National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
M. G. DeGroote Institute for Infectious Disease Research, Department of Biochemistry and Biomedical Sciences, DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada.
Proteomics Clin Appl. 2020 Jul;14(4):e1800182. doi: 10.1002/prca.201800182. Epub 2020 Feb 28.
Antimicrobial resistance (AMR), especially multidrug resistance, is one of the most serious global threats facing public health. The authors proof-of-concept study assessing the suitability of shotgun proteomics as an additional approach to whole-genome sequencing (WGS) for detecting AMR determinants.
Previously published shotgun proteomics and WGS data on four isolates of Campylobacter jejuni are used to perform AMR detection by searching the Comprehensive Antibiotic Resistance Database, and their detection ability relative to genomics screening and traditional phenotypic testing measured by minimum inhibitory concentration is assessed.
Both genomic and proteomic approaches identify the wild-type and variant molecular determinants responsible for resistance to tetracycline and ciprofloxacin, in agreement with phenotypic testing. In contrast, the genomic method identifies the presence of the β-lactamase gene, bla , in three isolates. However, its corresponding protein product is detected in only a single isolate, consistent with results obtained from phenotypic testing.
抗菌药物耐药性(AMR),尤其是多重耐药性,是全球公共卫生面临的最严重威胁之一。作者开展了一项概念验证研究,评估了 shotgun 蛋白质组学作为全基因组测序(WGS)的附加方法,用于检测 AMR 决定因素的适用性。
使用先前发表的空肠弯曲菌 4 株分离株的 shotgun 蛋白质组学和 WGS 数据,通过搜索综合抗生素耐药性数据库来进行 AMR 检测,并通过最小抑菌浓度评估其相对于基因组筛选和传统表型检测的检测能力。
基因组和蛋白质组方法都能识别四环素和环丙沙星耐药的野生型和变异分子决定因素,与表型检测结果一致。相比之下,基因组方法在 3 株分离株中鉴定出β-内酰胺酶基因 bla 的存在。然而,其对应的蛋白质产物仅在单个分离株中检测到,与表型检测结果一致。