4.5 Article

In vivo experimental drug resistance study in Trypanosoma vivax isolates from tsetse infested and non-tsetse infested areas of Northwest Ethiopia

Journal

ACTA TROPICA
Volume 146, Issue -, Pages 95-100

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.actatropica.2015.03.014

Keywords

Trypanosoma vivax; Drug resistance; Cattle; Northwest Ethiopia

Funding

  1. Ethio-Belgium VLIR Project [ZEIN2006PR324]
  2. GALVmed
  3. World Bank
  4. Addis Ababa University
  5. BBSRC [BB/K006495/1] Funding Source: UKRI
  6. Biotechnology and Biological Sciences Research Council [BB/K006495/1] Funding Source: researchfish

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Ethiopia, particularly in the Northwest region, is affected by both tsetse fly and non-tsetse fly transmitted trypanosomosis with a significant impact on livestock productivity. The control of trypanosomosis in Ethiopia relies on either curative or prophylactic treatment of animals with diminazene aceturate (DA) or isometamidium chloride (ISM), respectively. However, since these two trypanocides have been on the market for more than 40 years, this may have resulted in drug-resistance. Therefore, in vivo drug resistance tests on two Ethiopian isolates of Trypanosoma vivax were completed, one from an area where tsetse flies are present and one from an area where tsetse flies are not present. Twenty four cattle (Bos indicus) aged between 6 and 12 months, purchased from a trypanosome-free area (Debre Brehan: North-central Ethiopia) and confirmed to be trypanosome-negative, were randomly assigned into four groups of six animals, which were infected with T. vivax isolated from a tsetse-infested or non-tsetse infested area, and in each case treated with curative doses of DA or ISM. Each animal were inoculated intravenously 3 x 10(6) trypanosomes from donor animals. Parasitaemia became patent earlier in infections with non-tsetse T. vivax (similar to 7 days post-infection) than tsetse (similar to 14 days post-infection). Both groups were treated at the highest peak parasitaemia with DA or ISM and nine cattle, four with non-tsetse T. vivax (two ISM- and two DA-treated) and five with tsetse T. vivax (three ISM- and two DA-treated) showed relapses of parasitaemia. Moreover, treatment did not improve diagnostic host markers of trypanosome infections in these animals. In conclusion, in vivo drug tests indicated the presence of resistant parasites (>20% of treated animals in each group relapsed) against recommended doses of both available trypanocidal drugs. (C) 2015 Elsevier B.V. All rights reserved.

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