Affiliation:
1. Infectious Diseases Unit, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel
2. Sackler School of Medicine, Tel Aviv, Israel
3. Department of Molecular Microbiology and Biotechnology, George Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel
Abstract
ABSTRACT
Candida glabrata
causes persistent infections in patients treated with fluconazole and often acquires resistance following exposure to the drug. Here we found that clinical strains of
C. glabrata
exhibit cell-to-cell variation in drug response (heteroresistance). We used population analysis profiling (PAP) to assess fluconazole heteroresistance (FLC
HR
) and to ask if it is a binary trait or a continuous phenotype. Thirty (57.6%) of 52 fluconazole-sensitive clinical
C. glabrata
isolates met accepted dichotomous criteria for FLC
HR
. However, quantitative grading of FLC
HR
by using the area under the PAP curve (AUC) revealed a continuous distribution across a wide range of values, suggesting that all isolates exhibit some degree of heteroresistance. The AUC correlated with rhodamine 6G efflux and was associated with upregulation of the
CDR1
and
PDH1
genes, encoding ATP-binding cassette (ABC) transmembrane transporters, implying that HetR populations exhibit higher levels of drug efflux. Highly FLC
HR
C. glabrata
was recovered more frequently than nonheteroresistant
C. glabrata
from hematogenously infected immunocompetent mice following treatment with high-dose fluconazole (45.8% versus 15%,
P
= 0.029). Phylogenetic analysis revealed some phenotypic clustering but also variations in FLC
HR
within clonal groups, suggesting both genetic and epigenetic determinants of heteroresistance. Collectively, these results establish heteroresistance to fluconazole as a graded phenotype associated with ABC transporter upregulation and fluconazole efflux. Heteroresistance may explain the propensity of
C. glabrata
for persistent infection and the emergence of breakthrough resistance to fluconazole.
IMPORTANCE
Heteroresistance refers to variability in the response to a drug within a clonal cell population. This phenomenon may have crucial importance for the way we look at antimicrobial resistance, as heteroresistant strains are not detected by standard laboratory susceptibility testing and may be associated with failure of antimicrobial therapy. We describe for the first time heteroresistance to fluconazole in
C. glabrata
, a finding that may explain the propensity of this pathogen to acquire resistance following exposure to fluconazole and to persist despite treatment. We found that, rather than being a binary all-or-none trait, heteroresistance was a continuously distributed phenotype associated with increased expression of genes that encode energy-dependent drug efflux transporters. Moreover, we show that heteroresistance is associated with failure of fluconazole to clear infection with
C. glabrata
. Together, these findings provide an empirical framework for determining and quantifying heteroresistance in
C. glabrata
.
Funder
Ben Dov Physician Researcher Grant
European Union's 7th Framework Programme
EC | European Research Council
Publisher
American Society for Microbiology
Cited by
58 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献