Ej. Anaissie et al., COMPARATIVE EFFICACIES OF AMPHOTERICIN-B, TRIAZOLES, AND COMBINATION OF BOTH AS EXPERIMENTAL-THERAPY FOR MURINE TRICHOSPORONOSIS, Antimicrobial agents and chemotherapy, 38(11), 1994, pp. 2541-2544
We assessed the activities of amphotericin B deoxycholate, liposomal a
mphotericin B, fluconazole, and SCH 39304 against 10 strains of Tricho
sporon beigelii in mice dth hematogenous infections. Cyclophosphamide-
immunosuppressed CF1 male mice were challenged intravenously with a le
thal inoculum of T. beigelii (5 x 10(6) conidia per mouse) and were as
signed to different treatment groups or were left untreated. Amphoteri
cin B deoxycholate (1 mg/kg of body weight and liposomal amphotericin
B (1, 5, and 10 mg/kg) were given parenterally once daily. Escalating
doses (5, 10, and 20 mg/kg/day) of fluconazole and SCH 39304 were test
ed. We also compared the activity of amphotericin B deoxycholate plus
fluconazole (1 and 10 mg/kg/day, respectively) with that of each agent
alone. Fluconazole significantly prolonged the survival of mice infec
ted with each of the 10 strains tested. Amphotericin B deoxycholate ac
hieved various responses, improving the outcomes in mice infected with
seven of the strains. Liposomal amphotericin Il was not more effectiv
e than amphotericin B deoxycholate against the two strains tested. Bot
h fluconazole and SCH 39304 reduced the kidney fungal counts in a dose
-dependent pattern, with SCH 39304 being more active than fluconazole
against one of the two strains tested. The activity of the combination
of amphotericin B deoxycholate plus fluconazole appeared to be superi
or to that of either agent alone, especially in reducing the kidney fu
ngal burden. Fluconazole is more active than amphotericin B deoxychola
te against experimental murine trichosporonosis.