Divergence in fitness and evolution of drug resistance in experimental populations of Candida albicans

被引:85
作者
Cowen, LE [1 ]
Kohn, LM [1 ]
Anderson, JB [1 ]
机构
[1] Univ Toronto, Dept Bot, Mississauga, ON L5L 1C6, Canada
关键词
D O I
10.1128/JB.183.10.2971-2978.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The dissemination and persistence of drug-resistant organisms in nature depends on the relative fitness of sensitive and resistant genotypes, While resistant genotypes are expected to be at an advantage compared to less resistant genotypes in the presence of drug, resistance mag incur a cost; resistant genotypes may be at a disadvantage in the absence of drug. We measured the fitness of replicate experimental populations of the pathogenic yeast Candida albicans founded from a single progenitor cell in a previous study (L, E, Cowen, D, Sanglard, D, Calabrese, C, Sirjusingh, J.B. Anderson, and L. hi. Kohn, J, Bacteriol, 182:1515-1522, 2000) and evolved in the presence, and in the absence, of the antifungal agent fluconazole. Fitness was measured both in the presence and in the absence of fluconazole by placing each evolved population in direct competition with the drug-sensitive ancestor and measuring the reproductive output of each competitor in the mixture. Populations evolved in the presence of drug diverged in fitness, Any significant cost of resistance, indicated by reduced fitness in the absence of drug, was eliminated with further evolution. Populations evolved in the absence of drug showed more uniform increases in fitness under both conditions. Fitness in the competition assays was not predicted by measurements of the MICs, doubling times, or stationary-phase cell densities of the competitors in isolation, suggesting the importance of interactions between mixed genotypes in competitions.
引用
收藏
页码:2971 / 2978
页数:8
相关论文
共 45 条
[1]   OPPORTUNISTIC MYCOSES IN THE IMMUNOCOMPROMISED HOST - EXPERIENCE AT A CANCER CENTER AND REVIEW [J].
ANAISSIE, E .
CLINICAL INFECTIOUS DISEASES, 1992, 14 :S43-S53
[2]   The biological cost of antibiotic resistance [J].
Andersson, DI ;
Levin, BR .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (05) :489-493
[3]   The relationship between the volume of antimicrobial consumption in human communities and the frequency of resistance [J].
Austin, DJ ;
Kristinsson, KG ;
Anderson, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) :1152-1156
[4]   The impact of antibiotic use on resistance development and persistence [J].
Barbosa, TM ;
Levy, SB .
DRUG RESISTANCE UPDATES, 2000, 3 (05) :303-311
[5]   Single-copy IMH3 allele is sufficient to confer resistance to mycophenolic acid in Candida albicans and to mediate transformation of clinical candida species [J].
Beckerman, J ;
Chibana, H ;
Turner, J ;
Magee, PT .
INFECTION AND IMMUNITY, 2001, 69 (01) :108-114
[6]   The cost of antibiotic resistance from a bacterial perspective [J].
Björkman, J ;
Andersson, DI .
DRUG RESISTANCE UPDATES, 2000, 3 (04) :237-245
[7]   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
[8]   Resistance of human immunodeficiency virus type 1 to protease inhibitors: Selection of resistance mutations in the presence and absence of the drug [J].
Borman, AM ;
Paulous, S ;
Clavel, F .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :419-426
[9]   EVOLUTION OF A BACTERIA PLASMID ASSOCIATION [J].
BOUMA, JE ;
LENSKI, RE .
NATURE, 1988, 335 (6188) :351-352
[10]   Microbiology - Mice are not furry petri dishes [J].
Bull, J ;
Levin, B .
SCIENCE, 2000, 287 (5457) :1409-1410