Antiviral activity of bovine type III interferon against bovine viral diarrhea virus is greatly reduced in bovine turbinate cells due to limited expression of IFN lambda receptor 1 (IL-28Rα)

Front Immunol. 2024 Aug 19:15:1441908. doi: 10.3389/fimmu.2024.1441908. eCollection 2024.

Abstract

Introduction: The antiviral activity of recombinant bovine interferon lambda 3 (bovIFN-λ3) against bovine viral diarrhea virus (BVDV) has been demonstrated in vitro in Madin-Darby bovine kidney cells (MDBK) and in vivo in cattle. However, anti-BVDV activity of bovIFN-λ3 has not been studied in bovine respiratory tract epithelial cells, supposedly a primary target of BVDV infection when entering the host by the oronasal route.

Methods: Here we investigated the anti-BVDV activity of bovIFN-λ3 in bovine turbinate-derived primary epithelial cells (BTu) using BVDV infection and immunoperoxidase staining, TCID50, RT-qPCR, DNA and transcriptome sequencing, and transfection with plasmids containing the two subunits, IL-28Rα and IL-10Rβ that constitute the bovIFN-λ3 receptor.

Results: Our immunoperoxidase staining, RT-qPCR, and TCID50 results show that while BVDV was successfully cleared in MDBK cells treated with bovIFN-λ3 and bovIFN-α, only the latter, bovIFN-α, cleared BVDV in BTu cells. Preincubation of MDBK cells with bovIFN-λ3 before BVDV infection was needed to induce optimal antiviral state. Both cell types displayed intact type I and III IFN signaling pathways and expressed similar levels of IL-10Rβ subunit of the type III IFN receptor. Sequencing of PCR amplicon of the IL-28Rα subunit revealed intact transmembrane domain and lack of single nucleotide polymorphisms (SNPs) in BTu cells. However, RT-qPCR and transcriptomic analyses showed a lower expression of IL-28Rα transcripts in BTu cells as compared to MDBK cells. Interestingly, transfection of BTu cells with a plasmid encoding IL-28Rα subunit, but not IL-10Rβ subunit, established the bovIFN-λ3 sensitivity showing similar anti-BVDV activity to the response in MDBK cells.

Conclusion: Our results demonstrate that the sensitivity of cells to bovIFN-λ3 depends not only on the quality but also of the quantity of the IL-28Rα subunit of the heterodimeric receptor. A reduction in IL-28Rα transcript expression was detected in BTu as compared to MDBK cells, despite the absence of spliced variants or SNPs. The establishment of bovIFN-λ3 induced anti-BVDV activity in BTu cells transfected with an IL-28Rα plasmid suggests that the level of expression of this receptor subunit is crucial for the specific antiviral activity of type III IFN in these cells.

Keywords: IFN-λ3; IL-10Rβ; IL-28Rα; Madin-Darby bovine kidney cells; bovine turbinate primary epithelial cells; bovine type III interferon; bovine viral diarrhea virus.

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Bovine Virus Diarrhea-Mucosal Disease / immunology
  • Bovine Virus Diarrhea-Mucosal Disease / virology
  • Cattle
  • Cell Line
  • Diarrhea Viruses, Bovine Viral / immunology
  • Diarrhea Viruses, Bovine Viral / physiology
  • Epithelial Cells / immunology
  • Epithelial Cells / metabolism
  • Epithelial Cells / virology
  • Interferon Lambda*
  • Interferons* / immunology
  • Interferons* / metabolism
  • Interleukin-10 Receptor beta Subunit / genetics
  • Interleukin-10 Receptor beta Subunit / metabolism
  • Interleukins / genetics
  • Interleukins / immunology
  • Interleukins / metabolism
  • Interleukins / pharmacology
  • Receptors, Cytokine
  • Receptors, Interleukin / genetics
  • Receptors, Interleukin / metabolism
  • Recombinant Proteins / pharmacology
  • Turbinates* / immunology
  • Turbinates* / metabolism
  • Turbinates* / virology

Substances

  • Interferons
  • Interferon Lambda
  • interleukin 28alpha receptor
  • Antiviral Agents
  • Receptors, Interleukin
  • Interleukins
  • Recombinant Proteins
  • Interleukin-10 Receptor beta Subunit
  • Receptors, Cytokine

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was supported by funding through internal USDA research dollars (USDA/Agricultural Research Service, 5030-32000-229-000-D and 8064-32000-06 CRIS projects). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.