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Next-Generation Sequencing and Comparative Analysis of Sequential Outbreaks Caused by Multidrug-Resistant Acinetobacter baumannii at a Large Academic Burn Center

机译:大型学术烧伤中心的耐多药鲍曼不动杆菌引起的下一代暴发的下一代测序和比较分析

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摘要

Next-generation sequencing (NGS) analysis has emerged as a promising molecular epidemiological method for investigating health care-associated outbreaks. Here, we used NGS to investigate a 3-year outbreak of multidrug-resistant Acinetobacter baumannii (MDRAB) at a large academic burn center. A reference genome from the index case was generated using de novo assembly of PacBio reads. Forty-six MDRAB isolates were analyzed by pulsed-field gel electrophoresis (PFGE) and sequenced using an Illumina platform. After mapping to the index case reference genome, four samples were excluded due to low coverage, leaving 42 samples for further analysis. Multilocus sequence types (MLST) and the presence of acquired resistance genes were also determined from the sequencing data. A transmission network was inferred from genomic and epidemiological data using a Bayesian framework. Based on single-nucleotide variant (SNV) differences, this MDRAB outbreak represented three sequential outbreaks caused by distinct clones. The first and second outbreaks were caused by sequence type 2 (ST2), while the third outbreak was caused by ST79. For the second outbreak, the MLST and PFGE results were discordant. However, NGS-based SNV typing detected a recombination event and consequently enabled a more accurate phylogenetic analysis. The distribution of resistance genes varied among the three outbreaks. The first- and second-outbreak strains possessed a blaOXA-23-like group, while the third-outbreak strains harbored a blaOXA-40-like group. NGS-based analysis demonstrated the superior resolution of outbreak transmission networks for MDRAB and provided insight into the mechanisms of strain diversification between sequential outbreaks through recombination.
机译:下一代测序(NGS)分析已成为一种有前途的分子流行病学方法,用于调查与卫生保健相关的疾病暴发。在这里,我们使用NGS调查了一个大型学术性烧伤中心连续3年爆发的多药耐药鲍曼不动杆菌(MDRAB)。使用PacBio读数的从头装配从索引案例中获得参考基因组。通过脉冲场凝胶电泳(PFGE)分析了46个MDRAB分离株,并使用Illumina平台进行了测序。映射到索引病例参考基因组后,由于覆盖率低,排除了四个样本,剩下42个样本需要进一步分析。还从测序数据确定了多基因座序列类型(MLST)和获得的抗性基因的存在。使用贝叶斯框架从基因组和流行病学数据推断出传播网络。基于单核苷酸变异(SNV)差异,此MDRAB爆发代表了由不同克隆引起的三个连续爆发。第一次和第二次爆发是由序列类型2(ST2)引起的,而第三次爆发是由ST79引起的。对于第二次爆发,MLST和PFGE结果不一致。但是,基于NGS的SNV分型检测到重组事件,因此可以进行更准确的系统发育分析。抗性基因的分布在三个暴发中有所不同。第一次和第二次暴发菌株均带有blaOXA-23类,而第三次暴发菌株则具有blaOXA-40类。基于NGS的分析证明了MDRAB暴发传播网络的卓越分辨率,并为通过重组的连续暴发之间的菌株多样化机制提供了见解。

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