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Virus Res. 2014 Jun 24;185:72-6. doi: 10.1016/j.virusres.2014.03.006. Epub 2014 Mar 20.

Bovine herpesvirus 1 productive infection stimulates inflammasome formation and caspase 1 activity.

Author information

1
College of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Changcheng Road 700, Chengyang District, Qingdao 266109, PR China.
2
School of Veterinary Medicine and Biomedical Sciences, Nebraska Center for Virology, University of Nebraska, Lincoln Morisson Life Science Center, RM234, Lincoln, NE 68583-0900, United States.
3
School of Veterinary Medicine and Biomedical Sciences, Nebraska Center for Virology, University of Nebraska, Lincoln Morisson Life Science Center, RM234, Lincoln, NE 68583-0900, United States. Electronic address: cjones2@unl.edu.

Abstract

Bovine herpesvirus 1 (BoHV-1), a significant viral pathogen of cattle, causes inflammation in affected tissue during acute infection. Consequently, we tested whether productively infected bovine cells stimulate inflammasome formation. Expression of two components required for inflammasome formation, the DNA sensor IFI16 (gamma-interferon-inducible protein 16) and NLRP3 (NOD-like receptor family, pyrin domain containing 3), were induced in bovine kidney cells by eight hours after infection. IFI16 was detected in punctate granules localized to the cytoplasm and nucleus. During productive infection, more than ten times more cells were caspase 1 positive, which is activated following inflammasome formation. Two caspase 1 inhibitors had no effect on productive infection. Conversely, another caspase 1 inhibitor, glyburide, significantly inhibited virus infection suggesting it had off-target effects on related enzymes or interfered with infection via non-enzymatic mechanisms. Collectively, these studies demonstrated that BoHV-1 infection stimulated inflammasome formation, which we predict is important for clinical symptoms in cattle.

KEYWORDS:

BoHV-1; Caspase 1; DNA sensor IFI16; Inflammasome; NLRP3

PMID:
24657787
DOI:
10.1016/j.virusres.2014.03.006
[Indexed for MEDLINE]
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