Abstract

Canada has one of the lowest rates of tuberculosis (TB) in the world, however, among certain sub-populations, disease incidence rates approach those observed in sub-Saharan Africa, and other high incidence regions. In this study, we applied mycobacterial interspersed repetitive unit (MIRU) variable number of tandem repeat (VNTR) and whole genome sequencing (WGS) to the analysis of Mycobacterium tuberculosis isolates obtained from Northern communities in the territory of Nunavut. WGS was carried out using the Illumina MiSeq, with identified variants used to infer phylogenetic relationships and annotated to infer functional implications. Additionally, the sequencing data from these isolates were augmented with publically available WGS to evaluate data from the Nunavut outbreak in the broader Canadian context. In this study, isolates could be classified into four major clusters by MIRU-VNTR analysis. These could be further resolved into sub-clusters using WGS. No evidence for antimicrobial resistance, either genetic or phenotypic, was observed in this cohort. Among most subjects with multiple samples, reactivation/incomplete treatment likely contributed to recurrence. However, isolates from two subjects appeared more likely to have occurred via reinfection, based on the large number of genomic single nucleotide variants detected. Finally, although quite distinct from previously reported Canadian MTB strains, isolates obtained from Nunavut clustered most closely with a cohort of samples originating in the Nunavik region of Northern Quebec. This study demonstrates the benefit of using WGS for discriminatory analysis of MTB in Canada, especially in high incidence regions. It further emphasizes the importance of focusing epidemiological intervention efforts on interrupting transmission chains of endemic TB throughout Northern communities, rather than relying on strategies applied in regions where the majority of TB cases result from importation of foreign strains.

Highlights

  • Tuberculosis (TB) is a global disease with an estimated one third of the world’s population infected with the causative agent, Mycobacterium tuberculosis (MTB) [1]

  • The aims of this study were twofold: to characterize the amount of nucleotide-level diversity identified via whole genome sequencing (WGS) within the larger mycobacterial interspersed repetitive unit (MIRU) clusters in circulating MTB in Nunavut; and to perform a meta-analysis including our own data as well as all available Canadian MTB strains currently available in public reference databases, in order to better understand this epidemic within the Canadian context

  • 24-loci MIRU-variable number of tandem repeat (VNTR) performed on the 274 isolates from this region identified four clusters based on 100% pattern identity (Fig 1)

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Summary

Introduction

Tuberculosis (TB) is a global disease with an estimated one third of the world’s population infected with the causative agent, Mycobacterium tuberculosis (MTB) [1]. These Canadian subpopulations have dissimilar epidemiological profiles, with foreign-born individuals commonly infected in their home country and displaying restricted transmission of disease within Canadian communities, versus Canadian-born Indigenous Peoples infected by endemic clonal outbreak strains circulating through communities, and contributing to maintenance of transmission chains [4,5,6] Within this context, this study describes the ongoing TB epidemic in the territory of Nunavut, where, in 2003, a dramatic increase in the incidence of TB occurred, reaching a maximum rate of 299.8 per 100,000 in 2010 (Territory population of 33,353)[2]. To develop targeted medical and public health interventions, understanding and describing the molecular basis of the outbreak is required, as, to date, neither the epidemic nor the circulating strains in this region have been well characterized

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