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Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection
In 2015 Zika virus (ZIKV) emerged for the first time in South America. The following ZIKV epidemic resulted in the appearance of a clinical phenotype with microcephaly and other severe malformations in newborns. So far, mechanisms of ZIKV induced damage to the fetus are not completely understood. Pr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019633/ https://www.ncbi.nlm.nih.gov/pubmed/31936159 http://dx.doi.org/10.3390/v12010072 |
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author | Forster, Dominik Schwarz, Jan Hendrik Brosinski, Katrin Kalinke, Ulrich Sutter, Gerd Volz, Asisa |
author_facet | Forster, Dominik Schwarz, Jan Hendrik Brosinski, Katrin Kalinke, Ulrich Sutter, Gerd Volz, Asisa |
author_sort | Forster, Dominik |
collection | PubMed |
description | In 2015 Zika virus (ZIKV) emerged for the first time in South America. The following ZIKV epidemic resulted in the appearance of a clinical phenotype with microcephaly and other severe malformations in newborns. So far, mechanisms of ZIKV induced damage to the fetus are not completely understood. Previous data suggest that ZIKV may bypass the placenta to reach the fetus. Thus, animal models for ZIKV infection are important to facilitate studies about ZIKV infection during pregnancy. Here, we used ultrasound based imaging (USI) to characterize ZIKV induced pathogenesis in the pregnant Type I interferon receptor-deficient (IFNAR-/-) mouse model. Based on USI we suggest the placenta to be a primary target organ of ZIKV infection enabling ZIKV spreading to the fetus. Moreover, in addition to direct infection of the fetus, the placental ZIKV infection may cause an indirect damage to the fetus through reduced uteroplacental perfusion leading to intrauterine growth retardation (IUGR) and fetal complications as early as embryonic day (ED) 12.5. Our data confirmed the capability of USI to characterize ZIKV induced modifications in mouse fetuses. Data from further studies using USI to monitor ZIKV infections will contribute to a better understanding of ZIKV infection in pregnant IFNAR-/- mice. |
format | Online Article Text |
id | pubmed-7019633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70196332020-03-09 Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection Forster, Dominik Schwarz, Jan Hendrik Brosinski, Katrin Kalinke, Ulrich Sutter, Gerd Volz, Asisa Viruses Article In 2015 Zika virus (ZIKV) emerged for the first time in South America. The following ZIKV epidemic resulted in the appearance of a clinical phenotype with microcephaly and other severe malformations in newborns. So far, mechanisms of ZIKV induced damage to the fetus are not completely understood. Previous data suggest that ZIKV may bypass the placenta to reach the fetus. Thus, animal models for ZIKV infection are important to facilitate studies about ZIKV infection during pregnancy. Here, we used ultrasound based imaging (USI) to characterize ZIKV induced pathogenesis in the pregnant Type I interferon receptor-deficient (IFNAR-/-) mouse model. Based on USI we suggest the placenta to be a primary target organ of ZIKV infection enabling ZIKV spreading to the fetus. Moreover, in addition to direct infection of the fetus, the placental ZIKV infection may cause an indirect damage to the fetus through reduced uteroplacental perfusion leading to intrauterine growth retardation (IUGR) and fetal complications as early as embryonic day (ED) 12.5. Our data confirmed the capability of USI to characterize ZIKV induced modifications in mouse fetuses. Data from further studies using USI to monitor ZIKV infections will contribute to a better understanding of ZIKV infection in pregnant IFNAR-/- mice. MDPI 2020-01-07 /pmc/articles/PMC7019633/ /pubmed/31936159 http://dx.doi.org/10.3390/v12010072 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Forster, Dominik Schwarz, Jan Hendrik Brosinski, Katrin Kalinke, Ulrich Sutter, Gerd Volz, Asisa Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection |
title | Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection |
title_full | Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection |
title_fullStr | Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection |
title_full_unstemmed | Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection |
title_short | Obstetric Ultrasonography to Detect Fetal Abnormalities in a Mouse Model for Zika Virus Infection |
title_sort | obstetric ultrasonography to detect fetal abnormalities in a mouse model for zika virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019633/ https://www.ncbi.nlm.nih.gov/pubmed/31936159 http://dx.doi.org/10.3390/v12010072 |
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