Dokumentenserver der Freien Universität Berlin


Detection of multiple drug-resistant Trypanosoma congolense populations in village cattle of south-east Mali
Mungube, Erick O ;  Vitouley, Hervé S ;  Allegye-Cudjoe, Emmanuel ;  Diall, Oumar ;  Boucoum, Zakaria ;  Diarra, Boucader ;  Sanogo, Yousouf ;  Randolph, Thomas ;  Bauer, Burkhard ;  Zessin, Karl-Hans ;  Clausen, Peter Henning

Main titleDetection of multiple drug-resistant Trypanosoma congolense populations in village cattle of south-east Mali
AuthorMungube, Erick O
AuthorVitouley, Hervé S
AuthorAllegye-Cudjoe, Emmanuel
AuthorDiall, Oumar
AuthorBoucoum, Zakaria
AuthorDiarra, Boucader
AuthorSanogo, Yousouf
AuthorRandolph, Thomas
AuthorBauer, Burkhard
AuthorZessin, Karl-Hans
AuthorClausen, Peter Henning
No. of Pages9 S.
KeywordsCattle; Trypanosomosis risk; Trypanocide resistance; Mali
Classification (DDC)570 Life sciences
Also published inParasites and Vectors. 2012 Aug 1;5:155.
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.
If your browser can't open the file, please download the file first and then open it
FU DepartmentDepartment of Veterinary Medicine
Other affiliation(s)Institute for Parasitology and Tropical Veterinary Medicine
Year of publication2012
Type of documentScience article
Terms of use/Rights Creative Commons License
Dieses Werk ist unter einer Creative Commons-Lizenz lizenziert.
Authors commentsGefördert durch die Deutsche Forschungsgemeinschaft und den Open-Access-Publikationsfonds der Freien Universität Berlin
Created at2012-10-30 : 09:05:54
Last changed2014-01-10 : 10:29:01
Static URL