Literature DB >> 387610

Effects of low concentrations of zinc on the growth and dimorphism of Candida albicans: evidence for zinc-resistant and -sensitive pathways for mycelium formation.

G W Bedell, D R Soll.   

Abstract

In this analysis we have examined in detail the effects of low concentrations of zinc on the growth and dimorphism of Candida albicans. Evidence is presented that micromolar concentrations of zinc added to growth cultures grown at 25 degrees C (i) cause a twofold increase in the final concentration of spheres at sationary phase, (ii) result in an asynchronous block in the budding cycle at stationary phase, (iii) completely suppress mycelium formation in two independently isolated human strains which produce low but significant levels of mycelia at stationary phase, and (iv) completely suppress mycelium formation in cultures of mutant M10, in which over 60% of the cells form mycelia at stationary phase. In contrast, micromolar concentrations of zinc do not inhibit mycelium formation induced by releasing cells from stationary-phase cultures into fresh medium at 37 degrees C. In addition, if zinc is present in the growth medium of the initial culture at 25 degrees C, the average time of subsequent mycelium formation after release into fresh medium at 37 degrees C is halved. It is demonstrated that the above effects are specific to zinc. The possibility of alterante pathways for mycelium formation is suggested, and the medical implications of this possibility are discussed.

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Year:  1979        PMID: 387610      PMCID: PMC414618          DOI: 10.1128/iai.26.1.348-354.1979

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  11 in total

1.  Control of dimorphism in Candida albicans by zinc: effect on cell morphology and composition.

Authors:  H Yamaguchi
Journal:  J Gen Microbiol       Date:  1975-02

2.  PHOSPHATE DIRECTED Y-M VARIATION IN CANDIDA ALBICANS.

Authors:  A WIDRA
Journal:  Mycopathol Mycol Appl       Date:  1964-09-30

3.  Germ tube formation from zonal rotor fractions of Candida albicans.

Authors:  W L Chaffin; S J Sogin
Journal:  J Bacteriol       Date:  1976-05       Impact factor: 3.490

4.  Commitment to germ tube or bud formation during release from stationary phase in Candida albicans.

Authors:  L H Mitchell; D R Soll
Journal:  Exp Cell Res       Date:  1979-04       Impact factor: 3.905

5.  The regulation of nuclear migration and division during pseudo-mycelium outgrowth in the dimorphic yeast Candida albicans.

Authors:  D R Soll; M Stasi; G Bedell
Journal:  Exp Cell Res       Date:  1978-10-01       Impact factor: 3.905

6.  Genetic control of the cell division cycle in yeast.

Authors:  L H Hartwell; J Culotti; J R Pringle; B J Reid
Journal:  Science       Date:  1974-01-11       Impact factor: 47.728

7.  Growth stimulation and inhibition of Candida albicans by metabolic by-products.

Authors:  C G Saltarelli
Journal:  Mycopathol Mycol Appl       Date:  1973-09-28

8.  Zinc metabolism in infection.

Authors:  W R Beisel
Journal:  Prog Clin Biol Res       Date:  1977

9.  RNA synthesis and control of cell division in the yeast S. cerevisiae.

Authors:  G C Johnston; R A Singer
Journal:  Cell       Date:  1978-08       Impact factor: 41.582

10.  An amino acid liquid synthetic medium for the development of mycelial and yeast forms of Candida Albicans.

Authors:  K L Lee; H R Buckley; C C Campbell
Journal:  Sabouraudia       Date:  1975-07
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  109 in total

1.  Misexpression of the opaque-phase-specific gene PEP1 (SAP1) in the white phase of Candida albicans confers increased virulence in a mouse model of cutaneous infection.

Authors:  C Kvaal; S A Lachke; T Srikantha; K Daniels; J McCoy; D R Soll
Journal:  Infect Immun       Date:  1999-12       Impact factor: 3.441

2.  EFG1 null mutants of Candida albicans switch but cannot express the complete phenotype of white-phase budding cells.

Authors:  T Srikantha; L K Tsai; K Daniels; D R Soll
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

3.  The histone deacetylase genes HDA1 and RPD3 play distinct roles in regulation of high-frequency phenotypic switching in Candida albicans.

Authors:  T Srikantha; L Tsai; K Daniels; A J Klar; D R Soll
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

4.  Phenotypic switching in Candida albicans is controlled by a SIR2 gene.

Authors:  J Pérez-Martín; J A Uría; A D Johnson
Journal:  EMBO J       Date:  1999-05-04       Impact factor: 11.598

5.  Drug resistance is not directly affected by mating type locus zygosity in Candida albicans.

Authors:  Claude Pujol; Shawn A Messer; Michael Pfaller; David R Soll
Journal:  Antimicrob Agents Chemother       Date:  2003-04       Impact factor: 5.191

6.  Skin facilitates Candida albicans mating.

Authors:  Salil A Lachke; Shawn R Lockhart; Karla J Daniels; David R Soll
Journal:  Infect Immun       Date:  2003-09       Impact factor: 3.441

7.  Hemoglobin regulates expression of an activator of mating-type locus alpha genes in Candida albicans.

Authors:  Michael L Pendrak; S Steve Yan; David D Roberts
Journal:  Eukaryot Cell       Date:  2004-06

Review 8.  High-frequency switching in Candida albicans.

Authors:  D R Soll
Journal:  Clin Microbiol Rev       Date:  1992-04       Impact factor: 26.132

9.  The white cell response to pheromone is a general characteristic of Candida albicans strains.

Authors:  Nidhi Sahni; Song Yi; Claude Pujol; David R Soll
Journal:  Eukaryot Cell       Date:  2008-12-12

10.  Most frequent scenario for recurrent Candida vaginitis is strain maintenance with "substrain shuffling": demonstration by sequential DNA fingerprinting with probes Ca3, C1, and CARE2.

Authors:  S R Lockhart; B D Reed; C L Pierson; D R Soll
Journal:  J Clin Microbiol       Date:  1996-04       Impact factor: 5.948

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