Candida albicans Hyphal Formation and the Expression of the Efg1-Regulated Proteinases Sap4 to Sap6 Are Required for the Invasion of Parenchymal Organs

ABSTRACT The ability to change between yeast and hyphal cells (dimorphism) is known to be a virulence property of the human pathogen Candida albicans. The pathogenesis of disseminated candidosis involves adhesion and penetration of hyphal cells from a colonized mucosal site to internal organs. Parenchymal organs, such as the liver and pancreas, are invaded by C. albicans wild-type hyphal cells between 4 and 24 h after intraperitoneal (i.p.) infection of mice. In contrast, a hypha-deficient mutant lacking the transcription factor Efg1 was not able to invade or damage these organs. To investigate whether this was due to the inability to undergo the dimorphic transition or due to the lack of hypha-associated factors, we investigated the role of secreted aspartic proteinases during tissue invasion and their association with the different morphologies of C. albicans. Wild-type cells expressed a distinct pattern of SAP genes during i.p. infections. Within the first 72 h after infection, SAP1, SAP2, SAP4, SAP5, SAP6, and SAP9 were the most commonly expressed proteinase genes. Sap1 to Sap3 antigens were found on yeast and hyphal cells, while Sap4 to Sap6 antigens were predominantly found on hyphal cells in close contact with host cells, in particular, eosinophilic leukocytes. Mutants lacking EFG1 had either noticeably reduced or higher expressed levels of SAP4 to SAP6 transcripts in vitro depending on the culture conditions. During infection, efg1 mutants had a strongly reduced ability to produce hyphae, which was associated with reduced levels of SAP4 to SAP6 transcripts. Mutants lacking SAP1 to SAP3 had invasive properties indistinguishable from those of wild-type cells. In contrast, a triple mutant lacking SAP4 to SAP6 showed strongly reduced invasiveness but still produced hyphal cells. When the tissue damage of liver and pancreas caused by single sap4, sap5, and sap6 and double sap4 and -6, sap5 and -6, and sap4 and -5 double mutants was compared to the damage caused by wild-type cells, all mutants which lacked functional SAP6 showed significantly reduced tissue damage. These data demonstrate that strains which produce hyphal cells but lack hypha-associated proteinases, particularly that encoded by SAP6, are less invasive. In addition, it can be concluded that the reduced virulence of hypha-deficient mutants is not only due to the inability to form hyphae but also due to modified expression of the SAP genes normally associated with the hyphal morphology.

[1]  D. Soll,et al.  A characterization of pH-regulated dimorphism in Candida albicans , 1984, Mycopathologia.

[2]  A. Gillum,et al.  Isolation of the Candida albicans gene for orotidine-5′-phosphate decarboxylase by complementation of S. cerevisiae ura3 and E. coli pyrF mutations , 2004, Molecular and General Genetics MGG.

[3]  M. Schaller,et al.  Individual acid aspartic proteinases (Saps) 1-6 of Candida albicans are not essential for invasion and colonization of the gastrointestinal tract in mice. , 2002, Microbial pathogenesis.

[4]  B. Hube,et al.  Candida albicans proteinases: resolving the mystery of a gene family. , 2001, Microbiology.

[5]  Gerald R. Fink,et al.  The glyoxylate cycle is required for fungal virulence , 2001, Nature.

[6]  L. Hoyer,et al.  The ALS gene family of Candida albicans. , 2001, Trends in microbiology.

[7]  M. Whiteway,et al.  Repression of Hyphal Proteinase Expression by the Mitogen-Activated Protein (MAP) Kinase Phosphatase Cpp1p ofCandida albicans Is Independent of the MAP Kinase Cek1p , 2000, Infection and Immunity.

[8]  B. Hube,et al.  Secreted lipases of Candida albicans: cloning, characterisation and expression analysis of a new gene family with at least ten members , 2000, Archives of Microbiology.

[9]  J. Ernst Transcription factors in Candida albicans - environmental control of morphogenesis. , 2000, Microbiology.

[10]  S. Foundling,et al.  Enzymic characteristics of secreted aspartic proteases of Candida albicans. , 2000, Biochimica et biophysica acta.

[11]  S. Filler,et al.  Role of Hyphal Formation in Interactions ofCandida albicans with Endothelial Cells , 2000, Infection and Immunity.

[12]  T. Nichterlein,et al.  Differential activation of a Candida albicans virulence gene family during infection. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[13]  A. Brown,et al.  CIp10, an efficient and convenient integrating vector for Candida albicans. , 2000, Yeast.

[14]  T. Bertsch,et al.  Germ Tubes and Proteinase Activity Contribute to Virulence of Candida albicans in Murine Peritonitis , 1999, Infection and Immunity.

[15]  M. Schaller,et al.  Secreted aspartic proteinase (Sap) activity contributes to tissue damage in a model of human oral candidosis , 1999, Molecular microbiology.

[16]  P. Sundstrom,et al.  Adhesins in Candida albicans. , 1999, Current opinion in microbiology.

[17]  A. Brown,et al.  Regulatory networks controlling Candida albicans morphogenesis. , 1999, Trends in microbiology.

[18]  T. C. White,et al.  In Vivo Analysis of Secreted Aspartyl Proteinase Expression in Human Oral Candidiasis , 1999, Infection and Immunity.

[19]  D. Sanglard,et al.  Evidence that members of the secretory aspartyl proteinase gene family, in particular SAP2, are virulence factors for Candida vaginitis. , 1999, The Journal of infectious diseases.

[20]  J. Becker,et al.  Altered Expression of Selectable Marker URA3 in Gene-Disrupted Candida albicans Strains Complicates Interpretation of Virulence Studies , 1998, Infection and Immunity.

[21]  D. Hess,et al.  Differential regulation of SAP8 and SAP9, which encode two new members of the secreted aspartic proteinase family in Candida albicans. , 1998, Microbiology.

[22]  M. Schaller,et al.  Differential expression of secreted aspartyl proteinases in a model of human oral candidosis and in patient samples from the oral cavity , 1998, Molecular microbiology.

[23]  K. Boggian,et al.  The expression of the secreted aspartyl proteinases Sap4 to Sap6 from Candida albicans in murine macrophages , 1998, Molecular microbiology.

[24]  S. Kobayashi,et al.  Candida albicans hyphal formation and virulence: is there a clearly defined role? , 1998, Trends in microbiology.

[25]  J. Berman,et al.  Linkage of adhesion, filamentous growth, and virulence in Candida albicans to a single gene, INT1. , 1998, Science.

[26]  G. Fink,et al.  Nonfilamentous C. albicans Mutants Are Avirulent , 1997, Cell.

[27]  N. Gow,et al.  A triple deletion of the secreted aspartyl proteinase genes SAP4, SAP5, and SAP6 of Candida albicans causes attenuated virulence , 1997, Infection and immunity.

[28]  A. Brown,et al.  Disruption of each of the secreted aspartyl proteinase genes SAP1, SAP2, and SAP3 of Candida albicans attenuates virulence , 1997, Infection and immunity.

[29]  J. Ernst,et al.  Efg1p, an essential regulator of morphogenesis of the human pathogen Candida albicans, is a member of a conserved class of bHLH proteins regulating morphogenetic processes in fungi , 1997, The EMBO journal.

[30]  D. Soll Gene regulation during high-frequency switching in Candida albicans. , 1997, Microbiology.

[31]  D. Gozalbo,et al.  Molecular cloning and characterization of a Candida albicans gene (EFB1) coding for the elongation factor EF-1β , 1996 .

[32]  J. Ernst,et al.  Migration of the fungal pathogen Candida albicans across endothelial monolayers , 1996, Infection and immunity.

[33]  D. Gozalbo,et al.  Molecular cloning and characterization of a Candida albicans gene (EFB1) coding for the elongation factor EF-1 beta. , 1996, FEMS Microbiology Letters.

[34]  T. C. White,et al.  Candida albicans secreted aspartyl proteinases: isoenzyme pattern is determined by cell type, and levels are determined by environmental factors , 1995, Journal of bacteriology.

[35]  M. Ghannoum,et al.  Evidence implicating phospholipase as a virulence factor of Candida albicans , 1995, Infection and immunity.

[36]  A. Brown,et al.  Expression of seven members of the gene family encoding secretory aspartyl proteinases in Candida albicans , 1994, Molecular microbiology.

[37]  B. Hube,et al.  Multiplicity of genes encoding secreted aspartic proteinases in Candida species , 1994, Molecular microbiology.

[38]  D. Irwin,et al.  Isogenic strain construction and gene mapping in Candida albicans. , 1993, Genetics.

[39]  N. Gow,et al.  Contact sensing in Candida albicans: a possible aid to epithelial penetration. , 1992, Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology.

[40]  J. Cutler,et al.  Putative virulence factors of Candida albicans. , 1991, Annual review of microbiology.

[41]  N. Gow,et al.  Growth kinetics and morphology of colonies of the filamentous form of Candida albicans. , 1982, Journal of general microbiology.

[42]  F. Macdonald,et al.  Purified Candida albicans proteinase in the serological diagnosis of systemic candidosis. , 1980, JAMA.

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

[44]  D. Soll,et al.  A characterization of pH-regulated dimorphism in Candida albicans , 1984, Mycopathologia.

[45]  A. Gillum,et al.  Isolation of the Candida albicans gene for orotidine-5′-phosphate decarboxylase by complementation of S. cerevisiae ura3 and E. coli pyrF mutations , 2004, Molecular and General Genetics MGG.

[46]  M. Schaller,et al.  Individual acid aspartic proteinases (Saps) 1-6 of Candida albicans are not essential for invasion and colonization of the gastrointestinal tract in mice. , 2002, Microbial pathogenesis.

[47]  B. Hube,et al.  Candida albicans proteinases: resolving the mystery of a gene family. , 2001, Microbiology.

[48]  Gerald R. Fink,et al.  The glyoxylate cycle is required for fungal virulence , 2001, Nature.

[49]  L. Hoyer,et al.  The ALS gene family of Candida albicans. , 2001, Trends in microbiology.

[50]  M. Whiteway,et al.  Repression of Hyphal Proteinase Expression by the Mitogen-Activated Protein (MAP) Kinase Phosphatase Cpp1p ofCandida albicans Is Independent of the MAP Kinase Cek1p , 2000, Infection and Immunity.

[51]  B. Hube,et al.  Secreted lipases of Candida albicans: cloning, characterisation and expression analysis of a new gene family with at least ten members , 2000, Archives of Microbiology.

[52]  J. Ernst Transcription factors in Candida albicans - environmental control of morphogenesis. , 2000, Microbiology.

[53]  S. Foundling,et al.  Enzymic characteristics of secreted aspartic proteases of Candida albicans. , 2000, Biochimica et biophysica acta.

[54]  S. Filler,et al.  Role of Hyphal Formation in Interactions ofCandida albicans with Endothelial Cells , 2000, Infection and Immunity.

[55]  T. Nichterlein,et al.  Differential activation of a Candida albicans virulence gene family during infection. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[56]  A. Brown,et al.  CIp10, an efficient and convenient integrating vector for Candida albicans. , 2000, Yeast.

[57]  T. Bertsch,et al.  Germ Tubes and Proteinase Activity Contribute to Virulence of Candida albicans in Murine Peritonitis , 1999, Infection and Immunity.

[58]  M. Schaller,et al.  Secreted aspartic proteinase (Sap) activity contributes to tissue damage in a model of human oral candidosis , 1999, Molecular microbiology.

[59]  P. Sundstrom,et al.  Adhesins in Candida albicans. , 1999, Current opinion in microbiology.

[60]  A. Brown,et al.  Regulatory networks controlling Candida albicans morphogenesis. , 1999, Trends in microbiology.

[61]  T. C. White,et al.  In Vivo Analysis of Secreted Aspartyl Proteinase Expression in Human Oral Candidiasis , 1999, Infection and Immunity.

[62]  D. Sanglard,et al.  Evidence that members of the secretory aspartyl proteinase gene family, in particular SAP2, are virulence factors for Candida vaginitis. , 1999, The Journal of infectious diseases.

[63]  J. Becker,et al.  Altered Expression of Selectable Marker URA3 in Gene-Disrupted Candida albicans Strains Complicates Interpretation of Virulence Studies , 1998, Infection and Immunity.

[64]  D. Hess,et al.  Differential regulation of SAP8 and SAP9, which encode two new members of the secreted aspartic proteinase family in Candida albicans. , 1998, Microbiology.

[65]  M. Schaller,et al.  Differential expression of secreted aspartyl proteinases in a model of human oral candidosis and in patient samples from the oral cavity , 1998, Molecular microbiology.

[66]  K. Boggian,et al.  The expression of the secreted aspartyl proteinases Sap4 to Sap6 from Candida albicans in murine macrophages , 1998, Molecular microbiology.

[67]  S. Kobayashi,et al.  Candida albicans hyphal formation and virulence: is there a clearly defined role? , 1998, Trends in microbiology.

[68]  J. Berman,et al.  Linkage of adhesion, filamentous growth, and virulence in Candida albicans to a single gene, INT1. , 1998, Science.

[69]  G. Fink,et al.  Nonfilamentous C. albicans Mutants Are Avirulent , 1997, Cell.

[70]  N. Gow,et al.  A triple deletion of the secreted aspartyl proteinase genes SAP4, SAP5, and SAP6 of Candida albicans causes attenuated virulence , 1997, Infection and immunity.

[71]  J. Ernst,et al.  Efg1p, an essential regulator of morphogenesis of the human pathogen Candida albicans, is a member of a conserved class of bHLH proteins regulating morphogenetic processes in fungi , 1997, The EMBO journal.

[72]  D. Soll Gene regulation during high-frequency switching in Candida albicans. , 1997, Microbiology.

[73]  A. Brown,et al.  Disruption of each of the secreted aspartyl proteinase genes SAP1, SAP2, and SAP3 of Candida albicans attenuates virulence , 1997, Infection and immunity.

[74]  J. Ernst,et al.  Migration of the fungal pathogen Candida albicans across endothelial monolayers , 1996, Infection and immunity.

[75]  D. Gozalbo,et al.  Molecular cloning and characterization of a Candida albicans gene (EFB1) coding for the elongation factor EF-1 beta. , 1996, FEMS Microbiology Letters.

[76]  T. C. White,et al.  Candida albicans secreted aspartyl proteinases: isoenzyme pattern is determined by cell type, and levels are determined by environmental factors , 1995, Journal of bacteriology.

[77]  M. Ghannoum,et al.  Evidence implicating phospholipase as a virulence factor of Candida albicans , 1995, Infection and immunity.

[78]  A. Brown,et al.  Expression of seven members of the gene family encoding secretory aspartyl proteinases in Candida albicans , 1994, Molecular microbiology.

[79]  B. Hube,et al.  Multiplicity of genes encoding secreted aspartic proteinases in Candida species , 1994, Molecular microbiology.

[80]  D. Irwin,et al.  Isogenic strain construction and gene mapping in Candida albicans. , 1993, Genetics.

[81]  N. Gow,et al.  Contact sensing in Candida albicans: a possible aid to epithelial penetration. , 1992, Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology.

[82]  J. Cutler,et al.  Putative virulence factors of Candida albicans. , 1991, Annual review of microbiology.

[83]  F. Odds Candida and candidosis: a review and bibliography. 2nd edition. , 1988 .

[84]  N. Gow,et al.  Growth kinetics and morphology of colonies of the filamentous form of Candida albicans. , 1982, Journal of general microbiology.

[85]  F. Macdonald,et al.  Purified Candida albicans proteinase in the serological diagnosis of systemic candidosis. , 1980, JAMA.

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