首页> 美国卫生研究院文献>Frontiers in Microbiology >Genotypic and Antimicrobial Susceptibility of Carbapenem-resistant Acinetobacter baumannii: Analysis of ISAba Elements and blaOXA-23-like Genes Including a New Variant
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Genotypic and Antimicrobial Susceptibility of Carbapenem-resistant Acinetobacter baumannii: Analysis of ISAba Elements and blaOXA-23-like Genes Including a New Variant

机译:耐碳青霉烯鲍曼不动杆菌的基因型和抗菌药物敏感性:ISAba元素和blaOXA-23样基因的分析,包括一个新的变体

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摘要

Carbapenem-resistant Acinetobacter baumannii (CR-AB) causes serious nosocomial infections, especially in ICU wards of hospitals, worldwide. Expression of blaOXA genes is the chief mechanism of conferring carbapenem resistance among CR-AB. Although some blaOXA genes have been studied among CR-AB isolates from Iran, their blaOXA-23-like genes have not been investigated. We used a multiplex-PCR to detect Ambler class A, B, and D carbapenemases of 85 isolates, and determined that 34 harbored blaOXA-23-like genes. Amplified fragment length polymorphism (AFLP) genotyping, followed by DNA sequencing of blaOXA-23-like amplicons of CR-AB from each AFLP group was used to characterize their blaOXA-23-like genes. We also assessed the antimicrobial susceptibility pattern of CR-AB isolates, and tested whether they harbored insertion sequences ISAba1 and ISAba4. Sequence comparison with reference strain A. baumannii (NCTC12156) revealed five types of mutations in blaOXA-23-like genes; including one novel variant and four mutants that were already reported from China and the USA. All of the blaOXA-23-like genes mutations were associated with increased minimum inhibitory concentrations (MICs) against imipenem. ISAba1 and ISAba4 sequences were detected upstream of blaOXA-23 genes in 19 and 7% of isolates, respectively. The isolation of CR-AB with new blaOXA-23 mutations including some that have been reported from the USA and China highlights CR-AB pervasive distribution, which underscores the importance of concerted national and global efforts to control the spread of CR-AB isolates worldwide.
机译:耐碳青霉烯的鲍曼不动杆菌(CR-AB)引起严重的医院感染,尤其是在世界范围内的ICU医院病房中。 blaOXA基因的表达是CR-AB之间赋予碳青霉烯抗性的主要机制。尽管已经从伊朗的CR-AB分离物中研究了一些blaOXA基因,但尚未研究其blaOXA-23样基因。我们使用多重PCR检测了85个分离株的Ambler A,B和D类碳青霉烯酶,并确定了34个带有blaOXA-23样基因。使用扩增的片段长度多态性(AFLP)基因分型,然后对来自每个AFLP组的CR-AB的blaOXA-23样扩增子进行DNA测序,以表征其blaOXA-23样基因。我们还评估了CR-AB分离株的抗菌药敏模式,并测试了它们是否具有ISAba1和ISAba4插入序列。与参考菌株鲍曼不动杆菌(NCTC12156)的序列比较揭示了blaOXA-23-样基因中的五种突变。包括中国和美国已经报道的一种新型变体和四种突变体。所有blaOXA-23样基因突变均与对亚胺培南的最低抑菌浓度(MIC)升高有关。在blaOXA-23基因上游分别检测到ISAba1和ISAba4序列,分别为19和7%。带有新blaOXA-23突变的CR-AB的分离,包括美国和中国已报道的一些突变,突出了CR-AB的普遍分布,这突显了国家和全球共同努力控制CR-AB分离株在全球范围内传播的重要性。 。

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