Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon, Hong Kong, SAR China; State Key Lab of Chemical Biology and Drug Discovery and the Department of Food Science and Nutrition, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, SAR China.
Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon, Hong Kong, SAR China.
Microbiol Res. 2024 Jun;283:127666. doi: 10.1016/j.micres.2024.127666. Epub 2024 Feb 28.
The escalating prevalence of multidrug-resistant (MDR) bacteria pose a significant public health threat. Understanding the genomic features and deciphering the antibiotic resistance profiles of these pathogens is crucial for development of effective surveillance and treatment strategies. In this study, we employed the R10.4.1 nanopore sequencing technology, specifically through the use of the MinION platform, to analyze eight MDR bacterial strains originating from clinical, ecological and food sources. A single 72-hour sequencing run could yield approximately 12 million reads which covered a total of 34 gigabases (Gbp). The nanopore R10.4.1 data was processed using the Flye assembler, successfully assembling the genomes of eight bacterial strains and their 18 plasmids. Notably, the assemblies generated solely from R10.4.1 nanopore data closely matched those from next-generation sequencing data. Diverse antibiotic resistance patterns and specific resistance genes in the test strains were identified. Hospital strains that exhibited multidrug resistance were found to harbor various resistance genes that encode efflux pumps and extended-spectrum β-lactamases. Environmental and food sources were found to display resistance profiles in a species-specific manner. The composition of structurally complex plasmids in the test strains could also be revealed by analysis of nanopore long reads, which also suggested evidence of horizontal transfer of plasmids between different bacterial species. These findings provide valuable insights into the genetic characteristics of MDR bacteria and demonstrating the practicality of nanopore sequencing technology for detecting of resistance elements in bacterial pathogens.
多药耐药(MDR)细菌的流行呈上升趋势,对公共健康构成重大威胁。了解这些病原体的基因组特征并破译其抗生素耐药谱对于制定有效的监测和治疗策略至关重要。在这项研究中,我们使用 R10.4.1 纳米孔测序技术,特别是通过使用 MinION 平台,分析了来自临床、生态和食品来源的 8 株 MDR 细菌。单次 72 小时测序可产生约 1200 万条读数,总共覆盖 340 吉字节(Gbp)。使用 Flye 组装器处理纳米孔 R10.4.1 数据,成功组装了 8 株细菌及其 18 个质粒的基因组。值得注意的是,仅从 R10.4.1 纳米孔数据生成的组装与下一代测序数据非常匹配。在测试菌株中鉴定出不同的抗生素耐药模式和特定的耐药基因。表现出多药耐药性的医院菌株携带各种编码外排泵和扩展谱β-内酰胺酶的耐药基因。环境和食品来源显示出特定于物种的耐药谱。通过分析纳米孔长读长还可以揭示测试菌株中结构复杂质粒的组成,这也表明质粒在不同细菌物种之间发生水平转移的证据。这些发现为 MDR 细菌的遗传特征提供了有价值的见解,并证明了纳米孔测序技术在检测细菌病原体中的耐药元件的实用性。