Grant: Discovery Grants Program - Individual
University of Regina
$42,000.00
Discovering the networks that control cell wall integrity, cell division, morphogenesis and adhesion in Candida albicans using high content microscopy assays.
EF 2020-21
Résumé
The highly dynamic fungal cell envelope plays an important role in morphogenesis and virulence as the first line of defense for chemical challenge. Microbes use several strategies to maintain cell wall integrity (CWI), including signal-transduction cascades to monitor the cell wall and respond to environmental challenges. The specific molecular cues that initiate CWI cascades and delay or inhibit cell division in microbes are understudied. Over the past decade my lab has made significant strides in developing tools to probe CWI strategies in both fungi and bacteria.
We will develop novel microscopy assays to understand the role of yeast glycosylphosphatidylinositol (GPI)-anchored lipoproteins in response to essential oil components and derivatives, activating CWI pathways and regulating morphogenesis and cell division. Over the long-term we will identify the interrelationship between CWI pathways, cell division, morphology and virulence in response to numerous antifungals to inform the development of essential oil-based antifungal formulations for agriculture and medicine.
Our recently developed novel high-content assays use correlative atomic force-quantitative imaging-confocal laser scanning microscopy (AF-QI-CLSM) imaging to simultaneously monitor live cell envelope remodeling, cell wall elasticity and surface adhesion with nanometer (nm) and picoNewton (pN) resolution, respectively, while simultaneously tracking the organization and dynamics of at least three fluorescent protein (FP)-tagged molecules in real time. The correlative data provides insight into signal transduction across the cell envelope and into the cell in response to sub-lethal levels of xenobiotics.
Mutant strains of Candida albicans deficient in key CWI receptor proteins will pinpoint the pathways that respond to essential oils. Functionalized AFM tips will probe the localization, clustering and conformation of cell wall proteins, while FPs track intracellular signaling molecules and cell division proteins involved in the stress response and CWI signaling. Images will also reveal morphological changes such as yeast-hyphal transitions. Synchrotron-infrared nano-spectroscopy-AFM with Gough (UofM) will report on surface ultrastructure and cell wall biochemical composition with nm precision.
Correlative AFM-QI-CLSM of live cells is a completely novel analytical tool with broad application to cell biology for studying virtually any cell type and stress. This research will further our understanding of fungal CWI pathways and cell wall quality control at the molecular level. The cell wall is a primary target for antifungal agents, and its adaptive capabilities allow propagation of fungi that are a significant detriment to agriculture and medicine. Thus, understanding the impact of essential oils on fungal CWI will inform their use as environmentally safe antifungal alternatives.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Saskatchewan, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
RGPIN-2018-06649
Name nom
Dahms, Tanya
Department département
Chemistry and Biochemistry
Organization id
17
Institution établissement
University of Regina
Province en
Saskatchewan
Province fr
Saskatchewan
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2020
Competition year année de concours
2018
Award amount
42000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
100
Area of application group en
Agriculture and primary food production
Area of application group fr
Agriculture et produits alimentaires primaires
Area of application en
Agriculture and primary food production
Area of application fr
Agriculture et produits alimentaires primaires
Research subject code
5205
Research subject group en
Microbiology
Research subject group fr
Microbiologie
Research subject en
Mycology
Research subject fr
Mycologie
Installment
inst:3-5
Partie
3
Nb partie
5
Application title
Discovering the networks that control cell wall integrity, cell division, morphogenesis and adhesion in Candida albicans using high content microscopy assays.
Keyword
NSERC
Application summary
The highly dynamic fungal cell envelope plays an important role in morphogenesis and virulence as the first line of defense for chemical challenge. Microbes use several strategies to maintain cell wall integrity (CWI), including signal-transduction cascades to monitor the cell wall and respond to environmental challenges. The specific molecular cues that initiate CWI cascades and delay or inhibit cell division in microbes are understudied. Over the past decade my lab has made significant strides in developing tools to probe CWI strategies in both fungi and bacteria.
We will develop novel microscopy assays to understand the role of yeast glycosylphosphatidylinositol (GPI)-anchored lipoproteins in response to essential oil components and derivatives, activating CWI pathways and regulating morphogenesis and cell division. Over the long-term we will identify the interrelationship between CWI pathways, cell division, morphology and virulence in response to numerous antifungals to inform the development of essential oil-based antifungal formulations for agriculture and medicine.
Our recently developed novel high-content assays use correlative atomic force-quantitative imaging-confocal laser scanning microscopy (AF-QI-CLSM) imaging to simultaneously monitor live cell envelope remodeling, cell wall elasticity and surface adhesion with nanometer (nm) and picoNewton (pN) resolution, respectively, while simultaneously tracking the organization and dynamics of at least three fluorescent protein (FP)-tagged molecules in real time. The correlative data provides insight into signal transduction across the cell envelope and into the cell in response to sub-lethal levels of xenobiotics.
Mutant strains of Candida albicans deficient in key CWI receptor proteins will pinpoint the pathways that respond to essential oils. Functionalized AFM tips will probe the localization, clustering and conformation of cell wall proteins, while FPs track intracellular signaling molecules and cell division proteins involved in the stress response and CWI signaling. Images will also reveal morphological changes such as yeast-hyphal transitions. Synchrotron-infrared nano-spectroscopy-AFM with Gough (UofM) will report on surface ultrastructure and cell wall biochemical composition with nm precision.
Correlative AFM-QI-CLSM of live cells is a completely novel analytical tool with broad application to cell biology for studying virtually any cell type and stress. This research will further our understanding of fungal CWI pathways and cell wall quality control at the molecular level. The cell wall is a primary target for antifungal agents, and its adaptive capabilities allow propagation of fungi that are a significant detriment to agriculture and medicine. Thus, understanding the impact of essential oils on fungal CWI will inform their use as environmentally safe antifungal alternatives.