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Identification of bla KPC-2 on different plasmids of three Morganella morganii isolates.

机译:在三种摩根氏摩根氏菌分离物的不同质粒上鉴定bla KPC-2。

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Three Morganella morganii strains resistant to carbapenems were recovered from the surgical intensive care unit (SICU) in our hospital. Carbapenemases and extended-spectrum β-lactamases (ESBLs) were respectively detected by the modified Hodge test and the modified Clinical and Laboratory Standards Institute (CLSI) ESBL confirmatory test in all isolates. Amplification of whole-cell and plasmid DNAs extracted from isolates with primers specific for the bla (KPC) produced an amplicon confirmed to be bla (KPC-2) by sequence analysis. Pulsed-field gel electrophoresis (PFGE) typing revealed that three isolates belonged to two closely related types. Plasmids electrophoresis and restriction analysis revealed that the bla (KPC-2) was located on different plasmids. The transfer of carbapenem resistance from the three original isolates to Escherichia coli EC600 was successful by conjugation. An examination of the outer membrane proteins showed a lack of a 38-kDa outer membrane protein (OMP) compared with M. morganii susceptible to carbapenems. The production of KPC-2 and ESBLs, combined with OMP deficiency, resulted in high-level carbapenem resistance in the M. morganii strains. The genetic environment around bla (KPC-2) analysis revealed that this β-lactamase was located on the same mobile genetic elements which could transfer between different plasmids.
机译:从我院外科重症监护室(SICU)中回收了三株对碳青霉烯类耐药的摩根氏摩根氏菌。通过改良的Hodge检验和改良的临床和实验室标准协会(CLSI)ESBL确证试验分别检测了所有分离物中的碳青霉烯酶和广谱β-内酰胺酶(ESBLs)。用对bla(KPC)具有特异性的引物从分离物中提取的全细胞和质粒DNA进行扩增,产生的扩增子经序列分析证实为bla(KPC-2)。脉冲场凝胶电泳(PFGE)分型显示三种分离物属于两种密切相关的类型。质粒电泳和限制性酶切分析表明,bla(KPC-2)位于不同的质粒上。通过结合成功地将碳青霉烯抗性从三个原始分离株转移至大肠杆菌EC600。与对碳青霉烯易感的摩根摩根氏菌相比,对外膜蛋白的检查表明缺少38 kDa的外膜蛋白(OMP)。 KPC-2和ESBLs的产生,与OMP缺乏相结合,导致摩根氏菌株中对碳青霉烯类药物具有高水平的抗性。 bla周围的遗传环境(KPC-2)分析表明,这种β-内酰胺酶位于相同的可移动遗传元件上,可以在不同质粒之间转移。

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