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High-throughput Antiviral Assays to Screen for Inhibitors of Zika Virus Replication
Published on: October 30, 2021
DNAzymes Dz13 target the c-jun possess antiviral activity against influenza A viruses
Zhaopei Zhang1, Shouping Zhang2, Sanhu Wang1
1Henan Institute of Science and Technology, Xinxiang 453003, China.
Abstract:
The emergence of anti-influenza A virus drugs resistant strain highlights the need for more effective therapy. Our earlier study demonstrated that c-jun, a downstream molecule of JNK, might be important in viral infections and inflammatory responses. In the present study, we explored the function of DNAzymes Dz13 that target c-jun in influenza A virus infected mice. Dz13 displayed non-toxic side effects on A549 cells and BALB/c mice. Moreover, Dz13-treated mice had enhanced survival after influenza compared with untreated mice. Simultaneously, the pulmonary inflammatory responses and viral burden were decreased in Dz13 treated mice. Furthermore, proliferation levels of infection-induced CD4+ and CD8+ T cells were impaired. These data demonstrated that Dz13 could reduce viral replication and inflammatory response in vivo, suggesting that Dz13 may potentially be used to treat influenza A viral infection.
Insights
This study shows DNAzymes targeting c-jun (a molecule involved in inflammation) effectively reduced influenza A virus replication and inflammation in mice, improving survival rates.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Emerging drug-resistant influenza A virus strains necessitate novel therapeutic strategies.
- c-jun, a downstream molecule of JNK, plays a role in viral infections and inflammatory responses.
- Targeting c-jun presents a potential therapeutic avenue for influenza treatment.
Purpose of the Study:
- To investigate the efficacy of DNAzymes targeting c-jun (Dz13) in a mouse model of influenza A virus infection.
- To assess the safety and therapeutic potential of Dz13 against influenza A virus.
Main Methods:
- Administration of DNAzymes Dz13 to influenza A virus-infected BALB/c mice.
- Evaluation of Dz13 toxicity in A549 cells and mice.
- Assessment of survival rates, pulmonary inflammatory responses, viral load, and T cell proliferation in treated mice.
Main Results:
- Dz13 demonstrated no significant toxicity in cell cultures or in vivo.
- Dz13 treatment significantly enhanced survival rates in infected mice.
- Dz13 reduced pulmonary inflammation and viral burden.
- Dz13 treatment led to impaired proliferation of infection-induced CD4+ and CD8+ T cells.
Conclusions:
- DNAzymes targeting c-jun (Dz13) are effective in reducing influenza A virus replication and associated inflammation in vivo.
- Dz13 exhibits a favorable safety profile.
- Dz13 represents a promising therapeutic candidate for treating influenza A viral infections.
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