|
|
||||||||
Genetics and Molecular Biology |
Center for Medical Mycology, University Hospitals of Cleveland and Department of Dermatology, Case Western Reserve University, Cleveland, OH 44106-5028, USA1
Department of Microbiology and Immunology, Medical College of Ohio, Toledo, OH 43614-5806, USA2
Author for correspondence: Mahmoud A. Ghannoum. Tel: +1 216 844 8580. Fax: +1 216 844 1076. e-mail: mag3{at}po.cwru.edu
Phospholipases have been proposed to contribute to the virulence of Candida albicans. Recently, a candidal strain deleted for PLB1, the gene encoding the predominant phospholipase B (Plb1) secreted by C. albicans, was constructed and its virulence in an intravenous murine model of disseminated candidiasis was evaluated. In the present study, the PLB1 gene was reintroduced back into the plb1 null mutant to generate the revertant strain, which showed similar growth and morphology to its isogenic parent strain. Virulence of the revertant strain was found to be comparable to that of the parent strain in an intravenous murine model of disseminated candidiasis. To compare the abilities of the plb1 null mutant, the revertant and the isogenic parent strains to cross the gastrointestinal (GI) tract and cause systemic infection, an oralintragastric infant mouse model of candidiasis was used. Histological examinations and analysis of c.f.u. of the pathogen in liver homogenates revealed that the parental and revertant strains were able to invade and traverse the GI mucosa to a significantly greater extent than the plb1 null mutant. Immunofluorescence and immunoelectron microscopic studies of infected host tissue using anti-Plb1 antibody showed that Plb1 is secreted during invasion of the gastric mucosa by the parental and revertant strains. In contrast, little or no labelling was observed in the null mutant strain. The results indicate that the Plb1 secreted by C. albicans enhances the ability of this organism to cross the GI tract and disseminate haematogenously. These studies provide unequivocal evidence supporting a role for Plb1 during the course of infection by C. albicans.
Keywords: phospholipase B, virulence factor, candidal transmigration, in vivo localization of Plb1
Abbreviations: GI, gastrointestinal; PAS, periodic acidSchiff reagent
a These authors contributed equally to this work.
This article has been cited by other articles:
![]() |
S. Polakova, C. Blume, J. A. Zarate, M. Mentel, D. Jorck-Ramberg, J. Stenderup, and J. Piskur Formation of new chromosomes as a virulence mechanism in yeast Candida glabrata PNAS, February 24, 2009; 106(8): 2688 - 2693. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. L. Chaffin Candida albicans Cell Wall Proteins Microbiol. Mol. Biol. Rev., September 1, 2008; 72(3): 495 - 544. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Biswas, P. Van Dijck, and A. Datta Environmental Sensing and Signal Transduction Pathways Regulating Morphopathogenic Determinants of Candida albicans Microbiol. Mol. Biol. Rev., June 1, 2007; 71(2): 348 - 376. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. L. Richard and A. Plaine Comprehensive Analysis of Glycosylphosphatidylinositol-Anchored Proteins in Candida albicans Eukaryot. Cell, February 1, 2007; 6(2): 119 - 133. [Full Text] [PDF] |
||||
![]() |
S. Cheng, C. J. Clancy, M. A. Checkley, Z. Zhang, K. L. Wozniak, K. R. Seshan, H. Y. Jia, P. Fidel Jr, G. Cole, and M. H. Nguyen The Role of Candida albicans NOT5 in Virulence Depends upon Diverse Host Factors In Vivo Infect. Immun., November 1, 2005; 73(11): 7190 - 7197. [Abstract] [Full Text] [PDF] |
||||
![]() |
M Yordanov, P Dimitrova, S Patkar, S Falcocchio, E Xoxi, L Saso, and N Ivanovska Ibogaine reduces organ colonization in murine systemic and gastrointestinal Candida albicans infections J. Med. Microbiol., July 1, 2005; 54(7): 647 - 653. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y H Samaranayake, R S Dassanayake, J A. Jayatilake, B P. Cheung, J Y. Yau, K W. Yeung, and L P Samaranayake Phospholipase B enzyme expression is not associated with other virulence attributes in Candida albicans isolates from patients with human immunodeficiency virus infection J. Med. Microbiol., June 1, 2005; 54(6): 583 - 593. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Balish, T. F. Warner, P. J. Nicholas, E. E. Paulling, C. Westwater, and D. A. Schofield Susceptibility of Germfree Phagocyte Oxidase- and Nitric Oxide Synthase 2-Deficient Mice, Defective in the Production of Reactive Metabolites of Both Oxygen and Nitrogen, to Mucosal and Systemic Candidiasis of Endogenous Origin Infect. Immun., March 1, 2005; 73(3): 1313 - 1320. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Brand, D. M. MacCallum, A. J. P. Brown, N. A. R. Gow, and F. C. Odds Ectopic Expression of URA3 Can Influence the Virulence Phenotypes and Proteome of Candida albicans but Can Be Overcome by Targeted Reintegration of URA3 at the RPS10 Locus Eukaryot. Cell, August 1, 2004; 3(4): 900 - 909. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Timpe, M. M. Holm, S. L. Vanlerberg, V. Basrur, and E. R. Lafontaine Identification of a Moraxella catarrhalis Outer Membrane Protein Exhibiting Both Adhesin and Lipolytic Activities Infect. Immun., August 1, 2003; 71(8): 4341 - 4350. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. Noverr, G. M. Cox, J. R. Perfect, and G. B. Huffnagle Role of PLB1 in Pulmonary Inflammation and Cryptococcal Eicosanoid Production Infect. Immun., March 1, 2003; 71(3): 1538 - 1547. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. K. Mukherjee, J. Chandra, D. M. Kuhn, and M. A. Ghannoum Differential expression of Candida albicans phospholipase B (PLB1) under various environmental and physiological conditions Microbiology, January 1, 2003; 149(1): 261 - 267. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |