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  4. A salivary protein of Aedes aegypti promotes dengue-2 virus replication and transmission
 
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A salivary protein of Aedes aegypti promotes dengue-2 virus replication and transmission

Journal
Insect biochemistry and molecular biology
Journal Volume
111
Journal Volume
111
Start Page
article 103181
Date Issued
2019-08
Author(s)
Sri-In, Chalida
SHIH-CHE WENG  
Chen, Wen-Yu
BETTY AN-YE WU-HSIEH  
Tu, Wu-Chun
SHIN-HONG SHIAO  
DOI
10.1016/j.ibmb.2019.103181
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85068213840&doi=10.1016%2fj.ibmb.2019.103181&partnerID=40&md5=4528e132d2e6d26b387d5d1949df7fdb
https://scholars.lib.ntu.edu.tw/handle/123456789/414236
URL
https://api.elsevier.com/content/abstract/scopus_id/85068213840
Abstract
Although dengue is the most prevalent arthropod-borne viral disease in humans, no effective medication or vaccine is presently available. Previous studies suggested that mosquito salivary proteins influence infection by the dengue virus (DENV) in the mammalian host. However, the effects of salivary proteins on DENV replication within the Aedes aegypti mosquito remain largely unknown. In this study, we investigated the effect of a specific salivary protein (named AaSG34) on DENV serotype 2 (DENV2) replication and transmission. We showed that transcripts of AaSG34 were upregulated in the salivary glands of Aedes aegypti mosquitoes after a meal of blood infected with DENV2. Transcripts of the dengue viral genome and envelop protein in the salivary glands were significantly diminished after an infectious blood meal when AaSG34 was silenced. The effect of AaSG34 on DENV2 transmission was investigated in Stat1-deficient mice. The intradermal inoculation of infectious mosquito saliva induced hemorrhaging in the Stat1-deficient mice; however, saliva from the AaSG34-silenced mosquitoes did not induce hemorrhaging, suggesting that AaSG34 enhances DENV2 transmission. This is the first report to demonstrate that the protein AaSG34 promotes DENV2 replication in mosquito salivary glands and enhances the transmission of the virus to the mammalian host.
Subjects
Aedes aegypti; Dengue virus; Mosquito salivary proteins; Stat1(−/−) mice; Transmission
Aedes aegypti; Dengue virus; Mosquito salivary proteins; Stat1?/? mice; Transmission
SDGs

[SDGs]SDG3

Other Subjects
insect protein; saliva protein; Aedes; animal; C57BL mouse; dengue; Dengue virus; female; growth, development and aging; knockout mouse; mosquito vector; pathology; physiology; RNA interference; virology; virus replication; Aedes; Animals; Dengue; Dengue Virus; Female; Insect Proteins; Mice, Inbred C57BL; Mice, Knockout; Mosquito Vectors; RNA Interference; Salivary Proteins and Peptides; Virus Replication
Type
journal article

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