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High-throughput Antiviral Assays to Screen for Inhibitors of Zika Virus Replication
Published on: October 30, 2021
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Zika virus replication and cytopathic effects in liver cells
Kenneth E Sherman1, Susan D Rouster1, Ling X Kong1
1University of Cincinnati College of Medicine, Internal Medicine, Cincinnati, Ohio, United States of America.
Plos One
|March 21, 2019
Summary
Zika virus (ZIKV) replicates in human liver cells, causing cell damage similar to hepatitis. This study confirms liver cells are susceptible to ZIKV infection and injury.
Area of Science:
- Virology
- Hepatology
- Cell Biology
Background:
- Zika virus (ZIKV) is a global health concern, linked to microcephaly and neurological issues.
- ZIKV's homology to Hepaciviruses suggests potential for causing hepatitis.
- Understanding ZIKV's effect on liver cells is crucial for public health.
Purpose of the Study:
- To investigate Zika virus replication in hepatocyte-derived cell lines.
- To characterize the cytopathic effects and viral production in liver cells infected with ZIKV.
- To compare ZIKV replication in liver cells to that in standard viral replication models.
Main Methods:
- Infection of Huh7.5 and HepG2 (hepatocyte-derived) cells with ZIKV.
- Evaluation of viral replication using plaque assays, qRT-PCR, and NS1 protein detection.
- Assessment of viral particle production via transmission electron microscopy and negative staining.
- Comparison of growth curves in hepatocyte lines versus Vero cells.
Main Results:
- Hepatocyte-derived cell lines (Huh7.5, HepG2) supported ZIKV replication comparable to Vero cells.
- Cytopathic effects, including increased apoptosis markers, were observed in infected liver cells after 3 days.
- Viral capsids and ZIKV particles were identified within cells and in the supernatant, respectively.
Conclusions:
- Hepatocyte-derived cell lines are permissive to ZIKV replication.
- ZIKV infection in liver cells leads to overt cytopathic effects, suggesting acute viral hepatitis.
- Further research into ZIKV replication and pathogenesis in hepatocytes is warranted.
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