Abstract

The presence and expression of odorant-binding proteins (OBPs) in the olfactory organs suggest that they play an important role in mosquito olfaction. However, no direct evidence has been found for their involvement in the host-seeking behavior of mosquitoes. It is important to establish a method in which a loss-of-function test can be performed to determine the possible role of these genes in olfaction. In this study, a double subgenomic Sindbis virus expression system was used to reduce the expression of two Obp genes in Aedes aegypti L (Diptera: Culicidae), AaegObp1 and AaegObp2. Quantitative real-time PCR analysis showed predominant expression of both genes in the female antennae, the primary olfactory tissue of mosquitoes.Moreover, at 11 days post virus-inoculation, the mRNA levels of AaegObp1 and AaegObp2 were significantly reduced in olfactory tissues of recombinant virus-inoculated female mosquitoes compared to that of controls by approximately 8 and 100-fold, respectively. These data suggest that the double subgenomic Sindbis virus expression system can be efficiently used to knockdown Obp gene expression in olfactory tissues of mosquitoes. We discuss the potential for a systematic analysis of the molecular players involved in mosquito olfaction using this newly developed technique. Such analysis will provide an important step to interfere with the host-seeking behavior of mosquitoes to prevent the transmission of diseases.

Details

Title
Expression analysis and knockdown of two antennal odorant-binding protein genes in Aedes aegypti
Author
Sengul, Meryem S 1 ; Tu, Zhijian 2 

 Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA; Current address: Department of Biology, Bozok University, Yozgat, 66200, Turkey 
 Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA 
Publication year
2010
Publication date
2010
Publisher
Oxford University Press
e-ISSN
15362442
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3170718750
Copyright
This is an open access paper. We use the Creative Commons Attribution 3.0 license that permits unrestricted use, provided that the paper is properly attributed. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.