Comparison of the epidemiology, drug resistance mechanisms, and virulence of Candida dubliniensis and Candida albicans

被引:176
作者
Sullivan, DJ [1 ]
Moran, GP [1 ]
Pinjon, E [1 ]
Al-Mosaid, A [1 ]
Stokes, C [1 ]
Vaughan, C [1 ]
Coleman, DC [1 ]
机构
[1] Univ Dublin Trinity Coll, Dublin Dent Sch & Hosp, Dept Oral Med Oral Surg & Oral Pathol, Microbiol Res Unit, Dublin 2, Ireland
关键词
Candida dubliniensis; Candida albicans; epidemiology; virulence; resistance;
D O I
10.1016/S1567-1356(03)00240-X
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Candida dubliniensis is a pathogenic yeast species that was first identified as a distinct taxon in 1995. Epidemiological studies have shown that C dubliniensis is prevalent throughout the world and that it is primarily associated with oral carriage and oropharyngeal infections in human immunodeficiency virus (HIV)-infected and acquired immune deficiency syndrome (AIDS) patients. However, unlike Candida albicans, C dubliniensis is rarely found in the oral microflora of normal healthy individuals and is responsible for as few as 2% of cases of candidemia (compared to approximately 65% for C albicans). The vast majority of C dubliniensis isolates identified to date are susceptible to all of the commonly used antifungal agents, however, reduced susceptibility to azole drugs has been observed in clinical isolates and can be readily induced in vitro. The primary mechanism of fluconazole resistance in C dubliniensis has been shown to be overexpression of the major facilitator efflux pump Mdr1p. It has also been observed that a large number of C dubliniensis strains express a non-functional truncated form of Cdr1p, and it has been demonstrated that this protein does not play a significant role in fluconazole resistance in the majority of strains examined to date. Data from a limited number of infection models reflect findings from epidemiological studies and suggest that C dubliniensis is less pathogenic than C albicans. The reasons for the reduced virulence of C dubliniensis are not clear as it has been shown that the two species express a similar range of virulence factors. However, although C dubliniensis produces hyphae, it appears that the conditions and dynamics of induction may differ from those in C albicans. In addition, C. dubliniensis is less tolerant of environmental stresses such as elevated temperature and NaCl and H2O2 concentration, suggesting that C. albicans may have a competitive advantage when colonising and causing infection in the human body. It is our hypothesis that a genomic comparison between these two closely-related species will help to identify virulence factors responsible for the far greater virulence of C albicans and possibly identify factors that are specifically implicated in either superficial or systemic candidal infections. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:369 / 376
页数:8
相关论文
共 63 条
[1]   Differentiation of Candida dubliniensis from Candida albicans on Pal's agar [J].
Al Mosaid, A ;
Sullivan, DJ ;
Coleman, DC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (10) :4787-4789
[2]  
Alves SH, 2002, DIAGN MICR INFEC DIS, V43, P85
[3]   Racial distribution of Candida dubliniensis colonization among South Africans [J].
Blignaut, E ;
Pujol, C ;
Joly, S ;
Soll, DR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) :1838-1842
[4]   Adherence of different Candida dubliniensis isolates in the presence of fluconazole [J].
Borg-von Zepelin, M ;
Niederhaus, T ;
Gross, U ;
Seibold, M ;
Monod, M ;
Tintelnot, K .
AIDS, 2002, 16 (09) :1237-1244
[5]   Candida dubliniensis Fungemia:: the first four cases in North America [J].
Brandt, ME ;
Harrison, LH ;
Pass, M ;
Sofair, AN ;
Huie, S ;
Li, RK ;
Morrison, CJ ;
Warnock, DW ;
Hajjeh, RA .
EMERGING INFECTIOUS DISEASES, 2000, 6 (01) :46-49
[6]  
Coleman D, 1997, Oral Dis, V3 Suppl 1, pS96
[7]   Characterization of binding of Candida albicans to small intestinal mucin and its role in adherence to mucosal epithelial cells [J].
de Repentigny, L ;
Aumont, F ;
Bernard, K ;
Belhumeur, P .
INFECTION AND IMMUNITY, 2000, 68 (06) :3172-3179
[8]   Phylogenetic analysis and rapid identification of Candida dubliniensis based on analysis of ACT1 intron and exon sequences [J].
Donnelly, SM ;
Sullivan, DJ ;
Shanley, DB ;
Coleman, DC .
MICROBIOLOGY-UK, 1999, 145 :1871-1882
[9]   Rapid identification of Candida species with species-specific DNA probes [J].
Elie, CM ;
Lott, TJ ;
Reiss, E ;
Morrison, CJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (11) :3260-3265
[10]  
FISHER JM, 2001, AFR DENT J, V56, P599