This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ray, R.
Right arrow Articles by Belshe, R. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ray, R.
Right arrow Articles by Belshe, R. B.

 Previous Article  |  Next Article 

J. Virol., Mar 1995, 1959-1963, Vol 69, No. 3
Copyright © 1995, American Society for Microbiology

Characterization of a live, attenuated human parainfluenza type 3 virus candidate vaccine strain

R Ray, K Meyer, FK Newman and RB Belshe
Division of Infectious Diseases and Immunology, Saint Louis University Health Sciences Center, Missouri 63110.

Characterization of a temperature-sensitive and live, attenuated human parainfluenza type 3 virus strain (cp45) grown at a permissive temperature (32 degrees C) suggested that the virus efficiently multiplies in cell lines and retains antigenic and functional properties of the envelope glycoproteins. When grown at a nonpermissive temperature (39.5 degrees C), the cp45 virus exhibited poor replication; however, shifting to a permissive temperature allowed virus growth. Although at a nonpermissive temperature virus polypeptide synthesis was significantly reduced, the hemagglutinin-neuraminidase and fusion glycoproteins were transported to cell surfaces and retained their characteristic biologic activities. Studies on mRNA synthesis from the P protein gene suggested a poor transcriptional activity of the cp45 virus at a nonpermissive temperature. Results from this study indicate that the temperature sensitivity of cp45 virus is related to altered transcriptional activity and a marked reduction in virus polypeptide synthesis.


This article has been cited by other articles:

  • Ray, R. B., Steele, R., Meyer, K., Ray, R. (1997). Transcriptional Repression of p53 Promoter by Hepatitis C Virus Core Protein. J. Biol. Chem. 272: 10983-10986 [Abstract] [Full Text]