Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1997 Aug;179(16):4992–4999. doi: 10.1128/jb.179.16.4992-4999.1997

The glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase of Candida albicans is a surface antigen.

I Gil-Navarro 1, M L Gil 1, M Casanova 1, J E O'Connor 1, J P Martínez 1, D Gozalbo 1
PMCID: PMC179354  PMID: 9260938

Abstract

A lambda gt11 cDNA library from Candida albicans ATCC 26555 was screened by using pooled sera from two patients with systemic candidiasis and five neutropenic patients with high levels of anti-C. albicans immunoglobulin M antibodies. Seven clones were isolated from 60,000 recombinant phages. The most reactive one contained a 0.9-kb cDNA encoding a polypeptide immunoreactive only with sera from patients with systemic candidiasis. The whole gene was isolated from a genomic library by using the cDNA as a probe. The nucleotide sequence of the coding region showed homology (78 to 79%) to the Saccharomyces cerevisiae TDH1 to TDH3 genes coding for glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and their amino acid sequences showed 76% identity; thus, this gene has been named C. albicans TDH1. A rabbit polyclonal antiserum against the purified cytosolic C. albicans GAPDH (polyclonal antibody [PAb] anti-CA-GAPDH) was used to identify the GAPDH in the beta-mercaptoethanol extracts containing cell wall moieties. Indirect immunofluorescence demonstrated the presence of GAPDH at the C. albicans cell surface, particularly on the blastoconidia. Semiquantitative flow cytometry analysis showed the sensitivity of this GAPDH form to trypsin and its resistance to be removed with 2 M NaCl or 2% sodium dodecyl sulfate. The decrease in fluorescence in the presence of soluble GAPDH indicates the specificity of the labelling. In addition, a dose-dependent GAPDH enzymatic activity was detected in intact blastoconidia and germ tube cells. This activity was reduced by pretreatment of the cells with trypsin, formaldehyde, and PAb anti-CA-GAPDH. These observations indicate that an immunogenic, enzymatically active cell wall-associated form of the glycolytic enzyme GAPDH is found at the cell surface of C. albicans cells.

Full Text

The Full Text of this article is available as a PDF (675.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alloush H. M., López-Ribot J. L., Chaffin W. L. Dynamic expression of cell wall proteins of Candida albicans revealed by probes from cDNA clones. J Med Vet Mycol. 1996 Mar-Apr;34(2):91–97. [PubMed] [Google Scholar]
  2. Alloush H. M., López-Ribot J. L., Masten B. J., Chaffin W. L. 3-phosphoglycerate kinase: a glycolytic enzyme protein present in the cell wall of Candida albicans. Microbiology. 1997 Feb;143(Pt 2):321–330. doi: 10.1099/00221287-143-2-321. [DOI] [PubMed] [Google Scholar]
  3. Angiolella L., Facchin M., Stringaro A., Maras B., Simonetti N., Cassone A. Identification of a glucan-associated enolase as a main cell wall protein of Candida albicans and an indirect target of lipopeptide antimycotics. J Infect Dis. 1996 Mar;173(3):684–690. doi: 10.1093/infdis/173.3.684. [DOI] [PubMed] [Google Scholar]
  4. Baldari C., Cesareni G. Plasmids pEMBLY: new single-stranded shuttle vectors for the recovery and analysis of yeast DNA sequences. Gene. 1985;35(1-2):27–32. doi: 10.1016/0378-1119(85)90154-4. [DOI] [PubMed] [Google Scholar]
  5. Casanova M., Chaffin W. L. Cell wall glycoproteins of Candida albicans as released by different methods. J Gen Microbiol. 1991 May;137(5):1045–1051. doi: 10.1099/00221287-137-5-1045. [DOI] [PubMed] [Google Scholar]
  6. Casanova M., Gil M. L., Cardeñoso L., Martinez J. P., Sentandreu R. Identification of wall-specific antigens synthesized during germ tube formation by Candida albicans. Infect Immun. 1989 Jan;57(1):262–271. doi: 10.1128/iai.57.1.262-271.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Casanova M., Lopez-Ribot J. L., Martinez J. P., Sentandreu R. Characterization of cell wall proteins from yeast and mycelial cells of Candida albicans by labelling with biotin: comparison with other techniques. Infect Immun. 1992 Nov;60(11):4898–4906. doi: 10.1128/iai.60.11.4898-4906.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Casanova M., Lopez-Ribot J. L., Monteagudo C., Llombart-Bosch A., Sentandreu R., Martinez J. P. Identification of a 58-kilodalton cell surface fibrinogen-binding mannoprotein from Candida albicans. Infect Immun. 1992 Oct;60(10):4221–4229. doi: 10.1128/iai.60.10.4221-4229.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Costantino P. J., Franklyn K. M., Gare N. F., Warmington J. R. Production of antibodies to antigens of Candida albicans in CBA/H mice. Infect Immun. 1994 Apr;62(4):1400–1405. doi: 10.1128/iai.62.4.1400-1405.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Denis C. L., Ciriacy M., Young E. T. A positive regulatory gene is required for accumulation of the functional messenger RNA for the glucose-repressible alcohol dehydrogenase from Saccharomyces cerevisiae. J Mol Biol. 1981 Jun 5;148(4):355–368. doi: 10.1016/0022-2836(81)90181-9. [DOI] [PubMed] [Google Scholar]
  11. Ferdinand W. The isolation and specific activity of rabbit-muscle glyceraldehyde phosphate dehydrogenase. Biochem J. 1964 Sep;92(3):578–585. doi: 10.1042/bj0920578. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Fernandes P. A., Keen J. N., Findlay J. B., Moradas-Ferreira P. A protein homologous to glyceraldehyde-3-phosphate dehydrogenase is induced in the cell wall of a flocculent Kluyveromyces marxianus. Biochim Biophys Acta. 1992 Sep 4;1159(1):67–73. doi: 10.1016/0167-4838(92)90076-p. [DOI] [PubMed] [Google Scholar]
  13. Fernandes P. A., Sousa M., Moradas-Ferreira P. Flocculation of Kluyveromyces marxianus is induced by a temperature upshift. Yeast. 1993 Aug;9(8):859–866. doi: 10.1002/yea.320090806. [DOI] [PubMed] [Google Scholar]
  14. Goudot-Crozel V., Caillol D., Djabali M., Dessein A. J. The major parasite surface antigen associated with human resistance to schistosomiasis is a 37-kD glyceraldehyde-3P-dehydrogenase. J Exp Med. 1989 Dec 1;170(6):2065–2080. doi: 10.1084/jem.170.6.2065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Gozalbo D., Elorza M. V., Sanjuan R., Marcilla A., Valentín E., Sentandreu R. Critical steps in fungal cell wall synthesis: strategies for their inhibition. Pharmacol Ther. 1993 Nov;60(2):337–345. doi: 10.1016/0163-7258(93)90015-6. [DOI] [PubMed] [Google Scholar]
  16. Gutiérrez J., Maroto C., Piédrola G., Martín E., Perez J. A. Circulating Candida antigens and antibodies: useful markers of candidemia. J Clin Microbiol. 1993 Sep;31(9):2550–2552. doi: 10.1128/jcm.31.9.2550-2552.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Holland J. P., Holland M. J. Structural comparison of two nontandemly repeated yeast glyceraldehyde-3-phosphate dehydrogenase genes. J Biol Chem. 1980 Mar 25;255(6):2596–2605. [PubMed] [Google Scholar]
  18. Holland J. P., Labieniec L., Swimmer C., Holland M. J. Homologous nucleotide sequences at the 5' termini of messenger RNAs synthesized from the yeast enolase and glyceraldehyde-3-phosphate dehydrogenase gene families. The primary structure of a third yeast glyceraldehyde-3-phosphate dehydrogenase gene. J Biol Chem. 1983 Apr 25;258(8):5291–5299. [PubMed] [Google Scholar]
  19. Holland M. J., Holland J. P. Isolation and characterization of a gene coding for glyceraldehyde-3-phosphate dehydrogenase from Saccharomyces cerevisiae. J Biol Chem. 1979 Jun 25;254(12):5466–5474. [PubMed] [Google Scholar]
  20. Ishiguro A., Homma M., Torii S., Tanaka K. Identification of Candida albicans antigens reactive with immunoglobulin E antibody of human sera. Infect Immun. 1992 Apr;60(4):1550–1557. doi: 10.1128/iai.60.4.1550-1557.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Jones J. M. Laboratory diagnosis of invasive candidiasis. Clin Microbiol Rev. 1990 Jan;3(1):32–45. doi: 10.1128/cmr.3.1.32. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kuchler K. Unusual routes of protein secretion: the easy way out. Trends Cell Biol. 1993 Dec;3(12):421–426. doi: 10.1016/0962-8924(93)90030-5. [DOI] [PubMed] [Google Scholar]
  23. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  24. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  25. Lee K. L., Buckley H. R., Campbell C. C. An amino acid liquid synthetic medium for the development of mycelial and yeast forms of Candida Albicans. Sabouraudia. 1975 Jul;13(2):148–153. doi: 10.1080/00362177585190271. [DOI] [PubMed] [Google Scholar]
  26. López-Ribot J. L., Alloush H. M., Masten B. J., Chaffin W. L. Evidence for presence in the cell wall of Candida albicans of a protein related to the hsp70 family. Infect Immun. 1996 Aug;64(8):3333–3340. doi: 10.1128/iai.64.8.3333-3340.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. López-Ribot J. L., Chaffin W. L. Members of the Hsp70 family of proteins in the cell wall of Saccharomyces cerevisiae. J Bacteriol. 1996 Aug;178(15):4724–4726. doi: 10.1128/jb.178.15.4724-4726.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Matthews R., Burnie J. P., Lee W. The application of epitope mapping in the development of a new serological test for systemic candidosis. J Immunol Methods. 1991 Sep 20;143(1):73–79. doi: 10.1016/0022-1759(91)90274-j. [DOI] [PubMed] [Google Scholar]
  29. Matthews R., Burnie J. Diagnosis of systemic candidiasis by an enzyme-linked dot immunobinding assay for a circulating immunodominant 47-kilodalton antigen. J Clin Microbiol. 1988 Mar;26(3):459–463. doi: 10.1128/jcm.26.3.459-463.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Matthews R., Burnie J. The role of hsp90 in fungal infection. Immunol Today. 1992 Sep;13(9):345–348. doi: 10.1016/0167-5699(92)90169-8. [DOI] [PubMed] [Google Scholar]
  31. Matthews R., Wells C., Burnie J. P. Characterisation and cellular localisation of the immunodominant 47-Kda antigen of Candida albicans. J Med Microbiol. 1988 Dec;27(4):227–232. doi: 10.1099/00222615-27-4-227. [DOI] [PubMed] [Google Scholar]
  32. Meunier F. Candidiasis. Eur J Clin Microbiol Infect Dis. 1989 May;8(5):438–447. doi: 10.1007/BF01964058. [DOI] [PubMed] [Google Scholar]
  33. Morhart M., Rennie R., Ziola B., Bow E., Louie T. J. Evaluation of enzyme immunoassay for Candida cytoplasmic antigens in neutropenic cancer patients. J Clin Microbiol. 1994 Mar;32(3):766–776. doi: 10.1128/jcm.32.3.766-776.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Pancholi V., Fischetti V. A. A major surface protein on group A streptococci is a glyceraldehyde-3-phosphate-dehydrogenase with multiple binding activity. J Exp Med. 1992 Aug 1;176(2):415–426. doi: 10.1084/jem.176.2.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Pancholi V., Fischetti V. A. Glyceraldehyde-3-phosphate dehydrogenase on the surface of group A streptococci is also an ADP-ribosylating enzyme. Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8154–8158. doi: 10.1073/pnas.90.17.8154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Peñalver M. C., O'Connor J. E., Martinez J. P., Gil M. L. Binding of human fibronectin to Aspergillus fumigatus conidia. Infect Immun. 1996 Apr;64(4):1146–1153. doi: 10.1128/iai.64.4.1146-1153.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Reboli A. C. Diagnosis of invasive candidiasis by a dot immunobinding assay for Candida antigen detection. J Clin Microbiol. 1993 Mar;31(3):518–523. doi: 10.1128/jcm.31.3.518-523.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Reiss E., Morrison C. J. Nonculture methods for diagnosis of disseminated candidiasis. Clin Microbiol Rev. 1993 Oct;6(4):311–323. doi: 10.1128/cmr.6.4.311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Schwencke J., Canut H., Flores A. Simultaneous isolation of the yeast cytosol and well-preserved mitochondria with negligible contamination by vacuolar proteinases. FEBS Lett. 1983 Jun 13;156(2):274–280. doi: 10.1016/0014-5793(83)80512-2. [DOI] [PubMed] [Google Scholar]
  40. Sepulveda P., Cervera A. M., Lopez-Ribot J. L., Chaffin W. L., Martinez J. P., Gozalbo D. Cloning and characterization of a cDNA coding for Candida albicans polyubiquitin. J Med Vet Mycol. 1996 Sep-Oct;34(5):315–322. [PubMed] [Google Scholar]
  41. Shen H. D., Choo K. B., Lee H. H., Hsieh J. C., Lin W. L., Lee W. R., Han S. H. The 40-kilodalton allergen of Candida albicans is an alcohol dehydrogenase: molecular cloning and immunological analysis using monoclonal antibodies. Clin Exp Allergy. 1991 Nov;21(6):675–681. doi: 10.1111/j.1365-2222.1991.tb03195.x. [DOI] [PubMed] [Google Scholar]
  42. Stone E. M., Rothblum K. N., Alevy M. C., Kuo T. M., Schwartz R. J. Complete sequence of the chicken glyceraldehyde-3-phosphate dehydrogenase gene. Proc Natl Acad Sci U S A. 1985 Mar;82(6):1628–1632. doi: 10.1073/pnas.82.6.1628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Sundstrom P., Aliaga G. R. A subset of proteins found in culture supernatants of Candida albicans includes the abundant, immunodominant, glycolytic enzyme enolase. J Infect Dis. 1994 Feb;169(2):452–456. doi: 10.1093/infdis/169.2.452. [DOI] [PubMed] [Google Scholar]
  44. Swoboda R. K., Bertram G., Hollander H., Greenspan D., Greenspan J. S., Gow N. A., Gooday G. W., Brown A. J. Glycolytic enzymes of Candida albicans are nonubiquitous immunogens during candidiasis. Infect Immun. 1993 Oct;61(10):4263–4271. doi: 10.1128/iai.61.10.4263-4271.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Walsh T. J., Hathorn J. W., Sobel J. D., Merz W. G., Sanchez V., Maret S. M., Buckley H. R., Pfaller M. A., Schaufele R., Sliva C. Detection of circulating candida enolase by immunoassay in patients with cancer and invasive candidiasis. N Engl J Med. 1991 Apr 11;324(15):1026–1031. doi: 10.1056/NEJM199104113241504. [DOI] [PubMed] [Google Scholar]
  46. Winram S. B., Lottenberg R. The plasmin-binding protein Plr of group A streptococci is identified as glyceraldehyde-3-phosphate dehydrogenase. Microbiology. 1996 Aug;142(Pt 8):2311–2320. doi: 10.1099/13500872-142-8-2311. [DOI] [PubMed] [Google Scholar]
  47. Zöller L., Krämer I., Kappe R., Sonntag H. G. Enzyme immunoassays for invasive Candida infections: reactivity of somatic antigens of Candida albicans. J Clin Microbiol. 1991 Sep;29(9):1860–1867. doi: 10.1128/jcm.29.9.1860-1867.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. van Deventer A. J., van Vliet H. J., Voogd L., Hop W. C., Goessens W. H. Increased specificity of antibody detection in surgical patients with invasive candidiasis with cytoplasmic antigens depleted of mannan residues. J Clin Microbiol. 1993 Apr;31(4):994–997. doi: 10.1128/jcm.31.4.994-997.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES