Rapamycin inhibits pathogen transmission in mosquitoes by promoting immune activation

被引:9
|
作者
Feng, Yuebiao [1 ,2 ]
Chen, Lu [3 ]
Gao, Li [1 ,2 ]
Dong, Li [1 ,2 ]
Wen, Han [1 ,2 ]
Song, Xiumei [1 ,2 ]
Luo, Fang [1 ,2 ]
Cheng, Gong [3 ]
Wang, Jingwen [1 ,2 ]
机构
[1] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai, Peoples R China
[2] Fudan Univ, Sch Life Sci, Minist Educ, Key Lab Contemporary Anthropol, Shanghai, Peoples R China
[3] Tsinghua Univ, Beijing Adv Innovat Ctr Struct Biol, Sch Med, Tsinghua Peking Joint Ctr Life Sci, Beijing, Peoples R China
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
D O I
10.1371/journal.ppat.1009353
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Author summary Anautogenous mosquitoes must consume vertebrate blood meals to complete oogenesis. Repeated blood feeding makes the mosquitoes efficient disease-transmitting vectors. The TOR pathway activated by ingested blood is known as an important regulator for vitellogenesis in mosquitoes. Herein, we show that the protein kinase TOR is involved in the regulation of mosquitoes' susceptibility to Plasmodium infection. Inhibition of the TOR pathway by rapamycin upregulates the expression of REL2, a transcription factor controlling the expression of a variety of immune effectors. The enhanced immune responses in turn promote parasite elimination. Therefore, the TOR pathway plays a dual role in not only regulating mosquito reproduction but also in their vector potential. Repeated blood meals provide essential nutrients for mosquito egg development and routes for pathogen transmission. The target of rapamycin, the TOR pathway, is essential for vitellogenesis. However, its influence on pathogen transmission remains to be elucidated. Here, we show that rapamycin, an inhibitor of the TOR pathway, effectively suppresses Plasmodium berghei infection in Anopheles stephensi. An. stephensi injected with rapamycin or feeding on rapamycin-treated mice showed increased resistance to P. berghei infection. Exposing An. stephensi to a rapamycin-coated surface not only decreased the numbers of both oocysts and sporozoites but also impaired mosquito survival and fecundity. Transcriptome analysis revealed that the inhibitory effect of rapamycin on parasite infection was through the enhanced activation of immune responses, especially the NF-kappa B transcription factor REL2, a regulator of the immune pathway and complement system. Knockdown of REL2 in rapamycin-treated mosquitoes abrogated the induction of the complement-like proteins TEP1 and SPCLIP1 and abolished rapamycin-mediated refractoriness to Plasmodium infection. Together, these findings demonstrate a key role of the TOR pathway in regulating mosquito immune responses, thereby influencing vector competence.
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页数:18
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