Related Experiment Videos
Genome structure of mouse hepatitis virus: comparative analysis by oligonucleotide mapping
Advances in Experimental Medicine and Biology
|January 1, 1981
Summary
Mouse hepatitis virus (MHV) strains show significant genetic divergence, but MHV-3 and A59 are highly related. Specific genetic regions in MHV may correlate with viral pathogenicity and plaque variants.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Mouse hepatitis virus (MHV) is a significant pathogen with diverse natural variants.
- Understanding the genetic relatedness and variations among MHV strains is crucial for studying viral pathogenicity.
Purpose of the Study:
- To compare natural variants of mouse hepatitis viruses using T1-oligonucleotide fingerprinting.
- To identify genetic differences and similarities between specific MHV strains and plaque variants.
- To map unique oligonucleotides to specific regions of the MHV genome.
Main Methods:
- T1-oligonucleotide fingerprinting technique was employed to analyze MHV variants.
- RNA mapping was performed to locate specific oligonucleotides within the viral genome.
- Comparison of genomic sequences of different MHV strains and plaque variants.
Main Results:
- Most MHV variants showed extensive divergence, with notable exceptions like the relatedness of hepatotropic MHV-3 and nonpathogenic A59 strains.
- MHV-3 and A59 strains each contained 2-4 unique oligonucleotides, with some mapped near the 5' and 3' ends of the genome, potentially linked to pathogenicity.
- Two JHM plaque variants (DL and DS) shared most oligonucleotides but had one unique spot each, with the DL-specific oligonucleotide mapped near the 3' end.
- The MHV genome was confirmed to possess a 'cap' structure, characteristic of positive-stranded RNA viruses.
Conclusions:
- T1-oligonucleotide fingerprinting is effective in revealing genetic relationships and variations among MHV strains.
- Specific genetic regions, identified by unique oligonucleotides, may play a role in MHV pathogenicity and phenotypic variation.
- The MHV genome structure is consistent with a positive-stranded RNA virus.