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Characterising the Transcriptomic Response to Interferon and Infection in European Domestic Ferret Respiratory
Rubaiyea Farrukee1, Jessie J-Y Chang1, Jianshu Zhang1
1Department of Microbiology and Immunology, University of Melbourne, The Peter Doherty Institute for Infection and Immunity, Victoria, Australia.
Researchers characterized the ferret transcriptome response to interferon and influenza infection. This study identifies key interferon-stimulated genes (ISGs) and novel transcripts, enhancing the ferret model for influenza research.
Area of Science:
- Virology
- Immunology
- Genomics
Background:
- The domestic ferret is a key model for influenza virus studies.
- Limited data exists on the ferret's transcriptomic response to interferon (IFN) and influenza infection.
- Most interferon-stimulated genes (ISGs) in ferrets are computationally predicted, not experimentally verified.
Purpose of the Study:
- To comprehensively assess the ferret transcriptome response to IFN-α stimulation and influenza A virus (IAV) infection.
- To identify experimentally validated ferret ISGs and novel interferon-stimulated transcripts.
- To explore the role of poly(A) tail elongation in the ferret's antiviral response.
Main Methods:
- Utilized long-read RNA sequencing for transcriptome-wide analysis.
- Investigated ferret lung (FRL) cell lines treated with IFN-α in vitro.
- Analyzed nasal turbinate tissues from IAV-infected ferrets in vivo.
Main Results:
- Identified ferret genes orthologous to human ISGs upregulated by both IFN-α and IAV.
- Discovered novel interferon-stimulated genes and transcripts in ferrets.
- Observed poly(A) tail elongation in ribosome and COVID-19 pathways following IFN-α treatment, linking it to antiviral responses.
Conclusions:
- The study provides a detailed map of the ferret's transcriptional innate immune response.
- Identified validated ISGs and novel transcripts enhance the ferret model for influenza research.
- Findings suggest poly(A) tail elongation is involved in the host's antiviral mechanisms.
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