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. 2006 Jun;50(6):2058-63.
doi: 10.1128/AAC.01653-05.

Assessing resistance to the echinocandin antifungal drug caspofungin in Candida albicans by profiling mutations in FKS1

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Assessing resistance to the echinocandin antifungal drug caspofungin in Candida albicans by profiling mutations in FKS1

Sergey V Balashov et al. Antimicrob Agents Chemother. 2006 Jun.

Abstract

Resistance of clinical isolates of Candida albicans to the echinocandin drug caspofungin is slowly emerging and is linked to mutations in short conserved regions in the FKS1 gene. The most prominent changes occurred at the serine 645 position in Fks1p with substitutions of proline, tyrosine, and phenylalanine. An allele-specific real-time PCR molecular-beacon assay was developed for rapid identification of drug resistance by targeting FKS1 mutations. Mutations altering serine 645 were reliably identified in both heterozygous and homozygous states. The molecular-beacon assay was used to evaluate two large collections of spontaneous mutants from separate strains of C. albicans with resistance (MICs, >16 microg/ml) to caspofungin with the goal of understanding the relationship between FKS1 mutations and echinocandin resistance. Of 85 resistant isolates recovered, all were identified with mutations in FKS1; 93% showed changes at Ser645, with 62% displaying a characteristic S645P substitution expressed as either a homozygous or a heterozygous mutation in FKS1. Two other prominent amino acid substitutions, S645Y and S645F, were found at frequencies of 22% and 8%, respectively. Three new mutations were also identified: T1922C, G1932T, and C1934G, encoding F641S, L644F, and S645C substitutions, respectively. One strain had the double amino acid substitution L644F and S645C. Allele-specific probes were combined in a multiplex assay for reliable screening of known FKS1 mutations. These data support the importance of FKS1p substitutions in echinocandin resistance and demonstrate the feasibility of applying molecular screening for routine resistance assessment.

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Figures

FIG. 1.
FIG. 1.
Detection of the T1933C mutation in both the homozygous and heterozygous states. The graph summarizes results of four separate PCRs with individual allele-specific molecular beacons and DNA targets. Squares, FKS1(T1933C) beacon plus DNA of the FKS1 allele with a homozygous T1933C mutation; circles, FKS1(WT) beacon plus DNA of the FKS1 allele with a homozygous T1933C mutation; asterisks, FKS1(T1933C) beacon plus DNA of the FKS1 allele with a heterozygous T1933C mutation; diamonds, FKS1(WT) beacon plus DNA of the FKS1 allele with a heterozygous T1933C mutation.

References

    1. Bachmann, S. P., T. F. Patterson, and J. L. Lopez-Ribot. 2002. In vitro activity of caspofungin (MK-0991) against Candida albicans clinical isolates displaying different mechanisms of azole resistance. J. Clin. Microbiol. 40:2228-2230. - PMC - PubMed
    1. Balashov, S. V., R. Gardiner, S. Park, and D. S. Perlin. 2005. Rapid, high-throughput, multiplex, real-time PCR for identification of mutations in the cyp51A gene of Aspergillus fumigatus that confer resistance to itraconazole. J. Clin. Microbiol. 43:214-222. - PMC - PubMed
    1. Bonnet, G., S. Tyagi, A. Libchaber, and F. R. Kramer. 1999. Thermodynamic basis of the enhanced specificity of structured DNA probes. Proc. Natl. Acad. Sci. USA 96:6171-6176. - PMC - PubMed
    1. Cabello, M. A., G. Platas, J. Collado, M. T. Diez, I. Martin, F. Vicente, M. Meinz, J. C. Onishi, C. Douglas, J. Thompson, M. B. Kurtz, R. E. Schwartz, G. F. Bills, R. A. Giacobbe, G. K. Abruzzo, A. M. Flattery, L. Kong, and F. Pelaez. 2001. Arundifungin, a novel antifungal compound produced by fungi: biological activity and taxonomy of the producing organisms. Int. Microbiol. 4:93-102. - PubMed
    1. Chandrasekar, P. H., and E. K. Manavathu. 2002. Caspofungin. Drugs Today (Barcelona) 38:829-846. - PubMed

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