Interferon ɛ restricts Zika virus infection in the female reproductive tract

• Published in: PNAS nexus Vol. 2; no. 11; p. pgad350
• Main Authors: Xu, Chuan, Wang, Annie, Ebraham, Laith, Sullivan, Liam, Tasker, Carley, Pizutelli, Vanessa, Couret, Jennifer, Hernandez, Cyril, Kolli, Priyanka, Deb, Pratik Q, Fritzky, Luke, Subbian, Selvakumar, Gao, Nan, Lo, Yungtai, Salvatore, Mirella, Rivera, Amariliz, Lemenze, Alexander, Fitzgerald-Bocarsly, Patricia, Tyagi, Sanjay, Lu, Wuyuan, Beaulieu, Aimee, Chang, Theresa L
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.11.2023
• Subjects: Biological, Health, and Medical Sciences
• ISSN: 2752-6542; 2752-6542
• DOI: 10.1093/pnasnexus/pgad350

Interferon ɛ (IFNɛ) is a unique type I IFN that has been implicated in host defense against sexually transmitted infections. Zika virus (ZIKV), an emerging pathogen, can infect the female reproductive tract (FRT) and cause devastating diseases, particularly in pregnant women. How IFNɛ contributes to protection against ZIKV infection in vivo is unknown. In this study, we show that IFNɛ plays a critical role in host protection against vaginal ZIKV infection in mice. We found that IFNɛ was expressed not only by epithelial cells in the FRT but also by immune and stromal cells at baseline or after exposure to viruses or specific Toll-like receptor (TLR) agonists. IFNɛ-deficient mice exhibited abnormalities in the epithelial border and underlying tissue in the cervicovaginal tract, and these defects were associated with increased susceptibility to vaginal but not subcutaneous ZIKV infection. IFNɛ deficiency resulted in an increase in magnitude, duration, and depth of ZIKV infection in the FRT. Critically, intravaginal administration of recombinant IFNɛ protected mice and highly susceptible mice against vaginal ZIKV infection, indicating that IFNɛ was sufficient to provide protection even in the absence of signals from other type I IFNs and in an IFNAR1-independent manner. Our findings reveal a potentially critical role for IFNɛ in mediating protection against the transmission of ZIKV in the context of sexual contact.