A SUBSET OF PROTEINS FOUND IN CULTURE SUPERNATANTS OF CANDIDA-ALBICANS INCLUDES THE ABUNDANT, IMMUNODOMINANT, GLYCOLYTIC ENZYME ENOLASE

被引:53
作者
SUNDSTROM, P [1 ]
ALIAGA, GR [1 ]
机构
[1] UNIV N TEXAS,HLTH SCI CTR,DEPT BIOCHEM & MOLEC BIOL,FT WORTH,TX
关键词
D O I
10.1093/infdis/169.2.452
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunoblot analysis showed that enolase is one of a subset of proteins found in cell supernatants of Candida albicans. Enzyme assays on whole cell extracts indicated that enolase is an abundant protein, comprising 0.7% and 2.0% of the total protein from yeast and hyphal forms of C. albicans, respectively. Comparison of enolase enzyme activities in whole cell extracts and cell culture supernatants showed the enzyme to be located primarily within cells. Extracellular glyceraldehyde-3-phosphate dehydrogenase activity was absent or lower than that of enolase, despite equivalent intracellular levels. The results suggest that enolase, released from fungi in the absence of host factors, may contribute to enolase found circulating in the blood of patients with hematogenously disseminated candidiasis. In addition, the release from cells of highly immunogenic fungal proteins, such as enolase, may be important in defining the selective stimulation of host antifungal responses during infection.
引用
收藏
页码:452 / 456
页数:5
相关论文
共 15 条
[1]   COMPARISON OF ANTIBODY, ANTIGEN, AND METABOLITE ASSAYS FOR HOSPITALIZED-PATIENTS WITH DISSEMINATED OR PERIPHERAL CANDIDIASIS [J].
BOUGNOUX, ME ;
HILL, C ;
MOISSENET, D ;
DECHAUVIN, MF ;
BONNAY, M ;
VICENSSPRAUEL, I ;
PIETRI, F ;
MCNEIL, M ;
KAUFMAN, L ;
DUPOUYCAMET, J ;
BOHUON, C ;
ANDREMONT, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (05) :905-909
[2]   IDENTIFICATION OF CANDIDA-ALBICANS ANTIGENS REACTIVE WITH IMMUNOGLOBULIN-E ANTIBODY OF HUMAN SERA [J].
ISHIGURO, A ;
HOMMA, M ;
TORII, S ;
TANAKA, K .
INFECTION AND IMMUNITY, 1992, 60 (04) :1550-1557
[3]   SERUM NEURON SPECIFIC ENOLASE (NSE) IS A DETERMINANT OF RESPONSE DURATION IN SMALL-CELL LUNG-CANCER (SCLC) [J].
JORGENSEN, LGM ;
OSTERLIND, K ;
HANSEN, HH ;
COOPER, EH .
BRITISH JOURNAL OF CANCER, 1992, 66 (03) :594-598
[4]   INTEGRATIVE TRANSFORMATION OF CANDIDA-ALBICANS, USING A CLONED CANDIDA ADE2 GENE [J].
KURTZ, MB ;
CORTELYOU, MW ;
KIRSCH, DR .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (01) :142-149
[5]   METAL-ION SPECIFICITY AT THE CATALYTIC SITE OF YEAST ENOLASE [J].
LEE, ME ;
NOWAK, T .
BIOCHEMISTRY, 1992, 31 (07) :2172-2180
[6]   THE MAJOR EXOGLUCANASE FROM CANDIDA-ALBICANS - A NONGLYCOSYLATED SECRETORY MONOMER RELATED TO ITS COUNTERPART FROM SACCHAROMYCES-CEREVISIAE [J].
LUNAARIAS, JP ;
ANDALUZ, E ;
RIDRUEJO, JC ;
OLIVERO, I ;
LARRIBA, G .
YEAST, 1991, 7 (08) :833-841
[7]   ISOLATION OF IMMUNODOMINANT ANTIGENS FROM SERA OF PATIENTS WITH SYSTEMIC CANDIDIASIS AND CHARACTERIZATION OF SEROLOGICAL RESPONSE TO CANDIDA-ALBICANS [J].
MATTHEWS, RC ;
BURNIE, JP ;
TABAQCHALI, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (02) :230-237
[8]   PURIFICATION AND CHARACTERIZATION OF THE EXTRACELLULAR C3D-BINDING PROTEIN OF CANDIDA-ALBICANS [J].
SAXENA, A ;
CALDERONE, R .
INFECTION AND IMMUNITY, 1990, 58 (02) :309-314
[9]  
SHEKMAN R, 1982, MOL BIOL YEAST SACCH, P651
[10]   THE 40-KILODALTON ALLERGEN OF CANDIDA-ALBICANS IS AN ALCOHOL-DEHYDROGENASE - MOLECULAR-CLONING AND IMMUNOLOGICAL ANALYSIS USING MONOCLONAL-ANTIBODIES [J].
SHEN, HD ;
CHOO, KB ;
LEE, HH ;
HSIEH, JC ;
LIN, WL ;
LEE, WR ;
HAN, SH .
CLINICAL AND EXPERIMENTAL ALLERGY, 1991, 21 (06) :675-681