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Journal of Virology, August 2008, p. 7721-7724, Vol. 82, No. 15
0022-538X/08/$08.00+0 doi:10.1128/JVI.00304-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland 20892,1 Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB), Nacional de Biotecnología (CSIC), Campus Universidad Autónoma, Darwin 3, Cantoblanco, 28049 Madrid, Spain,2 Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina 27599,3 Infectious Diseases Pathology Activity, Centers for Disease Control and Prevention, Atlanta, Georgia 303334
Received 11 February 2008/ Accepted 29 April 2008
The immunogenicity and protective efficacy of a live attenuated vaccine consisting of a recombinant severe acute respiratory syndrome (SARS) coronavirus lacking the E gene (rSARS-CoV-
E) were studied using hamsters. Hamsters immunized with rSARS-CoV-
E developed high serum-neutralizing antibody titers and were protected from replication of homologous (SARS-CoV Urbani) and heterologous (GD03) SARS-CoV in the upper and lower respiratory tract. rSARS-CoV-
E-immunized hamsters remained active following wild-type virus challenge, while mock-immunized hamsters displayed decreased activity. Despite being attenuated in replication in the respiratory tract, rSARS-CoV-
E is an immunogenic and efficacious vaccine in hamsters.
Published ahead of print on 7 May 2008.
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