High precisionNeisseria gonorrhoeaevariant and antimicrobial resistance calling from metagenomic Nanopore sequencing
Sanderson ND., Swann J., Barker L., Kavanagh J., Hoosdally S., Crook D., Street TL., Eyre DW.
AbstractThe rise of antimicrobial resistantNeisseria gonorrhoeaeis a significant public health concern. Against this background, rapid culture-independent diagnostics may allow targeted treatment and prevent onward transmission. We have previously shown metagenomic sequencing of urine samples from men with urethral gonorrhoea can recover near-completeN. gonorrhoeaegenomes. However, disentangling theN. gonorrhoeaegenome from metagenomic samples and robustly identifying antimicrobial resistance determinants from error-prone Nanopore sequencing is a substantial bioinformatics challenge.Here we demonstrate anN. gonorrhoeaediagnostic workflow for analysis of metagenomic sequencing data obtained from clinical samples using R9.4.1 Nanopore sequencing. We compared results from simulated and clinical infections with data from known reference strains and Illumina sequencing of isolates cultured from the same patients. We evaluated three Nanopore variant callers and developed a random forest classifier to filter called SNPs. Clair was the most suitable variant caller after SNP filtering. A minimum depth of 20x reads was required to confidently identify resistant determinants over the entire genome. Our findings show that metagenomic Nanopore sequencing can provide reliable diagnostic information inN. gonorrhoeaeinfection.