首页> 外文期刊>Frontiers in Microbiology >A Novel IncA/C1 Group Conjugative Plasmid, Encoding VIM-1 Metallo-Beta-Lactamase, Mediates the Acquisition of Carbapenem Resistance in ST104 Klebsiella pneumoniae Isolates from Neonates in the Intensive Care Unit of V. Monaldi Hospital in Naples
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A Novel IncA/C1 Group Conjugative Plasmid, Encoding VIM-1 Metallo-Beta-Lactamase, Mediates the Acquisition of Carbapenem Resistance in ST104 Klebsiella pneumoniae Isolates from Neonates in the Intensive Care Unit of V. Monaldi Hospital in Naples

机译:编码VIM-1金属-β-内酰胺酶的新型IncA / C1基团结合质粒介导V. Monaldi医院重症监护病房新生儿ST104 <斜体>肺炎克雷伯菌菌株中碳青霉烯抗性的获得。那不勒斯

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The emergence of carbapenemase producing Enterobacteriaceae has raised major public health concern. The aim of this study was to investigate the molecular epidemiology and the mechanism of carbapenem resistance acquisition of multidrug-resistant Klebsiella pneumoniae isolates from 20 neonates in the neonatal intensive care unit (NICU) of the V. Monaldi Hospital in Naples, Italy, from April 2015 to March 2016. Genotype analysis by pulsed-field gel electrophoresis (PFGE) and multi-locus sequence typing (MLST) identified PFGE type A and subtypes A1 and A2 in 17, 2, and 1 isolates, respectively, and assigned all isolates to sequence type (ST) 104. K. pneumoniae isolates were resistant to all classes of β-lactams including carbapenems, fosfomycin, gentamicin, and trimethoprim–sulfamethoxazole, but susceptible to quinolones, amikacin, and colistin. Conjugation experiments demonstrated that resistance to third-generation cephems and imipenem could be transferred along with an IncA/C plasmid containing the extended spectrum β-lactamase bla _(SHV -12)and carbapenem-hydrolyzing metallo-β-lactamase bla _(V IM-1)genes. The plasmid that we called pIncAC_KP4898 was 156,252 bp in size and included a typical IncA/C backbone, which was assigned to ST12 and core genome (cg) ST12.1 using the IncA/C plasmid MLST (PMLST) scheme. pIncAC_KP4898 showed a mosaic structure with bla _(V IM-1)into a class I integron, bla _(SHV -12)flanked by IS6 elements, a mercury resistance and a macrolide 2′-phosphotransferase clusters, ant(3″), aph(3″), aacA4, qnrA1, sul1 , and dfrA14 conferring resistance to aminoglycosides, quinolones, sulfonamides, and trimethoprim, respectively, several genes predicted to encode transfer functions and proteins involved in DNA transposition. The acquisition of pIncAC_KP4898 carrying bla _(V IM-1)and bla _(SHV -12)contributed to the spread of ST104 K. pneumoniae in the NICU of V. Monaldi Hospital in Naples.
机译:产生碳青霉烯酶的肠杆菌科的出现引起了公众的重大关注。这项研究的目的是调查意大利那不勒斯V.Monaldi医院新生儿重症监护病房(NICU)从4月开始的20例新生儿的多药耐药肺炎克雷伯菌肺炎克雷伯菌的分子流行病学和耐药机制。 2015年至2016年3月。通过脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)进行基因型分析,分别在17、2和1个分离株中鉴定出PFGE A型以及A1和A2亚型,并将所有分离株分配给序列类型(ST)104.肺炎克雷伯菌分离株对所有种类的β-内酰胺类都有抗药性,包括碳青霉烯类,磷霉素,庆大霉素和甲氧苄啶-磺胺甲恶唑,但易受喹诺酮,丁胺卡那霉素和大肠粘菌素的影响。结合实验表明,对第三代头孢和亚胺培南的抗性可以与含有扩展谱β-内酰胺酶bla_(SHV -12)和碳青霉烯水解金属-β-内酰胺酶bla_(V IM)的IncA / C质粒一起转移-1)基因。我们称为pIncAC_KP4898的质粒大小为156,252 bp,包括一个典型的IncA / C主链,使用IncA / C质粒MLST(PMLST)方案将其分配给ST12和核心基因组(cg)ST12.1。 pIncAC_KP4898显示了一个带有bla _(V IM-1)进入I类整倍体的镶嵌结构,bla _(SHV -12)的侧面是IS6元素,具有耐汞性和大环内酯2'-磷酸转移酶簇,ant(3″), aph(3″),aacA4,qnrA1,sul1和dfrA14分别赋予氨基糖苷类,喹诺酮类,磺酰胺类和甲氧苄啶抗性,这几个基因预计可编码涉及DNA转座的转移功能和蛋白质。携带bla _(V IM-1)和bla _(SHV -12)的pIncAC_KP4898的收购有助于ST104肺炎克雷伯菌在那不勒斯V. Monaldi医院的重症监护病房中传播。

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