in the dissemination of ARGs, emphasizing the need for enhanced surveillance and improved health and hygiene practices for food handlers. This study provides a comprehensive molecular epidemiological framework for addressing multidrug-resistant Salmonella in globalized urban food hubs, offering a foundation for future surveillance and control efforts.
全球食品贸易中心多药耐药单相鼠伤寒沙门菌质粒驱动克隆扩增
深圳是一个进口食品供应严重的主要港口城市,为研究耐多药沙门氏菌1,4,bb1,1,12:i:- (S. 1,4,[5],12:i:-)的传播和适应提供了重要的环境。这项研究整合了17年来的基因组学、流行病学和食品安全数据。我们探讨了血清型的种群结构、抗生素耐药基因(ARG)模式以及本地和全球的传播动态。我们的分析显示,在过去的17年中,S. 1,4, bb0,12:i: -在非伤寒沙门氏菌分离株中的患病率大幅上升,从2007年的2.27%上升到2023年的24.79%。S. 1,4,[5],12:i: -以ST34(97.9%)为主,对氨基糖苷类(100%)、四环素类(96.6%)、β-内酰胺类(89.3%)和磺胺类(88.5%)具有较高的基因型抗性。系统发育分析将S. 1,4,[5],12:i: -分为4个支系。进化支4于2013年在深圳首次发现,到2023年成为优势谱系(56.9%)。该支系表现出最小的遗传多样性(≤38个核心snp),适应性性状与抗性相关质粒的获得有关。值得注意的是,质粒驱动的ARGs,包括碳青霉烯类耐药基因,已经越来越受到关注。传播分析确定了两种关键的传播动态:主要涉及食品处理人员的短暂暴发和通过当地和国际传播持续传播的持续谱系,通常由食品供应链促进。这些调查结果强调了职业携带者和进口食品在ARGs传播中的作用,强调需要加强监测并改善食品处理人员的健康和卫生习惯。本研究为解决全球化城市食品中心多重耐药沙门氏菌问题提供了一个全面的分子流行病学框架,为未来的监测和控制工作奠定了基础。
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来源期刊
Emerging Microbes & Infections
Emerging Microbes & Infections IMMUNOLOGY-MICROBIOLOGY
CiteScore
26.20
自引率
2.30%
发文量
276
审稿时长
20 weeks
期刊介绍: Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses. The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries. This journal addresses topics of critical biological and clinical importance, including but not limited to: - Epidemic surveillance - Clinical manifestations - Diagnosis and management - Cellular and molecular pathogenesis - Innate and acquired immune responses between emerging microbes and their hosts - Drug discovery - Vaccine development research Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.
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