Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, United States of America.
Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
PLoS One. 2020 Nov 9;15(11):e0236533. doi: 10.1371/journal.pone.0236533. eCollection 2020.
Mycobacterium chelonae is a rapidly growing nontuberculous mycobacterium that is a common cause of nosocomial infections. Here we describe investigation of a possible nosocomial transmission of M. chelonae at the Hospital of the University of Pennsylvania (HUP). M. chelonae strains with similar high-level antibiotic resistance patterns were isolated from two patients who developed post-operative infections at HUP in 2017, suggesting a possible point source infection. The isolates, along with other clinical isolates from other patients, were sequenced using the Illumina and Oxford Nanopore technologies. The resulting short and long reads were hybrid assembled into draft genomes. The genomes were compared by quantifying single nucleotide variants in the core genome and assessed using a control dataset to quantify error rates in comparisons of identical genomes. We show that all M. chelonae isolates tested were highly dissimilar, as indicated by high pairwise SNV values, consistent with environmental acquisition and not a nosocomial point source. Our control dataset determined a threshold for evaluating identity between strains while controlling for sequencing error. Finally, antibiotic resistance genes were predicted for our isolates, and several single nucleotide variants were identified that have the potential to modulated drug resistance.
龟分枝杆菌是一种快速生长的非结核分枝杆菌,是医院感染的常见原因。在这里,我们描述了对宾夕法尼亚大学医院(HUP)可能发生的龟分枝杆菌医院内传播的调查。2017 年,HUP 两名术后感染患者分离出具有相似高水平抗生素耐药模式的龟分枝杆菌菌株,提示可能存在同源点源感染。这些分离株与其他来自其他患者的临床分离株一起,使用 Illumina 和 Oxford Nanopore 技术进行测序。将产生的短读长和长读长混合组装成草图基因组。通过定量核心基因组中的单核苷酸变体并使用对照数据集评估比较相同基因组的错误率来比较基因组。我们表明,所有测试的龟分枝杆菌分离株都高度不同,这表明是环境获得的,而不是医院内的同源点源。我们的对照数据集确定了一个评估菌株间同一性的阈值,同时控制了测序错误。最后,预测了我们分离株的抗生素耐药基因,并鉴定出了一些可能调节耐药性的单核苷酸变异。