Molecular Confirmation of the Relationship between Candida guilliermondii Fks1p Naturally Occurring Amino Acid Substitutions and Its Intrinsic Reduced Echinocandin Susceptibility

被引:0
作者
Dudiuk, Catiana [1 ,2 ]
Macedo, Daiana [1 ]
Leonardelli, Florencia [1 ,2 ]
Theill, Laura [1 ]
Cabeza, Matias S. [1 ,2 ]
Gamarra, Soledad [1 ]
Garcia-Effron, Guillermo [1 ,2 ]
机构
[1] Univ Nacl Litoral, Fac Bioquim & Ciencias Biol, Catedra Parasitol & Micol, Lab Micol & Diagnost Mol, Santa Fe, Argentina
[2] Ctr Cient Tecnol Santa Fe, Consejo Nacl Invest Cient & Tecnol, Santa Fe, Argentina
关键词
Candida guilliermondii; FKS mutations; echinocandin resistance; molecular mechanism; INVASIVE CANDIDIASIS; SACCHAROMYCES-CEREVISIAE; ANIDULAFUNGIN; SURVEILLANCE; FLUCONAZOLE; RESISTANCE; THERAPY; PARAPSILOSIS; CASPOFUNGIN; MICAFUNGIN;
D O I
10.1128/AAC.02644-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Candida guilliermondii shows intrinsic reduced echinocandin susceptibility. It harbors two polymorphisms (L633M and T634A) in the Fks1p hot spot 1 region. Our objective was to confirm that the reduced echinocandin susceptibility of C. guilliermondii is due to those naturally occurring substitutions. We constructed a Saccharomyces cerevisiae mutant in which a region of the FKS1 gene (including hot spot 1) was replaced with that from C. guilliermondii. The chimeric mutants showed 32-fold increases in echinocandin MIC values, confirming the hypothesis.
引用
收藏
页数:5
相关论文
共 23 条
[1]  
[Anonymous], 2009, Method for Antifungal Disk Diffusion Susceptibility Testing of Yeasts
[2]  
Approved Guideline-Second Edition. CLSI document M44-A2
[3]  
Clinical and Laboratory Standards Institute (CLSI), 2012, M27S4 CLSI
[4]  
CLSI (Clinical and Laboratory Standards Institute), 2008, M27A3 CLSI
[5]  
Córdoba S, 2011, REV ARGENT MICROBIOL, V43, P176, DOI 10.1590/S0325-75412011000300003
[6]   Efficacy of micafungin in invasive candidiasis caused by common Candida species with special emphasis on non-albicans Candida species [J].
Cornely, Oliver A. ;
Vazquez, Jose ;
De Waele, Jan ;
Betts, Robert ;
Rotstein, Coleman ;
Nucci, Marcio ;
Pappas, Peter G. ;
Ullmann, Andrew J. .
MYCOSES, 2014, 57 (02) :79-89
[7]   THE SACCHAROMYCES-CEREVISIAE FKS1 (ETG1) GENE ENCODES AN INTEGRAL MEMBRANE-PROTEIN WHICH IS A SUBUNIT OF 1,3-BETA-D-GLUCAN SYNTHASE [J].
DOUGLAS, CM ;
FOOR, F ;
MARRINAN, JA ;
MORIN, N ;
NIELSEN, JB ;
DAHL, AM ;
MAZUR, P ;
BAGINSKY, W ;
LI, WL ;
ELSHERBEINI, M ;
CLEMAS, JA ;
MANDALA, SM ;
FROMMER, BR ;
KURTZ, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :12907-12911
[8]   Promoter-dependent disruption of genes: simple, rapid, and specific PCR-based method with application to three different yeast [J].
Edlind, TD ;
Henry, KW ;
Vermitsky, JP ;
Edlind, MP ;
Raj, S ;
Katiyar, SK .
CURRENT GENETICS, 2005, 48 (02) :117-125
[9]   A naturally occurring proline-to-alanine amino acid change in Fks1p in Candida parapsilosis, Candida orthopsilosis, and Candida metapsilosis accounts for reduced echinocandin susceptibility [J].
Garcia-Effron, Guillermo ;
Katiyar, Santosh K. ;
Park, Steven ;
Edlind, Thomas D. ;
Perlin, David S. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (07) :2305-2312
[10]   STUDIES ON THE TRANSFORMATION OF INTACT YEAST-CELLS BY THE LIAC/S-DNA/PEG PROCEDURE [J].
GIETZ, RD ;
SCHIESTL, RH ;
WILLEMS, AR ;
WOODS, RA .
YEAST, 1995, 11 (04) :355-360