Laboratory for Medical Microbiology and Immunology, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
Department of Infection Control, Amphia Hospital, Breda, The Netherlands.
PLoS One. 2020 May 18;15(5):e0233313. doi: 10.1371/journal.pone.0233313. eCollection 2020.
Knowledge of within-patient dynamics of resistance plasmids during outbreaks is important for understanding the persistence and transmission of plasmid-mediated antimicrobial resistance. During an outbreak of a Klebsiella pneumoniae carbapenemase-producing (KPC) K. pneumoniae, the plasmid and chromosomal dynamics of K. pneumoniae within-patients were investigated.
During the outbreak, all K. pneumoniae isolates of colonized or infected patients were collected, regardless of their susceptibility pattern. A selection of isolates was short-read and long-read sequenced. A hybrid assembly of the short-and long-read sequence data was performed. Plasmid contigs were extracted from the hybrid assembly, annotated, and within patient plasmid comparisons were performed.
Fifteen K. pneumoniae isolates of six patients were short-read whole-genome sequenced. Whole-genome multi-locus sequence typing revealed a maximum of 4 allele differences between the sequenced isolates. Within patients 1 and 2 the resistance gene- and plasmid replicon-content did differ between the isolates sequenced. Long-read sequencing and hybrid assembly of 4 isolates revealed loss of the entire KPC-gene containing plasmid in the isolates of patient 2 and a recombination event between the plasmids in the isolates of patient 1. This resulted in two different KPC-gene containing plasmids being simultaneously present during the outbreak.
During a hospital outbreak of a KPC-producing K. pneumoniae isolate, plasmid loss of the KPC-gene carrying plasmid and plasmid recombination was detected within the isolates from two patients. When investigating outbreaks, one should be aware that plasmid transmission can occur and the possibility of within- and between-patient plasmid variation needs to be considered.
了解爆发期间耐药质粒的患者内动力学对于理解质粒介导的抗菌耐药性的持续存在和传播非常重要。在产碳青霉烯酶肺炎克雷伯菌(KPC)肺炎克雷伯菌爆发期间,研究了患者体内肺炎克雷伯菌的质粒和染色体动力学。
在爆发期间,无论其药敏模式如何,均收集定植或感染患者的所有肺炎克雷伯菌分离株。对选择的分离株进行短读和长读测序。对短读和长读序列数据进行混合组装。从混合组装中提取质粒连续体,进行注释,并对患者内质粒进行比较。
对 6 名患者的 15 株肺炎克雷伯菌进行了短读全基因组测序。全基因组多位点序列分型显示,测序分离株之间的等位基因差异最大为 4 个。在患者 1 和 2 中,测序分离株之间的耐药基因和质粒复制子含量存在差异。对 4 株菌进行长读测序和混合组装发现,患者 2 的分离株中整个 KPC 基因携带质粒丢失,而患者 1 的分离株中质粒之间发生重组事件。这导致在爆发期间同时存在两种不同的含有 KPC 基因的质粒。
在产 KPC 的肺炎克雷伯菌分离株的医院爆发期间,在两名患者的分离株中检测到 KPC 基因携带质粒的丢失和质粒重组。在调查爆发时,应意识到质粒传播可能发生,并且需要考虑患者内和患者间质粒变异的可能性。