Abstract

Molecular typing based on variable-number tandem repeats (VNTR) analysis is a promising tool for identifying transmission of Mycobacterium tuberculosis. However, the currently proposed 15- and 24-locus VNTR sets (VNTR-15/24) only have limited resolution and contain too many loci for large-scale typing in high burden countries. To develop an optimal typing scheme in China, we evaluated the resolution and robustness of 25 VNTR loci, using population-based collections of 1362 clinical isolates from six provinces across the country. The resolution of most loci showed considerable variations among regions. By calculating the average resolution of all possible combinations of 20 robust loci, we identified an optimal locus set with a minimum of 9 loci (VNTR-9) that could achieve comparable resolution of the standard VNTR-15. The VNTR-9 had consistently high resolutions in all six regions, and it was highly concordant with VNTR-15 for defining both clustered and unique genotypes. Furthermore, VNTR-9 was phylogenetically informative for classifying lineages/sublineages of M. tuberculosis. Three hypervariable loci (HV-3), VNTR 3232, VNTR 3820 and VNTR 4120, were proved important for further differentiating unrelated clustered strains based on VNTR-9. We propose the optimized VNTR-9 as first-line method and the HV-3 as second-line method for molecular typing of M. tuberculosis in China and surrounding countries. The development of hierarchical VNTR typing methods that can achieve high resolution with a small number of loci could be suitable for molecular epidemiology study in other high burden countries.

Highlights

  • Tuberculosis (TB) remains a serious global public health issue, especially in the developing world

  • We systematically evaluated the discriminatory powers of 25 variable-number tandem repeats (VNTR) loci using population-based collections of M. tuberculosis strains from six field sites that cover different regions across China [4]

  • We found the variability for most VNTR loci varied considerably among the six sites, which could be explained by the genetic differences of M. tuberculosis between regions

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Summary

Introduction

Tuberculosis (TB) remains a serious global public health issue, especially in the developing world. In 2011, there were about one million new cases in China, which accounted for 12% of the global epidemic [1]. The TB epidemic in China was exacerbated by the dominance of the notorious M. tuberculosis Beijing strains [2], as well as the prevalence of multidrug resistant (MDR) cases [3]. Both the Beijing strains and MDR strains in China were found associate with ongoing transmissions [3,4]. There is an urgent need for reliable genotyping tools to identify and prevent transmissions of M. tuberculosis

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