School of Laboratory Medicine and Bioengineering, Hangzhou Medical College, Hangzhou, China.
Key Laboratory of Biomarkers and In Vitro Diagnosis Translation of Zhejiang Province, Hangzhou, China.
Ann Clin Microbiol Antimicrob. 2024 Jul 26;23(1):67. doi: 10.1186/s12941-024-00727-x.
The emergence of plasmid-mediated mobile colistin resistance (mcr) gene poses a great challenge to the clinical application of polymyxins. To date, mcr-1 to mcr-10 have been found in animals, humans, and the environment. Among them, mcr-8 was first identified in Klebsiella pneumoniae (K. pneumoniae) of swine origin, and then mcr-8.1 to mcr-8.5 were successively identified. Notably, K. pneumoniae is the major host of the mcr-8 gene in both animals and humans. This study aims to explore the characteristics of K. pneumoniae strains carrying the mcr-8 gene and tmexCD1-toprJ1 gene cluster and investigate the correlation between these two antibiotic resistance genes.
The isolates from the poultry farms and the surrounding villages were identified by mass spectrometer, and the strains positive for mcr-1 to mcr-10 were screened by polymerase chain reaction (PCR). The size of the plasmid and the antimicrobial resistance genes carried were confirmed by S1-nuclease pulsed-field gel electrophoresis (S1-PFGE) and Southern hybridization, and the transferability of the plasmid was verified by conjugation experiments. Antimicrobial susceptibility testing (AST) and whole genome sequencing (WGS) were used to characterize the strains.
Two K. pneumoniae isolates (KP26 and KP29) displaying polymyxin resistance were identified as mcr-8 gene carriers. Besides that, tigecycline-resistant gene cluster tmexCD1-toprJ1 was also found on the other plasmid which conferred strain resistance to tigecycline. Through epidemiological analysis, we found that the mcr-8 gene has dispersed globally, circulating in the human, animals, and the environment. Furthermore, our analysis suggests that the coexistence of mcr-8 and tmexCD1-toprJ1 on a single plasmid might evolved through plasmid recombination.
Although the mcr-8 and tmexCD1-toprJ1 gene clusters in the two strains of K. pneumoniae in this study were on two different plasmids, they still pose a potential threat to public health, requiring close monitoring and further study.
质粒介导的多黏菌素耐药性(mcr)基因的出现对多黏菌素的临床应用构成了巨大挑战。迄今为止,已在动物、人类和环境中发现了 mcr-1 至 mcr-10。其中,mcr-8 最初在猪源肺炎克雷伯菌(K. pneumoniae)中被发现,随后相继鉴定出 mcr-8.1 至 mcr-8.5。值得注意的是,K. pneumoniae 是动物和人类中 mcr-8 基因的主要宿主。本研究旨在探讨携带 mcr-8 基因和 tmexCD1-toprJ1 基因簇的肺炎克雷伯菌菌株的特征,并研究这两种抗生素耐药基因之间的相关性。
通过质谱仪鉴定来自家禽养殖场和周边村庄的分离株,并通过聚合酶链反应(PCR)筛选 mcr-1 至 mcr-10 阳性菌株。通过 S1-核酸酶脉冲场凝胶电泳(S1-PFGE)和 Southern 杂交确认质粒的大小和携带的抗生素耐药基因,并通过接合实验验证质粒的可转移性。药敏试验(AST)和全基因组测序(WGS)用于对菌株进行特征描述。
鉴定出两株对多黏菌素耐药的肺炎克雷伯菌(KP26 和 KP29)为 mcr-8 基因携带者。此外,另一个质粒上还发现了替加环素耐药基因簇 tmexCD1-toprJ1,该基因簇赋予菌株对替加环素的耐药性。通过流行病学分析发现,mcr-8 基因已在全球范围内传播,存在于人类、动物和环境中。此外,我们的分析表明,单个质粒上 mcr-8 和 tmexCD1-toprJ1 的共存可能是通过质粒重组进化而来的。
尽管本研究中两株肺炎克雷伯菌的 mcr-8 和 tmexCD1-toprJ1 基因簇位于两个不同的质粒上,但它们仍然对公共健康构成潜在威胁,需要密切监测和进一步研究。