Effect of rpoB mutations conferring rifampin resistance on fitness of Mycobacterium tuberculosis

被引:193
作者
Mariam, DH
Mengistu, Y
Hoffner, SE
Andersson, DI [1 ]
机构
[1] Swedish Inst Infect Dis Control, Dept Bacteriol, S-17182 Solna, Sweden
[2] Karolinska Inst, Ctr Microbiol & Tumor Biol, S-17177 Solna, Sweden
[3] Univ Addis Ababa, Fac Med, Dept Microbiol & Parasitol, Addis Ababa, Ethiopia
[4] Univ Addis Ababa, Armauer Hansen Res Inst, Addis Ababa, Ethiopia
关键词
D O I
10.1128/AAC.48.4.1289-1294.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Rifampin is a major drug used in the treatment of tuberculosis infections, and increasing rifampin resistance represents a worldwide clinical problem. Resistance to rifampin is caused by mutations in the rpoB gene, encoding the beta-subunit of RNA polymerase. We examined the effect of three different rpoB mutations on the fitness of Mycobacterium tuberculosis. Rifampin-resistant mutants were isolated from a virulent clinical isolate of M. tuberculosis (strain Harlingen) in vitro at a mutation frequency of 2.3 X 10(-8). Mutations in the rpoB gene were identified, and the growth rates of three defined mutants were measured by competition with the susceptible parent strain in laboratory medium and by single cultures in a macrophage cell line and in laboratory medium. All of the mutants showed a decreased growth rate in the three assays. The relative fitness of the mutants varied between 0.29 and 0.96 (that of the susceptible strain was set to 1.0) depending on the specific mutant and assay system. Unexpectedly, the relative fitness ranking of the mutants differed between the different assays. In conclusion, rifampin resistance is associated with a cost that is conditional.
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收藏
页码:1289 / 1294
页数:6
相关论文
共 32 条
[1]   Persistence of antibiotic resistant bacteria [J].
Andersson, DI .
CURRENT OPINION IN MICROBIOLOGY, 2003, 6 (05) :452-456
[2]   Physiological cost of rifampin resistance induced in vitro in Mycobacterium tuberculosis [J].
Billington, OJ ;
McHugh, TD ;
Gillespie, SH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (08) :1866-1869
[3]   Mutation frequency and biological cost of antibiotic resistance in Helicobacter pylori [J].
Björkholm, B ;
Sjölund, M ;
Falk, PG ;
Berg, OG ;
Engstrand, L ;
Andersson, DI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14607-14612
[4]   Effects of environment on compensatory mutations to ameliorate costs of antibiotic resistance [J].
Björkman, J ;
Nagaev, I ;
Berg, OG ;
Hughes, D ;
Andersson, DI .
SCIENCE, 2000, 287 (5457) :1479-1482
[5]   Virulence of antibiotic-resistant Salmonella typhimurium [J].
Björkman, J ;
Hughes, D ;
Andersson, DI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3949-3953
[6]   Fitness of antibiotic-resistant microorganisms and compensatory mutations [J].
Böttger, EC ;
Springer, B ;
Pletschette, M ;
Sander, P .
NATURE MEDICINE, 1998, 4 (12) :1343-1344
[7]   Persistence of sulphonamide resistance in Escherichia coli in the UK despite national prescribing restriction [J].
Enne, VI ;
Livermore, DM ;
Stephens, P ;
Hall, LMC .
LANCET, 2001, 357 (9265) :1325-1328
[8]   Global trends in resistance to antituberculosis drugs [J].
Espinal, MA ;
Laszlo, A ;
Simonsen, L ;
Boulahbal, F ;
Kim, SJ ;
Reniero, A ;
Hoffner, S ;
Rieder, HL ;
Binkin, N ;
Dye, C ;
Williams, R ;
Raviglione, MC .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (17) :1294-1303
[9]   Evolution of drug resistance in Mycobacterium tuberculosis:: Clinical and molecular perspective [J].
Gillespie, SH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (02) :267-274
[10]   Evolutionary barriers to quinolone resistance in Streptococcus pneumoniae [J].
Gillespie, SH ;
Voelker, LL ;
Dickens, A .
MICROBIAL DRUG RESISTANCE, 2002, 8 (02) :79-84