Clonal expansion of a globally disseminated lineage of Mycobacterium tuberculosis with low IS6110 copy numbers

Date
2004
Authors
Warren R.M.
Victor T.C.
Streicher E.M.
Richardson M.
Van Der Spuy G.D.
Johnson R.
Chihota V.N.
Locht C.
Supply P.
Van Helden P.D.
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
Knowledge of the clonal expansion of Mycobacterium tuberculosis and accurate identification of predominant evolutionary lineages in this species remain limited, especially with regard to low-IS6110-copy-number strains. In this study, 170 M. tuberculosis isolates with ≤6 IS6110 insertions identified in Cape Town, South Africa, were characterized by principal genetic grouping, restriction fragment length polymorphism analysis, spoligotyping, IS6110 insertion site mapping, and variable-number tandem repeat (VNTR) typing. These analyses indicated that all but one of the isolates analyzed were members of principal genetic group 2 and of the same low-IS6110-copy-number lineage. The remaining isolate was a member of principal genetic group 1 and a different low-IS6110-copy-number lineage. Phylogenetic reconstruction suggests clonal expansion through sequential acquisition of additional IS6110 copies, expansion and contraction of VNTR sequences, and the deletion of specific direct-variable-repeat sequences. Furthermore, comparison of the genotypic data of 91 representative low-IS6110-copy-number isolates from Cape Town, other southern African regions, Europe, and the United States suggests that certain low-IS6110-copy-number strain spoligotypes and IS6110 fingerprints were acquired in the distant past. These clones have subsequently become widely disseminated and now play an important role in the global tuberculosis epidemic.
Description
Keywords
article, bacterial genetics, bacterial genome, bacterial strain, clonal variation, Europe, evolutionary adaptation, gene deletion, gene insertion, gene mapping, gene number, gene sequence, genetic analysis, genetic epidemiology, genetic variability, genotype, molecular cloning, Mycobacterium tuberculosis, nonhuman, phylogeny, priority journal, restriction fragment length polymorphism, sequential analysis, South Africa, tandem repeat, United States, DNA Transposable Elements, Europe, Evolution, Molecular, Gene Dosage, Humans, Minisatellite Repeats, Mycobacterium tuberculosis, Oligonucleotides, Phylogeny, Polymerase Chain Reaction, Polymorphism, Restriction Fragment Length, South Africa, Tuberculosis, United States, Actinobacteria (class), Bacteria (microorganisms), insertion sequences, Mycobacterium, Mycobacterium tuberculosis, uncultured actinomycete
Citation
Journal of Clinical Microbiology
42
12