Literature DB >> 23743309

Sublineages of lineage 4 (Euro-American) Mycobacterium tuberculosis differ in genotypic clustering.

J Anderson1, L G Jarlsberg, J Grindsdale, D Osmond, M Kawamura, P C Hopewell, M Kato-Maeda.   

Abstract

SETTING: Mycobacterium tuberculosis is classified into six phylogenetic lineages, each of which can be divided into sublineages. Sublineages of the same lineage have phenotypic differences, including their capacity to cause disease (pathogenicity).
OBJECTIVE: 1) To test the hypothesis that different sublineages of lineage 4, which causes most of the tuberculosis (TB) in the United States, have varying ability to cause secondary cases as determined by genotypic clustering, a proxy for pathogenicity; and 2) to determine if spoligotype and mycobacterial interspersed repetitive units (MIRU) typing could infer sublineage.
DESIGN: We included TB cases caused by lineage 4 strains from our community-based study in San Francisco. Sublineage was determined by regions of difference. Genotypic clustering was determined by insertion sequence 6110 and polymorphic guanine-cytosine-rich sequence. Associations between sublineages and patient characteristics were evaluated with adjusted and unadjusted analyses.
RESULTS: The most frequent sublineage was H37Rv-like. In the adjusted analysis, sublineage 183 was associated with clustering and homelessness. We found that strains from different sublineages had convergent spoligotype and MIRU types.
CONCLUSIONS: Sublineage 183 is associated with genotypic clustering, evidence of its being more able to cause secondary cases than the other lineage 4 sublineages. This finding suggests that bacterial factors contribute to the pathogenesis of TB. Spoligotype and MIRU type cannot be used to infer sublineage.

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Year:  2013        PMID: 23743309     DOI: 10.5588/ijtld.12.0960

Source DB:  PubMed          Journal:  Int J Tuberc Lung Dis        ISSN: 1027-3719            Impact factor:   2.373


  4 in total

1.  Phylogenetic Analysis of Mycobacterium tuberculosis Strains in Wales by Use of Core Genome Multilocus Sequence Typing To Analyze Whole-Genome Sequencing Data.

Authors:  R C Jones; L G Harris; S Morgan; M C Ruddy; M Perry; R Williams; T Humphrey; M Temple; A P Davies
Journal:  J Clin Microbiol       Date:  2019-05-24       Impact factor: 5.948

Review 2.  Consequences of genomic diversity in Mycobacterium tuberculosis.

Authors:  Mireia Coscolla; Sebastien Gagneux
Journal:  Semin Immunol       Date:  2014-10-22       Impact factor: 11.130

3.  Early alveolar macrophage response and IL-1R-dependent T cell priming determine transmissibility of Mycobacterium tuberculosis strains.

Authors:  Arianne Lovey; Sheetal Verma; Vaishnavi Kaipilyawar; Rodrigo Ribeiro-Rodrigues; Seema Husain; Moises Palaci; Reynaldo Dietze; Shuyi Ma; Robert D Morrison; David R Sherman; Jerrold J Ellner; Padmini Salgame
Journal:  Nat Commun       Date:  2022-02-16       Impact factor: 14.919

4.  A Major Mycobacterium tuberculosis outbreak caused by one specific genotype in a low-incidence country: Exploring gene profile virulence explanations.

Authors:  Dorte Bek Folkvardsen; Anders Norman; Åse Bengård Andersen; Erik Michael Rasmussen; Troels Lillebaek; Lars Jelsbak
Journal:  Sci Rep       Date:  2018-08-08       Impact factor: 4.379

  4 in total

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