SARS-CoV-2 nsp13 suppresses hepatitis B virus replication by targeting cccDNA transcription

To effectively combat hepatitis B virus (HBV), it is imperative to develop potent antiviral medications targeting covalently closed circular DNA (cccDNA). Our investigation aimed to assess the impact of SARS-CoV-2 nsp13 on HBV replication across diverse HBV models, confirming its ability to significantly reduce several HBV replication markers. Additionally, our identification of the interaction between nsp13 and SMC4 opens the door for further mechanistic exploration. This marks a paradigm shift in our approach to HBV antiviral therapy, introducing an entirely novel perspective. Our findings propose a novel strategy for developing anti-HBV drugs that specifically target HBV cccDNA.

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Publication Details

Journal
Journal of Virology
Published
2024-10-07
DOI
https://doi.org/10.1128/jvi.01042-24
Citations
2
Primary Topic
Hepatitis B Virus Studies
Type
article
Field-Weighted Citation Impact
0.77

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article

SARS-CoV-2 nsp13 suppresses hepatitis B virus replication by targeting cccDNA transcription

Yuchen Xia, Aixin Li, Yingcheng Zheng, Cheng‐Liang Zhu et al.
2 citations
Journal of Virology
Hepatitis B Virus Studies
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article

SARS-CoV-2 nsp13 suppresses hepatitis B virus replication by targeting cccDNA transcription

Yuchen Xia, Aixin Li, Yingcheng Zheng, Cheng‐Liang Zhu, Qiongrong Chen, Kaitao Zhao, Wenbo Liu, Bei Zhang, Xiaoming Cheng, Yurong Duan, Lixia Hui
article en
2 citations

Abstract

To effectively combat hepatitis B virus (HBV), it is imperative to develop potent antiviral medications targeting covalently closed circular DNA (cccDNA). Our investigation aimed to assess the impact of SARS-CoV-2 nsp13 on HBV replication across diverse HBV models, confirming its ability to significantly reduce several HBV replication markers. Additionally, our identification of the interaction between nsp13 and SMC4 opens the door for further mechanistic exploration. This marks a paradigm shift in our approach to HBV antiviral therapy, introducing an entirely novel perspective. Our findings propose a novel strategy for developing anti-HBV drugs that specifically target HBV cccDNA.

Journal of VirologyVol. 98(11)
Weifang Medical University (CN), Wuhan University (CN), Hubei Provincial Center for Disease Control and Prevention (CN), Wuhan Institute of Virology (CN), Zhongnan Hospital of Wuhan University (CN), Renmin Hospital of Wuhan University (CN), State Key Laboratory of Virology, Hubei University (CN)
National Natural Science Foundation of China, Wuhan University, Zhongnan Hospital of Wuhan University, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Good health and well-being
Openalex Percentile: Top 25%
Hepatitis B Virus Studies
0.77
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