Infection by chikungunya virus modulates the expression of several proteins in Aedes aegypti salivary glands
1 Unité de Génétique Moléculaire des Bunyavirus, 25 rue du Dr Roux, 75724, Paris cedex 15
2 Unité de Biochimie et de Biologie Moléculaire des Insectes, Institut Pasteur, 28 rue du Dr Roux, 75724 cedex 15, Paris, France
3 Plate-forme protéomique PF5, Institut Pasteur, 28 rue du Dr Roux, 75724 cedex 15, Paris, France
4 present address: Unité Interactions Moléculaires Flavivirus-Hôtes, Institut Pasteur, 25, rue du Dr Roux, 75724 cedex 15, Paris, France
Parasites & Vectors 2012, 5:264 doi:10.1186/1756-3305-5-264Published: 15 November 2012
Arthropod-borne viral infections cause several emerging and resurging infectious diseases. Among the diseases caused by arboviruses, chikungunya is responsible for a high level of severe human disease worldwide. The salivary glands of mosquitoes are the last barrier before pathogen transmission.
We undertook a proteomic approach to characterize the key virus/vector interactions and host protein modifications that occur in the salivary glands that could be responsible for viral transmission by using quantitative two-dimensional electrophoresis.
We defined the protein modulations in the salivary glands of Aedes aegypti that were triggered 3 and 5 days after an oral infection (3 and 5 DPI) with chikungunya virus (CHIKV). Gel profile comparisons showed that CHIKV at 3 DPI modulated the level of 13 proteins, and at 5 DPI 20 proteins. The amount of 10 putatively secreted proteins was regulated at both time points. These proteins were implicated in blood-feeding or in immunity, but many have no known function. CHIKV also modulated the quantity of proteins involved in several metabolic pathways and in cell signalling.
Our study constitutes the first analysis of the protein response of Aedes aegypti salivary glands infected with CHIKV. We found that the differentially regulated proteins in response to viral infection include structural proteins and enzymes for several metabolic pathways. Some may favour virus survival, replication and transmission, suggesting a subversion of the insect cell metabolism by arboviruses. For example, proteins involved in blood-feeding such as the short D7, an adenosine deaminase and inosine-uridine preferring nucleoside hydrolase, may favour virus transmission by exerting an increased anti-inflammatory effect. This would allow the vector to bite without the bite being detected. Other proteins, like the anti-freeze protein, may support vector protection.