Evidence for a role for secreted aspartate proteinase of Candida albicans in vulvovaginal candidiasis.

The presence of the secretory aspartate (acid) proteinase in the vaginal fluid of candidal vaginitis patients and controls was studied by ELISA and immunoblot (Western blot). In addition, a proteinase-deficient mutant strain of Candida albicans (IR24) was compared with the wild-type parent strain (10261) for ability to infect the vagina of pseudoestrus rats under estradiol treatment. Among the 67 women examined, proteinase was detected only in 22 harboring C. albicans (range, 42-233 ng/ml of vaginal fluid), at concentrations significantly higher in the 14 vaginitis patients than in the 8 asymptomatic fungal carriers. Western blots confirmed the presence of only one protein band of approximately 43 kDa, corresponding to that of the purified proteinase, in the ELISA-positive vaginal fluids. Experimental vaginal infection was significantly more extensive and persistent in rats infected with the proteinase-producer strain than in those challenged with the proteinase-deficient mutant, and the enzyme was detected in the vaginas of the former but not of the latter animals. Both strains 10261 and IR24 developed hyphal forms to a roughly similar extent during infection, and both showed a comparable adherence in vitro to vaginal and buccal epithelial cells. The clinical and experimental evidence support a role for secretory proteinase as a virulence factor in the pathogenesis of candidal vaginitis.

[1]  A. Cassone,et al.  The secreted aspartate proteinase of Candida albicans: physiology of secretion and virulence of a proteinase-deficient mutant. , 1990, Journal of general microbiology.

[2]  A. Cassone,et al.  Experimental pathogenicity and acid proteinase secretion of vaginal isolates of Candida parapsilosis. , 1990, Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology.

[3]  A. Cassone,et al.  Isolation, acid proteinase secretion, and experimental pathogenicity of Candida parapsilosis from outpatients with vaginitis , 1989, Journal of clinical microbiology.

[4]  A. Cassone,et al.  Experimental rat vaginal infection with Candida parapsilosis. , 1989, FEMS microbiology letters.

[5]  K. Hazen Participation of yeast cell surface hydrophobicity in adherence of Candida albicans to human epithelial cells , 1989, Infection and immunity.

[6]  J. Burnie,et al.  Assessment of DNA fingerprinting for rapid identification of outbreaks of systemic candidiasis. , 1989, BMJ.

[7]  J. Mestecky,et al.  Induction of the mucosal immune response. , 1988, Reviews of infectious diseases.

[8]  M. Ghannoum,et al.  Correlative relationship between proteinase production, adherence and pathogenicity of various strains of Candida albicans. , 1986, Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology.

[9]  G. Carruba,et al.  Nutrition-dependent modulations of protein synthesis in Candida albicans during germ-tube formation or maintenance of the yeast form in N-acetyl glucosamine media , 1986 .

[10]  R. Rüchel,et al.  Characterization of a secretory proteinase of Candida parapsilosis and evidence for the absence of the enzyme during infection in vitro , 1986, Infection and immunity.

[11]  P. T. Magee,et al.  Genetic evidence for role of extracellular proteinase in virulence of Candida albicans , 1985, Infection and immunity.

[12]  J. Sobel Epidemiology and pathogenesis of recurrent vulvovaginal candidiasis. , 1985, American journal of obstetrics and gynecology.

[13]  R. Sweet,et al.  Importance of differential diagnosis in acute vaginitis. , 1985, American journal of obstetrics and gynecology.

[14]  J. Sobel,et al.  Experimental chronic vaginal candidosis in rats. , 1985, Sabouraudia.

[15]  R. Rüchel A variety of Candida proteinases and their possible targets of proteolytic attack in the host. , 1984, Zentralblatt fur Bakteriologie, Mikrobiologie, und Hygiene. Series A, Medical microbiology, infectious diseases, virology, parasitology.

[16]  J. Sobel,et al.  Critical role of germ tube formation in the pathogenesis of candidal vaginitis , 1984, Infection and immunity.

[17]  F. Macdonald,et al.  Virulence for mice of a proteinase-secreting strain of Candida albicans and a proteinase-deficient mutant. , 1983, Journal of general microbiology.

[18]  R. Rüchel Properties of a purified proteinase from the yeast Candida albicans. , 1981, Biochimica et biophysica acta.

[19]  F. Macdonald,et al.  Inducible proteinase of Candida albicans in diagnostic serology and in the pathogenesis of systemic candidosis. , 1980, Journal of medical microbiology.

[20]  D. Ahearn,et al.  Genus 4. Candida Berkhout. , 1984 .

[21]  F. Odds,et al.  Candida and candidosis , 1979 .