Mosquito Saliva in Dengue Virus Pathogenesis. Dengue virus is a single-stranded RNA Flavivirus that causes dengue fever (DF), the most prevalent arthropod-borne viral illness in humans. Dengue viruses cause an estimated 5 million new cases of DF and 250,000 cases of dengue hemorrhagic fever (DHF) per year in tropical and subtropical areas of the world, with >100 countries with endemic transmission. Currently, no specific treatment or licensed vaccine is available for either DF or DHF. Given its global burden, increased travel and military activity in dengue-endemic areas, there is an urgent need for animal models of disease, to understand the basics of dengue pathogenesis, especially the mechanisms that lead to the more severe DHF, and whether vaccination might actually enhance disease. This is the first revision of a 5-year grant proposal to study the effect of mosquito salia on dengue virus pathogenesis. We have recently established a mouse model of dengue fever, using humanized mice (transplanted with human immune system stem cells), and we infect these mice by mosquito bite. Our preliminary data point to a major enhancement of dengue virus replication and pathogenesis in these mice, due to mosquito saliva components;the mice develop the typical "saddleback", prolonged viremia and rash that occurs in humans, before going on to develop severe disease, or DHF. These mice also develop human antibodies to dengue after mosquito bite, in contrast with no antibodies after virus injection by syringe, providing evidence that these mice can mount an adaptive immune response. These results have led us to propose studies to define the specific mechanisms of infection and pathogenesis in this unique laboratory system that mimics the natural cycle of dengue transmission.
The specific aims are: 1). Define dengue virus pathogenicity in mosquito-bitten, humanized mice. Definition of determinants of dengue pathogenesis in humanized mice, including pinpointing specific genome regions involved in viral replication and tropism, measurement of human antibodies and cellular immunity after mosquito infection, and the possibility of inducing typical DHF, with hemorrhagic signs of disease, after serial infection;and 2). Measure the effect of specific saliva components on immune response in humanized mice. Evaluation of the individual and combined effects of mosquito saliva components on rates of infection and dengue pathogenesis in humanized mice, including using injection of recombinant saliva proteins (9 total) and overexpression of some (4 max.) of these saliva proteins, in engineered mosquitoes. Dengue is a category A Priority Pathogen in the NIAID Biodefense Research Program;the results of this project would benefit many other arbovirus and parasite studies, especially those that concern the role of arthropod saliva in disease progression.

Public Health Relevance

This is a 5-year grant proposal to study the immune reaction of mice transplanted with human cord blood stem cells to infection by dengue virus, via mosquito bite, and to measure the effect of mosquito saliva proteins on dengue virus pathogenesis. There is evidence that some vector-borne microorganisms that infect humans may have enhanced virulence due to our immune reaction to saliva injected during mosquito bite. Our humanized mouse model of dengue infection is a unique, innovative and realistic way to study pathogenesis of dengue virus, one of the most important mosquito-transmitted viruses of humans. We have preliminary evidence that mosquito saliva enhances dengue virus replication in these mice, and that it may be a factor in producing severe dengue disease. The results of this project could lead to understanding dengue virus pathogenesis and transmission dynamics, and to develop effective drugs and vaccines to combat dengue fever and dengue hemorrhagic fever.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI099483-01A1
Application #
8439456
Study Section
Vector Biology Study Section (VB)
Program Officer
Cassetti, Cristina
Project Start
2012-12-12
Project End
2017-11-30
Budget Start
2012-12-12
Budget End
2013-11-30
Support Year
1
Fiscal Year
2013
Total Cost
$451,173
Indirect Cost
$158,811
Name
Baylor College of Medicine
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Andrus, Jon; Bottazzi, Maria Elena; Chow, Jennifer et al. (2013) Ears of the Armadillo: Global Health Research and Neglected Diseases in Texas. PLoS Negl Trop Dis 7:e2021