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首页> 外文期刊>Antimicrobial Resistance and Infection Control >Co-existence of bla OXA-23 and bla NDM-1 genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance
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Co-existence of bla OXA-23 and bla NDM-1 genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance

机译:尼泊尔鲍曼不动杆菌bla OXA-23和bla NDM-1基因的共存:耐药性及其临床意义

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Background Molecular analysis of carbapenem-resistant genes in Acinetobacter baumannii , an emerging pathogen, is less commonly reported from Nepal. In this study we determined the antibiotic susceptibility profile and genetic mechanism of carbapenem resistance in clinical isolates of A. baumannii. Methods A. baumannii were isolated from various clinical specimens and identified based on Gram staining, biochemical tests, and PCR amplification of organism specific 16S rRNA and bla OXA-51 genes. The antibiotic susceptibility testing was performed using disc diffusion and E-test method. Multiplex PCR assays were used to detect the following β-lactamase genes: four class D carbapenem hydrolyzing oxacillinases ( bla OXA-51, bla OXA-23, bla OXA-24 and bla OXA-58). Uniplex PCRs were used to detect three class B metallo-β-lactamases genes ( bla IMP, bla VIM and bla NDM-1), class C cephalosporin resistance genes ( bla ADC), aminoglycoside resistance gene ( aphA6 ), and IS Aba1 of all isolates. Insertion sequence IS Aba125 among NDM-1 positive strains was detected. Clonal relatedness of all isolates were analyzed using repetitive sequence-based PCR (rep-PCR). Results Of total 44 analyzed isolates, 97.7% ( n =?43) were carbapenem-resistant A. baumannii (CR-AB) and 97.7% ( n =?43) were multidrug resistant A. baumannii (MDR-AB). One isolate was detected to be extremely drug resistant A. baumannii (XDR-AB). All the isolates were fully susceptible to colistin (MICs?OXA-23 gene was detected in all isolates, while bla NDM-1 was detected in 6 isolates (13.6%). Insertion sequence, IS Aba1 was detected in all of bla OXA-23 positive isolates. IS Aba125 was detected in all bla NDM-1 positive strains. The bla ADC and aphA6 genes were detected in 90.1 and 40.1%, respectively. The rep-PCR of all isolates represented 7 different genotypes. Conclusion We found high prevalence of CR-AB and MDR-AB with bla OXA-23 gene in a tertiary care hospital in Nepal. Systemic network surveillance should be established for monitoring and controlling the spread of these resistant strains.
机译:背景技术尼泊尔很少报道鲍曼不动杆菌(一种新兴病原体)中对碳青霉烯类耐药基因的分子分析。在这项研究中,我们确定了鲍曼不动杆菌临床分离株中对碳青霉烯类药物的耐药性和遗传机制。方法从各种临床标本中分离鲍曼不动杆菌,并根据革兰氏染色,生化试验和PCR扩增生物特异性16S rRNA和bla OXA-51 基因进行鉴定。使用纸片扩散和E-test方法进行抗生素敏感性测试。使用多重PCR分析检测以下β-内酰胺酶基因:四个D类碳青霉烯水解草酸酶(bla OXA-51 ,bla OXA-23 ,bla OXA -24 和bla OXA-58 )。 Uniplex PCR用于检测三个B类金属β-内酰胺酶基因(bla IMP ,bla VIM 和bla NDM-1 )所有分离株的C头孢菌素抗性基因(bla ADC ),氨基糖苷抗性基因(aphA6)和IS Aba1。在NDM-1阳性菌株中检测到插入序列IS Aba125。使用基于重复序列的PCR(rep-PCR)分析所有分离株的克隆相关性。结果分析的44种分离株中,耐碳青霉烯的鲍曼不动杆菌(CR-AB)为97.7%(n =?43),耐多药的鲍曼不动杆菌(MDR-AB)为97.7%(n =?43)。检测到一种分离物具有极强的耐药性鲍曼不动杆菌(XDR-AB)。所有分离株均对大肠菌素完全敏感(在所有分离株中均检测到MICs?OXA-23 基因,而在6个分离株中检测到bla NDM-1 (13.6%)。在所有bla OXA-23 阳性菌株中均检测到IS Aba1,在所有bla NDM-1 阳性菌株中均检测到IS Aba125。 >和aphA6基因的检出率分别为90.1%和40.1%,所有分离株的rep-PCR代表7种不同的基因型。结论我们发现bla OXA-23 应该建立系统的网络监视以监视和控制这些耐药菌株的传播。

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