National Food Institute, Technical University of Denmark, 2800 Kgs Lyngby, Denmark.
Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark, 2800 Kgs Lyngby, Denmark.
J Antimicrob Chemother. 2017 Oct 1;72(10):2764-2768. doi: 10.1093/jac/dkx217.
Antibiotic resistance is a major health problem, as drugs that were once highly effective no longer cure bacterial infections. WGS has previously been shown to be an alternative method for detecting horizontally acquired antimicrobial resistance genes. However, suitable bioinformatics methods that can provide easily interpretable, accurate and fast results for antimicrobial resistance associated with chromosomal point mutations are still lacking.
Phenotypic antimicrobial susceptibility tests were performed on 150 isolates covering three different bacterial species: Salmonella enterica, Escherichia coli and Campylobacter jejuni. The web-server ResFinder-2.1 was used to identify acquired antimicrobial resistance genes and two methods, the novel PointFinder (using BLAST) and an in-house method (mapping of raw WGS reads), were used to identify chromosomal point mutations. Results were compared with phenotypic antimicrobial susceptibility testing results.
A total of 685 different phenotypic tests associated with chromosomal resistance to quinolones, polymyxin, rifampicin, macrolides and tetracyclines resulted in 98.4% concordance. Eleven cases of disagreement between tested and predicted susceptibility were observed: two C. jejuni isolates with phenotypic fluoroquinolone resistance and two with phenotypic erythromycin resistance and five colistin-susceptible E. coli isolates with a detected pmrB V161G mutation when assembled with Velvet, but not when using SPAdes or when mapping the reads.
PointFinder proved, with high concordance between phenotypic and predicted antimicrobial susceptibility, to be a user-friendly web tool for detection of chromosomal point mutations associated with antimicrobial resistance.
抗生素耐药性是一个主要的健康问题,因为曾经非常有效的药物不再能治愈细菌感染。全基因组测序(WGS)以前被证明是一种替代方法,用于检测水平获得的抗菌药物耐药基因。然而,仍然缺乏能够提供易于解释、准确和快速的结果的合适生物信息学方法,用于与染色体点突变相关的抗菌药物耐药性。
对涵盖三个不同细菌物种的 150 个分离株进行了表型抗菌药物敏感性测试:肠炎沙门氏菌、大肠杆菌和空肠弯曲菌。使用 ResFinder-2.1 网络服务器来识别获得的抗菌药物耐药基因,并用两种方法,即新的 PointFinder(使用 BLAST)和内部方法(原始 WGS 读数的映射)来识别染色体点突变。将结果与表型抗菌药物敏感性测试结果进行比较。
总共 685 种不同的与喹诺酮类、多粘菌素、利福平、大环内酯类和四环素类药物的染色体耐药相关的表型测试结果显示出 98.4%的一致性。在测试和预测的敏感性之间观察到 11 个不一致的情况:两个空肠弯曲菌分离株具有表型氟喹诺酮耐药性和两个具有表型红霉素耐药性,以及五个粘菌素敏感的大肠杆菌分离株,当用 Velvet 组装时检测到 pmrB V161G 突变,但当用 SPAdes 或映射读数时则没有。
PointFinder 证明了与表型和预测抗菌药物敏感性之间具有高度一致性,是一种用户友好的网络工具,用于检测与抗菌药物耐药性相关的染色体点突变。