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首页> 外文期刊>Biotechnology & Biotechnological Equipment >Investigation of mutations in adeR and adeS gene regions in gentamicine resistant Acinetobacter baumannii isolates
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Investigation of mutations in adeR and adeS gene regions in gentamicine resistant Acinetobacter baumannii isolates

机译:常常蛋白抗性分离物中诱剂抗性抗菌剂突变的研究及抗裂解基因区

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ABSTRACT This study evaluated the relationship between aminoglycoside resistance and the active efflux pump and investigated the role of the active efflux pump in resistance mechanisms. In addition, the mutations related to aminoglycoside resistance were investigated in Acinetobacter baumannii isolates obtained from different clinical specimens. The study included 32 A . baumannii isolates. They were identified and their susceptibilities were determined using conventional techniques and an automated system. Total genomic RNA, DNA and cDNA were obtained using commercial extraction kits. Primers for adeR and adeS were designed using sequences in GenBank. All isolates were subjected to polymerase chain reaction (PCR) to determine the presence of adeR and adeS . The PCR products were electrophoresed for the optimization study. Subsequently, real-time PCR was performed to determine the expression levels of the adeR and adeS genes. Sequence analysis of the two adeRS operons in our isolates showed five mutations differing from those of other isolates. Isolate A21 had three mutations: (Tyr31Phe), (Val136Ala) and (Leu142Ile); isolate A24 had two mutations: (Asn115His) and (Leu142Ile). In our study, the examined gene regions that play a role in the resistance mechanisms of A . baumannii were considered important. The results indicated that adeR and adeS expression clearly affect aminoglycoside resistance. However, gene expression alone does not seem sufficient to explain that. These results could help to design improved active efflux pump inhibitors.
机译:摘要本研究评估了氨基糖苷抗性和活性流出泵之间的关系,并研究了活性流出泵在电阻机构中的作用。此外,在从不同临床标本获得的肺杆菌Baumannii分离物中研究了与氨基糖苷抗性相关的突变。该研究包括32个。 Baumannii孤立。它们被识别出,并使用常规技术和自动化系统确定它们的敏感性。使用商业提取试剂盒获得总基因组RNA,DNA和cDNA。使用Genbank中的序列设计了Ader和Ades的引物。对所有分离物进行聚合酶链式反应(PCR)以确定涂剂和脂肪的存在。 PCR产物被电泳用于优化研究。随后,进行实时PCR以确定Ader和Ades基因的表达水平。我们分离株中的两个涂剂操纵子的序列分析显示了与其他分离物不同的五个突变。分离物A21有三个突变:(Tyr31phe),(Val136Ala)和(Leu142ile);分离物A24有两个突变:(Asn115His)和(Leu142ile)。在我们的研究中,检查了在抗性机制中发挥作用的研究。 Baumannii被认为是重要的。结果表明,Ader和Ades表达明显影响氨基糖苷抗性。然而,单独的基因表达似乎不足以解释这一点。这些结果有助于设计改进的活性流出泵抑制剂。

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