Project Number: 1931-22000-009-02-R
Project Type: Reimbursable
Start Date: Oct 1, 2009
End Date: Dec 31, 2012
1. Characterize the kinetics of host ROS production and changes in the expression of genes related to ROS production or scavenging in fruit tissue as a response to yeast antagonist cells and exogenous ROS. Focus will be on NADPH oxidase, SOD, and peroxidase. 2. Characterize the effect of ROS on host genes associated with MAPK signaling cascade leading to host defense reactions. Focus will be on salicylic acid-induced protein kinase (SIPK) and wound-induced protein kinase (WIPK) orthologues in apple and citrus fruit tissue. 3. Determine the implications of elevated ROS production (induced by antagonist yeasts or other factors) at the infection sites (surface wounds) on the ability of pathogenic fungi to infect host tissue. 4. Examine the effects of ROS on the tolerance of yeast antagonists to stress conditions (dehydration, nutrient starvation, osmotic stress) and on their ability to proliferate, colonize, and form biofilms in or on wounded and intact fruit tissue, respectively. In this regard, we will examine the activity and gene expression of three enzymes known to be involved in oxidative and stress tolerance in yeasts: catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPX), and also, characterize the overall proteomic response of yeast antagonists to exogenous ROS.
Kinetics and mechanism of ROS production and scavenging in fruit tissue as affected by yeast antagonist cells (Candida oleophila and Metschnikowia fructicola), fruit type (apple and citrus), and maturity/ripening stage will be studied using assays for superoxide anions and hydrogen peroxide, laser confocal microscopy, apple and citrus microarrays, and Real-Time qPCR analysis of the expression of oxidative stress related genes. Expression of key genes in the MAPK signaling cascade (orthologues of SIPK and WIPK in apple and citrus) will be investigated by means of Real-Time qPCR. The implication of ROS in wound sites on infection and development of the pathogens (Penicillium digitatum and Penicillium expansum) will be assessed using various elicitors and inhibitors of ROS. Production of ROS by yeast cells, and the expression and activity of ROS-related genes and proteins, respectively, will be determined using Real-Time qPCR techniques and spectrophotometric assays. DIGE technology and MALDI-TOF analysis will be utilized to investigate changes in the yeast proteome as affected by ROS and other stressors.