College of Veterinary Medicine, National Risk Assessment Laboratory for Antimicrobial Resistance of Microorganisms in Animals, South China Agricultural University, Guangzhou, China.
Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Veterinary Medicine, China Agricultural University, Beijing, China.
Lancet Infect Dis. 2016 Feb;16(2):161-8. doi: 10.1016/S1473-3099(15)00424-7. Epub 2015 Nov 19.
Until now, polymyxin resistance has involved chromosomal mutations but has never been reported via horizontal gene transfer. During a routine surveillance project on antimicrobial resistance in commensal Escherichia coli from food animals in China, a major increase of colistin resistance was observed. When an E coli strain, SHP45, possessing colistin resistance that could be transferred to another strain, was isolated from a pig, we conducted further analysis of possible plasmid-mediated polymyxin resistance. Herein, we report the emergence of the first plasmid-mediated polymyxin resistance mechanism, MCR-1, in Enterobacteriaceae.
The mcr-1 gene in E coli strain SHP45 was identified by whole plasmid sequencing and subcloning. MCR-1 mechanistic studies were done with sequence comparisons, homology modelling, and electrospray ionisation mass spectrometry. The prevalence of mcr-1 was investigated in E coli and Klebsiella pneumoniae strains collected from five provinces between April, 2011, and November, 2014. The ability of MCR-1 to confer polymyxin resistance in vivo was examined in a murine thigh model.
Polymyxin resistance was shown to be singularly due to the plasmid-mediated mcr-1 gene. The plasmid carrying mcr-1 was mobilised to an E coli recipient at a frequency of 10(-1) to 10(-3) cells per recipient cell by conjugation, and maintained in K pneumoniae and Pseudomonas aeruginosa. In an in-vivo model, production of MCR-1 negated the efficacy of colistin. MCR-1 is a member of the phosphoethanolamine transferase enzyme family, with expression in E coli resulting in the addition of phosphoethanolamine to lipid A. We observed mcr-1 carriage in E coli isolates collected from 78 (15%) of 523 samples of raw meat and 166 (21%) of 804 animals during 2011-14, and 16 (1%) of 1322 samples from inpatients with infection.
The emergence of MCR-1 heralds the breach of the last group of antibiotics, polymyxins, by plasmid-mediated resistance. Although currently confined to China, MCR-1 is likely to emulate other global resistance mechanisms such as NDM-1. Our findings emphasise the urgent need for coordinated global action in the fight against pan-drug-resistant Gram-negative bacteria.
Ministry of Science and Technology of China, National Natural Science Foundation of China.
到目前为止,多粘菌素耐药性涉及染色体突变,但从未通过水平基因转移报道过。在中国进行的一项关于食品动物共生大肠杆菌抗菌药物耐药性的常规监测项目中,观察到多粘菌素耐药性显著增加。当从猪中分离出携带可转移至另一菌株的多粘菌素耐药性的大肠杆菌菌株 SHP45 时,我们对可能的质粒介导多粘菌素耐药性进行了进一步分析。在此,我们报道了肠杆菌科中第一个质粒介导的多粘菌素耐药机制 MCR-1 的出现。
通过全质粒测序和亚克隆鉴定大肠杆菌 SHP45 菌株中的 mcr-1 基因。通过序列比较、同源建模和电喷雾电离质谱对 MCR-1 机制进行研究。在 2011 年 4 月至 2014 年 11 月期间,从五个省份收集大肠杆菌和肺炎克雷伯菌菌株,调查 mcr-1 的流行情况。在鼠大腿模型中检测 MCR-1 体内赋予多粘菌素耐药性的能力。
多粘菌素耐药性仅归因于质粒介导的 mcr-1 基因。通过接合,携带 mcr-1 的质粒以 10(-1)至 10(-3)个受体细胞/细胞的频率转移到大肠杆菌受体中,并在肺炎克雷伯菌和铜绿假单胞菌中保持。在体内模型中,MCR-1 的产生使多粘菌素失去疗效。MCR-1 是磷酸乙醇胺转移酶家族的成员,在大肠杆菌中的表达导致脂质 A 中添加磷酸乙醇胺。我们观察到 2011-14 年间从生肉 523 个样本和动物 804 个样本中分离的大肠杆菌分离株中携带 mcr-1 的有 78(15%),从感染住院患者的 1322 个样本中有 16(1%)。
MCR-1 的出现标志着质粒介导的耐药性突破了最后一组抗生素-多粘菌素。尽管目前仅限于中国,MCR-1 可能会效仿其他全球耐药机制,如 NDM-1。我们的研究结果强调了迫切需要协调全球行动,以对抗泛耐药性革兰氏阴性菌。
中国科学技术部、国家自然科学基金。