West Nile virus (WNV) is a neurotropic flavivirus that is the leading cause of arboviral encephalitis in the United States. The need to study WNV pathogenesis and the host immune response to infection is imperative as there are no specific therapies or vaccines available for human use. The search for effective intervention strategies relies on a better basic science understanding of the pathogenesis of WNV. Inflammatory monocytes are critical mediators of the antiviral response against WNV and accumulate in the CNS during WNV encephalitis. In preliminary data, we show that efficient accumulation of monocytes in the CNS first requires the release of monocyte from the bone marrow, a step that is entirely dependent on chemokine receptor CCR2. In this application, we will evaluate the relative contribution of the CCR2 ligands, chemokines CCL2 and CCL7, in mediating this monocytosis during WNV infection (Aim 1), and evaluate the extent to which these ligands, given exogenously, can promote monocyte accumulation in the CNS and alter the outcome of infection (Aim 2). Since monocytes appear to play a protective role within the CNS, understanding the chemokines that regulate their release from the bone marrow, and the potential to exploit this step to modulate monocyte accumulation in the CNS, is an important goal with translational implications.

Public Health Relevance

This proposal seeks to understand how chemokines control WNV-induced monocytosis, which is required for efficient monocyte accumulation in the CNS and survival. Understanding the specific roles of the chemokines involved in this step will provide new insight into the fundamental biology of the host response to WNV and promote the development of more effective, targeted therapeutics.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31AI110071-01
Application #
8652697
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Adger-Johnson, Diane S
Project Start
2014-01-17
Project End
2017-01-16
Budget Start
2014-01-17
Budget End
2015-01-16
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10029
Bardina, Susana V; Brown, Julia A; Michlmayr, Daniela et al. (2017) Chemokine Receptor Ccr7 Restricts Fatal West Nile Virus Encephalitis. J Virol 91:
Hoffman, Kevin W; Sachs, David; Bardina, Susana V et al. (2016) Differences in Early Cytokine Production Are Associated With Development of a Greater Number of Symptoms Following West Nile Virus Infection. J Infect Dis 214:634-43
Michlmayr, Daniela; Bardina, Susana V; Rodriguez, Carlos A et al. (2016) Dual Function of Ccr5 during Langat Virus Encephalitis: Reduction in Neutrophil-Mediated Central Nervous System Inflammation and Increase in T Cell-Mediated Viral Clearance. J Immunol 196:4622-31
Bardina, Susana V; Michlmayr, Daniela; Hoffman, Kevin W et al. (2015) Differential Roles of Chemokines CCL2 and CCL7 in Monocytosis and Leukocyte Migration during West Nile Virus Infection. J Immunol 195:4306-18