Ferreira Roberta Carvalho, Kessler Rafael Luis, Lorenzo Marcelo Gustavo, Paim Rafaela Magalhães Macedo, Ferreira Luciana De Lima, Probst Christian Macagnan, Alves-Silva Juliana, Guarneri Alessandra Aparecida
Vector Behavior and Pathogen Interaction Group,Centro de Pesquisas René Rachou,Fiocruz,Av. Augusto de Lima,1715,Belo Horizonte,Minas Gerais,Brazil.
Laboratory of Functional Genomic,Instituto Carlos Chagas,Fiocruz,Rua Prof. Algacyr Munhoz Mader,3775, 81350-010 Curitiba,Paraná,Brazil.
Parasitology. 2016 Apr;143(4):434-43. doi: 10.1017/S0031182015001857. Epub 2016 Jan 28.
Trypanosoma cruzi, the etiological agent of Chagas disease, is ingested by triatomines during their bloodmeal on an infected mammal. Aiming to investigate the development and differentiation of T. cruzi inside the intestinal tract of Rhodnius prolixus at the beginning of infection we fed insects with cultured epimastigotes and blood trypomastigotes from infected mice to determine the amount of recovered parasites after ingestion. Approximately 20% of the ingested parasites was found in the insect anterior midgut (AM) 3 h after feeding. Interestingly, a significant reduction (80%) in the numbers of trypomastigotes was observed after 24 h of infection suggesting that parasites were killed in the AM. Moreover, few parasites were found in that intestinal portion after 96 h of infection. The evaluation of the numbers of parasites in the posterior midgut (PM) at the same periods showed a reduced parasite load, indicating that parasites were not moving from the AM. Additionally, incubation of blood trypomastigotes with extracts from R. prolixus AMs revealed that components of this tissue could induce significant death of T. cruzi. Finally, we observed that differentiation from trypomastigotes to epimastigotes is not completed in the AM; instead we suggest that trypomastigotes change to intermediary forms before their migration to the PM, where differentiation to epimastigotes takes place. The present work clarifies controversial points concerning T. cruzi development in insect vector, showing that parasite suffers a drastic decrease in population size before epimastigonesis accomplishment in PM.
克氏锥虫是恰加斯病的病原体,在吸血时被锥蝽摄取,此时锥蝽吸食受感染哺乳动物的血液。为了研究感染初期克氏锥虫在红带锥蝽肠道内的发育和分化情况,我们用培养的上鞭毛体和来自受感染小鼠的血液型锥鞭毛体喂养昆虫,以确定摄取后回收的寄生虫数量。喂食后3小时,在昆虫前中肠(AM)中发现约20%的摄取寄生虫。有趣的是,感染24小时后观察到锥鞭毛体数量显著减少(80%),这表明寄生虫在前中肠中被杀死。此外,感染96小时后,在该肠道部位发现的寄生虫很少。同期对后中肠(PM)中寄生虫数量的评估显示寄生虫负荷降低,表明寄生虫没有从前中肠迁移。此外,将血液型锥鞭毛体与红带锥蝽前中肠提取物一起孵育发现,该组织的成分可诱导克氏锥虫大量死亡。最后,我们观察到锥鞭毛体向前鞭毛体的分化在前中肠中并未完成;相反,我们认为锥鞭毛体在迁移到后中肠之前会转变为中间形式,而后中肠是向前鞭毛体分化发生的地方。本研究澄清了关于克氏锥虫在昆虫媒介中发育的争议点,表明在寄生虫在后中肠完成前鞭毛体形成之前,其种群数量会急剧减少。