A spontaneous, cerulenin-resistant mutant of Candida albicans (strain 4918-10) was found to adhere less readily to human vaginal mucosal cells in vitro than a wild type C. albicans (strain 4918). In a murine model of vaginal infection, strain 4918-10 was found to be less virulent than wild type C. albicans, i.e., the infection rate caused by 4918-10 was only 31% of that observed with wild type, 4918. A chitin-soluble extract (CSE) prepared from 4918 blocked attachment of yeast cells to human vaginal epithelial cells, while CSE from 4918-10 did not significantly reduce the attachment of yeasts to vaginal cells. Both 4918 and 4918-10 produced hyphae in vitro and in vivo, were negative for proteinase production and grew equally well at 28"C and 37"C. The data suggest that adherence to vaginal mueosa may be an important determinant in the pathogenesis of vaginal infection eaused by C. albicans.The attachment of Candida albicans yeast cells in vitro to human vaginal mucosa epithelial (VME) cells has been described by several investigators [4,[7][8][9][12][13][14][15][16][17]. Attachment of yeast cells to human VME cells in vitro was reduced if yeast cells were killed by UV irradiation, formalin or treated with proteinases (but not pepsin). Adherence was not influenced by pH [7] or if yeast cells were pretreated with salts or divalent cations, detergents, urea, lipase or a-mannosidase [8]. However, fl-mercaptoethanol did reduce adherence significantly [8].The nature of the surface component promoting yeast attachment to vaginal mucosa is not known. Lee & King [8] suggested that cell wall mannan-protein may be involved in attachment. Contrary to that, our previous studies revealed that chitin, chitin derivatives, a chitin soluble extract and amino sugars [9,12,13] blocked in-vitro adherence to human VME.Animal models have been used to study the pathogenesis of vaginal infection [9,13,15,18]. We have shown in a murine model of vaginal candidiasis that animals, pretreated with vaginal rinses consisting of a chitin-soluble extract (CSE) or N-acetyl-glucosamine, did not develop infection upon subsequent inoculation of C. albicans [9,13].