Abstract
Of the 55 point mutations which distinguish the type 1 poliovirus vaccine strain (Sabin 1) from its neurovirulent progenitor (P1/Mahoney), two have been strongly implicated by previous studies as determinants of the attenuation phenotype. A change of an A to a G at position 480, located within the 5' noncoding region, has been suggested to be the major attenuating mutation, analogous to the mutations at positions 481 and 472 in poliovirus types 2 and 3, respectively. In addition, the change of a U to a C at position 6203, resulting in an amino acid change in the polymerase protein 3D, has also been implicated as a determinant of attenuation, albeit to a lesser extent. To assess the contributions of these mutations to attenuation and temperature sensitivity, reciprocal changes were generated at these positions in infectious cDNA clones of Sabin 1 and P1/Mahoney. Assays in tissue culture and primates indicated that the two mutations make some contribution to the temperature sensitivity of the Sabin 1 strain but that neither is a strong determinant of attenuation.
Original language | English |
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Pages (from-to) | 7601-5 |
Number of pages | 5 |
Journal | Journal of Virology |
Volume | 69 |
Issue number | 12 |
Publication status | Published - Dec 1995 |
Keywords
- Cell Line
- Cloning, Molecular
- Cytosine
- DNA, Complementary
- Genome, Viral
- Guanine
- Humans
- Nucleic Acid Conformation
- Phenotype
- Point Mutation
- Poliovirus
- Poliovirus Vaccine, Oral
- RNA, Viral
- Tumor Cells, Cultured
- Uracil
- Vaccines, Attenuated
- Virulence