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THE FOREST BEHIND THE TREE: PHYLOGENETIC EXPLORATION OF A DOMINANT MYCOBACTERIUM TUBERCULOSIS STRAIN LINEAGE FROM A HIGH TUBERCULOSIS BURDEN COUNTRY
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Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Molecular Aplicada a Micobacterias. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Molecular Aplicada a Micobacterias. Rio de Janeiro, RJ, Brasil.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
Fundação Estadual de Produção e Pesquisa em Saúde. Centro de Desenvolvimento Científico e Tecnológico. Porto Alegre, RS, Brasil.
Instituto Evandro Chagas. Belém, PA, Brasil.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
Institut Pasteur. Department of Infection and Epidemiology. Paris, France.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France / Institut Pasteur. Department of Infection and Epidemiology. Paris, France..
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Molecular Aplicada a Micobacterias. Rio de Janeiro, RJ, Brasil.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Molecular Aplicada a Micobacterias. Rio de Janeiro, RJ, Brasil.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
Fundação Estadual de Produção e Pesquisa em Saúde. Centro de Desenvolvimento Científico e Tecnológico. Porto Alegre, RS, Brasil.
Instituto Evandro Chagas. Belém, PA, Brasil.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
Institut Pasteur. Department of Infection and Epidemiology. Paris, France.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France / Institut Pasteur. Department of Infection and Epidemiology. Paris, France..
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Molecular Aplicada a Micobacterias. Rio de Janeiro, RJ, Brasil.
INSERM U1019, Lille, France. CNRS UMR 8204, Lille, France. Univ Lille Nord de France, Lille, France. Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
Abstract
Background: Genotyping of Mycobacterium tuberculosis isolates is a powerful tool for epidemiological control of tuberculosis
(TB) and phylogenetic exploration of the pathogen. Standardized PCR-based typing, based on 15 to 24 mycobacterial
interspersed repetitive unit-variable number of tandem repeat (MIRU-VNTR) loci combined with spoligotyping, has been
shown to have adequate resolution power for tracing TB transmission and to be useful for predicting diverse strain lineages in
European settings. Its informative value needs to be tested in high TB-burden countries, where the use of genotyping is often
complicated by dominance of geographically specific, genetically homogeneous strain lineages.
Methodology/Principal Findings: We tested this genotyping system for molecular epidemiological analysis of 369 M.
tuberculosis isolates from 3 regions of Brazil, a high TB-burden country. Deligotyping, targeting 43 large sequence
polymorphisms (LSPs), and the MIRU-VNTRplus identification database were used to assess phylogenetic predictions. High
congruence between the different typing results consistently revealed the countrywide supremacy of the Latin-American-
Mediterranean (LAM) lineage, comprised of three main branches. In addition to an already known RDRio branch, at least one
other branch characterized by a phylogenetically informative LAM3 spoligo-signature seems to be globally distributed
beyond Brazil. Nevertheless, by distinguishing 321 genotypes in this strain population, combined MIRU-VNTR typing and
spoligotyping demonstrated the presence of multiple distinct clones. The use of 15 to 24 loci discriminated 21 to 25% more
strains within the LAM lineage, compared to a restricted lineage-specific locus set suggested to be used after SNP analysis.
Noteworthy, 23 of the 28 molecular clusters identified were exclusively composed of patient isolates from a same region,
consistent with expected patterns of mostly local TB transmission.
Conclusions/Significance: Standard MIRU-VNTR typing combined with spoligotyping can reveal epidemiologically
meaningful clonal diversity behind a dominant M. tuberculosis strain lineage in a high TB-burden country and is useful
to explore international phylogenetical ramifications.
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