Biomimetic Placenta-Fetus Model Demonstrating Maternal–Fetal Transmission and Fetal Neural Toxicity of Zika Virus

2018 ◽  
Vol 46 (12) ◽  
pp. 1963-1974 ◽  
Author(s):  
Navein Arumugasaamy ◽  
Leila E. Ettehadieh ◽  
Che-Ying Kuo ◽  
Dominic Paquin-Proulx ◽  
Shannon M. Kitchen ◽  
...  
2019 ◽  
Vol 167 ◽  
pp. 104-109 ◽  
Author(s):  
Satoru Watanabe ◽  
Nicole Wei Wen Tan ◽  
Kitti Wing Ki Chan ◽  
Subhash G. Vasudevan

2019 ◽  
Vol 39 (2) ◽  
pp. 89-90
Author(s):  
L. Pomar ◽  
M. Vouga ◽  
V. Lambert ◽  
C. Pomar ◽  
N. Hcini ◽  
...  

2018 ◽  
Vol 6 (1) ◽  
pp. e1402143 ◽  
Author(s):  
Camila Zanluca ◽  
Lucia de Noronha ◽  
Claudia Nunes Duarte dos Santos

BMJ ◽  
2018 ◽  
pp. k4431 ◽  
Author(s):  
Léo Pomar ◽  
Manon Vouga ◽  
Véronique Lambert ◽  
Céline Pomar ◽  
Najeh Hcini ◽  
...  

AbstractObjectivesTo estimate the rates of maternal-fetal transmission of Zika virus, adverse fetal/neonatal outcomes, and subsequent rates of asymptomatic/symptomatic congenital Zika virus infections up to the first week of life.DesignCohort study with prospective data collection and subsequent review of fetal/neonatal outcomes.SettingsReferral centre for prenatal diagnosis of the French Guiana Western Hospital.ParticipantsPregnant women at any stage of pregnancy with a laboratory confirmed symptomatic or asymptomatic Zika virus infection during the epidemic period in western French Guiana. The cohort enrolled 300 participants and prospectively followed their 305 fetuses/newborns.Main outcome measuresRate of maternal-fetal transmission of Zika virus (amniotic fluid, fetal and neonatal blood, urine, cerebrospinal fluid, and placentas); clinical, biological, and radiological outcomes (blindly reviewed); and adverse outcomes defined as moderate signs potentially related to congenital Zika syndrome (CZS), severe complications compatible with CZS, or fetal loss. Associations between a laboratory confirmed congenital Zika virus infection and adverse fetal/neonatal outcomes were evaluated.ResultsMaternal-fetal transmission was documented in 26% (76/291) of fetuses/newborns with complete data. Among the Zika virus positive fetuses/newborns, 45% (34/76) presented with no signs/complications at birth, 20% (15/76) with moderate signs potentially related to CZS, 21% (16/76) with severe complications compatible with CZS, and 14% (11/76) with fetal loss. Compared with the Zika virus positive fetuses/neonates, those that were identified as negative for Zika virus (215/291) were less likely to present with severe complications (5%; 10/215) or fetal loss (0.5%; 1/215; relative risk 6.9, 95% confidence interval 3.6 to 13.3). Association between a positive Zika virus test and any adverse fetal/neonatal outcome was also significant (relative risk 4.4, 2.9 to 6.6). The population attributable fraction estimates that a confirmed congenital Zika virus infection contributes to 47% of adverse outcomes and 61% of severe adverse outcomes observed.ConclusionIn cases of a known maternal Zika virus infection, approximately a quarter of fetuses will become congenitally infected, of which a third will have severe complications at birth or fetal loss. The burden of CZS might be lower than initially described in South America and may not differ from other congenital infections.


2017 ◽  
Vol 214 (8) ◽  
pp. 2303-2313 ◽  
Author(s):  
Bin Cao ◽  
Lindsay A. Parnell ◽  
Michael S. Diamond ◽  
Indira U. Mysorekar

Zika virus (ZIKV) infection during pregnancy leads to devastating fetal outcomes, including intrauterine growth restriction and microcephaly. Greater understanding of mechanisms underlying ZIKV maternal-fetal transmission is needed to develop new therapeutic interventions. Here, we define an important role for the autophagy pathway in ZIKV vertical transmission. ZIKV infection induced autophagic activity in human trophoblasts and pharmacological inhibition limited ZIKV infectivity. Furthermore, deficiency in an essential autophagy gene, Atg16l1, in mice limited ZIKV vertical transmission and placental and fetal damage and overall improved placental and fetal outcomes. This protection was due to a placental trophoblast cell-autonomous effect of autophagic activity, not to alterations in systemic maternal ZIKV infection. Finally, an autophagy inhibitor, hydroxychloroquine, approved for use in pregnant women, attenuated placental and fetal ZIKV infection and ameliorated adverse placental and fetal outcomes. Our study reveals new insights into the mechanism of ZIKV vertical transmission and suggests that an autophagy-based therapeutic warrants possible evaluation in humans to diminish the risks of ZIKV maternal-fetal transmission.


2019 ◽  
Author(s):  
Valeria DeGiorgi ◽  
Jennifer Tan ◽  
Sarah Fowler ◽  
Sonia Maciejewski ◽  
David Gordon ◽  
...  

Abstract BACKGROUND: Zika virus (ZIKV) is primarily mosquito-borne, but can also be transfusion- and sexually transmitted. Maternal-fetal transmission may result in fetal loss or severe congenital defects. METHODS: We surveyed blood recipients enrolled in a donor-recipient-linked study of transfusion-transmitted infections to assess potential risk of ZIKV maternal-fetal transmission following transfusion. Participants were tested for antibodies to ZIKV, dengue and chikungunya viruses. Positive serology from post- and pre-transfusion samples and from linked donors were tested using real-time PCR. RESULTS: The mean age of female recipients was 65 years (36-80). Only one was < 50 years. None reported having sexual intercourse within the first month and none became pregnant within six months following transfusion. Male recipients were a mean 62 years of age (31-81). Twenty percent of males had sexual intercourse with a female partner within three months of transfusion; no pregnancies resulted. Females and males most commonly reported that they were no longer sexually active or felt too ill after transfusion. All of the respondents were IgM and RT-PCR negative. CONCLUSIONS: Our survey of blood recipients, combined with derived data and the literature, suggest that most transfused women are beyond the age of likely pregnancy and most transfused women and men are too infirm from the underlying condition to engage in sex. However, 20% of male recipients did report having sexual intercourse during the ZIKV infectious period.


2017 ◽  
Vol 37 (7) ◽  
pp. 287-294 ◽  
Author(s):  
Bin Cao ◽  
Michael S. Diamond ◽  
Indira U. Mysorekar

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