Oral biologists at the University at Buffalo have shown for the first time how histatin kills the oral pathogen Candida albicans, the fungus responsible for most HIV-related oral infections. This, the researchers believe, could lead to a better drug for candidiasis.
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Researchers led by Dr Mira Edgerton, discovered that histatin binds to a specific membrane protein called TRK1p, which regulates potassium ion flow through the cell membrane of the pathogenic fungus Candida albicans and allows the cell to regulate its volume.
The binding action of histatin acts like a “foot in the door,” said Edgerton, UB research associate professor of oral biology in the UB School of Dental Medicine and senior author on the study. “This is the first identification of a specific target for histatin,” she said, “the finding paves the way for eventually developing a better therapeutic drug for candidiasis.”
Candidias, also known as thrush, is a disease characterized by whitish spots and ulcers on the membranes of the mouth, tongue and throat. It affects primarily people with weakened immune systems caused by antibiotics, chemotherapy or by diseases such as AIDS. Thrush also affects many denture wearers.
The condition can be treated with antifungal medication in otherwise healthy people, but it is difficult to treat in persons with compromised immunity and can be deadly if it infects vital organs.