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首页> 外文期刊>Medical Journal Armed Forces India >Molecular detection of bla_(NDM-1) (New Delhi metallobetalactamase-1) in nosocomial Enterobacteriaceae isolates by nested, multiplex polymerase chain reaction
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Molecular detection of bla_(NDM-1) (New Delhi metallobetalactamase-1) in nosocomial Enterobacteriaceae isolates by nested, multiplex polymerase chain reaction

机译:通过嵌套,多重聚合酶链式反应在医院肠杆菌菌分离株中的Bla_(Ndm-1)(新Delhi金属酰胺酰胺酶-1)的分子检测

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Background: Carbapenems are considered "drugs of last resort" in many life-threatening infections. Advent of carbapenemases like KPC, OXA-48, VIM, IMP, and NDM have greatly affected the efficacy of these drugs, posing serious threat to global health and infection control. NDM bears special significance to the India subcontinent, labeled as place of origin and reservoir. NDM tends to escape detection by routine phenotypic methods, requiring molecular confirmation. This study utilizes nested, multiplex polymerase chain reaction (PCR) for reliable detection of bla_(NDM-1) in nosocomial Enterobacteriaceae isolates. Methods: This study was conducted to detect prevalence of bla_(NDM-1)>bla_(IMP), bla_(VIM) and bla_(KpC) genes by multiplex PGR among multidrug/carbapenem-resistant nosocomial Enterobacteriaceae isolates. From March 2013 to April 2014, 100 consecutive non-repeat isolates of Enterobacteriaceae from various inpatient clinical samples were analyzed. Imipenem-resis-tant isolates identified by Kirby Bauer disk diffusion method with Clinical and Laboratory Standards Institute guidelines were further subjected to nested, multiplex PCR to simultaneously detect bla_(NDM-1), bla_(IMP), bla_(VIM) and bla_(KPc) genes. Results: Out of 100 isolates, 17 (17%) were found to be imipenem-resistant. bla_(NDM-1) was detected in all 17 isolates by nested, multiplex PCR. bla_(VIM) was co-carried in 4 isolates while one isolate co-harbored bla_(IMP) with bIa_(NDM-1). Imipenem resistance and NDM-1 carriage was predominant amongst Klebsiella isolates. Maximum NDM-1 producers were isolated from the intensive care unit (70.6%). Conclusion: NDM-1 prevalence in nosocomial Enterobacteriaceae isolates in our hospital was found to be 17%. A nested, multiplex PCR was used for rapid detection of various carbapenemase genes with high sensitivity and specificity which is essential not only for favorable patient outcome but also for timely implementation of appropriate infection control practices to prevent further spread of such organisms. ^g>Carbapenemases,New Delhi Metallobetalactamase, (NDM), Multiplex, bla_(IMp), bla_(VIM) and bIa_(KPC), ICU
机译:背景:在许多危及生命的感染中,Carbapenems被认为是“持续前手段的药物”。 KPC,OXA-48,Vim,Imp和NDM等碳蔗糖酶的出现极大地影响了这些药物的疗效,对全球健康和感染控制构成严重威胁。 NDM对印度次大陆具有特殊意义,标记为原产地和水库。 NDM倾向于通过常规表型方法逃逸检测,需要分子确认。该研究利用嵌套,多重聚合酶链反应(PCR)在医院肠杆菌区分离株中可靠地检测Bla_(Ndm-1)。方法:通过多重PGR在多药/抵抗医院内肠杆菌分离株中检测该研究以检测BLA_(NDM-1)> BLA_(IMP),BLA_(VIM)和BLA_(KPC)基因的患病率。从2013年3月至2014年4月,分析了来自各种住院性临床样品的100个连续的非重复分离肠杆菌的分离物。通过临床和实验室标准研究所的Kirby Bauer磁盘扩散方法识别的Imipenem-Resis-Tantations进一步进行嵌套,多重PCR以同时检测Bla_(NDM-1),BLA_(IMP),BLA_(VIM)和BLA_( KPC)基因。结果:17个分离物中,发现17个(17%)是抗亚胺尼的抗性。通过嵌套的多重PCR在所有17个分离物中检测到BLA_(NDM-1)。 Bla_(Vim)在4个分离物中共同携带,而一个分离与BIA_(NDM-1)的共同覆盖的BLA_(IMP)。 Inipenem抗性和NDM-1携带在Klebsiella隔离物中是主要的。最大NDM-1生产商与重症监护病房(70.6%)分离出来。结论:发现我们院医院内肠杆菌的NDM-1流行率为17%。嵌套的多重PCR用于快速检测具有高敏感性和特异性的各种碳碱酶基因,这对于有利的患者结果至关重要,也必不可少地实施适当的感染控制实践,以防止这种生物进一步扩散。 ^ g>碳结甲酶,新德里金属酰胺酰亚胺酶,(ndm),多路复用,bla_(imp),bla_(vim)和bia_(kpc),ICU

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