Department of Infectious Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310016, China; Key Laboratory of Microbial Technology and Bioinformatics of Zhejiang Province, Hangzhou 310016, China.
Biomedicine Discovery Institute, Department of Microbiology, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne 3800, Australia; Department of Infectious Diseases, The Alfred Hospital and Central Clinical School, Monash University, Melbourne 3004, Australia.
Genomics Proteomics Bioinformatics. 2020 Oct;18(5):539-548. doi: 10.1016/j.gpb.2020.12.002. Epub 2020 Dec 30.
Plasmids remain important microbial components mediating the horizontal gene transfer (HGT) and dissemination of antimicrobial resistance. To systematically explore the relationship between mobile genetic elements (MGEs) and antimicrobial resistance genes (ARGs), a novel strategy using single-molecule real-time (SMRT) sequencing was developed. This approach was applied to pooled conjugative plasmids from clinically isolated multidrug-resistant (MDR) Klebsiella pneumoniae from a tertiary referral hospital over a 9-month period. The conjugative plasmid pool was obtained from transconjugants that acquired antimicrobial resistance after plasmid conjugation with 53 clinical isolates. The plasmid pool was then subjected to SMRT sequencing, and 82 assembled plasmid fragments were obtained. In total, 124 ARGs (responsible for resistance to β-lactam, fluoroquinolone, and aminoglycoside, among others) and 317 MGEs [including transposons (Tns), insertion sequences (ISs), and integrons] were derived from these fragments. Most of these ARGs were linked to MGEs, allowing for the establishment of a relationship network between MGEs and/or ARGs that can be used to describe the dissemination of resistance by mobile elements. Key elements involved in resistance transposition were identified, including IS26, Tn3, IS903B, ISEcp1, and ISKpn19. As the most predominant IS in the network, a typical IS26-mediated multicopy composite transposition event was illustrated by tracing its flanking 8-bp target site duplications (TSDs). The landscape of the pooled plasmid sequences highlights the diversity and complexity of the relationship between MGEs and ARGs, underpinning the clinical value of dominant HGT profiles.
质粒仍然是介导水平基因转移 (HGT) 和抗生素耐药性传播的重要微生物成分。为了系统地研究移动遗传元件 (MGE) 与抗生素耐药基因 (ARGs) 之间的关系,开发了一种使用单分子实时 (SMRT) 测序的新策略。该方法应用于 9 个月内从一家三级转诊医院临床分离的多药耐药 (MDR) 肺炎克雷伯菌中汇集的可接合质粒。可接合质粒池是从通过质粒与 53 株临床分离株的接合获得抗生素耐药性的转导体中获得的。然后对质粒池进行 SMRT 测序,获得 82 个组装的质粒片段。总共从这些片段中获得了 124 个 ARGs(负责对β-内酰胺、氟喹诺酮和氨基糖苷类药物等的耐药性)和 317 个 MGEs[包括转座子 (Tns)、插入序列 (ISs) 和整合子]。这些 ARGs 大多数与 MGEs 相连,从而可以建立 MGEs 和/或 ARGs 之间的关系网络,用于描述移动元件介导的耐药性传播。确定了与耐药性转位有关的关键元件,包括 IS26、Tn3、IS903B、ISEcp1 和 ISKpn19。作为网络中最主要的 IS,通过追踪其侧翼 8 个碱基对的靶位重复序列 (TSD),说明了典型的 IS26 介导的多拷贝复合转位事件。汇集质粒序列的景观突出了 MGEs 和 ARGs 之间关系的多样性和复杂性,为主要 HGT 图谱的临床价值提供了依据。