Phaeohyphomycosis due to Veronaea botryosa in cultured white sturgeon (Acipenser transmontanus Richardson) from California USA during 2006 to 2015.

Infection with Veronaea botryosa can result in rare cutaneous or disseminated, granulomatous to pyogranulomatous phaeohyphomycosis in humans, although disease due to the fungus has also been reported in non-mammalian vertebrates. This report documents disease due to V. botryosa in captive, juvenile to subadult or young adult white sturgeon (Acipenser transmontanus Richardson) from California USA and complements a previous report of the disease in captive Siberian sturgeon (Acipenser baerii) from Florida USA. Pathological examinations revealed granulomatous to pyogranulomatous inflammation of multiple organs. Isolates of the fungal agent were phenotypically consistent with V. botryosa, and molecular analyses of the D1/D2 region of the fungal 28S rRNA gene and the internal transcribed spacer (ITS) region located between the fungal 18S and 28S rRNA genes confirmed the aetiologic agent as V. botryosa. The disease in captive sturgeon results in a considerable economic encumbrance to the producer due to the loss of the cumulative financial resources invested in the production of older subadult to young adult sturgeon.

Single-dose pharmacokinetics of ceftazidime and fluconazole during concurrent clinical use in cold-stunned Kemp's ridley turtles (Lepidochelys kempii).

Single-dose pharmacokinetics of intramuscularly administered ceftazidime (22 mg/kg) and subcutaneously administered fluconazole (21 mg/kg) were investigated during concurrent clinical use in naturally cold-stunned Kemp's ridley turtles (Lepidochelys kempii). Maximum mean concentration for ceftazidime was 61.31 µg/mL, and time of maximum concentration was 1.56 h postinjection. Maximum mean concentration for fluconazole was 26.16 µg/mL, and time of maximum concentration was 0.79 h postinjection. Results indicate that the ceftazidime dose and dosing interval used in this study are likely to be effective in treating susceptible strains of bacteria in Kemp's ridley turtles. However, the fluconazole dose and dosing interval are not likely to be effective against filamentous fungal pathogens that are often involved in marine turtle fungal infections.