Li Zhouxun, Wu Chunyan, Cai Xuemei, Song Yongli, Zheng Xingping, He Yuan, Song Guibo
Department of Clinical Laboratory, The First Affiliated Hospital of Kunming Medical University; Yunnan Key Laboratory of Laboratory Medicine; Yunnan Province Clinical Research Center for Laboratory Medicine; Kunming, China.
Department of Nuclear Medicine, The Affiliated Hospital of Yunnan University, Kunming, China.
Pol J Microbiol. 2025 Mar 26;74(1):82-94. doi: 10.33073/pjm-2025-007. eCollection 2025 Mar 1.
Globally, the infection rate of carbapenem-resistant (CRKP) producing OXA-48-like carbapenemase is increasing, posing a significant public health threat due to its high antibiotic resistance. Between December 2019 and April 2023, ten CRKP strains carrying the OXA-48-like carbapenemase were isolated from inpatients at the First Affiliated Hospital of Kunming Medical University. Wholegenome sequencing (WGS) revealed that all strains carried the OXA-232 gene, a variant of OXA-48-like, located on the non-conjugative ColKP3 plasmid. Sequence typing identified nine strains as ST231 and one as ST11. The ST231 strains carried common virulence genes, including yersiniabactin (ybtA, fyuA, irp2) and aerobactin (iucABCD, iutA), while the ST11 strain carried high-virulence genes (rmpA, rmpA2, peg-344) as well as KPC-2 and OXA-232 carbapenemase genes on separate plasmids, suggesting that CRKP can harbor multiple plasmids with carbapenemase genes. Sequence typing of 264 global ST231 CRKP isolates (n = 264) showed a distinct clonal relationship between our strains and Indian CRKP isolates, indicating potential cross-border transmission. The virulence potential and immune response of the ST231 strains were assessed using a mouse respiratory infection model. The concentrations of inflammatory factors CCL2/MCP-1, IL-6, and TNF-α in the alveolar lavage fluid and blood of the model mice were detected. Combined with the pathological analysis of lung and liver tissues, it reveals variability in virulence and immune response despite carrying identical resistance and virulence genes. This underscores the urgent need for monitoring and tailored public health strategies to combat the global spread of drug-resistant strains.
在全球范围内,产OXA - 48样碳青霉烯酶的耐碳青霉烯肺炎克雷伯菌(CRKP)的感染率正在上升,因其高度的抗生素耐药性对公共卫生构成了重大威胁。2019年12月至2023年4月期间,从昆明医科大学第一附属医院的住院患者中分离出10株携带OXA - 48样碳青霉烯酶的CRKP菌株。全基因组测序(WGS)显示,所有菌株都携带位于非接合型ColKP3质粒上的OXA - 232基因,这是OXA - 48样的一个变体。序列分型鉴定出9株为ST231,1株为ST11。ST231菌株携带常见的毒力基因,包括耶尔森菌素(ybtA、fyuA、irp2)和气杆菌素(iucABCD、iutA),而ST11菌株在不同质粒上携带高毒力基因(rmpA、rmpA2、peg - 344)以及KPC - 2和OXA - 232碳青霉烯酶基因,这表明CRKP可以携带多个带有碳青霉烯酶基因的质粒。对264株全球ST231 CRKP分离株(n = 264)进行的序列分型显示,我们的菌株与印度CRKP分离株之间存在明显的克隆关系,表明存在潜在的跨境传播。使用小鼠呼吸道感染模型评估了ST231菌株的毒力潜力和免疫反应。检测了模型小鼠肺泡灌洗液和血液中炎症因子CCL2/MCP - 1、IL - 6和TNF - α的浓度。结合肺和肝组织的病理分析,结果显示尽管携带相同的耐药和毒力基因,但毒力和免疫反应存在差异。这凸显了监测和制定针对性公共卫生策略以对抗耐药菌株全球传播的迫切需求。