Lei Deru, Dong Xu, Yang Ting, Jin Ye, Zhou Wangxiao
Clinical Laboratory Center, The Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, People's Republic of China.
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, People's Republic of China.
mSystems. 2025 Sep 24:e0084825. doi: 10.1128/msystems.00848-25.
sequence type (ST) 188 is a globally distributed lineage frequently associated with colonization and bloodstream infection in both humans and animals, yet its evolutionary dynamics and genomic adaptations remain poorly understood. In this study, we conducted a comprehensive genomic analysis of 808 ST188 isolates collected from 24 countries between 2004 and 2023. Phylogenetic reconstruction identified seven clades, with clades I and VII showing independent clonal expansions in China. Frequent cross-regional, international, and cross-host transmission events were observed, supporting the emergence of ST188 as a host-generalist lineage. A distinct methicillin-resistant subclade within clade VI likely emerged from a methicillin-susceptible ancestor through the acquisition of SCC IVa. This event was accompanied by co-acquisition of resistance transposon Tn and fluoroquinolone-resistance mutations, alongside truncation of the adhesion-related gene and loss of the serine protease genes . Preliminary phenotypic assays confirmed reduced adhesion and colonization in clade VI isolates. Comparative analysis revealed clade-specific patterns of mobile genetic elements, including vertical inheritance of SaPI1 and SaPI2 in the Chinese subclade of clade VII. In contrast, the novel prophage φST188-1, found exclusively in clade VII isolates, appeared to have been independently acquired. However, accessory genome variation across clades was limited, and the overall population structure was primarily shaped by core genome single-nucleotide polymorphisms. These findings provide a detailed view of the evolution and adaptation of ST188, underscore the role of clade-specific resistance and virulence patterns, and highlight the importance of continued genomic surveillance of this emerging lineage.
The global emergence of ST188 poses new challenges to public health due to its ability to infect both humans and animals and spread across regions and continents. Despite its growing prevalence, little has been known about its evolutionary history and dissemination patterns. In this study, we analyzed 808 ST188 genomes from 24 countries and found evidence of frequent cross-regional and cross-host transmission. Two major clades, showing clear clonal expansion, were dominated by isolates from China. We also identified a newly emerged methicillin-resistant subclade likely derived from a methicillin-susceptible ancestor, characterized by the acquisition of SCC IVa, multiple resistance genes, and fluoroquinolone-resistance mutations. This subclade exhibited reduced adhesion and colonization capacity due to structural loss of key virulence genes. These findings provide new insights into the clade-specific adaptation and global spread of ST188 and underscore the need for genomic surveillance of multidrug-resistant emerging from traditionally susceptible lineages.
序列类型(ST)188是一种全球分布的谱系,在人类和动物中都经常与定植和血流感染相关,但对其进化动态和基因组适应性的了解仍然很少。在本研究中,我们对2004年至2023年间从24个国家收集的808株ST188分离株进行了全面的基因组分析。系统发育重建确定了七个分支,其中分支I和VII在中国显示出独立的克隆扩张。观察到频繁的跨区域、国际和跨宿主传播事件,支持ST188作为一种宿主泛化谱系的出现。分支VI内一个独特的耐甲氧西林亚分支可能通过获得SCC IVa从一个甲氧西林敏感祖先中出现。这一事件伴随着抗性转座子Tn和氟喹诺酮抗性突变的共同获得,同时粘附相关基因的截断和丝氨酸蛋白酶基因的缺失。初步表型分析证实分支VI分离株的粘附和定植减少。比较分析揭示了移动遗传元件的分支特异性模式,包括分支VII的中国亚分支中SaPI1和SaPI2的垂直遗传。相比之下,仅在分支VII分离株中发现的新型噬菌体φST188-1似乎是独立获得的。然而,各分支间的辅助基因组变异有限,总体种群结构主要由核心基因组单核苷酸多态性塑造。这些发现提供了ST188进化和适应性的详细视图,强调了分支特异性抗性和毒力模式的作用,并突出了对这一新兴谱系持续进行基因组监测的重要性。
ST188在全球范围内的出现因其能够感染人类和动物并在不同地区和大陆传播,给公共卫生带来了新的挑战。尽管其流行率不断上升,但对其进化历史和传播模式却知之甚少。在本研究中,我们分析了来自24个国家的808个ST188基因组,发现了频繁的跨区域和跨宿主传播的证据。两个主要分支显示出明显的克隆扩张,以来自中国的分离株为主。我们还鉴定出一个新出现的耐甲氧西林亚分支,可能源自一个甲氧西林敏感祖先,其特征是获得了SCC IVa、多个抗性基因和氟喹诺酮抗性突变。由于关键毒力基因的结构缺失,该亚分支表现出粘附和定植能力降低。这些发现为ST188的分支特异性适应性和全球传播提供了新的见解,并强调了对从传统敏感谱系中出现的多重耐药菌进行基因组监测的必要性。