In recent years, dengue fever has emerged as one of the most serious vector-borne viral diseases. The molecular biology of dengue virus propagation in the mosquito vector is largely unknown, but the genome sequence, reverse genetic and functional genomics tools as well as high throughput screening methodologies that are now available provide a means of dissecting the mosquito's interactions with the virus in greater detail. In this proposal, we will apply a highly innovative interdisciplinary approach to discover and develop small molecules (compounds) that can render the Aedes aegypti vector mosquito resistant to the virus and thereby incapable of transmitting disease. A previous collaboration between the groups of Drs. Garcia-Blanco and Dimopoulos identified over 300 potential dengue virus host and restriction factors through a high throughput RNAi screen in a Drosophila cell line. We will now expand on these findings and identify homologues of these factors in the Aedes mosquito in specific Aim 1.
In Aim 2 we will assess the anti-dengue potential of selected factors in the Aedes cell line and mosquito to select those that are most suitable for small molecule discovery. We will then use a powerful established yeast-based platform to identify compounds that can repress dengue virus host factors, and an established insect cell line -based system to identify compounds that can activate expression of dengue virus restriction factors in Aim 3.
In Aim 4 we will test a selected set of these compounds for anti-dengue activity in Aedes cell lines and adult female mosquitoes through different routes of exposure. We will finally investigate the potential influence of selected compounds on mosquito fitness parameters and assess their anti-dengue activity in field -derived mosquito strains in Aim 5. The completion of this highly innovative work will lead to a transition into translational studis on the delivery of potent anti-dengue compounds to natural dengue vector populations, as a prelude towards the development of a novel dengue control strategy.

Public Health Relevance

Despite the dramatic surge in dengue prevalence, surprisingly little is known about the molecular biology and genetic basis of the virus interactions with the mosquito vectors that enable transmission. This research proposal aims at the discovery and development of small molecules (compounds) that can target dengue virus host and restriction factors of the Aedes aegypti mosquito, and thereby renders it incapable of transmitting the disease. The knowledge generated from this study will furthermore contribute to the development of control methods for dengue and other viruses such as yellow fever and West Nile viruses.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
3R01AI101431-03S1
Application #
8839070
Study Section
Program Officer
Costero-Saint Denis, Adriana
Project Start
2014-05-01
Project End
2017-04-30
Budget Start
2014-09-01
Budget End
2015-04-30
Support Year
3
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Microbiology/Immun/Virology
Type
Schools of Public Health
DUNS #
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Short, Sarah M; van Tol, Sarah; Smith, Brendan et al. (2018) The mosquito adulticidal Chromobacterium sp. Panama causes transgenerational impacts on fitness parameters and elicits xenobiotic gene responses. Parasit Vectors 11:229
Barrows, Nicholas J; Campos, Rafael K; Liao, Kuo-Chieh et al. (2018) Biochemistry and Molecular Biology of Flaviviruses. Chem Rev 118:4448-4482
Reid, David W; Campos, Rafael K; Child, Jessica R et al. (2018) Dengue Virus Selectively Annexes Endoplasmic Reticulum-Associated Translation Machinery as a Strategy for Co-opting Host Cell Protein Synthesis. J Virol 92:
Short, Sarah M; van Tol, Sarah; MacLeod, Hannah J et al. (2018) Hydrogen cyanide produced by the soil bacterium Chromobacterium sp. Panama contributes to mortality in Anopheles gambiae mosquito larvae. Sci Rep 8:8358
Soto-Acosta, Ruben; Xie, Xuping; Shan, Chao et al. (2018) Fragile X mental retardation protein is a Zika virus restriction factor that is antagonized by subgenomic flaviviral RNA. Elife 7:
Angleró-Rodríguez, Yesseinia I; Talyuli, Octavio Ac; Blumberg, Benjamin J et al. (2017) An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity. Elife 6:
Angleró-Rodríguez, Yesseinia I; MacLeod, Hannah J; Kang, Seokyoung et al. (2017) Aedes aegypti Molecular Responses to Zika Virus: Modulation of Infection by the Toll and Jak/Stat Immune Pathways and Virus Host Factors. Front Microbiol 8:2050
Campos, Rafael K; Wong, Benjamin; Xie, Xuping et al. (2017) RPLP1 and RPLP2 Are Essential Flavivirus Host Factors That Promote Early Viral Protein Accumulation. J Virol 91:
Ward, Alex Michael; Calvert, Meredith E K; Read, Leah R et al. (2016) The Golgi associated ERI3 is a Flavivirus host factor. Sci Rep 6:34379
Saraiva, Raúl G; Kang, Seokyoung; Simões, Maria L et al. (2016) Mosquito gut antiparasitic and antiviral immunity. Dev Comp Immunol 64:53-64

Showing the most recent 10 out of 23 publications