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This review article focuses on the mechanisms underlying temperature adaptation and virulence of the etiologic agents of blastomycosis, , , and . In response to temperature, undergoes a reversible morphologic switch between hyphae and yeast known as the phase transition. The conversion to yeast for and related thermally dimorphic fungi is essential for virulence. In the yeast phase, upregulates the essential virulence factor, BAD1, which promotes attachment to host cells, impairs activation of immune cells, and blunts cytokine release. yeast also secrete dipeptidyl-peptidase IVA (DPPIVA), a serine protease that blunts the action of cytokines released from host immune cells. transcriptional profiling of yeast has uncovered genes such as and involved in zinc scavenging that contribute to virulence during murine pulmonary infection. The discovery and characterization of genes important for virulence has led to advances at the bedside regarding novel diagnostics, vaccine development, and new targets for drug discovery.
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http://dx.doi.org/10.1080/21505594.2018.1449506 | DOI Listing |
ACS Synth Biol
September 2025
ARC Centre of Excellence in Synthetic Biology, Queensland University of Technology, Brisbane, QLD 4000, Australia.
Fluorescent proteins (FPs) are commonly used as reporters to examine intracellular genetic, molecular, and biochemical status. Flow cytometry is a powerful technique for accurate quantification of single-cell fluorescent levels. Here, we characterize green, red, and blue FPs for use in yeast .
View Article and Find Full Text PDFJ Biosci Bioeng
September 2025
Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8565, Japan.
We have developed the methylotrophic yeast Ogataea minuta as a useful host for producing heterologous proteins. In this study, a double mutant that lacks the Prb1 protease and alcohol oxidase was generated and applied for heterologous protein production. Upon our optimization of the fermentation conditions, such as feeding of carbon and nitrogen sources and pH control, this mutant showed increased production of human serum albumin, resulting in a yield of approximately 7.
View Article and Find Full Text PDFmSystems
September 2025
Department of Biological Sciences and BioDiscovery Institute, University of North Texas, Denton, Texas, USA.
is a human fungal pathogen that survives and proliferates within phagocytic immune cells. To sustain growth in the nutrient-limited phagosome environment, the pathogenic yeast scavenges available carbon sources, which must be metabolized through central carbon metabolism for respiration and biomass synthesis. However, carbon metabolic pathways operating in the pathogenic yeast phase have not been extensively mapped.
View Article and Find Full Text PDFJ Food Sci Technol
October 2025
Centro de Referencia en Levaduras y Tecnología Cervecera (CRELTEC), Instituto Andino Patagónico de Tecnologías Biológicas y Geoambientales (IPATEC), CONICET - Universidad Nacional del Comahue, Quintral 1250, CP8400 San Carlos de Bariloche, Argentina.
Unlabelled: The wild yeast (parental of the lager brewing hybrid yeast) has been intensively studied for brewing applications since its discovery in Patagonia (Argentina), and then in other parts of the world. In this work, cultures of this non-conventional yeast in different physiological conditions were tested in terms of viability and vitality, to understand its behavior and provide tools for biomass quality assessment for brewing. Four dyes were analyzed, and alkaline methylene violet turned out to be the most accurate for viability measurements.
View Article and Find Full Text PDFAnal Bioanal Chem
September 2025
Department of Chemistry, School of Chemistry, Food and Pharmacy, University of Reading, Reading, RG6 6DX, UK.
Fungal pathogens pose a growing threat to global health, necessitating rapid and accurate identification methods. Here, liquid atmospheric pressure matrix-assisted laser desorption/ionisation (LAP-MALDI) mass spectrometry (MS) is applied to fast lipid and protein profiling of Candida albicans and Saccharomyces cerevisiae from cultured colonies. Species-specific lipid profiles were observed in the m/z 600-1100 range, dominated by phospholipids as confirmed by tandem mass spectrometry (MS/MS).
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