By exclusion of other possible aetiological agents, strong circumstantial evidence is presented of Trypanosoma evansi infection being the cause of late gestation abortion and stillbirth in buffaloes.
Clinical, parasitological and serological findings of Trypanosoma evansi infections in buffaloes (Bubalis bubalis) from north-eastern Thailand are reported. The overall infection rate was found to be around 20% with a distinct peak of acute infections during the rainy season. The disease is aggravated by normally well tolerated concomitant infections such as liver fluke infestations and by other stress factors.
Two methods of trypanosome control in Boran cattle kept under very high trypanosomiasis risk were compared: the traditional intramuscular isometamidium chloride prophylaxis with a parasite detection and intravenous isometamidium chloride treatment method. The results were related to a control group under diminazene aceturate treatment. Isometamidium chloride at 0.25 mg/kg as routinely used by the ranch was of little benefit by either method, with breakthrough infections occurring as early as one week after treatment. When isometamidium chloride at 1 mg/kg was used, the curative intravenous method appeared to be superior to the intramuscular prophylaxis with regard to cost of drugs and to a 31% higher weight gain over a 30 week period. Weekly infection rates in the intravenous group decreased over time, despite an increasing trypanosomiasis challenge, with a mean interval of 6.4 weeks between treatments as compared with 4.3 weeks in a diminazene aceturate control group. It was concluded that isometamidium chloride given intravenously had not only a very good therapeutic but also a considerable prophylactic effect of not less than four weeks.
SYNOPSIS
Two groups of 5 and 6 Babesia bigemina“vaccine donor” animals of which 8 had been splenectomized were challenged 6 and 12 months respectively after they had lost their carrier state. All animals of the former, and 3 of the latter group survived; the remaining 3 animals succumbed to the challenge and died. It was concluded that premunity to B. bigemina is followed by sterile immunity which lasts for at least 6 months. Thereafter it fades gradually with time, depending on the immune response of the host, but can last for at least 12 months.
Six splenectomized animals, which had lost their infectivity after treatment of their initial B. bigemina parasitemia at the rapidly rising phase with 1 mg/kg Berenil, died on challenge. It was concluded that a minimum period of contact between host and parasite is required for the acquisition of immunity to B. bigemina.
Capillary tube agglutination titers were generally higher in the protected than in the unprotected animals. They remained fairly high for a long period after animals had lost their carrier state, which indicated the sensitivity of the CA test but rendered it unreliable for the detection of carrier animals.
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