Publication

Zika Virus Infects Human Placental Macrophages

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Last modified
  • 03/03/2025
Type of Material
Authors
    Kendra M. Quicke, Emory UniversityJames R. Bowen, Emory UniversityErica Johnson, Emory UniversityCirce E. McDonald, Emory UniversityHuailiang Ma, Yerkes National Primate Research CenterJustin T. O'Neal, Emory UniversityAugustine Rajakumar, Emory UniversityJens Wrammert, Emory UniversityBassam Rimawi, Emory UniversityBali Pulendran, Emory UniversityRaymond Schinazi, Emory UniversityRana Chakraborty, Emory UniversityMehul Suthar, Emory University
Language
  • English
Date
  • 2016-07-13
Publisher
  • Elsevier (Cell Press)
Publication Version
Copyright Statement
  • © 2016 Elsevier Inc.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1931-3128
Volume
  • 20
Issue
  • 1
Start Page
  • 83
End Page
  • 90
Grant/Funding Information
  • This work was funded in part by NIH grants U19AI083019 (M.S.S), R56AI110516 (M.S.S), R21AI113485 (M.S.S.), 2U19AI090023 (B.P), 5R37DK057665 (B.P), 5R37AI048638 (B.P), and 2U19AI057266 (B.P); Children’s Healthcare of Atlanta (M.S.S); Emory Vaccine Center (M.S.S); The Georgia Research Alliance (M.S.S); Multi-Center NICHD International Maternal Pediatric Adolescent AIDS Clinical Trials Network (R.C); and P30AI050409 Center for AIDS Research at Emory University (R.F.S).
Supplemental Material (URL)
Abstract
  • The recent Zika virus (ZIKV) outbreak in Brazil has been directly linked to increased cases of microcephaly in newborns. Current evidence indicates that ZIKV is transmitted vertically from mother to fetus. However, the mechanism of intrauterine transmission and the cell types involved remain unknown. We demonstrate that the contemporary ZIKV strain PRVABC59 (PR 2015) infects and replicates in primary human placental macrophages, called Hofbauer cells, and to a lesser extent in cytotrophoblasts, isolated from villous tissue of full-term placentae. Viral replication coincides with induction of type I interferon (IFN), pro-inflammatory cytokines, and antiviral gene expression, but with minimal cell death. Our results suggest a mechanism for intrauterine transmission in which ZIKV gains access to the fetal compartment by directly infecting placental cells and disrupting the placental barrier.
Author Notes
Keywords
Research Categories
  • Health Sciences, Public Health
  • Health Sciences, Immunology
  • Biology, Virology

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