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Cell cycle perturbations induced by infection with the coronavirus infectious bronchitis virus and their effect on virus replication

Dove, B., Brooks, G., Bicknell, K. A., Wurm, T. and Hiscox, J. A. (2006) Cell cycle perturbations induced by infection with the coronavirus infectious bronchitis virus and their effect on virus replication. Journal of Virology, 80 (8). pp. 4147-4156. ISSN 0022-538X

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To link to this article DOI: 10.1128/jvi.80.8.4147-4156.2006

Abstract/Summary

In eukaryotic cells, cell growth and division occur in a stepwise, orderly fashion described by a process known as the cell cycle. The relationship between positive-strand RNA viruses and the cell cycle and the concomitant effects on virus replication are not clearly understood. We have shown that infection of asynchronously replicating and synchronized replicating cells with the avian coronavirus infectious bronchitis virus (IBV), a positive-strand RNA virus, resulted in the accumulation of infected cells in the G(2)/M phase of the cell cycle. Analysis of various cell cycle-regulatory proteins and cellular morphology indicated that there was a down-regulation of cyclins D1 and D2 (G(2) regulatory cyclins) and that a proportion of virus-infected cells underwent aberrant cytokinesis, in which the cells underwent nuclear, but not cytoplasmic, division. We assessed the impact of the perturbations on the cell cycle for virus-infected cells and found that IBV-infected G(2)/M-phase-synchronized cells exhibited increased viral protein production when released from the block when compared to cells synchronized in the Go phase or asynchronously replicating cells. Our data suggested that IBV induces a G(2)/M phase arrest in infected cells to promote favorable conditions for viral replication.

Item Type:Article
Refereed:Yes
Divisions:Faculty of Life Sciences > School of Biological Sciences
Faculty of Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy
Interdisciplinary centres and themes > Institute for Cardiovascular and Metabolic Research (ICMR)
ID Code:10150
Uncontrolled Keywords:HUMAN-IMMUNODEFICIENCY-VIRUS, RIBOSOME ENTRY SITE, MURINE, HEPATITIS-VIRUS, AVIAN CORONAVIRUS, NUCLEOCAPSID PROTEIN, HOST-CELL, TRANSLATIONAL REGULATION, P53-MEDIATED APOPTOSIS, SARS CORONAVIRUS, DNA-REPLICATION

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