This proposal is for a new R21, and we are responding to the NIAID's Interest to Highlight High-Priority Zika virus (ZIKV) Research Areas (NOT-AI-16-026). ZIKV is a rapidly emerging flavivirus that is spread primarily by the mosquito vector, Aedes aegypti. The current ZIKV outbreak in South America has been associated with a 20-fold increase in the rate of babies born with microcephaly and has also been linked with the development of Guillain-Barre syndrome. The regions involved in the current outbreak are known to be endemic for another flavivirus, dengue virus (DENV). This indicates that a large percentage of the population may have preexisting DENV immunity. It has been shown that preexisting immunity to DENV can enhance infection with other closely related flaviviruses. ZIKV is genetically very close to DENV. The purpose of this study is to identify potential enhancement of ZIKV infection by antibodies recognizing DENV. As the World Health Organization considers the current ZIKV epidemic and related microcephaly association an international public health emergency, investigations into ZIKV infection and behavior in human immune cells, with and without preexisting flaviviral immunity, are a priority area of research. Our central hypothesis is that antibodies recognizing DENV can complex with ZIKV and that this immune complex is able to infect monocytes and other Fc receptor-bearing cells, which would result in higher viremia. Specifically, Aim 1 will establish a model of antibody-dependent enhancement using ZIKV infection and sera from South American DENV patients, collected prior to the current ZIKV outbreak.
Aim 2 will characterize the role preexisting DENV immunity may play in ZIKV infection of neural cells. We will examine avidity and affinity between ZIKV and DENV antibodies; evaluate ZIKV infection in primary human immune cells and neural cells in the presence of antibodies recognizing DENV 1-4; and examine cytokine and chemokine production by ZIKV infected cells with and without anti-DENV immune sera. Together, these aims will provide a more comprehensive picture of ZIKV infection in the presence of preexisting DENV immunity.

Public Health Relevance

Zika virus (ZIKV) is a rapidly emerging flavivirus mainly spread by Aedes mosquitoes. The current outbreak in South and Central America has been associated with neurological complications, including Guillain-Barre syndrome and cases of microcephaly. The regions involved in the current ZIKV outbreak are known to be endemic for dengue virus (DENV), and preexisting immunity to DENV has been shown to enhance infections with other flaviviruses. In this project, we will characterize interactions between ZIKV and antibodies that recognize DENV. Additionally, we will examine the ability of preexisting DENV antibodies to enhance ZIKV infection in primary human immune cells. If successful, this project could have a major impact on the field and on global health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI129881-01
Application #
9280227
Study Section
Special Emphasis Panel (ZAI1)
Program Officer
Challberg, Mark D
Project Start
2017-08-07
Project End
2019-07-31
Budget Start
2017-08-07
Budget End
2018-07-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Boston University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Londono-Renteria, Berlin; Troupin, Andrea; Cardenas, Jenny C et al. (2017) A relevant in vitro human model for the study of Zika virus antibody-dependent enhancement. J Gen Virol 98:1702-1712