Loss of cell wall mannosylphosphate in Candida albicans does not influence macrophage recognition

R P Hobson, C A Munro, S Bates, D M MacCallum, J E Cutler, S E M Heinsbroek, G D Brown, F C Odds, N A R Gow

Research output: Contribution to journalArticle

91 Citations (Scopus)

Abstract

The outer layer of the cell wall of the human pathogenic fungus Candida albicans is enriched with heavily mannosylated glycoproteins that are the immediate point of contact between the fungus and cells of the host, including phagocytes. Previous work had identified components of the acid-labile fraction of N-linked mannan, comprising beta-1,2-linked mannose residues attached via a phosphodiester bond, as potential ligands for macrophage receptors and modulators of macrophage function. We therefore isolated and disrupted the CaMNN4 gene, which is required for mannosyl phosphate transfer and hence the attachment of beta-1,2 mannose oligosaccharides to the acid-labile N-mannan side chains. With the mannosylphosphate eliminated, the mnn4Delta null mutant was unable to bind the charged cationic dye Alcian Blue and was devoid of acid-labile beta-1,2-linked oligomannosaccharides. The mnn4Delta mutant was unaffected in cell growth and morphogenesis in vitro and in virulence in a murine model of systemic C. albicans infection. The null mutant was also not affected in its interaction with macrophages. Mannosylphosphate is therefore not required for macrophage interactions or for virulence of C. albicans.

Original languageEnglish
Pages (from-to)39628-39635
Number of pages8
JournalThe Journal of Biological Chemistry
Volume279
Early online date22 Jul 2004
DOIs
Publication statusPublished - 17 Sep 2004

Keywords

  • selectable marker URA3
  • beta-glucan receptor
  • saccharomyces-cerevisiae
  • beta-1,2-linked oligomannosides
  • yeast mannan
  • adhesin activity
  • host-defense
  • serotype-A
  • MNN4 gene
  • virulence

Cite this

Loss of cell wall mannosylphosphate in Candida albicans does not influence macrophage recognition. / Hobson, R P ; Munro, C A ; Bates, S ; MacCallum, D M ; Cutler, J E ; Heinsbroek, S E M ; Brown, G D ; Odds, F C ; Gow, N A R .

In: The Journal of Biological Chemistry, Vol. 279, 17.09.2004, p. 39628-39635.

Research output: Contribution to journalArticle

Hobson, R P ; Munro, C A ; Bates, S ; MacCallum, D M ; Cutler, J E ; Heinsbroek, S E M ; Brown, G D ; Odds, F C ; Gow, N A R . / Loss of cell wall mannosylphosphate in Candida albicans does not influence macrophage recognition. In: The Journal of Biological Chemistry. 2004 ; Vol. 279. pp. 39628-39635.
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AU - Odds, F C

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AB - The outer layer of the cell wall of the human pathogenic fungus Candida albicans is enriched with heavily mannosylated glycoproteins that are the immediate point of contact between the fungus and cells of the host, including phagocytes. Previous work had identified components of the acid-labile fraction of N-linked mannan, comprising beta-1,2-linked mannose residues attached via a phosphodiester bond, as potential ligands for macrophage receptors and modulators of macrophage function. We therefore isolated and disrupted the CaMNN4 gene, which is required for mannosyl phosphate transfer and hence the attachment of beta-1,2 mannose oligosaccharides to the acid-labile N-mannan side chains. With the mannosylphosphate eliminated, the mnn4Delta null mutant was unable to bind the charged cationic dye Alcian Blue and was devoid of acid-labile beta-1,2-linked oligomannosaccharides. The mnn4Delta mutant was unaffected in cell growth and morphogenesis in vitro and in virulence in a murine model of systemic C. albicans infection. The null mutant was also not affected in its interaction with macrophages. Mannosylphosphate is therefore not required for macrophage interactions or for virulence of C. albicans.

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