Abstract
BackgroundTrypanosoma evansi is mechanically transmitted by biting flies and affects camels, equines, and other domestic and wild animals in which it causes a disease called surra. At least two types of Trypanosoma evansi circulate in Ethiopia: type A, which is present in Africa, Latin America and Asia, and type B, which is prevalent in Eastern Africa. Currently, no information is available about the drug sensitivity of any Ethiopian T. evansi type.Methodology/principal findingsThis study was conducted with the objective of determining the in vivo drug sensitivity of two T. evansi type A and two type B stocks that were isolated from camels from the Tigray and Afar regions of Northern Ethiopia. We investigated the efficacy of four trypanocidal drugs to cure T. evansi infected mice: melarsamine hydrochloride (Cymelarsan), diminazene diaceturate (Veriben and Sequzene), isometamidium chloride (Veridium) and homidium chloride (Bovidium). Per experimental group, 6 mice were inoculated intraperitoneally with trypanosomes, treated at first peak parasitemia by daily drug injections for 4 consecutive days and followed-up for 60 days. Cymelarsan at 2 mg/kg and Veriben at 20 mg/kg cured all mice infected with any T. evansi stock, while Sequzene at 20 mg/kg caused relapses in all T. evansi stocks. In contrast, Veridium and Bovidium at 1 mg/kg failed to cure any T. evansi infection in mice.Conclusions/significanceWe conclude that mice infected with Ethiopian T. evansi can be cured with Cymelarsan and Veriben regardless of T. evansi type. In contrast, Veridium and Bovidium are not efficacious to cure any T. evansi type. Although innate resistance to phenanthridines was previously described for T. evansi type A, this report is the first study to show that this phenomenom also occurs in T. evansi type B infections.
Highlights
African trypanosomoses (AT) are neglected parasitic diseases of humans and animals caused by various subgenera of pathogenic trypanosomes (Trypanozoon, Dutonella and Nannomonas)
At least two types of Trypanosoma evansi circulate in Ethiopia: type A, which is present in Africa, Latin America and Asia, and type B, which is prevalent in Eastern Africa
TTAT are due to Trypanosoma (T). congolense, T. vivax, and T. brucei brucei, whereas non tsetse-transmitted African trypanosomiasis (NTTAT) are due to mechanically transmitted T. evansi and T. vivax, and the sexually transmitted T. equiperdum [5,6,7,8,9,10,11,12]
Summary
African trypanosomoses (AT) are neglected parasitic diseases of humans and animals caused by various subgenera of pathogenic trypanosomes (Trypanozoon, Dutonella and Nannomonas). In Ethiopia, AAT has been described as a major impediment to livestock development and agricultural production, contributing negatively to development in general and to food self-reliance efforts of the country in particular. Both tsetsetransmitted (TTAT) and non tsetse-transmitted African trypanosomiasis (NTTAT) are endemic to the country. Surra is the number one protozoan disease of camels and is caused by T. evansi. Infected camels and equines may die within 3 months after onset of the disease. Trypanosoma evansi is mechanically transmitted by biting flies and affects camels, equines, and other domestic and wild animals in which it causes a disease called surra. No information is available about the drug sensitivity of any Ethiopian T. evansi type
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