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DOI 10.1186/s13071-017-2040-9

Медицинская библиотека · Parasites & vectors · 2017

Microbiota activates IMD pathway and limits Sindbis infection in Aedes aegypti.

Barletta Ana Beatriz Ferreira, Nascimento-Silva Maria Clara L, Talyuli Octávio A C, Oliveira José Henrique M, Pereira Luiza Oliveira Ramos, Oliveira Pedro L, Sorgine Marcos Henrique F

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Aedes aegypti is the main vector of important arboviruses such as dengue, Zika and chikungunya. During infections mosquitoes can activate the immune pathways Toll, IMD and JAK/STAT to limit pathogen replication.

RESULTS

Here, we evaluate the immune response profile of Ae. aegypti against Sindbis virus (SINV). We analyzed gene expression of components of Toll, IMD and JAK/STAT pathways and showed that a blood meal and virus infection upregulated aaREL2 in a microbiota-dependent fashion, since this induction was prevented by antibiotic. The presence of the microbiota activates IMD and impaired the replication of SINV in the midgut. Constitutive activation of the IMD pathway, by Caspar depletion, leads to a decrease in microbiota levels and an increase in SINV loads.

CONCLUSION

Together, these results suggest that a blood meal is able to activate innate immune pathways, through a nutrient induced growth of microbiota, leading to upregulation of aaREL2 and IMD activation. Microbiota levels seemed to have a reciprocal interaction, where the proliferation of the microbiota activates IMD pathway that in turn controls bacterial levels, allowing SINV replication in Ae. aegypti mosquitoes. The activation of the IMD pathway seems to have an indirect effect in SINV levels that is induced by the microbiota.

Для цитирования: Barletta Ana Beatriz Ferreira, Nascimento-Silva Maria Clara L, Talyuli Octávio A C, Oliveira José Henrique M, Pereira Luiza Oliveira Ramos, Oliveira Pedro L, Sorgine Marcos Henrique F. Microbiota activates IMD pathway and limits Sindbis infection in Aedes aegypti.. Parasites & vectors. 2017. DOI: 10.1186/s13071-017-2040-9.

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