Fluconazole resistance in Candida species: a current perspective

被引:358
作者
Berkow, Elizabeth L. [1 ]
Lockhart, Shawn R. [1 ]
机构
[1] Ctr Dis Control & Prevent, Mycot Dis Branch, Atlanta, GA USA
关键词
Candida; fluconazole resistance; ERG11; drug efflux; ergosterol; ANTIFUNGAL-DRUG-RESISTANCE; AMINO-ACID SUBSTITUTIONS; AZOLE RESISTANCE; MOLECULAR-MECHANISMS; MULTIDRUG-RESISTANCE; UP-REGULATION; ERG11; GENE; IN-VIVO; ABC TRANSPORTERS; CROSS-RESISTANCE;
D O I
10.2147/IDR.S118892
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Candida albicans and the emerging non-albicans Candida spp. have significant clinical relevance among many patient populations. Current treatment guidelines include fluconazole as a primary therapeutic option for the treatment of these infections, but it is only fungistatic against Candida spp. and both inherent and acquired resistance to fluconazole have been reported. Such mechanisms of resistance include increased drug efflux, alteration or increase in the drug target, and development of compensatory pathways for producing the target sterol, ergosterol. While many mechanisms of resistance observed in C. albicans are also found in the non-albicans species, there are also important and unexpected differences between species. Furthermore, mechanisms of fluconazole resistance in emerging Candida spp., including the global health threat Candida auris, are largely unknown. In order to preserve the utility of one of our fundamental antifungal drugs, fluconazole, it is essential that we fully appreciate the manner by which Candida spp. manifest resistance to it.
引用
收藏
页码:237 / 245
页数:9
相关论文
共 108 条
[1]   The bZip transcription factor Cap1p is involved in multidrug resistance and oxidative stress response in Candida albicans [J].
Alarco, AM ;
Raymond, M .
JOURNAL OF BACTERIOLOGY, 1999, 181 (03) :700-708
[2]   Evolution of antifungal-drug resistance: Mechanisms and pathogen fitness [J].
Anderson, JB .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (07) :547-556
[3]   Experimental induction of fluconazole resistance in Candida tropicalis ATCC 750 [J].
Barchiesi, F ;
Calabrese, D ;
Sanglard, D ;
Di Francesco, LF ;
Caselli, F ;
Giannini, D ;
Giacometti, A ;
Gavaudan, S ;
Scalise, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) :1578-1584
[4]   Multidrug Transporters and Alterations in Sterol Biosynthesis Contribute to Azole Antifungal Resistance in Candida parapsilosis [J].
Berkow, Elizabeth L. ;
Manigaba, Kayihura ;
Parker, Josie E. ;
Barker, Katherine S. ;
Kelly, Stephen L. ;
Rogers, P. David .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (10) :5942-5950
[5]   Comparative Pathogenicity of United Kingdom Isolates of the Emerging Pathogen Candida auris and Other Key Pathogenic Candida Species [J].
Borman, Andrew M. ;
Szekely, Adrien ;
Johnson, Elizabeth M. .
MSPHERE, 2016, 1 (04)
[6]  
Calderone RA, 2012, CANDIDA CANDIDIASIS
[7]   Reversible fluconazole resistance in Candida albicans: A potential in vitro model [J].
Calvet, HM ;
Yeaman, MR ;
Filler, SG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (03) :535-539
[8]   First report of Candida auris in America: Clinical and microbiological aspects of 18 episodes of candidemia [J].
Calvo, Belinda ;
Melo, Analy S. A. ;
Perozo-Mena, Armindo ;
Hernandez, Martin ;
Francisco, Elaine Cristina ;
Hagen, Ferry ;
Meis, Jacques F. ;
Colombo, Arnaldo Lopes .
JOURNAL OF INFECTION, 2016, 73 (04) :369-374
[9]   Genomewide Expression Profile Analysis of the Candida glabrata Pdr1 Regulon [J].
Caudle, Kelly E. ;
Barker, Katherine S. ;
Wiederhold, Nathan P. ;
Xu, Lijing ;
Homayouni, Ramin ;
Rogers, P. David .
EUKARYOTIC CELL, 2011, 10 (03) :373-383
[10]   Inactivation of sterol Δ5,6-desaturase attenuates virulence in Candida albicans [J].
Chau, AS ;
Gurnani, M ;
Hawkinson, R ;
Laverdiere, M ;
Cacciapuoti, A ;
McNicholas, PM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (09) :3646-3651