While Zika virus (ZIKV) is well known for its transmission through the Aedes mosquitoes, recent evidence highlights sexual contact with an infected partner as another important route of transmission. There have been multiple confirmed and suspected cases of sexual transmission in humans, all of which involve transmission from infected men to their female partners through vaginal intercourse (1-7). ZIKV has been detected in semen of infected men (4, 6, 8). Collectively, these studies indicate that sexual transmission from infected male to uninfected female occurs in humans. An important clinical concern is whether ZIKV can be transmitted sexually in pregnant women, and what the consequence of such infections may be on the outcome of pregnancy. The CDC urges men with ZIKV disease to wait at least 6 months after symptom onset to attempt conception (5). However, the consequences of sexual transmission of ZIKV during pregnancy are unknown. Three recent studies using the mouse model of ZIKV have revealed that type I interferon (IFN) receptor (IFNAR) is critical in host resistance against ZIKV (9-11), and that persistent replication of the virus within the testes of infected IFNAR-deficient male mice (9). Subcutaneous ZIKV infection of Ifnar-/- dams mated with WT sires results in intrauterine growth restriction (IUGR) (12). However, virtually nothing is known about either the pathogenesis of sexual Zika virus transmission, or the defense mechanisms that prevent sexual transmission of ZIKV in pregnant women or the fetus. To this end, we developed the first vaginal ZIKV transmission model in mice. Remarkably, vaginal infection of pregnant mice results in IUGR and infection within the cerebellum and cortex of the fetal brain. Moreover, by using mice that lack various innate sensor and signaling pathways, we unveiled the role of each pathway in controlling ZIKV replication and spread from the vaginal mucosa to the fetus. Using this unique approach, we will find urgently needed answers to the following key questions - 1) which innate signaling pathways block ZIKV in the virgin vs. pregnant female mice; and 2) what innate antiviral pathways are important to restrict ZIKV infection within the fetus?

Public Health Relevance

While Zika virus (ZIKV) is well known for its transmission through the Aedes mosquitoes, recent evidence highlights another important route of transmission through sexual contact with an infected partner. This project proposes to examine the mechanism by which the innate antiviral pathways control ZIKV transmission and replication in the female reproductive tract, and to understand the maternal vs. fetal intrinsic defense mechanisms that control ZIKV during pregnancy - the understanding obtained through the project will help to establish critical foundation with which to design immunological interventions and preventative measures against ZIKV induced fetal abnormalities including microcephaly in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AI131284-02
Application #
9407774
Study Section
Special Emphasis Panel (ZAI1)
Program Officer
Challberg, Mark D
Project Start
2017-01-06
Project End
2018-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Yale University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
Yockey, Laura J; Iwasaki, Akiko (2018) Interferons and Proinflammatory Cytokines in Pregnancy and Fetal Development. Immunity 49:397-412
Gopinath, Smita; Kim, Myoungjoo V; Rakib, Tasfia et al. (2018) Topical application of aminoglycoside antibiotics enhances host resistance to viral infections in a microbiota-independent manner. Nat Microbiol 3:611-621
Yockey, Laura J; Jurado, Kellie A; Arora, Nitin et al. (2018) Type I interferons instigate fetal demise after Zika virus infection. Sci Immunol 3:
Uraki, Ryuta; Jurado, Kellie Ann; Hwang, Jesse et al. (2017) Fetal Growth Restriction Caused by Sexual Transmission of Zika Virus in Mice. J Infect Dis 215:1720-1724
Iwasaki, Akiko (2017) Immune Regulation of Antibody Access to Neuronal Tissues. Trends Mol Med 23:227-245
Hastings, Andrew K; Yockey, Laura J; Jagger, Brett W et al. (2017) TAM Receptors Are Not Required for Zika Virus Infection in Mice. Cell Rep 19:558-568
Uraki, Ryuta; Hwang, Jesse; Jurado, Kellie Ann et al. (2017) Zika virus causes testicular atrophy. Sci Adv 3:e1602899