Institut de Recherche en Elevage pour le Développement (IRED), Ndjaména, Chad.
Université de Montpellier, Cirad, IRD, Intertryp, Montpellier, France.
Parasit Vectors. 2023 Mar 22;16(1):111. doi: 10.1186/s13071-023-05721-4.
Human African trypanosomiasis (HAT) is a neglected tropical disease caused by Trypanosoma brucei gambiense transmitted by tsetse flies in sub-Saharan West Africa. In southern Chad the most active and persistent focus is the Mandoul focus, with 98% of the reported human cases, and where African animal trypanosomosis (AAT) is also present. Recently, a control project to eliminate tsetse flies (Glossina fuscipes fuscipes) in this focus using the sterile insect technique (SIT) was initiated. However, the release of large numbers of sterile males of G. f. fuscipes might result in a potential temporary increase in transmission of trypanosomes since male tsetse flies are also able to transmit the parasite. The objective of this work was therefore to experimentally assess the vector competence of sterile males treated with isometamidium for Trypanosoma brucei brucei.
An experimental infection was set up in the laboratory, mimicking field conditions: the same tsetse species that is present in Mandoul was used. A T. b. brucei strain close to T. b. gambiense was used, and the ability of the sterile male tsetse flies fed on blood with and without a trypanocide to acquire and transmit trypanosomes was measured.
Only 2% of the experimentally infected flies developed an immature infection (midgut) while none of the flies developed a metacyclic infection of T. b. brucei in the salivary glands. We did not observe any effect of the trypanocide used (isometamidium chloride at 100 mg/l) on the development of infection in the flies.
Our results indicate that sterile males of the tested strain of G. f. fuscipes were unable to cyclically transmit T. b. brucei and might even be refractory to the infection. The data of the research indicate that the risk of cyclical transmission of T. brucei by sterile male G. f. fuscipes of the strain colonized at IAEA for almost 40 years appears to be small.
人类非洲锥虫病(HAT)是一种由布氏锥虫冈比亚亚种通过撒哈拉以南西非的采采蝇传播的被忽视的热带病。在乍得南部,最活跃和最持久的焦点是 Mandoul 焦点,报告的人类病例中有 98%,并且也存在非洲动物锥虫病(AAT)。最近,启动了一个使用不育昆虫技术(SIT)消除该焦点中的采采蝇( Glossina fuscipes fuscipes )的控制项目。然而,大量不育雄性 G. f. fuscipes 的释放可能导致锥虫传播的潜在暂时增加,因为雄性采采蝇也能够传播寄生虫。因此,这项工作的目的是实验评估用异米替丁处理的不育雄性感染布氏锥虫布鲁斯氏菌的媒介能力。
在实验室中建立了一个实验感染,模拟野外条件:使用在 Mandoul 存在的相同采采蝇物种。使用与布氏锥虫冈比亚亚种接近的布氏锥虫布鲁斯氏菌菌株,测量了吸食含和不含杀锥虫剂的血液的不育雄性采采蝇获得和传播锥虫的能力。
只有 2%的实验感染的苍蝇发育出不成熟的感染(中肠),而没有苍蝇在唾液腺中发育出布氏锥虫布鲁斯氏菌的循环感染。我们没有观察到所用杀锥虫剂(100mg/l 的异米替丁)对苍蝇感染发展的任何影响。
我们的结果表明,测试的 G. f. fuscipes 菌株的不育雄性无法周期性传播 T. b. brucei ,甚至可能对感染具有抗性。研究数据表明,在 IAEA 近 40 年殖民的菌株的 G. f. fuscipes 不育雄性周期性传播 T. brucei 的风险似乎很小。