Abstract

Whole-genome sequencing (WGS) with next-generation DNA sequencing (NGS) is an increasingly accessible and affordable method for genotyping hundreds of Mycobacterium tuberculosis (Mtb) isolates, leading to more effective epidemiological studies involving single nucleotide variations (SNVs) in core genomic sequences based on molecular evolution. We developed an all-in-one web-based tool for genotyping Mtb, referred to as the Total Genotyping Solution for TB (TGS-TB), to facilitate multiple genotyping platforms using NGS for spoligotyping and the detection of phylogenies with core genomic SNVs, IS6110 insertion sites, and 43 customized loci for variable number tandem repeat (VNTR) through a user-friendly, simple click interface. This methodology is implemented with a KvarQ script to predict MTBC lineages/sublineages and potential antimicrobial resistance. Seven Mtb isolates (JP01 to JP07) in this study showing the same VNTR profile were accurately discriminated through median-joining network analysis using SNVs unique to those isolates. An additional IS6110 insertion was detected in one of those isolates as supportive genetic information in addition to core genomic SNVs. The results of in silico analyses using TGS-TB are consistent with those obtained using conventional molecular genotyping methods, suggesting that NGS short reads could provide multiple genotypes to discriminate multiple strains of Mtb, although longer NGS reads (≥300-mer) will be required for full genotyping on the TGS-TB web site. Most available short reads (~100-mer) can be utilized to discriminate the isolates based on the core genome phylogeny. TGS-TB provides a more accurate and discriminative strain typing for clinical and epidemiological investigations; NGS strain typing offers a total genotyping solution for Mtb outbreak and surveillance. TGS-TB web site: https://gph.niid.go.jp/tgs-tb/.

Highlights

  • An estimated 8.6 million people developed tuberculosis (TB) in 2012, and 1.3 million individuals died from this disease

  • Spoligotyping has less resolving power to discriminate among Mycobacterium tuberculosis (Mtb) strains compared with IS6110 genotyping [5]

  • Whole-genome sequencing (WGS) provides an adequate solution for molecular epidemiology, traditional genotyping methods are still used effectively

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Summary

Introduction

An estimated 8.6 million people developed tuberculosis (TB) in 2012, and 1.3 million individuals died from this disease. Molecular genotyping of Mtb has been well developed [2]; three main typing methods, IS6110 restriction fragment length polymorphism (RFLP), spoligotyping (spacer oligonucleotide typing), and variable-number tandem repeat (VNTR) analysis, are currently used for fingerprinting Mtb strains to detect recent transmission. Spoligotyping has less resolving power to discriminate among Mtb strains compared with IS6110 genotyping [5]. MIRU-VNTR typing has progressed and is currently used to visualize the transmission of multiple Mtb strains, yielding intrinsically digital results that can be catalogued in a computer database [6]. The discriminatory power of this technique is not sufficient in countries such as East Asia and Russia with a high proportion of Beijing-type Mtb. Lineage- or sublineage-specific loci should be investigated to increase the discriminative power of genotyping [8]

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