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Individuals infected with ZIKV generate an immune response composed of antibodies which bind to the envelope (E) protein. These anti-E antibodies are critical in protecting individuals from subsequent infection. Multiple groups have found that many ZIKV antibodies bind to domain III of E (EDIII), suggesting that this region is an important target of neutralizing antibodies. Here, we generated a chimeric virus containing ZIKV EDIII in a dengue virus backbone to measure ZIKV EDIII-specific antibody responses. We found that while polyclonal ZIKV immune serum contains antibodies targeting EDIII, they constitute only a small fraction of the total population of antibodies that neutralize ZIKV. Further studies are needed to define the main targets on the viral envelope recognized by human neutralizing antibodies, which is critical for guiding the development of ZIKV vaccines.<\/jats:p>","DOI":"10.1128\/mbio.01485-19","type":"journal-article","created":{"date-parts":[[2019,9,16]],"date-time":"2019-09-16T14:13:52Z","timestamp":1568643232000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":40,"title":["Role of Zika Virus Envelope Protein Domain III as a Target of Human Neutralizing Antibodies"],"prefix":"10.1128","volume":"10","author":[{"given":"Emily N.","family":"Gallichotte","sequence":"first","affiliation":[{"name":"Department of Epidemiology, University of North Carolina at Chapel Hill School of Public Health, Chapel Hill, North Carolina, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ellen F.","family":"Young","sequence":"additional","affiliation":[{"name":"Department of 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