Large-scale genomic analysis places Chinese CC398 as a persistent human-associated MSSA lineage apart from the dominant global LA-MRSA clade.

IF 5.2 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2026-10-20 Epub Date: 2026-09-11 DOI:10.1128/msystems.00621-26
Guilai Jiang, Changyuan Guo, Yulin Hua, Chaoshen Wu, Shengkai Li, Yuezhuo Wang, Jun Zhao, Linli Ji, Yijie Cheng, Zhemin Zhou, Xuejie Wu, Heng Li
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引用次数: 0

Abstract

Staphylococcus aureus clonal complex (CC)398 has emerged as a dominant livestock-associated methicillin-resistant S. aureus (LA-MRSA) lineage worldwide; however, its evolutionary trajectory and regional diversification remain incompletely understood. We developed a core-genome multilocus sequence typing (cgMLST) scheme with hierarchical clustering and applied it to over 30,000 S. aureus genomes, revealing frequent cross-border transmission of CC398. Subsequent time-calibrated phylogenetic analysis placed the most recent common ancestor at 1942 (95% CI: 1939-1945), with the human-to-livestock host jump around 1969 (95% CI: 1968-1972). Chinese CC398 exhibits a distinct trajectory: unlike the LA-MRSA lineages dominating Europe and North America, Chinese isolates are predominantly human-associated methicillin-susceptible S. aureus (HA-MSSA), forming unique East Asia-specific phylogroups (SAP1, SAP2, and AP1-AP3), with distinct resistance and virulence profiles. The LA lineage remains limited in China, with multinational mixed clusters emerging only after 2019. Analysis of global transmission networks revealed a significant correlation between LA-CC398 spread and international trade in fresh swine products, while no such correlation was observed for the human-associated lineage. Beyond the established lineage markers tet(M) and scn, our analysis identified additional differentially distributed genes, including cadC-a chromosomal cadmium resistance regulator-as a novel HA-lineage-enriched gene whose functional role in host adaptation remains to be determined. This study reveals that CC398 followed fundamentally different evolutionary paths in China versus Western countries, challenging a one-size-fits-all model of its dissemination.IMPORTANCEThis study illustrates how large-scale microbial genomics can resolve the evolutionary origins and regional diversification of bacterial pathogens. By applying a novel cgMLST scheme to over 30,000 S. aureus genomes, we show that CC398 followed fundamentally different evolutionary paths in China versus Western countries-challenging the prevailing model of uniform global dissemination-and that livestock-associated MRSA expansion is closely linked to international trade in fresh pork products. These findings highlight the need for integrated surveillance across human, animal, and trade interfaces to anticipate the emergence and spread of zoonotic pathogens.

大规模基因组分析表明,中国的CC398与全球的LA-MRSA分支不同,是一个持久的与人类相关的MSSA谱系。
金黄色葡萄球菌克隆复合体(CC)398已成为世界范围内主要的家畜相关耐甲氧西林金黄色葡萄球菌(LA-MRSA)谱系;然而,其演化轨迹和区域多样化仍不完全清楚。我们开发了一种核心基因组多位点序列分型(cgMLST)方案,并将其应用于30,000多个金黄色葡萄球菌基因组,揭示了CC398频繁的跨境传播。随后经过时间校准的系统发育分析认为,最近的共同祖先出现在1942年(95% CI: 1939-1945),人-牲畜宿主在1969年左右跳跃(95% CI: 1968-1972)。中国CC398表现出独特的发展轨迹:与欧洲和北美的LA-MRSA谱系不同,中国分离株主要是人类相关的甲氧西林敏感金黄色葡萄球菌(HA-MSSA),形成了独特的东亚特异性系统群(SAP1, SAP2和AP1-AP3),具有独特的抗性和毒力特征。洛杉矶的血统在中国仍然有限,直到2019年之后才出现跨国混合集群。对全球传播网络的分析显示,LA-CC398的传播与生猪产品的国际贸易之间存在显著相关性,而在人类相关谱系中没有观察到这种相关性。除了已建立的谱系标记tet(M)和scn之外,我们的分析还发现了其他差异分布的基因,包括cadc -染色体抗镉调节因子-作为一种新的ha谱系富集基因,其在宿主适应中的功能作用仍有待确定。本研究表明,CC398在中国和西方国家遵循了根本不同的进化路径,挑战了其传播的一刀切模式。这项研究阐明了大规模微生物基因组学如何解决细菌病原体的进化起源和区域多样化。通过对超过30,000个金黄色葡萄球菌基因组应用新的cgMLST方案,我们发现CC398在中国和西方国家遵循了根本不同的进化路径,挑战了全球统一传播的主流模式,并且家畜相关的MRSA扩展与新鲜猪肉产品的国际贸易密切相关。这些发现强调需要对人、动物和贸易界面进行综合监测,以预测人畜共患病原体的出现和传播。
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
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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