尼日利亚伊巴丹市肺炎克雷伯菌质粒编码blaKPC和blaNDM菌株引起的卫生保健相关感染

Abigail T. Okunlola, O. Olowe, S. Taiwo
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引用次数: 2

摘要

碳青霉烯酶产生肺炎克雷伯菌(CPKP)最近成为卫生保健相关感染(HAIs)的主要原因。这些菌株现在被美国疾病控制中心列为需要紧急关注的超级细菌。本研究调查了伊巴丹市大学附属学院医院(UCH)住院患者HAIs中CPKP的发生情况。方法:采用标准微生物学方法对250例临床HAIs患者的非重复标本进行6个月的培养。采用GNB 24E微生物试剂盒鉴定肺炎克雷伯菌,采用纸片扩散试验检测对选定抗生素的体外药敏。采用改良霍奇法测定碳青霉烯酶的产量。采用常规PCR法检测肺炎克雷伯菌碳青霉烯酶(blaKPC)和新德里金属β-内酰胺酶(blaNDM)基因。对50例(20%)肺炎克雷伯菌感染培养阳性患者的数据进行分析。结果:分离株对氨苄西林(100%)、头孢呋辛(96%)、阿莫西林(92%)、庆大霉素(86%)、呋喃妥英(80%)、环丙沙星(80%)、头孢他啶(78%)、氧氟沙星(72%)耐药,对美罗培南敏感76%。碳青霉烯酶未检出,但12株美罗培南耐药异黄酮中8株携带blaKPC基因,2株同时携带blaKPC和blaNDM基因。研究表明,blaKPC和blaNDM K肺炎与伊巴丹地区的临床感染有关。结论:本研究报告了尼日利亚第二例肺炎克氏菌NDM临床感染病例。有必要加强尼日利亚医院的感染控制方案,以防止这些微生物在全国范围内传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Healthcare associated infections caused by plasmid-encoded blaKPC and blaNDM strains of Klebsiella pneumoniae in Ibadan, Nigeria
Introduction: Carbapenemase producing Klebsiella pneumoniae (CPKP) has recently emerged as major cause of healthcare associated infections (HAIs). These strains are now classified by the US Center for Disease Control as superbugs of urgent concern. This study investigated the occurrence of CPKP in HAIs among hospitalized patients in University College Hospital (UCH), Ibadan. Methods: Non-duplicate specimens obtained from 250 patients with clinical HAIs were cultured by standard microbiological methods over a period of 6 months. K. pneumoniae was identified using GNB 24E Microbact kit and invitro susceptibility to selected antibiotics was performed by the disk diffusion test. Carbapenemase production was tested by Modified Hodge technique. K pneumoniae carbapenemase (blaKPC) and New Delhi Metallo-β-lactamase (blaNDM) genes were detected by conventional PCR assay. Data were analyzed for the 50 (20%) patients who were culture positive for K pneumoniae infections. Results: Isolates were resistant to ampicillin (100%), cefuroxime (96%), amoxicillin (92%), gentamicin (86%), nitrofurantoin (80%), ciprofloxacin (80%), ceftazidime (78%) and ofloxacin (72%) but 76% were sensitive to meropenem. No carbapenemase enzyme was detected but 8 of 12 iso-lates resistant to meropenem carried blaKPC while 2 carried both blaKPC and blaNDM genes. The study shows that blaKPC and blaNDM K pneumoniae are involved in clinical infections in Ibadan. Conclusion: This study reports the second case of K pneumoniae NDM clinical infection in Nigeria. There is need to strengthen the infection control programme of Nigerian hospitals to prevent nationwide spread of these organisms.
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