Detection of multiple drug-resistant Trypanosoma congolense populations in village cattle of south-east Mali

Parasites and Vectors - Tập 5 - Trang 1-9 - 2012
Erick O Mungube1,2, Hervé S Vitouley3, Emmanuel Allegye-Cudjoe4, Oumar Diall5, Zakaria Boucoum6, Boucader Diarra7, Yousouf Sanogo6, Thomas Randolph8, Burkhard Bauer1, Karl-Hans Zessin9, Peter-Henning Clausen1
1Institute for Parasitology and Tropical Veterinary Medicine, Freie Universität Berlin, Berlin, Germany
2Kenya Agricultural Research Institute, Katumani Research Centre, Machakos, Kenya
3Centre International de Recherche-Développement sur l’Elevage en Zone subhumide (CIRDES), Burkina Faso
4Central Veterinary Laboratory, Pong-Tamale, Tamale, Ghana
5FAO Regional Office, Accra, Ghana
6Laboratoire Central Vétérinaire (LCV), Bamako, Mali
7Pan African Tsetse and Typanosomosis Eradication Programme (PATTEC) Mali, Bamako, Mali
8International Livestock Research Institute (ILRI), Nairobi, Kenya
9International Animal Health, Freie Universität Berlin, Berlin, Germany

Tóm tắt

Tsetse fly-transmitted African animal trypanosomosis causes annual losses that run into billions of dollars. The disease is assumed to cause hunger and poverty in most sub-Saharan countries since it represents a serious impediment to sustainable livestock production. Both a cross-sectional and a longitudinal study were carried out from November to December 2007 to evaluate trypanosomosis risk and susceptibility of trypanosomes to trypanocidal drug treatment in village cattle populations in south-east Mali. Eight purposively selected villages participated in the study. In each village, eight traps deployed along drainage lines over 24hour duration were used to catch tsetse. One hundred systematically selected cattle in the study villages were examined for trypanosomes. All trypanosome-positive cattle were randomly allocated into two treatment groups: a group treated with 0.5 mg/kg bw. isometamidium chloride (ISMM) and a group treated with 3.5 mg/kg bw. diminazene aceturate (DIM). The cattle were monitored for trypanosomes at day 14 and 28 post-treatment. Of the 796 cattle examined, 125 (15.7%) were trypanosome-positive. Village trypanosome prevalences ranged between 11% and 19%. There were no significant (p > 0.05) differences in the village trypanosome prevalences. Trypanosoma congolense was the dominant trypanosome species accounting for 73% (91/125) of the infections and T. vivax the remainder. Twenty (31.7%) of the 63 cattle on 0.5 mg/kg bw. ISMM treatment were still positive14 days post-treatment. Of the 43 aparasitaemic cattle monitored to day 28, 25.6% (11) became parasitaemic, resulting in a cumulative failure rate of 49.2% (31/63). Trypanosoma congolense accounted for 77.4% (24/31) of failed ISMM treatments. The 62 cattle treated with 3.5 mg/kg bw. DIM resulted in 30.6% (19/62) failed treatments. Although 42.2% (19/45) of T. congolense positive cattle did not respond to DIM treatment, all T. vivax positive cattle responded positively to DIM treatment. The overreliance on trypanocides in the control of trypanosomosis will ultimately lead to multiple drug-resistant trypanosome populations as detected in villages in south-east Mali rendering the use of drugs doubtful. Effective alternative methods for trypanosomosis control ought to substitute chemotherapy to ensure sustainable cattle production in these villages. Since there is no single strategy for containing trypanocidal drug resistance, promotion of an integrated approach combining proven trypanosomosis control approaches in high trypanosomosis risk areas is most desirous. The best-bet strategy this study recommended for areas with multiple drug resistance included area-wide community tsetse control, control of co-infections to exploit self-cure against resistant trypanosome populations and the rational use of trypanocidal drugs which should be urgently promoted at all levels as a way of containing or reversing resistance.

Tài liệu tham khảo

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