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Emergence of Mobile Colistin Resistance ( mcr-8 ) in a Highly Successful Klebsiella pneumoniae Sequence Type 15 Clone from Clinical Infections in Bangladesh

机译:在高度成功的Klebsiella肺炎血管素序列中出现的流动乳突抗性(MCR-8),来自孟加拉国临床感染的15型克隆

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The emergence of mobilized colistin resistance genes ( mcr ) has become a serious concern in clinical practice, compromising treatment options for life-threatening infections. In this study, colistin-resistant Klebsiella pneumoniae harboring mcr-8.1 was recovered from infected patients in the largest public hospital of Bangladesh, with a prevalence of 0.3% (3/1,097). We found mcr-8.1 in an identical highly stable multidrug-resistant IncFIB(pQil) plasmid of ~113?kb, which belonged to an epidemiologically successful K. pneumoniae clone, ST15. The resistance mechanism was proven to be horizontally transferable, which incurred a fitness cost to the host. The core genome phylogeny suggested the clonal spread of mcr-8.1 in a Bangladeshi hospital. Core genome single-nucleotide polymorphisms among the mcr-8.1 -positive K. pneumoniae isolates ranged from 23 to 110. It has been hypothesized that mcr-8.1 was inserted into IncFIB(pQil) with preexisting resistance loci, bla TEM-1b and bla CTX-M-15 , by IS 903B . Coincidentally, all resistance determinants in the plasmid [ mcr-8.1 , ampC , sul2 , 1d-APH(6) , APH(3′′)-Ib , bla TEM-1b , bla CTX-M-15 ] were bracketed by IS 903B , demonstrating the possibility of intra- and interspecies and intra- and intergenus transposition of entire resistance loci. This is the first report of an mcr -like mechanism from human infections in Bangladesh. However, given the acquisition of mcr-8.1 by a sable conjugative plasmid in a successful high-risk clone of K. pneumoniae ST15, there is a serious risk of dissemination of mcr-8.1 in Bangladesh from 2017 onwards. IMPORTANCE There is a marked paucity in our understanding of the epidemiology of colistin-resistant bacterial pathogens in South Asia. A report by Davies and Walsh (Lancet Infect Dis 18:256–257, https://doi.org/10.1016/S1473-3099(18)30072-0, 2018) suggests the export of colistin from China to India, Vietnam, and South Korea in 2016 was approximately 1,000 tons and mainly used as a poultry feed additive. A few reports forecast that the prevalence of mcr in humans and livestock will increase in South Asia. Given the high prevalence of bla CTX-M-15 and bla NDM in India, Bangladesh, and Pakistan, colistin has become the invariable option for the management of serious infections, leading to the emergence of mcr -like mechanisms in South Asia. Systematic scrutiny of the prevalence and transmission of mcr variants in South Asia is vital to understanding the drivers of mcr genes and to initiate interventions to overcome colistin resistance.
机译:动员的乳霉素抗性基因(MCR)的出现已成为临床实践的严重关切,损害治疗危及生命感染的治疗方案。在这项研究中,从孟加拉国最大的公共医院的感染患者中回收了含有MCR-8.1的Colistin抗性Klebsiella肺炎,患病率为0.3%(3 / 1,097)。我们发现MCR-8.1在一个相同的高度稳定的多药抗性INCFIB(PQIL)质粒,其属于流行病学成功的K.肺炎克隆ST15。证明抵抗机制是水平可转移的,这对宿主产生了健身成本。核心基因组系统提出了MCR-8.1在孟加拉国医院中的克隆扩散。 MCR-8.1的核心基因组单核苷酸多态性,肺炎氏肺炎的分离物中的23-110。已经假设将MCR-8.1插入Incfib(PQIL)中,具有预先存在的抗性基因座,BLA TEM-1B和BLA CTX -m-15,是903b。巧合,质粒中的所有抗性决定簇[MCR-8.1,AMPC,SUL2,1D-APH(6),APH(3') - IB,BLA TEM-1B,BLA CTX-M-15是903B的,展示了整个抵抗基因座的内部和间隔和和和和中间型血管内的可能性。这是孟加拉国人类感染的MCR般的机制的第一个报告。然而,鉴于在K.Pneumoniae ST15的成功高危克隆中获得MCR-8.1,在K.Pneumoniae ST15的成功高危克隆中,从2017年开始,孟加拉国的MCR-8.1发生严重风险。我们对我们对南亚耐药细菌病原体的流行病学的理解有明显缺乏缺乏症。 Davies和Walsh的报告(柳叶葡萄牙感染者18:256-257,https://doi.org/10.1016/s1473-3099(18)30072-0,2018)表明,从中国到印度,越南的Colistin出口, 2016年韩国约为1000吨,主要用作家禽饲料添加剂。一些报告预测,人类和牲畜中MCR的患病率将在南亚增加。鉴于BLA CTX-M-15和BLA NDM在印度,孟加拉国和巴基斯坦的普及率高,Colistin已成为管理严重感染的不变选择,导致南亚MCR的出现。系统审查南亚MCR变体的患病率和传播至关重要,以了解MCR基因的驱动程序,并开始干预措施克服菌落抗性。

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