Chelerythrine inhibits HSV-1 infection by suppressing virus binding to the cells

Hu，Ziwei1,2,3; Zhang，Chaowei2; Zhong，Jianfeng2; Hu，Hao2; Li，Chenyang2; Zhao，Yunshi2; Wang，Lu2; Ye，Liang2; Yan，Cong2; Wang，Mingzhong1; Zhu，Qinchang1; Wen，Bo4; He，Longxia5; Rajoka，Muhammad Shahid Riaz2; Song，Xun1,2; He，Zhendan1,2

2023-03-01

10.1016/j.prmcm.2023.100223

Pharmacological Research - Modern Chinese Medicine   影响因子和分区

2667-1425

Objective: Herpes simplex virus type 1 (HSV-1) is a worldwide pathogen and mainly puts immunocompromised patients at higher risk of various complications. This research aims to demonstrate the antiviral activity of chelerythrine (CHE), an alkaloid compound derived from the traditional Chinese medicine Mcleaya cordata, towards the HSV-1 F strain. Methods: Bioassay-guided fractionation was carried out in order to isolate the antiviral compound CHE. The plaque reduction assay was used to evaluate the antiviral activity of CHE. The combination of quantitative PCR (qPCR) and western blot was used to elucidate whether CHE interferes with viral DNA synthesis, followed by time-of-addition assay to examine which steps of HSV-1 infection CHE affected. The immunofluorescent assay and transmission electron microscopy assay were performed to further analyze the intracellular localization and the ultrastructural features of HSV-1 virions with the treatment of CHE. The binding affinity in CHE to targeted viral glycoprotein was investigated by surface plasmon resonance (SPR) assay and docking simulation. Results: CHE displayed a significant antiviral effect against HSV-1 at 0.312 to 2.5 µM with a viral titer reduction of 29.38% to 61.02%. CHE had an EC value of 1.78 µM against HSV-1, and the selectivity index (SI) for CHE was 4.07. Additionally, CHE inhibits ICP0 expression in the immediate early stage of infection, which further affected the early stage of infection, and subsequent viral replication. Results of the SPR assay showed that CHE had strong-binding affinity to gB with a KD value of 7.80 × 10 M, while gD with a value of 1.18 × 10 M. TEM revealed that CHE can clearly inhibit the virion release. In silico experiments further confirmed that CHE had low binding free energy in the activity sites of gB and gD. Conclusion: This study revealed that CHE directly targeted viral gB or gD as a potent glycoprotein inhibitor, which suggested that CHE could be a virus entry inhibitor for HSV-1 treatment.

Antiviral Chelerythrine Glycoprotein B Glycoprotein D Herpes simplex virus type 1

英语

其他

2-s2.0-85147218923

Scopus

1.College of Pharmacy,Shenzhen Technology University,Shenzhen,518118,China
2.Health Science Center,School of Basic Medicine,School of Pharmaceutical Sciences,Shenzhen University General Hospital,Shenzhen University,Shenzhen,518000,China
3.Department of Biochemistry,School of Medicine,Southern University of Science and Technology,Shenzhen,Guangdong,518055,China
4.The Key Laboratory of Optimal Utilization of Natural Medicine Resources,School of Pharmaceutical Sciences,Guizhou Medical University,University Town,Guian New District,Guizhou,550025,China
5.Department of Otorhinolaryngology-Head and Neck Surgery,Chengdu Integrated TCM&Western Medicine Hospital,Chengdu,610017,China

Hu，Ziwei,Zhang，Chaowei,Zhong，Jianfeng,et al. Chelerythrine inhibits HSV-1 infection by suppressing virus binding to the cells[J]. Pharmacological Research - Modern Chinese Medicine,2023,6.

Hu，Ziwei.,Zhang，Chaowei.,Zhong，Jianfeng.,Hu，Hao.,Li，Chenyang.,...&He，Zhendan.(2023).Chelerythrine inhibits HSV-1 infection by suppressing virus binding to the cells.Pharmacological Research - Modern Chinese Medicine,6.

Hu，Ziwei,et al."Chelerythrine inhibits HSV-1 infection by suppressing virus binding to the cells".Pharmacological Research - Modern Chinese Medicine 6(2023).