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Updated: Jan 26, 2026

Zika Virus Specific Diagnostic Epitope Discovery
Published on: December 12, 2017
Developing animal models of Zika virus infection for novel drug discovery
Cristine Marie Yde Ohki1, Cecilia Benazzato1,2, Fabiele Baldino Russo1
1a Department of Microbiology, Institute of Biomedical Sciences , University of São Paulo , São Paulo , Brazil.
Introduction:
Just before the Brazilian outbreak, Zika virus was related to a mild infection, causing fever and skin rash. Congenital Zika Syndrome was first described in Brazil, causing microcephaly and malformations in newborns. Three years after the outbreak, the mechanisms of Zika pathogenesis are still not completely elucidated. Moreover, as of today, there is still no approved vaccine that can be administered to the susceptible population. Considering the unmet clinical need, animal models represent an unprecedented opportunity to study Zika pathophysiology and test drugs for the treatment and prevention of vertical transmission. Areas covered: The authors explore the current knowledge about Zika through animal models and advancements in drug discovery by highlighting drugs with the greatest potential to treat ZIKV infection and block vertical transmission. Expert opinion: Some drugs used to treat other infections have been repurposed to treat Zika infection, reducing the cost and time for clinical application. One promising example is Sofosbuvir, which protected mice models against Zika pathogenesis by preventing vertical transmission. Importantly, there is a lack on exploration on the long-term effects of Zika Congenital Syndrome, as well as the possible ways to treat its sequelae.
Insights
Animal models are crucial for understanding Zika virus pathogenesis and developing treatments. Sofosbuvir shows promise in preventing Zika
Area of Science:
- Virology
- Infectious Diseases
- Neuroscience
Background:
- Zika virus (ZIKV) infection was initially mild but became associated with Congenital Zika Syndrome (CZS) causing microcephaly and malformations.
- Despite the 2015 Brazilian outbreak, ZIKV pathogenesis mechanisms remain unclear, and no approved vaccine exists.
- There is a significant need for effective treatments to prevent ZIKV infection and vertical transmission.
Purpose of the Study:
- To review current knowledge on ZIKV pathophysiology using animal models.
- To highlight advancements in drug discovery for ZIKV infection and vertical transmission prevention.
- To identify potential therapeutic agents for ZIKV and CZS sequelae.
Main Methods:
- Literature review of studies utilizing animal models for ZIKV research.
- Analysis of drug discovery efforts, including repurposed medications.
- Focus on drugs demonstrating efficacy in preclinical models for ZIKV treatment and prevention of vertical transmission.
Main Results:
- Animal models are essential for studying ZIKV pathophysiology and testing interventions.
- Repurposed drugs offer a faster, cost-effective approach to ZIKV treatment.
- Sofosbuvir demonstrated efficacy in mouse models, preventing ZIKV pathogenesis and vertical transmission.
Conclusions:
- Animal models are vital for advancing ZIKV research and therapeutic development.
- Repurposed drugs like Sofosbuvir show potential for treating ZIKV infection and preventing vertical transmission.
- Further research is needed on long-term CZS effects and treatment strategies for its sequelae.
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