上海某教学医院耐碳青霉烯高毒力肺炎克雷伯菌表型与基因型分析

Wei Ma, Yuxiang Wan, Xuejiao Li, Xiaochun Huang, Changzi Deng, Qin Qin
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摘要

介绍。耐碳青霉烯高致病性肺炎克雷伯菌(CR-hvKP)是一种与严重临床结果相关的新兴病原体,促使对其基因组特征和致病潜力进行紧急调查。假设/差距语句。我们推测,CR-hvKP菌株表现出高耐药性和高毒力,导致其在临床环境中迅速传播,并对临床治疗构成严重威胁。本研究旨在研究CR-hvKP菌株的表型和基因型,揭示其耐药和毒力相关的基因组特征,阐明高毒力和高耐药菌株的生物学特性,为临床提供分子流行病学资料。2013年1月至2018年12月从临床样本中获得耐碳青霉烯类肺炎克雷伯菌(CRKP)菌株。PCR扩增筛选碳青霉烯类基因。为了评估分离株的毒力潜力,我们进行了一系列试验,包括串试验、mellonella幼虫感染试验、荚膜多糖合成基因分型和基因测序分析。采用PFGE、多位点序列分型和新一代测序等方法检测菌株的亲缘关系和同源性。本研究共获得500株CRKP,其中鉴定为CR-hvKP的有18株。所有CR-hvKP菌株均具有多重耐药,对大多数β-内酰胺类抗生素(包括碳青霉烯类)表现出高度耐药。除N5株外,所有CR-hvKP株blaKPC-2阳性,其中14株为荚膜血清型K64。通过PFGE分析鉴定出10种不相关的PFGE类型。根据PFGE结果,从18株分离株中筛选出12株CR-hvKP进行进一步检测,9株分离株与pLVPK毒力相关质粒具有高度同源性。所有CR-hvKP菌株均表现出高毒力。该研究揭示了CR-hvKP菌株的抗性和毒力相关的基因组特征,并证实了这些菌株的高毒力。这些结果对了解CR-hvKP的流行病学特征和临床治疗具有重要意义,为制定相应的防控策略提供基础数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenotype and genotype of carbapenem-resistant hypervirulent Klebsiella pneumoniae in a teaching hospital in Shanghai, China.

Introduction. Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP) is an emerging pathogen associated with severe clinical outcomes, prompting an urgent investigation into its genomic characteristics and pathogenic potential.Hypothesis/Gap Statement. We hypothesize that CR-hvKP strains exhibit high-level resistance and high virulence, leading to their rapid spread in clinical settings and posing a serious threat to clinical treatment.Aim. The aim of the study was to investigate the phenotype and genotype of CR-hvKP strains, reveal their resistance- and virulence-related genomic characteristics and elucidate the biological characteristics of high-virulence and high-resistance strains to provide molecular epidemiological data for clinical use.Methodology. Carbapenem-resistant K. pneumoniae (CRKP) strains were obtained from clinical samples, from January 2013 to December 2018. PCR amplification was conducted to screen for carbapenem genes. To evaluate the virulence potential of the isolates, we conducted various tests, including a string test, Galleria mellonella larvae infection test, capsular polysaccharide synthesis genotyping and genetic sequencing analyses. We used PFGE, multilocus sequence typing and next-generation sequencing to detect the genetic relationship and homology of the strains.Results. In this study, we obtained 500 strains of CRKP, among which 18 strains were identified as CR-hvKP. All CR-hvKP strains were multidrug-resistant, exhibiting high-level resistance to most β-lactam antibiotics, including carbapenems. All CR-hvKP strains except N5 were positive for blaKPC-2, of which 14 isolates belonged to capsular serotype K64. Ten unrelated PFGE types were identified by PFGE analysis. Based on the results of PFGE, a total of 12 CR-hvKP isolates were selected from the 18 isolates for further testing, and 9 isolates had high homology with pLVPK virulence-related plasmids. All CR-hvKP strains showed high virulence in the Galleria mellonella infection model.Conclusions. The study revealed the resistance- and virulence-related genomic characteristics of CR-hvKP strains and confirmed the high virulence of these strains. These results are of great significance for understanding the epidemiological characteristics and clinical treatment of CR-hvKP and provide basic data for the formulation of corresponding prevention and control strategies.

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