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Covert dissemination of carbapenemase-producing Klebsiella pneumoniae (KPC) in a successfully controlled outbreak: long and short-read whole-genome sequencing demonstrate multiple genetic modes of transmission

机译:在成功控制的爆发中秘密传播产生碳青霉烯酶的肺炎克雷伯菌(KpC):长读和短读全基因组测序证明了多种遗传传播模式

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摘要

Background: Carbapenemase-producing Enterobacteriaceae (CPE), including KPC-producing Klebsiella pneumoniae (KPC-Kpn), are an increasing threat to patient safety. Objectives: To use WGS to investigate the extent and complexity of carbapenemase gene dissemination in a controlled KPC outbreak. Materials and methods: Enterobacteriaceae with reduced ertapenem susceptibility recovered from rectal screening swabs/clinical samples, during a 3 month KPC outbreak (2013–14), were investigated for carbapenemase production, antimicrobial susceptibility, variable-number-tandem-repeat profile and WGS [short-read (Illumina), long-read (MinION)]. Short-read sequences were used for MLST and plasmid/Tn4401 fingerprinting, and long-read sequence assemblies for plasmid identification. Phylogenetic analysis used IQTree followed by ClonalFrameML, and outbreak transmission dynamics were inferred using SCOTTI. Results: Twenty patients harboured KPC-positive isolates (6 infected, 14 colonized), and 23 distinct KPC-producing Enterobacteriaceae were identified. Four distinct KPC plasmids were characterized but of 20 KPC-Kpn (from six STs), 17 isolates shared a single pKpQIL-D2 KPC plasmid. All isolates had an identical transposon (Tn4401a), except one KPC-Kpn (ST661) with a single nucleotide variant. A sporadic case of KPC-Kpn (ST491) with Tn4401a-carrying pKpQILD2 plasmid was identified 10 months before the outbreak. This plasmid was later seen in two other species and other KPC-Kpn (ST14,ST661) including clonal spread of KPC-Kpn (ST661) from a symptomatic case to nine ward contacts. Conclusions: WGS of outbreak KPC isolates demonstrated blaKPC dissemination via horizontal transposition (Tn4401a), plasmid spread (pKpQIL-D2) and clonal spread (K. pneumoniae ST661). Despite rapid outbreak control, considerable dissemination of blaKPC still occurred among K. pneumoniae and other Enterobacteriaceae, emphasizing its high transmission potential and the need for enhanced control efforts.
机译:背景:产生碳青霉烯酶的肠杆菌科(CPE),包括生产KPC的肺炎克雷伯菌(KPC-Kpn),对患者安全的威胁日益增加。目的:使用WGS研究在受控的KPC暴发中碳青霉烯酶基因传播的程度和复杂性。材料和方法:在3个月KPC爆发期间(2013-14年),从直肠筛查拭子/临床样本中回收的厄他培南敏感性降低的肠杆菌科细菌进行了碳青霉菌酶生产,抗菌药敏感性,可变数目串联重复谱和WGS的研究[短读(Illumina),长读(MinION)]。短读序列用于MLST和质粒/ Tn4401指纹图谱,长读序列用于质粒鉴定。系统发育分析使用IQTree,然后使用ClonalFrameML,并使用SCOTTI推断暴发传播动力学。结果:20例患者携带KPC阳性分离株(6例感染,14例定植),鉴定出23种不同的KPC产肠杆菌科。表征了四个不同的KPC质粒,但是在20个KPC-Kpn(来自六个ST)中,有17个分离株共享一个pKpQIL-D2 KPC质粒。除一个带有单个核苷酸变异体的KPC-Kpn(ST661)外,所有分离株均具有相同的转座子(Tn4401a)。在疫情爆发前10个月,发现了零星的KPC-Kpn(ST491)携带Tn4401a的pKpQILD2质粒。后来在另外两个物种和其他KPC-Kpn(ST14,ST661)中发现了该质粒,包括KPC-Kpn(ST661)从有症状病例到九个病房接触的克隆传播。结论:爆发的KPC分离株的WGS证明了blaKPC通过水平转座(Tn4401a),质粒扩散(pKpQIL-D2)和克隆扩散(肺炎克雷伯氏菌ST661)传播。尽管控制了迅速的暴发,但在肺炎克雷伯菌和其他肠杆菌科中仍大量传播blaKPC,强调了其高传播潜力,需要加强控制力度。

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