Wen Yongxian, Wu Jingtong, You Lv, Wei Xiaoyu, Wang Junhua, Li Shijun
School of Public Health, The Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang, China.
Laboratory of Bacterial Disease, Experimental Center, Guizhou Provincial Center for Disease Control and Prevention, Guiyang, China.
Front Microbiol. 2025 Mar 27;16:1532036. doi: 10.3389/fmicb.2025.1532036. eCollection 2025.
The emergence of extensively drug-resistant (XDR) in humans poses a significant public health and therapeutic challenge. However, limited data are available on XDR isolates from Guizhou province, China. This study aimed to investigate the molecular epidemiology and resistance patterns of XDR isolates from clinical samples in this region.
A total of 931 isolates were screened for XDR isolates through antimicrobial susceptibility testing. These XDR isolates were subjected to whole-genome sequencing (WGS) and bioinformatic analysis to further systematically investigating the molecular epidemiology and resistance patterns of XDR isolates.
Between 2019 and 2023, 931 isolates were collected from clinical samples in Guizhou. Of these isolates, 51 (5.5%) were identified as XDR and classified into 16 serovars. Among the serovars, 15 corresponded to a specific sequence type, except for serovars. The predominant serovars, . 1,4,[5],12:i:-, , and . Kentucky, were divided into ST34, ST11, and ST198, respectively. Genomic analysis showed that all XDR isolates harbored at least eight antimicrobial resistance genes (ARGs) and multidrug efflux pumps. Highly prevalent point mutations in (D87 and S83) and (S80I) were detected, along with eight plasmid-mediated quinolone resistance () genes. The gene was the most common (43.1%), followed by , variant, , , , , and . The predominant -lactamase gene was (54.9%), and (35.3%) was the most prevalent extended-spectrum -lactamase subtype. Notably, gene was identified for the first time in from Guizhou, and one 1,4,[5],12:i:- isolate contained the gene. ARGs profiles varied by serovars, with 1,4,[5],12:i:- isolates carrying the highest number. Ten plasmid types were identified, predominantly IncHI2/IncHI2A (47.5%). Key resistance genes such as , , , , and were located on IncHI2/IncHI2A plasmids. Notably, 75.0% of the conjugative plasmids belonged to IncHI2/IncHI2A, indicating that horizontal gene transfer through conjugation facilitates ARGs dissemination. Core genome multilocus sequence typing (cgMLST) analysis revealed significant genetic diversity, with 39 core genome sequence types (cgSTs) identified and no evidence of outbreaks.
The rising prevalence of XDR in Guizhou province is concerning. Initial whole-genome sequencing (WGS) data provide critical insights for understanding and controlling XDR infections, aiding public health officials in identifying emerging threats and trends.
广泛耐药(XDR)菌株在人类中的出现对公共卫生和治疗构成了重大挑战。然而,关于中国贵州省XDR菌株的可用数据有限。本研究旨在调查该地区临床样本中XDR菌株的分子流行病学和耐药模式。
通过抗菌药物敏感性试验对总共931株菌株进行XDR菌株筛查。对这些XDR菌株进行全基因组测序(WGS)和生物信息学分析,以进一步系统地研究XDR菌株的分子流行病学和耐药模式。
2019年至2023年期间,从贵州的临床样本中收集了931株菌株。在这些菌株中,51株(5.5%)被鉴定为XDR,并分为16个血清型。在这些血清型中,除了某些血清型外,15个对应于特定的序列类型。主要的血清型,即1,4,[5],12:i: -、[未提及的血清型]和肯塔基血清型,分别分为ST34、ST11和ST198。基因组分析表明,所有XDR菌株至少携带8个抗菌耐药基因(ARGs)和多药外排泵。检测到gyrA(D87和S83)和parC(S80I)中高度流行的点突变,以及8个质粒介导的喹诺酮耐药(qnr)基因。qnrS基因最常见(43.1%),其次是qnrB、qnrVC变体、qnrD、qnrA、qnrC、qnrE和qnrS1。主要的β-内酰胺酶基因是blaCTX-M(54.9%),blaCTX-M-15(35.3%)是最流行的超广谱β-内酰胺酶亚型。值得注意的是,qnrD基因首次在贵州的[未提及的菌株名称]中被鉴定,并且一株1,4,[5],12:i: -菌株含有mcr-1基因。ARGs谱因血清型而异,1,4,[5],12:i: -菌株携带的数量最多。鉴定出10种质粒类型,主要是IncHI2/IncHI2A(47.5%)。关键耐药基因如blaCTX-M、blaNDM、mcr-1、qnrS和armA位于IncHI2/IncHI2A质粒上。值得注意的是,75.0%的接合性质粒属于IncHI2/IncHI2A,表明通过接合进行的水平基因转移促进了ARGs的传播。核心基因组多位点序列分型(cgMLST)分析显示出显著的遗传多样性,鉴定出39种核心基因组序列类型(cgSTs),没有爆发的证据。
贵州省XDR菌株患病率的上升令人担忧。初步的全基因组测序(WGS)数据为理解和控制XDR菌株感染提供了关键见解,有助于公共卫生官员识别新出现的威胁和趋势。