Literature DB >> 16215175

The Candida albicans vacuole is required for differentiation and efficient macrophage killing.

G E Palmer1, M N Kelly, J E Sturtevant.   

Abstract

Yeast-hypha differentiation is believed to be necessary for the normal progression of Candida albicans infections. The emergence and extension of a germ tube from a parental yeast cell are accompanied by dynamic changes in vacuole size and morphology. Although vacuolar function is required during this process, it is unclear if it is vacuolar expansion or some other vacuolar function that is important. We previously described a C. albicans vps11Delta mutant which lacked a recognizable vacuole compartment and with defects in multiple vacuolar functions. These include sensitivities to stress, reduced proteolytic activities, and severe defects in filamentation. Herein we utilize a partially functional VPS11 allele (vps11hr) to help define which vacuolar functions are required for differentiation and which influence interaction with macrophages. Mutant strains harboring this allele are not osmotically or temperature sensitive and have normal levels of secreted aspartyl protease and carboxypeptidase Y activity but have a fragmented vacuole morphology. Moreover, this mutant is defective in filamentation, suggesting that the major role the vacuole plays in yeast-hypha differentiation may relate directly to its morphology. The results of this study support the hypothesis that vacuole expansion is required during germ tube emergence. Both vps11 mutants were severely attenuated in their ability to kill a macrophage cell line. The viability of the vps11delta mutant was significantly reduced during macrophage interaction compared to that in the control strains, while the vps11hr mutant was unaffected. This implies some vacuolar functions are required for Candida survival within the macrophage, while additional vacuolar functions are required to inflict injury on the macrophage.

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Year:  2005        PMID: 16215175      PMCID: PMC1265890          DOI: 10.1128/EC.4.10.1677-1686.2005

Source DB:  PubMed          Journal:  Eukaryot Cell        ISSN: 1535-9786


  35 in total

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Journal:  Yeast       Date:  1996-01       Impact factor: 3.239

2.  Nonfilamentous C. albicans mutants are avirulent.

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Journal:  Cell       Date:  1997-09-05       Impact factor: 41.582

3.  Rapid hypothesis testing with Candida albicans through gene disruption with short homology regions.

Authors:  R B Wilson; D Davis; A P Mitchell
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

4.  ABG1, a novel and essential Candida albicans gene encoding a vacuolar protein involved in cytokinesis and hyphal branching.

Authors:  Verónica Veses; Manuel Casanova; Amelia Murgui; Angel Domínguez; Neil A R Gow; José P Martínez
Journal:  Eukaryot Cell       Date:  2005-06

5.  A novel RING finger protein complex essential for a late step in protein transport to the yeast vacuole.

Authors:  S E Rieder; S D Emr
Journal:  Mol Biol Cell       Date:  1997-11       Impact factor: 4.138

6.  The expression of the secreted aspartyl proteinases Sap4 to Sap6 from Candida albicans in murine macrophages.

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Journal:  Mol Microbiol       Date:  1998-05       Impact factor: 3.501

7.  Random mutagenesis of an essential Candida albicans gene.

Authors:  Glen E Palmer; Joy E Sturtevant
Journal:  Curr Genet       Date:  2004-11-10       Impact factor: 3.886

8.  Apg9p/Cvt7p is an integral membrane protein required for transport vesicle formation in the Cvt and autophagy pathways.

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Journal:  J Cell Biol       Date:  2000-02-07       Impact factor: 10.539

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Journal:  J Cell Sci       Date:  1998-08       Impact factor: 5.285

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Authors:  T A Vida; S D Emr
Journal:  J Cell Biol       Date:  1995-03       Impact factor: 10.539

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  29 in total

1.  Trafficking through the late endosome significantly impacts Candida albicans tolerance of the azole antifungals.

Authors:  Arturo Luna-Tapia; Morgan E Kerns; Karen E Eberle; Branko S Jursic; Glen E Palmer
Journal:  Antimicrob Agents Chemother       Date:  2015-02-09       Impact factor: 5.191

2.  Endosomal and AP-3-dependent vacuolar trafficking routes make additive contributions to Candida albicans hyphal growth and pathogenesis.

Authors:  Glen E Palmer
Journal:  Eukaryot Cell       Date:  2010-09-24

3.  Vocation, location, vocation: researching Candida pathogenesis.

Authors:  Joy Sturtevant
Journal:  Virulence       Date:  2014       Impact factor: 5.882

4.  Candida albicans VPS4 contributes differentially to epithelial and mucosal pathogenesis.

Authors:  Hallie S Rane; Sarah Hardison; Claudia Botelho; Stella M Bernardo; Floyd Wormley; Samuel A Lee
Journal:  Virulence       Date:  2014-10-31       Impact factor: 5.882

5.  Candida albicans SUR7 contributes to secretion, biofilm formation, and macrophage killing.

Authors:  Stella M Bernardo; Samuel A Lee
Journal:  BMC Microbiol       Date:  2010-04-30       Impact factor: 3.605

6.  Candida albicans AGE3, the ortholog of the S. cerevisiae ARF-GAP-encoding gene GCS1, is required for hyphal growth and drug resistance.

Authors:  Thomas Lettner; Ute Zeidler; Mario Gimona; Michael Hauser; Michael Breitenbach; Arnold Bito
Journal:  PLoS One       Date:  2010-08-05       Impact factor: 3.240

7.  Candida albicans VPS1 contributes to protease secretion, filamentation, and biofilm formation.

Authors:  Stella M Bernardo; Zachary Khalique; John Kot; Jason K Jones; Samuel A Lee
Journal:  Fungal Genet Biol       Date:  2008-01-26       Impact factor: 3.495

8.  Deletion of vacuolar proton-translocating ATPase V(o)a isoforms clarifies the role of vacuolar pH as a determinant of virulence-associated traits in Candida albicans.

Authors:  Summer M Raines; Hallie S Rane; Stella M Bernardo; Jessica L Binder; Samuel A Lee; Karlett J Parra
Journal:  J Biol Chem       Date:  2013-01-11       Impact factor: 5.157

9.  Three prevacuolar compartment Rab GTPases impact Candida albicans hyphal growth.

Authors:  Douglas A Johnston; Arturo Luna Tapia; Karen E Eberle; Glen E Palmer
Journal:  Eukaryot Cell       Date:  2013-05-24

10.  The contribution of Candida albicans vacuolar ATPase subunit V₁B, encoded by VMA2, to stress response, autophagy, and virulence is independent of environmental pH.

Authors:  Hallie S Rane; Stella M Bernardo; Summer R Hayek; Jessica L Binder; Karlett J Parra; Samuel A Lee
Journal:  Eukaryot Cell       Date:  2014-07-18
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