Massachusetts Host-Microbiome Center, Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Clinical Microbiology Laboratory, Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Clin Microbiol Infect. 2018 Sep;24(9):1016.e7-1016.e13. doi: 10.1016/j.cmi.2017.12.024. Epub 2018 Jan 9.
Corynebacterium striatum is an emerging multidrug-resistant (MDR) pathogen of immunocompromised and chronically ill patients. The objective of these studies was to provide a detailed genomic analysis of disease-causing C. striatum and determine the genomic drivers of resistance and resistance-gene transmission.
A multi-institutional and prospective pathogen genomics programme flagged seven MDR C. striatum infections occurring close in time, and specifically in immunocompromised patients with underlying respiratory diseases. Whole genome sequencing was used to identify clonal relationships among strains, genetic causes of antimicrobial resistance, and their mobilization capacity. Matrix-assisted linear desorption/ionization-time-of-flight analyses of sequenced isolates provided curated content to improve rapid clinical identification in subsequent cases.
Epidemiological and genomic analyses identified a related cluster of three out of seven C. striatum among lung transplant patients who had common procedures and exposures at an outlying institution. Genomic analyses further elucidated drivers of the MDR phenotypes, including resistance genes mobilized by IS3504 and ISCg9a-like insertion sequences. Seven mobilizable resistance genes were localized to a common chromosomal region bounded by unpaired insertion sequences, suggesting that a single recombination event could spread resistance to aminoglycosides, macrolides, lincosamides and tetracyclines to naive strains.
In-depth genomic studies of MDR C. striatum reveal its capacity for clonal spread within and across healthcare institutions and identify novel vectors that can mobilize multiple forms of drug resistance, further complicating efforts to treat infections in immunocompromised populations.
棒状杆菌属是一种新兴的多药耐药(MDR)病原体,感染对象为免疫功能低下和患有慢性疾病的患者。本研究的目的是对致病的 C. striatum 进行详细的基因组分析,确定耐药性和耐药基因传播的基因组驱动因素。
一项多机构和前瞻性的病原体基因组学计划标记了 7 例时间上接近的 MDR C. striatum 感染,这些感染发生在患有潜在呼吸道疾病的免疫功能低下的患者中。全基因组测序用于确定菌株之间的克隆关系、抗菌药物耐药的遗传原因及其移动能力。对测序分离株进行基质辅助线性解吸/电离-飞行时间分析,提供了经过整理的内容,以提高随后病例的快速临床鉴定能力。
流行病学和基因组分析在肺移植患者中发现了 7 例 C. striatum 中有 3 例具有相关性,这些患者在一家偏远的机构进行了共同的手术和暴露。基因组分析进一步阐明了 MDR 表型的驱动因素,包括由 IS3504 和 ISCg9a 样插入序列移动的耐药基因。7 个可移动的耐药基因定位于一个由未配对插入序列包围的共同染色体区域,表明单个重组事件可将氨基糖苷类、大环内酯类、林可酰胺类和四环素类耐药传播到未感染的菌株。
对 MDR C. striatum 的深入基因组研究揭示了其在医疗机构内部和跨医疗机构传播的能力,并确定了可移动多种形式耐药性的新型载体,进一步增加了治疗免疫功能低下人群感染的难度。