Severe Acute Respiratory Syndrome Coronavirus 7a Accessory Protein Is a Viral Structural Protein
Open Access
- 1 August 2006
- journal article
- research article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 80 (15), 7287-7294
- https://doi.org/10.1128/jvi.00414-06
Abstract
Severe acute respiratory syndrome coronavirus (SCoV) 7a protein is one of the viral accessory proteins. In expressing cells, 7a protein exhibits a variety of biological activities, including induction of apoptosis, activation of the mitogen-activated protein kinase signaling pathway, inhibition of host protein translation, and suppression of cell growth progression. Analysis of SCoV particles that were purified by either sucrose gradient equilibrium centrifugation or a virus capture assay, in which intact SCoV particles were specifically immunoprecipitated by anti-S protein monoclonal antibody, demonstrated that 7a protein was associated with purified SCoV particles. Coexpression of 7a protein with SCoV S, M, N, and E proteins resulted in production of virus-like particles (VLPs) carrying 7a protein, while 7a protein was not released from cells expressing 7a protein alone. Although interaction between 7a protein and another SCoV accessory protein, 3a, has been reported, 3a protein was dispensable for assembly of 7a protein into VLPs. S protein was not required for the 7a protein incorporation into VLPs, and yet 7a protein interacted with S protein in coexpressing cells. These data established that, in addition to 3a protein, 7a protein was a SCoV accessory protein identified as a SCoV structural protein.Keywords
This publication has 56 references indexed in Scilit:
- The putative protein 6 of the severe acute respiratory syndrome‐associated coronavirus: Expression and functional characterizationFEBS Letters, 2005
- Bats Are Natural Reservoirs of SARS-Like CoronavirusesScience, 2005
- The severe acute respiratory syndrome coronavirus 3a is a novel structural proteinBiochemical and Biophysical Research Communications, 2005
- Efficient assembly and release of SARS coronavirus‐like particles by a heterologous expression systemFEBS Letters, 2004
- Characterization of the 3a Protein of SARS-associated Coronavirus in Infected Vero E6 Cells and SARS PatientsJournal of Molecular Biology, 2004
- Phosphorylation of p38 MAPK and its downstream targets in SARS coronavirus-infected cellsBiochemical and Biophysical Research Communications, 2004
- Assembly of human severe acute respiratory syndrome coronavirus-like particlesBiochemical and Biophysical Research Communications, 2004
- Identification of a novel protein 3a from severe acute respiratory syndrome coronavirusFEBS Letters, 2004
- The Genome Sequence of the SARS-Associated CoronavirusScience, 2003
- Characterization of a Novel Coronavirus Associated with Severe Acute Respiratory SyndromeScience, 2003