Nanopore ultra-long read sequencing technology for antimicrobial resistance detection in Mannheimia haemolytica

纳米孔 DNA测序 全基因组测序 抗菌剂 放大器 基因组 细菌
作者
Alexander Lim,Bryan Naidenov,Haley Bates,Karyn Willyerd,Timothy A. Snider,M. B. Couger,Charles Chen,Akhilesh Ramachandran
出处
期刊:Journal of Microbiological Methods [Elsevier BV]
卷期号:159: 138-147 被引量:13
标识
DOI:10.1016/j.mimet.2019.03.001
摘要

Disruptive innovations in long-range, cost-effective direct template nucleic acid sequencing are transforming clinical and diagnostic medicine. A multidrug resistant strain and a pan-susceptible strain of Mannheimia haemolytica, isolated from pneumonic bovine lung samples, were sequenced at 146× and 111× coverage, respectively with Oxford Nanopore Technologies MinION. De novo assembly produced a complete genome for the non-resistant strain and a nearly complete assembly for the drug resistant strain. Functional annotation using RAST (Rapid Annotations using Subsystems Technology), CARD (Comprehensive Antibiotic Resistance Database) and ResFinder databases identified genes conferring resistance to different classes of antibiotics including β-lactams, tetracyclines, lincosamides, phenicols, aminoglycosides, sulfonamides and macrolides. Resistance phenotypes of the M. haemolytica strains were determined by minimum inhibitory concentration (MIC) of the antibiotics. Sequencing with a highly portable MinION device corresponded to MIC assays with most of the antimicrobial resistant determinants being identified with as few as 5437 reads, except for the genes responsible for resistance to Fluoroquinolones. The resulting quality assemblies and AMR gene annotation highlight the efficiency of ultra-long read, whole-genome sequencing (WGS) as a valuable tool in diagnostic veterinary medicine.

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