A single species Candida albicans, causes half of all invasive fungal infections in humans. The ability of C. albicans to switch reversibly between yeast and hyphe is a major virulence trait that helps it disseminate into the bloodstream (yeast) and invade target organs (filaments). Yeast to hyphae morphogenesis has been extensively studied and its regulation well understood. To the contrary, little is known about the reverse process: hyphae to yeast growth. C. albicans hyphae produce yeast cells from their lateral septal regions, coined as ?lateral yeasts?. These lateral yeasts are always found with hyphae at the site of active infection, are the major cells that re- enter the bloodstream and establish distal foci of infection. In fact, lateral yeast cells released from the hyphal layers of biofilm-contaminated catheters have direct access into the bloodstream. We identified the first regulator of hyphae-to-lateral yeast growth, PES1 and have shown that blocking the process (by depleting PES1 in vivo) can abrogate disseminated candidiasis as well as biofilm- associated candidemia. Nothing is known on the regulatory aspects pf PES1. Our preliminary studies show that phosphorylation of Pes1 by Ras-PKA inhibits lateral yeast growth while its dephosphorylation by a Ras- linked phosphatase Yvh1 activates lateral yeast emergence from hyphae and induces biofilm dispersal. Using PES1 as a target for identifying small molecule inhibitors of lateral yeast growth, identified alexidine dihydrochloride that directly inhibited both Pes1 and Yvh1 and protected mice from biofilm-associated disseminated candidiasis. Here, using protein biochemistry assays, we propose to delineate how signaling through Ras-PKA regulates Pes1. We will identify other cognate regulators that interact with Pes1 to control lateral yeast growth, and use this information to discover novel compounds that can interrupt hyphae to lateral yeast growth and disseminated candidiasis. Ultimately, better outcomes for patients with indwelling medical devices is the goal of this application.
A single species Candida albicans causes half of all invasive fungal infections in humans. Hyphae to lateral yeast morphogenetic switching plays a vital role in causing disseminated candidiasis. The current proposal will identify novel proteins that regulate lateral yeast growth and use them as targets to identify small molecule inhibitors of the C. albicans infectious cycle, in vivo.
