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Rapid detection of Acinetobacter baumannii and molecular epidemiology of carbapenem-resistant A. baumannii in two comprehensive hospitals of Beijing, China

机译:碳青霉烯耐药性 A的鲍曼不动杆菌的快速检测和分子流行病学。北京市两家综合医院的鲍曼氏菌

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Acinetobacter baumannii is an important opportunistic pathogen associated with a variety of nosocomial infections. A rapid and sensitive molecular detection in clinical isolates is quite needed for the appropriate therapy and outbreak control of A. baumannii . Group 2 carbapenems have been considered the agents of choice for the treatment of multiple drug-resistant A. baumannii . But the prevalence of carbapenem-resistant A. baumannii (CRAB) has been steadily increasing in recent years. Here, we developed a loop-mediated isothermal amplification (LAMP) assay for the rapid detection of A. baumannii in clinical samples by using high-specificity primers of the bla _(OXA-51)gene. Then we investigated the OXA-carbapenemases molecular epidemiology of A. baumannii isolates in two comprehensive hospitals in Beijing. The results showed that the LAMP assay could detect target DNA within 60 min at 65°C. The detection limit was 50 pg/μl, which was about 10-fold greater than that of PCR. Furthermore, this method could distinguish A. baumannii from the homologous A. nosocomialis and A. pittii . A total of 228 positive isolates were identified by this LAMP-based method for A. baumannii from 335 intensive care unit patients with clinically suspected multi-resistant infections in two hospitals in Beijing. The rates of CRAB are on the rise and are slowly becoming a routine phenotype for A. baumannii. Among the CRABs, 92.3% harbored both the bla _(OXA-23)and bla _(OXA-51)genes. Thirty-three pulsotypes were identified by pulsed-field gel electrophoresis, and the majority belonged to clone C. In conclusion, the LAMP method developed for detecting A. baumannii was faster and simpler than conventional PCR and has great potential for both point-of-care testing and basic research. We further demonstrated a high distribution of class D carbapenemase-encoding genes, mainly OXA-23, which presents an emerging threat in hospitals in China.
机译:鲍曼不动杆菌是与多种医院感染相关的重要机会病原体。为了对鲍曼不动杆菌进行适当的治疗和控制暴发,非常需要对临床分离株进行快速灵敏的分子检测。第2组碳青霉烯类被认为是治疗多重耐药鲍曼不动杆菌的首选药物。但是,近年来,对碳青霉烯类耐药的鲍曼不动杆菌(CRAB)的发病率一直在稳定增长。在这里,我们通过使用bla _(OXA-51)基因的高特异性引物开发了一种环介导的等温扩增(LAMP)分析法,用于快速检测临床样品中的鲍曼不动杆菌。然后,我们在北京的两家综合医院调查了鲍曼不动杆菌菌株的OXA-卡宾戊烯分子流行病学。结果表明,LAMP检测可以在65°C下60分钟内检测到目标DNA。检测限为50 pg /μl,比PCR的检测限高约10倍。此外,该方法可以将鲍曼不动杆菌与同源的医院内不动杆菌和皮氏不动杆菌区分开。通过这种基于LAMP的方法,在北京两家医院的335名重症监护病房中,临床上怀疑具有多重耐药性感染的鲍曼不动杆菌共鉴定出228株阳性菌。 CRAB的比率正在上升,并逐渐成为鲍曼不动杆菌的常规表型。在CRAB中,有92.3%的人同时具有bla _(OXA-23)和bla _(OXA-51)基因。通过脉冲场凝胶电泳鉴定了33种脉冲型,大多数属于克隆C。总之,开发的用于检测鲍曼不动杆菌的LAMP方法比常规PCR更快,更简单,并且在两个检测点上都具有巨大潜力。护理测试和基础研究。我们进一步证明了高分布的D类碳青霉烯酶编码基因,主要是OXA-23,这在中国的医院中正面临着新的威胁。

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