p53 suppresses the inflammatory response following respiratory syncytial virus infection by inhibiting TLR2

Virology. 2024 May:593:110018. doi: 10.1016/j.virol.2024.110018. Epub 2024 Feb 10.

Abstract

-Respiratory syncytial virus (RSV) is a pivotal virus leading to acute lower respiratory tract infections in children under 5 years old. This study aimed to explore the correlation between p53 and Toll-like receptors (TLRs) post RSV infection. p53 levels exhibited a substantial decrease in nasopharyngeal aspirates (NPAs) from infants with RSV infection compared to control group. Manipulating p53 expression had no significant impact on RSV replication or interferon signaling pathway. Suppression of p53 expression led to heightened inflammation following RSV infection in A549 cells or airways of BALB/c mice. while stabilizing p53 expression using Nutlin-3a mitigated the inflammatory response in A549 cells. Additionally, Inhibiting p53 expression significantly increased Toll-like receptor 2 (TLR2) expression in RSV-infected epithelial cells and BALB/c mice. Furthermore, the TLR2 inhibitor, C29, effectively reduced inflammation mediated by p53 in A549 cells. Collectively, our results indicate that p53 modulates the inflammatory response after RSV infection through TLR2.

Keywords: Inflammation; Respiratory syncytial virus; Toll-like receptor 2; p53.

MeSH terms

  • A549 Cells / metabolism
  • A549 Cells / virology
  • Animals
  • Child
  • Child, Preschool
  • Humans
  • Inflammation
  • Mice
  • Respiratory Syncytial Virus Infections* / genetics
  • Respiratory Syncytial Virus Infections* / metabolism
  • Respiratory Syncytial Virus, Human* / metabolism
  • Toll-Like Receptor 2* / genetics
  • Toll-Like Receptor 2* / metabolism
  • Tumor Suppressor Protein p53* / genetics
  • Tumor Suppressor Protein p53* / metabolism

Substances

  • TLR2 protein, human
  • Toll-Like Receptor 2
  • Tumor Suppressor Protein p53