Abstract

Understanding Mycobacterium tuberculosis (Mtb) transmission is essential to guide efficient tuberculosis control strategies. Traditional strain typing lacks sufficient discriminatory power to resolve large outbreaks. Here, we tested the potential of using next generation genome sequencing for identification of outbreak-related transmission chains. During long-term (1997 to 2010) prospective population-based molecular epidemiological surveillance comprising a total of 2,301 patients, we identified a large outbreak caused by an Mtb strain of the Haarlem lineage. The main performance outcome measure of whole genome sequencing (WGS) analyses was the degree of correlation of the WGS analyses with contact tracing data and the spatio-temporal distribution of the outbreak cases. WGS analyses of the 86 isolates revealed 85 single nucleotide polymorphisms (SNPs), subdividing the outbreak into seven genome clusters (two to 24 isolates each), plus 36 unique SNP profiles. WGS results showed that the first outbreak isolates detected in 1997 were falsely clustered by classical genotyping. In 1998, one clone (termed "Hamburg clone") started expanding, apparently independently from differences in the social environment of early cases. Genome-based clustering patterns were in better accordance with contact tracing data and the geographical distribution of the cases than clustering patterns based on classical genotyping. A maximum of three SNPs were identified in eight confirmed human-to-human transmission chains, involving 31 patients. We estimated the Mtb genome evolutionary rate at 0.4 mutations per genome per year. This rate suggests that Mtb grows in its natural host with a doubling time of approximately 22 h (400 generations per year). Based on the genome variation discovered, emergence of the Hamburg clone was dated back to a period between 1993 and 1997, hence shortly before the discovery of the outbreak through epidemiological surveillance. Our findings suggest that WGS is superior to conventional genotyping for Mtb pathogen tracing and investigating micro-epidemics. WGS provides a measure of Mtb genome evolution over time in its natural host context.

Highlights

  • Mortality due to infectious diseases remains a major burden, especially in low- and middle-income countries

  • Our findings suggest that whole genome sequencing (WGS) is superior to conventional genotyping for Mycobacterium tuberculosis (Mtb) pathogen tracing and investigating micro-epidemics

  • WGS provides a measure of Mtb genome evolution over time in its natural host context

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Summary

Introduction

Mortality due to infectious diseases remains a major burden, especially in low- and middle-income countries. In an increasingly globalized world, the free movement of humans favors the continuous spread of human pathogens such as Mycobacterium tuberculosis (Mtb), which is still among the most devastating pathogens [1,2] To detect this spread, understand the dynamics of the disease, and develop optimized tuberculosis (TB) control strategies, accurate tracing of pathogen transmission in the host population is of outmost importance [3]. Concerning Mtb, three reliable typing methods are used most often: IS6110 RFLP (restriction fragment length polymorphism) [4], spoligotyping (interspaced palindromic repeats; CRISPRs) [5], and MIRU-VNTR (mycobacterial interspersed repetitive unit– variable number of tandem repeats) typing [6] of up to 24 loci These methods have been successfully applied to a wide variety of research questions, e.g., investigation of laboratory cross-contaminations, investigation of outbreaks, and population-based analysis of recent transmission in metropolitan settings or country-wide [7,8,9]. Tuberculosis can be cured by taking several antibiotics daily for at least six months, the recent emergence of multidrug-resistant M. tuberculosis is making tuberculosis harder to treat

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