首页> 外文期刊>International Journal of Microbiology >Molecular Detection of Carbapenemase-Encoding Genes in Multidrug-Resistant Acinetobacter baumannii Clinical Isolates in South Africa
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Molecular Detection of Carbapenemase-Encoding Genes in Multidrug-Resistant Acinetobacter baumannii Clinical Isolates in South Africa

机译:南非多药物抗性临床临床分离株中的碳结构酶 - 编码基因的分子检测

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Introduction. Carbapenem-resistant Acinetobacter baumannii has been responsible for an increasing number of hospital-acquired infections globally. The study investigated the prevalence of carbapenemase-encoding genes in clinical multidrug-resistant A. baumannii strains. Materials and Methods. A total of 100 nonduplicate multidrug-resistant A. baumannii strains were cultured from clinical samples obtained from healthcare facilities in the O. R. Tambo district. The strains were confirmed by detecting the intrinsic blaOXA-51-like gene. Antimicrobial susceptibility testing was performed by VITEK? 2 and autoSCAN-4 systems. The MIC of imipenem and meropenem was rechecked by E-test. Colistin MIC was confirmed by the broth microdilution method. Real-time PCR was performed to investigate the presence of carbapenemase-encoding genes. Results. Most strains showed high resistance rates (80%) to the antibiotics tested. Resistance to amikacin, tetracycline, and tigecycline were 50%, 64%, and 48%, respectively. All strains were fully susceptible to colistin. The blaOXA-51-like was detected in all strains whilst blaOXA-23-like, blaOXA-58-like, blaOXA-24-like, blaIMP-1, blaVIM, and blaNDM-1 were found in 70%, 8%, 5%, 4%, 3%, and 2% of strains, respectively. None of the tested strains harboured the genes blaSIM and blaAmpC. The coexistence of blaOXA-23-like, and blaIMP-1 or blaOXA-58-like was detected in 1% and 2% strains, respectively. A distinct feature of our findings was the coharbouring of the genes blaOXA-23-like, blaOXA-58-like, and blaIMP-1 in 2% strains, and this is the first report in the Eastern Cape Province, South Africa. The intI1 was carried in 80% of tested strains whilst ISAba1/blaOXA-51-like and ISAba1/blaOXA-23-like were detected in 15% and 40% of the strains, respectively. The detection of blaOXA-23-like, ISAba1/blaOXA-51-like, ISAba1/blaOXA-23-like, and blaOXA-23-like, blaOXA-58-like, and blaIMP-1 carbapenemases in strains had a significant effect on both imipenem and meropenem MICs. Conclusions. Results showed a high level of oxacillinases producing A. baumannii circulating in our study setting, highlighting the need for local molecular surveillance to inform appropriate management and prevention strategies.
机译:介绍。抗抵抗肺癌的肺病鲍曼尼负责全球医院收养的感染越来越多。该研究研究了临床多药抗性A. Baumannii菌株中碳结构酶 - 编码基因的患病率。材料和方法。总共100份不保蛋白的多药抗性A.Baumannii菌株从O. R. Tambo区的医疗保健设施中获得的临床样品中培养。通过检测固有的Blaoxa-51样基因来确认菌株。 Vitek进行抗微生物易感性测试? 2和AutoScan-4系统。通过电子试验重新检查Imipenem和Meropenem的MIC。 Colistin MIC通过肉汤微稀释方法确认。进行实时PCR以研究编码碳碱酶的存在。结果。大多数菌株向测试的抗生素显示出高抗性率(> 80%)。对阿米卡星,四环素和脱癸锌素的抵抗力分别为50%,64%和48%。所有菌株都完全易于肥钠。在所有菌株中检测到Blaoxa-51样,虽然Blaoxa-23样,Blaoxa-58样,Blaoxa-24样,Blaimp-1,Blavim和Blandm-1在70%,8%,5分别分别为4%,3%和2%的菌株。没有测试的菌株覆盖了Blasim和Blaampc基因。 Blaoxa-23样的共存和Blaimp-1或Blaoxa-58样品分别以1%和2%的菌株检测。我们研究结果的一种独特的特点是Blaoxa-23样,Blaoxa-58样的基因的Coharbouring,以及2%菌株中的Blaimp-1,这是南非东开普省的第一个报告。 INTI1在80%的测试菌株中携带,而ISABA1 / BLAOXA-51样和ISABA1 / Blaoxa-23样品分别以15%和40%的菌株检测。类似于Blaoxa-23的isaBa1 / Blaoxa-51样,isaba1 / blaoxa-23样,以及Blaoxa-23样,Blaoxa-58样,菌株中的Blaimp-1碳丙烯酶酶对菌株有显着影响inipenem和meropenem mics。结论。结果表明,在我们的研究环境中产生了高水平的氧化酶酶,在我们的研究环境中循环,突出了局部分子监测的需求,以提供适当的管理和预防策略。

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