Frontiers in Microbiology (Jun 2023)

Cathelicidin-derived antiviral peptide inhibits herpes simplex virus 1 infection

  • Xiaomin Guo,
  • Yanxing An,
  • Wanmin Tan,
  • Ling Ma,
  • Mingyang Wang,
  • Juyan Li,
  • Binghong Li,
  • Wei Hou,
  • Li Wu

DOI
https://doi.org/10.3389/fmicb.2023.1201505
Journal volume & issue
Vol. 14

Abstract

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Herpes simplex virus 1 (HSV-1) is a widely distributed virus. HSV-1 is a growing public health concern due to the emergence of drug-resistant strains and the current lack of a clinically specific drug for treatment. In recent years, increasing attention has been paid to the development of peptide antivirals. Natural host-defense peptides which have uniquely evolved to protect the host have been reported to have antiviral properties. Cathelicidins are a family of multi-functional antimicrobial peptides found in almost all vertebrate species and play a vital role in the immune system. In this study, we demonstrated the anti-HSV-1 effect of an antiviral peptide named WL-1 derived from human cathelicidin. We found that WL-1 inhibited HSV-1 infection in epithelial and neuronal cells. Furthermore, the administration of WL-1 improved the survival rate and reduced viral load and inflammation during HSV-1 infection via ocular scarification. Moreover, facial nerve dysfunction, involving the abnormal blink reflex, nose position, and vibrissae movement, and pathological injury were prevented when HSV-1 ear inoculation-infected mice were treated with WL-1. Together, our findings demonstrate that WL-1 may be a potential novel antiviral agent against HSV-1 infection-induced facial palsy.

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