Clinical and parasitological evaluations of levamisole as a treatment for bovine stephanofilariasis

Abstract

Field trials were carried out with two formulations of levamisole for treatment of chronic inflammatory lesions on the muzzle and teats of cattle, caused by Stephanofilaria okinawaensis in the enzootic area of the disease, Ishigaki Island, Okinawa Prefecture, Japan. Cattle were treated orally with levamisole hydrochloride (10% powder) at a dose of 7.5 g/100 kg of body weight once (64 cattle) or twice with an interval of 3 or 4 weeks (five cattle each). Lesions on the muzzle and tests disappeared or were reduced within 4 weeks of the first medication. In some cattle a sign of recurrence was observed 8 weeks after medication. Parasitological and histological examinations were carried out 1 week carried out 1 week (10 cattle), 4 weeks (12 cattle), and 8 weeks (13 cattle) after single oral administration of levamisole hydrochloride. No Stephanofilaria worms were detected at 1 week after medication. A small number of worms were detected at 4 weeks and more were observed 8 weeks after medication. A levamisole phosphate solution (18.2%) was injected subcutaneously once into one teat of each of three cattle, or twice into the neck with a 4-week interval between treatments (five cattle). The dose was 2 ml/teat (364 mg of active ingredient) or 2 ml/45 kg of body weight for the side of the neck. There was marked improvement as with oral medication with levamisole hydrochloride powder.