Dengue viruses binding proteins from Aedes aegypti and Aedes polynesiensis salivary glands

被引:33
作者
Cao-Lormeau, Van-Mai [1 ]
机构
[1] Inst Louis Malarde, Lab Rech Virol Med, POB 30, Papeete 98713, Tahiti, France
关键词
SENSITIVE METHOD; MOSQUITO; POTENTIATION; TRANSMISSION; ENCEPHALITIS; INFECTION; RECEPTORS; MOLECULES; TARGETS; APYRASE;
D O I
10.1186/1743-422X-6-35
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dengue virus (DENV), the etiological agent of dengue fever, is transmitted to the human host during blood uptake by an infective mosquito. Infection of vector salivary glands and further injection of infectious saliva into the human host are key events of the DENV transmission cycle. However, the molecular mechanisms of DENV entry into the mosquito salivary glands have not been clearly identified. Otherwise, although it was demonstrated for other vector-transmitted pathogens that insect salivary components may interact with host immune agents and impact the establishment of infection, the role of mosquito saliva on DENV infection in human has been only poorly documented. To identify salivary gland molecules which might interact with DENV at these key steps of transmission cycle, we investigated the presence of proteins able to bind DENV in salivary gland extracts (SGE) from two mosquito species. Using virus overlay protein binding assay, we detected several proteins able to bind DENV in SGE from Aedes aegypti (L.) and Aedes polynesiensis (Marks). The present findings pave the way for the identification of proteins mediating DENV attachment or entry into mosquito salivary glands, and of saliva-secreted proteins those might be bound to the virus at the earliest step of human infection. The present findings might contribute to the identification of new targets for anti-dengue strategies.
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