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Early gene expression events in ferrets in response to SARS coronavirus infection versus direct interferon-alpha2b stimulation.


ABSTRACT: Type I interferons (IFNs) are essential to the clearance of viral diseases, however, a clear distinction between genes upregulated by direct virus-cell interactions and genes upregulated by secondary IFN production has not been made. Here, we investigated differential gene regulation in ferrets upon subcutaneous administration of IFN-?2b and during SARS-CoV infection. In vivo experiments revealed that IFN-?2b causes STAT1 phosphorylation and upregulation of abundant IFN response genes (IRGs), chemokine receptors, and other genes that participate in phagocytosis and leukocyte transendothelial migration. During infection with SARS-CoV not only a variety of IRGs were upregulated, but also a significantly broader range of genes involved in cell migration and inflammation. This work allowed dissection of several molecular signatures present during SARS-CoV which are part of a robust IFN antiviral response. These signatures can be useful markers to evaluate the status of IFN responses during a viral infection and specific features of different viruses.

SUBMITTER: Danesh A 

PROVIDER: S-EPMC7111932 | biostudies-literature | 2011 Jan

REPOSITORIES: biostudies-literature

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Early gene expression events in ferrets in response to SARS coronavirus infection versus direct interferon-alpha2b stimulation.

Danesh Ali A   Cameron Cheryl M CM   León Alberto J AJ   Ran Longsi L   Xu Luoling L   Fang Yuan Y   Kelvin Alyson A AA   Rowe Thomas T   Chen Honglin H   Guan Yi Y   Jonsson Colleen B CB   Cameron Mark J MJ   Kelvin David J DJ  

Virology 20101028 1


Type I interferons (IFNs) are essential to the clearance of viral diseases, however, a clear distinction between genes upregulated by direct virus-cell interactions and genes upregulated by secondary IFN production has not been made. Here, we investigated differential gene regulation in ferrets upon subcutaneous administration of IFN-α2b and during SARS-CoV infection. In vivo experiments revealed that IFN-α2b causes STAT1 phosphorylation and upregulation of abundant IFN response genes (IRGs), ch  ...[more]

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