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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Emergence of Serratia marcescens, Klebsiella pneumoniae, and Escherichia coli Isolates possessing the plasmid-mediated carbapenem-hydrolyzing beta-lactamase KPC-2 in intensive care units of a Chinese hospital.
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Emergence of Serratia marcescens, Klebsiella pneumoniae, and Escherichia coli Isolates possessing the plasmid-mediated carbapenem-hydrolyzing beta-lactamase KPC-2 in intensive care units of a Chinese hospital.

机译:在一家中国医院的重症监护病房中,具有质粒介导的碳青霉烯水解β-内酰胺酶KPC-2的粘质沙雷氏菌,肺炎克雷伯菌和大肠杆菌分离株的出现。

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Twenty-one Serratia marcescens, ten Klebsiella pneumoniae, and one Escherichia coli isolate with carbapenem resistance or reduced carbapenem susceptibility were recovered from intensive care units (ICUs) in our hospital. Enterobacterial repetitive intergenic consensus-PCR and pulsed-field gel electrophoresis demonstrated that all the S. marcescens isolates belonged to a clonal strain and the 10 K. pneumoniae isolates were indistinguishable or closely related to each other. The MICs of imipenem, meropenem, and ertapenem for all isolates were 2 to 8 microg/ml, except for K. pneumoniae K10 (MICs of 128, 256, and >256 microg/ml). Isoelectric focusing, PCRs, and DNA sequencing indicated that all S. marcescens isolates produced KPC-2 and a beta-lactamase with a pI of 6.5. All K. pneumoniae isolates produced TEM-1, KPC-2, CTX-M-14, and a beta-lactamase with a pI of 7.3. The E. coli E1 isolate produced KPC-2, CTX-M-15, and a beta-lactamase with a pI of 7.3. Conjugation studies with E. coli (EC600) resulted in the transfer of reduced carbapenem susceptibility compared to that of the original isolates, and only the bla(KPC-2) gene was detected in E. coli transconjugants. Plasmid restriction analysis showed identical restriction patterns among all E. coli transconjugants. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and ompK35/36 gene sequence analysis of outer membrane proteins revealed that K. pneumoniae K10 failed to express OmpK36, because of insertional inactivation by an insertion sequence ISEcp1. All these results indicate that KPC-2-producing S. marcescens, K. pneumoniae, and E. coli isolates emerged in ICUs in our hospital. KPC-2 combined with porin deficiency results in high-level carbapenem resistance in K. pneumoniae. The same bla(KPC-2)-encoding plasmid was spread among the three different genera.
机译:从我院的重症监护病房(ICU)中回收了21株粘质沙雷氏菌,10株肺炎克雷伯菌和1株具有碳青霉烯耐药性或碳青霉烯敏感性降低的大肠杆菌。肠细菌重复基因间共有-PCR和脉冲场凝胶电泳表明,所有的粘液链球菌均属于克隆菌株,而10株肺炎克雷伯菌则无法区分或彼此密切相关。除肺炎克雷伯菌K10(MIC分别为128、256和> 256 microg / ml)外,所有分离物的亚胺培南,美洛培南和厄他培南的MIC均为2至8 microg / ml。等电聚焦,PCR和DNA测序表明,所有的marcescens分离株均产生KPC-2和β-内酰胺酶,pI为6.5。所有肺炎克雷伯菌分离株均产生TEM-1,KPC-2,CTX-M-14和β-内酰胺酶,pI为7.3。大肠杆菌E1分离株产生KPC-2,CTX-M-15和β-内酰胺酶,pI为7.3。与大肠杆菌(EC600)的结合研究导致碳青霉烯敏感性降低(与原始分离株相比)的转移,并且在大肠杆菌转导结合物中仅检测到bla(KPC-2)基因。质粒限制性内切酶分析显示在所有大肠杆菌转导结合物中相同的限制性内切酶模式。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和外膜蛋白的ompK35 / 36基因序列分析显示,肺炎克雷伯菌K10无法表达OmpK36,这是由于插入序列ISEcp1导致的插入失活。所有这些结果表明,在我们医院的ICU中出现了生产KPC-2的粘液链球菌,肺炎克雷伯菌和大肠杆菌分离株。 KPC-2与孔蛋白缺乏症相结合导致肺炎克雷伯菌具有高水平的碳青霉烯抗性。相同的bla(KPC-2)编码质粒分布在三个不同的属中。

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