AI Article Synopsis

  • Trypanosomosis is a disease caused by parasites that affects people and animals in Africa, mainly spread by tsetse flies, but some types can be found outside of Africa too.
  • In a study, researchers tested a drug called ascofuranone (AF) on six male cattle calves infected with two different types of parasites, T. vivax and T. congolense.
  • The results showed that AF worked well against T. vivax but didn’t clear T. congolense, suggesting a need for new treatments for this disease.*

Article Abstract

Trypanosomosis is a disease complex which affects both humans and animals in sub-Saharan Africa, transmitted by the tsetse fly and distributed within the tsetse belt of Africa. But some trypanosome species, for example, Trypanosoma brucei evansi, T. vivax, T. theileri and T. b. equiperdum are endemic outside the tsetse belt of Africa transmitted by biting flies, for example, Tabanus and Stomoxys, or venereal transmission, respectively. Trypanocidal drugs remain the principal method of animal trypanosomosis control in most African countries. However, there is a growing concern that their effectiveness may be severely curtailed by widespread drug resistance. A minimum number of six male cattle calves were recruited for the study. They were randomly grouped into two (T. vivax and T. congolense groups) of three calves each. One calf per group served as a control while two calves were treatment group. They were inoculated with 105 cells/mL parasites in phosphate buffered solution (PBS) in 2 mL. When parasitaemia reached 1 × 107.8 cells/mL trypanosomes per mL in calves, treatment was instituted with 20 mL (25 mg/kg in 100 kg calf) ascofuranone (AF) for treatment calves, while the control ones were administered a placebo (20 mL PBS) intramuscularly. This study revealed that T. vivax was successfully cleared by AF but the T. congolense group was not cleared effectively.Contribution: There is an urgent need to develop new drugs which this study sought to address. It is suggested that the AF compound can be developed further to be a sanative drug for T. vivax in non-tsetse infested areas like South Americas.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11005941PMC
http://dx.doi.org/10.4102/ojvr.v91i1.2115DOI Listing

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