4.7 Article

Major Mycobacterium tuberculosis Lineages Associate with Patient Country of Origin

Journal

JOURNAL OF CLINICAL MICROBIOLOGY
Volume 47, Issue 4, Pages 1119-1128

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JCM.02142-08

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Funding

  1. Canadian Institutes of Health Research [MOP82931, RRD153877, MOP53184]
  2. Montreal Chest Institute
  3. Canadian Institutes of Health Research
  4. Fonds de la Recherche en Sante du Quebec (FRSQ)

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Over recent years, there has been an increasing acknowledgment of the diversity that exists among Mycobacterium tuberculosis clinical isolates. To facilitate comparative studies aimed at deciphering the relevance of this diversity to human disease, an unambiguous and easily interpretable method of strain classification is required. Presently, the most effective means of assigning isolates into a series of unambiguous lineages is the method of Gagneux et al. (S. Gagneux et al., Proc. Natl. Acad. Sci. USA 103: 2869-2873, 2006) that involves the PCR-based detection of large sequence polymorphisms (LSPs). In this manner, isolates are classified into six major lineages, the majority of which display a high degree of geographic restriction. Here we describe an independent replicate of the Gagneux study carried out on 798 isolates collected over a 6-year period from mostly foreign-born patients resident on the island of Montreal, Canada. The original trends in terms of bacterial genotype and patient ethnicity are remarkably conserved within this Montreal cohort, even though the patient distributions between the two populations are quite distinct. In parallel with the LSP analysis, we also demonstrate that clustered tuberculosis (TB) cases defined through restriction fragment length polymorphism (RFLP) analysis (for isolates with >= 6 IS6110 copies) or RFLP in combination with spoligotyping (for isolates with <6 IS6110 copies) do not stray across the LSP-defined lineage boundaries. However, our data also demonstrate the poor discriminatory power of either RFLP or spoligotyping alone for these low-IS6110-copy-number isolates. We believe that this independent validation of the LSP method should encourage researchers to adopt this system in investigations aimed at elucidating the role of strain variation in TB.

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