Thonningianin A disrupts pA104R−DNA binding and inhibits African swine fever virus replication

African swine fever is a highly lethal disease caused by the African swine fever virus (ASFV), posing a significant threat to the global pig industry, wherease no approved treatments are currently available. The ASFV DNA-binding protein, pA104R, plays a critical role in viral genome packaging and replication, making it a key target for drug discovery. Through structure-based virtual screening, we identified a polyphenolic compound, thonningianin A, which disrupts the pA104R-DNA binding and significantly inhibits ASFV replication. Mechanistic study revealed that thonningianin A binds to the DNA-binding region of pA104R, forming strong hydrogen bonds with H100 and occupying the vital DNA-binding residues K92, R94, and K97. In addition, we resolved the high-resolution (1.8 Å) structure of pA104R (PDB ID 9JS5), providing valuable insights for future drug screening. Together, these results demonstrate that thonningianin A holds great potential for the development of anti-ASFV drug, as a herb extract with favourable pharmacokinetic properties and safety.

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Publication Details

Journal
Emerging Microbes & Infections
Published
2025-03-27
DOI
https://doi.org/10.1080/22221751.2025.2482697
Citations
5
Primary Topic
Animal Disease Management and Epidemiology
Type
article
Field-Weighted Citation Impact
9.51
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article

Thonningianin A disrupts pA104R−DNA binding and inhibits African swine fever virus replication

Quanjie Li, Dongrong Yi, Linlin Zheng, Qian Liu et al.
5 citations
Emerging Microbes & Infections
Animal Disease Management and Epidemiology
9.51
article

Thonningianin A disrupts pA104R−DNA binding and inhibits African swine fever virus replication

Quanjie Li, Dongrong Yi, Linlin Zheng, Qian Liu, Tao Feng, Huabin Shao, Shan Cen, Chenxi Huo
article en
5 citations

Abstract

African swine fever is a highly lethal disease caused by the African swine fever virus (ASFV), posing a significant threat to the global pig industry, wherease no approved treatments are currently available. The ASFV DNA-binding protein, pA104R, plays a critical role in viral genome packaging and replication, making it a key target for drug discovery. Through structure-based virtual screening, we identified a polyphenolic compound, thonningianin A, which disrupts the pA104R-DNA binding and significantly inhibits ASFV replication. Mechanistic study revealed that thonningianin A binds to the DNA-binding region of pA104R, forming strong hydrogen bonds with H100 and occupying the vital DNA-binding residues K92, R94, and K97. In addition, we resolved the high-resolution (1.8 Å) structure of pA104R (PDB ID 9JS5), providing valuable insights for future drug screening. Together, these results demonstrate that thonningianin A holds great potential for the development of anti-ASFV drug, as a herb extract with favourable pharmacokinetic properties and safety.

Emerging Microbes & InfectionsVol. 14(1)
Academy of Medical Sciences (GB), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN), Lanzhou Veterinary Research Institute (CN), Chinese Academy of Agricultural Sciences (CN), Lanzhou University (CN)
Zero hunger
Openalex Percentile: Top 2%
Animal Disease Management and Epidemiology
9.51
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