Infection of PRRSV inhibits CSFV C-strain replication by inducing macrophages polarization to M1

Vet Microbiol. 2024 Feb:289:109957. doi: 10.1016/j.vetmic.2023.109957. Epub 2023 Dec 20.

Abstract

It is a common sense that porcine reproductive and respiratory syndrome virus (PRRSV) infection could cause immune failure of classical swine fever (CSF) vaccine, and porcine alveolar macrophages (PAMs) are the target cells of both. To elucidate the role of macrophage polarization in PRRSV infection induced CSF vaccine failure, an immortal porcine alveolar macrophage line PAM39 cell line was used to investigate the effect of PRRSV or/and CSFV C-strain (CSFV-C) infection on macrophage polarization in vitro. Interestingly, PRRSV single infection or PRRSV co-infection with CSFV-C promoted PAM39 cells to M1, while CSFV-C single infection induced PAM39 cells to M2. After the construction of M1 and M2 PAM39 cells polarization models, M1 polarized PAM39 cells were found to inhibit the replication of CSFV-C, and Chinese medicine such as matrine, ginsenosides and astragalus polysaccharides could alleviate the polarization of PAM39 cells and the replication of CSFV-C. Furthermore, interferon (IFN)-γ and lipopolysaccharide (LPS) co-stimulation induced NF-κB activation while matrine treatment blocked M1 polarization-induced NF-κB pathway activation. These findings provided a theoretical basis for designing a new strategy to improve the immune effect of CSFV-C based on porcine alveolar macrophage polarization subtypes.

Keywords: CSFV-C; Co-infection; Matrine; PAM39 cells; PRRSV; Polarization; TLR4/NF-κB.

MeSH terms

  • Animals
  • Classical Swine Fever* / prevention & control
  • Macrophages, Alveolar
  • Matrines
  • NF-kappa B / metabolism
  • Porcine Reproductive and Respiratory Syndrome* / metabolism
  • Porcine respiratory and reproductive syndrome virus*
  • Swine
  • Swine Diseases* / metabolism
  • Vaccines*
  • Virus Replication

Substances

  • NF-kappa B
  • Matrines
  • Vaccines