Literature DB >> 29267916

Zika Virus Infection in Pregnancy: Maternal, Fetal, and Neonatal Considerations.

Carmen D Zorrilla1, Inés García García2, Lourdes García Fragoso2, Alberto De La Vega1.   

Abstract

An infection with the Zika virus (ZIKV) is usually mild, with nonspecific symptoms and most often asymptomatic. However, because of its causal relationship with severe congenital malformations, the ZIKV epidemic became an imperative for mobilization, renewed strategies for vector control, and biomedical research. A congenital Zika syndrome (CZS) has been characterized with 5 distinctive features that focus on brain development abnormalities (including microcephaly and brain calcifications), retinal manifestations, and defects on extremities including congenital contractures and hypertonia. The CZS could be just "the tip of the iceberg", pending the documentation of a spectrum of disease that could manifest later in life, from mild dysfunction to severe disease. It will be a matter of time for neurodevelopmental abnormalities, learning disabilities, and other unknown but yet-to-be-described outcomes to be associated with intrauterine ZIKV infection. In addition, ZIKV infection during pregnancy has been associated with other adverse outcomes. Reports mostly include ZIKV-affected pregnancies, and it will be difficult to clearly establish causality without appropriate control groups. We are summarizing some of the known or reported consequences of such infection during pregnancy. Women of reproductive age and particularly pregnant women are the most vulnerable to the adverse consequences of the ZIKV epidemic. Vector control programs need to be expanded to curtail new infections. Research is needed to develop safe and effective treatments, a preventive or therapeutic vaccine, and specific and sensitive tests and to diagnose and identify correlates of long-term immunity. Vaccines and treatments should be safe to be used in pregnancy. To do nothing would allow thousands of pregnant women to expose their fetuses to an infection that causes birth defects and other problems. Prenatal diagnosis technology development is necessary to be able to predict or diagnose adverse fetal outcomes related to ZIKV. Moreover, these tests should be used in a manner similar to the testing/screening method for neural tube defects and common chromosomal anomalies during prenatal care.
© The Author(s) 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  ZIKV; Zika in pregnancy; pregnancy

Mesh:

Year:  2017        PMID: 29267916      PMCID: PMC5853951          DOI: 10.1093/infdis/jix448

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  40 in total

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Authors:  Emily E Petersen; Dana Meaney-Delman; Robyn Neblett-Fanfair; Fiona Havers; Titilope Oduyebo; Susan L Hills; Ingrid B Rabe; Amy Lambert; Julia Abercrombie; Stacey W Martin; Carolyn V Gould; Nadia Oussayef; Kara N D Polen; Matthew J Kuehnert; Satish K Pillai; Lyle R Petersen; Margaret A Honein; Denise J Jamieson; John T Brooks
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2016-10-07       Impact factor: 17.586

9.  Ocular Findings in Infants With Microcephaly Associated With Presumed Zika Virus Congenital Infection in Salvador, Brazil.

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4.  Pandemic Zika: A Formidable Challenge to Medicine and Public Health.

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6.  Transfusion-Transmitted Zika Virus Infection in Pregnant Mice Leads to Broad Tissue Tropism With Severe Placental Damage and Fetal Demise.

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7.  Identification of Novel Natural Products as Effective and Broad-Spectrum Anti-Zika Virus Inhibitors.

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8.  Role of Prenatal Ultrasonography and Amniocentesis in the Diagnosis of Congenital Zika Syndrome: A Systematic Review.

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Review 9.  Evolution of Two Major Zika Virus Lineages: Implications for Pathology, Immune Response, and Vaccine Development.

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10.  The Robust Restriction of Zika Virus by Type-I Interferon in A549 Cells Varies by Viral Lineage and Is Not Determined by IFITM3.

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