Abstract
The poliovirus type 3 Sabin oral poliovirus vaccine strain P3/Leon/12a1b differs in nucleotide sequence from its neurovirulent progenitor P3/Leon/37 by just 10 point mutations. The contribution of each mutation to the attenuation phenotype of the vaccine strain was determined by the construction of a series of recombinant viruses from infectious cDNA clones. The neurovirulence testing of recombinant viruses indicated that the attenuation phenotype is determined by just two point mutations: a C to U in the noncoding region at position 472 and a C to U at nucleotide 2034 which results in a serine-to-phenylalanine amino acid substitution in the structural protein VP3.
MeSH Terms
Amino Acid Sequence
Animals
Biological Assay
Cloning, Molecular
DNA/genetics
DNA Mutational Analysis
Genes, Viral
Nervous System/microbiology
Poliovirus/genetics,pathogenicity
Poliovirus Vaccine, Oral/genetics
RNA, Viral/genetics
Regulatory Sequences, Nucleic Acid
Structure-Activity Relationship
Vaccines, Attenuated/genetics
Chemicals
Poliovirus Vaccine, Oral
RNA, Viral
Vaccines, Attenuated
DNA
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Westrop G D
Department of Microbiology, University of Reading, United Kingdom.
Wareham K A
Evans D M
Dunn G
Minor P D
Magrath D I
Taffs F
Marsden S
Skinner M A
Schild G C
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