Dissemination dynamics of colistin resistance genes mcr-9 and mcr-10 across diverse Inc plasmid backbones.

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Odion O Ikhimiukor, Manuela Montoya-Giraldo, Stephanie S R Souza, Ifeoluwa J Akintayo, Nicole I Zac Soligno, Maitiú Marmion, Elissa M Eckhardt, Nisalda Carreiro, Adrienne A Workman, Isabella W Martin, Cheryl P Andam
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Abstract

Background: The polymyxin antibiotic colistin is used as a final line of treatment for life threatening infections caused by multidrug resistant and carbapenem-resistant Gram-negative bacteria. Mobile colistin resistance genes mcr-9 and mcr-10 are increasingly detected in Enterobacteriaceae but their epidemiology is poorly understood.

Methods: The genetic characteristics of mcr-9 and mcr-10, being the only mobile colistin resistance genes detected in a local population of Enterobacter species isolated from bloodstream infections in Dartmouth Hitchcock Medical Center, USA, were elucidated and contextualized against a global dataset of mcr-9/10-bearing plasmids using genomic and phylogenetic tools.

Results: Seven out of 59 Enterobacter isolates carry either an mcr-9 or mcr-10 on a plasmid with distinct single and multiple replicon configurations, including IncFIB(pECLA), IncFIB(K), IncFIA(HI1)-IncFIB(K), IncFIB(pECLA)--IncFII(pECLA) and IncFIB(K)--IncFII(pECLA), whereas two genomes harbor mcr-9 on their chromosome. Global contextualization reveals that allelic variants of mcr-9 and mcr-10 are widely disseminated across diverse Inc-type plasmids, transcending geographic and taxonomic boundaries. Plasmid-borne genes conferring resistance to other antimicrobial agents, such as aminoglycoside, tetracycline and trimethoprim, tend to co-occur with mcr-9.1 and mcr-9.2 alleles.

Conclusions: Findings from this study enhance our understanding of the plasmid backgrounds of mcr-9 and mcr-10, their associated antimicrobial resistance gene carriage and co-occurrence. This knowledge may be critical to inform scalable and effective public health interventions aimed at preserving the efficacy of colistin.

黏菌素耐药基因mcr-9和mcr-10在不同Inc质粒主干间的传播动力学。
背景:多粘菌素抗生素粘菌素被用作治疗由多重耐药和碳青霉烯耐药革兰氏阴性菌引起的危及生命的感染的最后一线。移动粘菌素耐药基因mcr-9和mcr-10在肠杆菌科中越来越多地被检测到,但对其流行病学了解甚少。方法:利用基因组学和系统发育工具,对美国达特茅斯希区柯克医学中心从血液感染中分离的当地肠杆菌种群中检测到的mcr-9和mcr-10的遗传特征进行了阐明,并与全球mcr-9/10携带质粒的数据集进行了背景分析。结果:59株肠杆菌中有7株在具有不同的单复制子和多复制子配置的质粒上携带mcr-9或mcr-10,包括IncFIB(pECLA), IncFIB(K), IncFIA(HI1)-IncFIB(K), IncFIB(pECLA)- IncFII(pECLA)和IncFIB(K)- IncFII(pECLA),而两个基因组在其染色体上携带mcr-9。全球背景分析表明,mcr-9和mcr-10的等位基因变异在不同的inc型质粒中广泛传播,超越了地理和分类的界限。质粒携带的对其他抗菌剂(如氨基糖苷、四环素和甲氧苄啶)具有耐药性的基因往往与mcr-9.1和mcr-9.2等位基因共同出现。结论:本研究结果增强了我们对mcr-9和mcr-10的质粒背景及其相关的耐药基因携带和共现的认识。这一知识可能对旨在保持粘菌素功效的可扩展和有效的公共卫生干预措施至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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