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Genetic basis of attenuation of the Sabin type 3 oral poliovirus vaccine.
Authors:G D Westrop   K A Wareham   D M Evans   G Dunn   P D Minor   D I Magrath   F Taffs   S Marsden   M A Skinner   G C Schild  et al.
Affiliation:Department of Microbiology, University of Reading, United Kingdom.
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.
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