TY - JOUR KW - DNA-Directed RNA Polymerases KW - Drug Resistance, Bacterial KW - Genome, Bacterial KW - Models, Molecular KW - Mutation KW - Mycobacterium tuberculosis KW - Rifampin KW - Sequence Analysis, DNA KW - Tuberculosis, Multidrug-Resistant AU - Comas I AU - Borrell S AU - Roetzer A AU - Rose G AU - Malla B AU - Kato-Maeda M AU - Galagan J AU - Niemann S AU - Gagneux S AB -
Epidemics of drug-resistant bacteria emerge worldwide, even as resistant strains frequently have reduced fitness compared to their drug-susceptible counterparts. Data from model systems suggest that the fitness cost of antimicrobial resistance can be reduced by compensatory mutations; however, there is limited evidence that compensatory evolution has any significant role in the success of drug-resistant bacteria in human populations. Here we describe a set of compensatory mutations in the RNA polymerase genes of rifampicin-resistant M. tuberculosis, the etiologic agent of human tuberculosis (TB). M. tuberculosis strains harboring these compensatory mutations showed a high competitive fitness in vitro. Moreover, these mutations were associated with high fitness in vivo, as determined by examining their relative clinical frequency across patient populations. Of note, in countries with the world's highest incidence of multidrug-resistant (MDR) TB, more than 30% of MDR clinical isolates had this form of mutation. Our findings support a role for compensatory evolution in the global epidemics of MDR TB.
BT - Nature genetics C1 -http://www.ncbi.nlm.nih.gov/pubmed/22179134?dopt=Abstract
DO - 10.1038/ng.1038 IS - 1 J2 - Nat. Genet. LA - eng N2 -Epidemics of drug-resistant bacteria emerge worldwide, even as resistant strains frequently have reduced fitness compared to their drug-susceptible counterparts. Data from model systems suggest that the fitness cost of antimicrobial resistance can be reduced by compensatory mutations; however, there is limited evidence that compensatory evolution has any significant role in the success of drug-resistant bacteria in human populations. Here we describe a set of compensatory mutations in the RNA polymerase genes of rifampicin-resistant M. tuberculosis, the etiologic agent of human tuberculosis (TB). M. tuberculosis strains harboring these compensatory mutations showed a high competitive fitness in vitro. Moreover, these mutations were associated with high fitness in vivo, as determined by examining their relative clinical frequency across patient populations. Of note, in countries with the world's highest incidence of multidrug-resistant (MDR) TB, more than 30% of MDR clinical isolates had this form of mutation. Our findings support a role for compensatory evolution in the global epidemics of MDR TB.
PY - 2012 SP - 106 EP - 10 T2 - Nature genetics TI - Whole-genome sequencing of rifampicin-resistant Mycobacterium tuberculosis strains identifies compensatory mutations in RNA polymerase genes. UR - http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246538/pdf/nihms339089.pdf VL - 44 SN - 1546-1718 ER -