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Author Notes:

Correspondence: elizabeth_stringer@med.unc.edu (ES) or matthew.collins@emory.edu (MC)

MC: Conceptualization, Data curation, Formal analysis, Investigation, Writing – original draft. OZ: Data curation, Investigation, Writing – review & editing. BB: Data curation, Formal analysis, Methodology, Writing – review & editing. RJ: Data curation, Formal analysis, Writing – review & editing.

MM: Data curation, Investigation, Writing – review & editing. RP: Investigation, Project administration, Resources, Writing – review & editing. G-JL: Data curation, Formal analysis, Investigation, Methodology, Writing – review & editing. MM-C: Data curation, Formal analysis, Investigation, Writing – original draft, Writing – review & editing.

EH:Conceptualization, Funding acquisition, Investigation, Project administration, Resources, Writing – review & editing. SB-D:Conceptualization, Funding acquisition, Investigation, Project administration, Resources, Writing – review & editing.

AMS: Conceptualization, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Supervision, Writing – review & editing. JS: Conceptualization, Investigation, Writing – review & editing.

FB: Conceptualization, Funding acquisition, Investigation, Project administration, Resources, Supervision, Writing – review & editing. ES: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Supervision, Writing – review & editing.

The authors wish to acknowledge the invaluable contribution of the study participants and also the immense effort of the study team (Lic. Hernan Vanegas, Licda. Nancy Corea, Licda. Celeste Perez and Licda. Yorling Picado), who monitored the Labor and Delivery room at all hours to obtain cord blood samples.

The assistance of Dra. Karla Vilchez and Dra. Candida Chavez from Perla Maria Health Center in subject recruitment and study implementation is much appreciated.

Subjects:

Research Funding:

Understanding Maternal Fetal Transmission of Zika virus ECBR_003 6/2016-6/2017 UNC Pilot to PI E. Stringer for startup supplies and recruitment of pregnancy cohort in Nicaragua.

F Bucardo received a Fogarty fellowship from UNC that supported some of his effort on this work.

Structure based design of recombinant Zika virus antigens for serodiagnosis R21 AI134073 (MPI: de Silva) NIH/NIAID.

00HVCLJB-2017-04191 (PI: de Silva) CDC Diagnosis of recent and remote Zika infections supported assay development and serologic testing of cohort specimens at UNC.

NIH P01 AI106695 (EH); funders played no role in the writing of the manuscript or the decision to submit it for publication.

S. Becker-Dreps was supported by NIAID 5R21AI129532-02.

MHC is supported by NIH 1K22AI137306-01 and Thrasher Research Fund.

Keywords:

  • Science & Technology
  • Multidisciplinary Sciences
  • Science & Technology - Other Topics
  • Virus
  • Brazil
  • Antibodies

Serologic surveillance of maternal Zika infection in a prospective cohort in Leon, Nicaragua during the peak of the Zika epidemic

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Journal Title:

PLoS ONE

Volume:

Volume 15, Number 4

Publisher:

, Pages e0230692-e0230692

Type of Work:

Article | Final Publisher PDF

Abstract:

Background Zika virus caused thousands of congenital anomalies during a recent epidemic. Because Zika emerged in areas endemic for dengue and these related flaviviruses elicit cross-reactive antibodies, it is challenging to serologically monitor pregnant women for Zika infection. Methods A prospective cohort of 253 pregnant women was established in León, Nicaragua. Women were followed during prenatal care through delivery. Serologic specimens were obtained at each visit, and birth outcome was recorded. Established flavivirus serologic methods were adapted to determine Zika seroprevalence, and a stepwise testing algorithm estimated timing of Zika infection in relation to pregnancy. Results Zika seroprevalence was approximately 59% among women tested. Neutralization testing was highly concordant with Zika NS1 BOB results. Per study algorithm, 21% (40/187) of women were classified as experiencing Incident ZIKV infection during pregnancy. Importantly, the Incident ZIKV group included mostly women pregnant during the 2016 Zika epidemic peak and the only 3 subjects in the cohort with RT-PCR-confirmed infections. Approximately 17% of births had complications; 1.5% (3/194) manifesting clinical criteria of congenital Zika syndrome, one was RT-PCR-confirmed as a case of congenital Zika syndrome. Adverse birth outcome did not correlate with timing of Zika infection. Conclusions By leveraging prenatal care systems, we developed a simple algorithm for identifying women who were likely infected by Zika during pregnancy.

Copyright information:

© 2020 Collins et al.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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