Mosquitoes are important vectors for a number of infectious diseases caused by arboviruses including West Nile virus, dengue virus, yellow fever virus, LaCrosse virus, and Venezuelan, eastern and western equine encephalitis viruses. Mosquitoes acquire arboviruses from vertebrate hosts during blood feeding, and after entry into the mosquito vector, the virus must first infect, replicate in, and escape from the epithelial cells of the midgut before it can be disseminated to other organs. Dissemination to the salivary glands is necessary for transmission to another host. Thus, the midgut epithelium constitutes a potential barrier to infection and subsequent transmission, and is therefore a target for interrupting the transmission cycle. It is well documented that only certain vector-virus combinations result in efficient transmission of disease, and data exist indicating that arboviruses must overcome the immune defenses of the insect vector in order to be transmitted successfully. However, little is known about anti-viral defenses in insects. For several years the Clem laboratory has been studying the role of apoptosis in defense against baculovirus infection in lepidopteran insects. This application seeks to explore the question of whether apoptosis can serve as a defense against arbovirus invasion in the mosquito midgut. In order to accomplish this goal a strong and diverse team has been assembled that includes expertise in apoptosis, mosquito vector biology, and arboviruses.
In Aim 1, midguts and other tissues from arbovirus-infected mosquitoes will be examined for apoptosis, including a collection of Aedes aegypti strains that vary in their ability to vector dengue virus.
In Aim 2, the hypothesis that apoptosis can limit virus replication and spread will be directly tested by manipulating apoptotic pathways in the mosquito and examining the effects on the ability of arboviruses to successfully cause disseminated infections. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI067642-01
Application #
7020173
Study Section
Special Emphasis Panel (ZRG1-VB (01))
Program Officer
Repik, Patricia M
Project Start
2006-05-01
Project End
2008-04-30
Budget Start
2006-05-01
Budget End
2007-04-30
Support Year
1
Fiscal Year
2006
Total Cost
$182,500
Indirect Cost
Name
Kansas State University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
929773554
City
Manhattan
State
KS
Country
United States
Zip Code
66506
Wang, Hua; Clem, Rollie J (2011) The role of IAP antagonist proteins in the core apoptosis pathway of the mosquito disease vector Aedes aegypti. Apoptosis 16:235-48
Liu, Qingzhen; Clem, Rollie J (2011) Defining the core apoptosis pathway in the mosquito disease vector Aedes aegypti: the roles of iap1, ark, dronc, and effector caspases. Apoptosis 16:105-13
Bartholomay, Lyric C; Waterhouse, Robert M; Mayhew, George F et al. (2010) Pathogenomics of Culex quinquefasciatus and meta-analysis of infection responses to diverse pathogens. Science 330:88-90
Bryant, Bart; Ungerer, Mark C; Liu, Qingzhen et al. (2010) A caspase-like decoy molecule enhances the activity of a paralogous caspase in the yellow fever mosquito, Aedes aegypti. Insect Biochem Mol Biol 40:516-23
Bryant, B; Zhang, Y; Zhang, C et al. (2009) A lepidopteran orthologue of reaper reveals functional conservation and evolution of IAP antagonists. Insect Mol Biol 18:341-51
Wang, Hua; Blair, Carol D; Olson, Ken E et al. (2008) Effects of inducing or inhibiting apoptosis on Sindbis virus replication in mosquito cells. J Gen Virol 89:2651-61
Bryant, Bart; Blair, Carol D; Olson, Ken E et al. (2008) Annotation and expression profiling of apoptosis-related genes in the yellow fever mosquito, Aedes aegypti. Insect Biochem Mol Biol 38:331-45