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Published on: May 18, 2016
Trypanosoma brucei: infectivity and immunogenicity of cultured parasites
Abstract:
Trypanosoma brucei brucei, derived from the salivary glands of infected tsetse flies (Glossina morsitans morsitans) and maintained in culture for over 4 years, were infective to both albino rats and tsetse flies. Virulence was markedly enhanced during the first passage in albino rats or tsetse flies. Irradiated cultured trypanosomes induced immunity to homologous challenge but not to tsetse fly or blood-induced challenge with the same stock.
Insights
Cultured Trypanosoma brucei brucei remain infective and show enhanced virulence after passage in rats or tsetse flies. Irradiated parasites induced homologous immunity but not cross-immunity to other challenge types.
Area of Science:
- Parasitology
- Immunology
- Tropical medicine
Background:
- Trypanosoma brucei brucei is a protozoan parasite transmitted by tsetse flies.
- Long-term in vitro culture of trypanosomes can alter their characteristics.
- Understanding parasite infectivity and virulence is crucial for disease control.
Purpose of the Study:
- To assess the infectivity and virulence of cultured Trypanosoma brucei brucei.
- To investigate the immunogenicity of irradiated cultured trypanosomes.
Main Methods:
- Trypanosomes were cultured for over 4 years.
- Infectivity was tested in albino rats and tsetse flies.
- Virulence was assessed after initial passages.
- Immunity was evaluated using irradiated trypanosomes and homologous/heterologous challenge.
Main Results:
- Cultured trypanosomes remained infective to rats and tsetse flies.
- Virulence significantly increased after the first passage in vivo.
- Irradiated cultured trypanosomes conferred immunity against homologous challenge.
- No cross-immunity was observed against tsetse fly or blood-induced challenge.
Conclusions:
- Long-term culture of Trypanosoma brucei brucei maintains infectivity and can lead to enhanced virulence upon host passage.
- Irradiated cultured trypanosomes show potential for inducing specific immunity, but cross-protection is limited.
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