Department of Clinical Laboratory, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Antimicrob Resist Infect Control. 2024 Jun 18;13(1):66. doi: 10.1186/s13756-024-01423-3.
Carbapenem-resistant E. coli (CREco) pose a significant public health threat due to their multidrug resistance. Colistin is often a last-resort treatment against CREco; however, the emergence of colistin resistance gene mcr-1 complicates treatment options.
Two E. coli strains (ECO20 and ECO21), recovered from hospitalized patients in distinct wards, exhibited resistance to carbapenems and colistin. Whole-genome sequencing and phenotypic characterization were employed to study resistance patterns, plasmid profiles, transferability of resistance and virulence genes, and siderophore production capabilities. Comparative genome analysis was used to investigate the genetic environment of mcr-1, bla, and virulence clusters.
Both E. coli strains exhibited thr presence of both mcr-1 and bla genes, showing high resistance to multiple antibiotics. Genomic analysis revealed the clonal transmission of these strains, possessing identical plasmid profiles (pMCR, pNDM, and pVir) associated with colistin resistance, carbapenem resistance, and virulence factors. Conjugation experiments confirmed the transferability of these plasmids, indicating their potential to disseminate resistance and virulence traits to other strains. Comparative genomic analyses unveiled the distribution of mcr-1 (IncX4-type) and bla (IncX3-type) plasmids across diverse bacterial species, emphasizing their adaptability and threat. The novelty of pVir indicates its potential role in driving the evolution of highly adaptable and pathogenic strains.
Our findings underscore the co-occurrence of mcr-1, bla, and siderophore-producing plasmids in E. coli, which poses a significant concern for global health. This research is crucial to unravel the complex mechanisms governing plasmid transfer and recombination and to devise robust strategies to control their spread in healthcare settings.
耐碳青霉烯类大肠杆菌(CREco)由于其对多种药物的耐药性,对公共健康构成重大威胁。多粘菌素通常是治疗 CREco 的最后手段;然而,粘菌素耐药基因 mcr-1 的出现使治疗选择复杂化。
从不同病房住院患者中分离出两株大肠杆菌(ECO20 和 ECO21),它们对碳青霉烯类和多粘菌素表现出耐药性。采用全基因组测序和表型特征分析研究耐药模式、质粒图谱、耐药和毒力基因的可转移性以及铁载体产生能力。比较基因组分析用于研究 mcr-1、bla 和毒力基因簇的遗传环境。
两株大肠杆菌均携带 mcr-1 和 bla 基因,对多种抗生素表现出高度耐药性。基因组分析显示这些菌株的克隆传播,具有相同的质粒图谱(pMCR、pNDM 和 pVir)与多粘菌素耐药、碳青霉烯类耐药和毒力因子相关。接合实验证实了这些质粒的可转移性,表明它们有可能将耐药性和毒力特征传播给其他菌株。比较基因组分析揭示了 mcr-1(IncX4 型)和 bla(IncX3 型)质粒在不同细菌种属中的分布,强调了它们的适应性和威胁。pVir 的新颖性表明其在驱动高度适应性和致病性菌株进化方面的潜在作用。
我们的研究结果强调了 mcr-1、bla 和产铁载体质粒在大肠杆菌中的共同存在,这对全球健康构成了重大关注。这项研究对于揭示质粒转移和重组的复杂机制以及制定控制其在医疗机构中传播的强大策略至关重要。