Molecular Characterization of Attenuated Vaccine Strains of Transmissible Gastroenteritis Virus
Open Access
- 1 January 1994
- journal article
- research article
- Published by SAGE Publications in Journal of Veterinary Diagnostic Investigation
- Vol. 6 (1) , 16-22
- https://doi.org/10.1177/104063879400600104
Abstract
Previous studies in our laboratory demonstrated that 2 attenuated strains of transmissible gastroenteritis virus (TGEV) contain deletions affecting messenger (m) RNAs 2, 3, or 4. In this report, we have compared mRNAs of four modified-live virus vaccines for TGEV with the virulent Miller PP3 isolate to determine whether any transcriptional patterns are shared among attenuated strains. Using northern blot analysis, all vaccine viruses expressed mRNAs indistinguishable in size from those of Miller PP3. However, using S1 nuclease protection experiments, alterations in the regions of the genome from which mRNAs 2 and 3 are transcribed were detected in 2 of the vaccine strains. When genomic cDNA fragments derived from the coding region for mRNA 2 were sequenced, a 6-nucleotide deletion, also found in the attenuated strain Purdue- 115, was discovered. The product of mRNA 2, a spike glycoprotein, was visualized by western blotting for each vaccine strain, and no profound differences in mobility were detected relative to Miller PP3. Alterations in the region of the genome from which mRNA 3 is transcribed appear to be identical or very similar to sequence alterations already described in this region for Purdue- 115, one of which is likely to alter the polypeptide product of mRNA 3. Insertions or deletions in mRNAs 2 or 3 may contribute to attenuation but are not a prerequisite for this phenotype. The S1 nuclease protection analysis is a sensitive tool for differentiating particular strains of TGEV.Keywords
This publication has 41 references indexed in Scilit:
- The cloning and sequencing of the virion protein genes from a British isolate of porcine respiratory coronavirus: comparison with transmissible gastroenteritis virus genesVirus Research, 1991
- Residues involved in the antigenic sites of transmissible gastroenteritis coronavirus S glycoproteinVirology, 1991
- Modification of a discontinuous and highly porous sodium dodecyl sulfate-polyacrylamide gel system for minigel electrophoresisAnalytical Biochemistry, 1990
- CORONAVIRUS: ORGANIZATION, REPLICATION AND EXPRESSION OF GENOMEAnnual Review of Microbiology, 1990
- Four major antigenic sites of the coronavirus transmissible gastroenteritis virus are located on the amino-terminal half of spike glycoprotein SJournal of General Virology, 1990
- Sequence of the coding regions from the 3.0 kb and 3.9 kb mRNAArchiv für die gesamte Virusforschung, 1989
- Antigenic Differentiation between Transmissible Gastroenteritis Virus of Swine and a Related Porcine Respiratory CoronavirusJournal of General Virology, 1988
- The nucleotide sequence of the peplomer gene of porcine transmissible gastroenteritis virus (TGEV): comparison with the sequence of the peplomer protein of feline infectious peritonitis virus (FIPV)Virus Research, 1987
- Monoclonal antibodies to murine hepatitis virus-4 (strain JHM) define the viral glycoprotein responsible for attachment and cell-cell fusionVirology, 1982
- Antigenicity of structural components from porcine transmissible gastroenteritis virusVeterinary Microbiology, 1979