Literature DB >> 8133102

Comparative pathogenesis of clinical and nonclinical isolates of Saccharomyces cerevisiae.

K V Clemons1, J H McCusker, R W Davis, D A Stevens.   

Abstract

Although considered nonpathogenic, Saccharomyces cerevisiae is being encountered more frequently in the clinical setting. To assess pathogenic potential, 13 clinical isolates, 10 nonclinical isolates, and 5 constructed strains of S. cerevisiae were analyzed. All were S. cerevisiae by biochemical profiles, sporulation, or genetic evidence. Intravenous inoculation of yeasts into CD-1 mice showed that some clinical isolates proliferated in the brain (5-fold) but nonclinical isolates were cleared (1000-fold) by day 7 after infection. Comparison of burdens with those of YJM128 (clinical) and Y55 (laboratory strain) revealed three virulence groupings: virulent, those greater than or equal to YJM128 (5 clinical and 2 genetic constructs); intermediate virulent, those less than YJM128 and greater than Y55 (5 clinical, 3 genetic constructs, and 4 nonclinical); and avirulent, those less than or equal to Y55 (1 clinical and 6 nonclinical). Genetic crosses indicated that virulence was a dominant trait. Growth of various isolates at 37 degrees C and 39 degrees C indicated that temperature is associated with but not solely responsible for differences in virulence. These data demonstrate that some clinical isolates of S. cerevisiae can proliferate and resist clearance in vivo and support the potential of S. cerevisiae as a cause of clinical disease.

Entities:  

Mesh:

Year:  1994        PMID: 8133102     DOI: 10.1093/infdis/169.4.859

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  39 in total

1.  Known mutator alleles do not markedly increase mutation rate in clinical Saccharomyces cerevisiae strains.

Authors:  Daniel A Skelly; Paul M Magwene; Brianna Meeks; Helen A Murphy
Journal:  Proc Biol Sci       Date:  2017-04-12       Impact factor: 5.349

2.  Sequential elimination of major-effect contributors identifies additional quantitative trait loci conditioning high-temperature growth in yeast.

Authors:  Himanshu Sinha; Lior David; Renata C Pascon; Sandra Clauder-Münster; Sujatha Krishnakumar; Michelle Nguyen; Getao Shi; Jed Dean; Ronald W Davis; Peter J Oefner; John H McCusker; Lars M Steinmetz
Journal:  Genetics       Date:  2008-09-09       Impact factor: 4.562

3.  Genome-wide association analysis of clinical vs. nonclinical origin provides insights into Saccharomyces cerevisiae pathogenesis.

Authors:  L A H Muller; J E Lucas; D R Georgianna; J H McCusker
Journal:  Mol Ecol       Date:  2011-08-31       Impact factor: 6.185

4.  Microsatellite typing as a new tool for identification of Saccharomyces cerevisiae strains.

Authors:  C Hennequin; A Thierry; G F Richard; G Lecointre; H V Nguyen; C Gaillardin; B Dujon
Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

5.  Epidemiological investigation of vaginal Saccharomyces cerevisiae isolates by a genotypic method.

Authors:  M J McCullough; K V Clemons; C Farina; J H McCusker; D A Stevens
Journal:  J Clin Microbiol       Date:  1998-02       Impact factor: 5.948

6.  Role of nitrogen and carbon transport, regulation, and metabolism genes for Saccharomyces cerevisiae survival in vivo.

Authors:  Joanne M Kingsbury; Alan L Goldstein; John H McCusker
Journal:  Eukaryot Cell       Date:  2006-05

7.  Saccharomyces cerevisiae virulence phenotype as determined with CD-1 mice is associated with the ability to grow at 42 degrees C and form pseudohyphae.

Authors:  J H McCusker; K V Clemons; D A Stevens; R W Davis
Journal:  Infect Immun       Date:  1994-12       Impact factor: 3.441

8.  Development of Saccharomyces cerevisiae as a model pathogen. A system for the genetic identification of gene products required for survival in the mammalian host environment.

Authors:  A L Goldstein; J H McCusker
Journal:  Genetics       Date:  2001-10       Impact factor: 4.562

9.  Typing of Saccharomyces cerevisiae clinical strains by using microsatellite sequence polymorphism.

Authors:  J Y Malgoire; S Bertout; F Renaud; J M Bastide; M Mallié
Journal:  J Clin Microbiol       Date:  2005-03       Impact factor: 5.948

10.  Species identification and virulence attributes of Saccharomyces boulardii (nom. inval.).

Authors:  M J McCullough; K V Clemons; J H McCusker; D A Stevens
Journal:  J Clin Microbiol       Date:  1998-09       Impact factor: 5.948

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.