Article
Molecular analysis of yellow fever virus 17DD vaccine strain
Registro en:
POST, Paulo R. et al. Molecular analysis of yellow fever virus 17DD vaccine strain. Memórias do Instituto Oswaldo Cruz, Rio de Janeiro, v. 96, n. 2, p. 239-246, Apr./June 1991.
0074-0276
10.1590/S0074-02761991000200015
1678-8060
Autor
Post, Paulo R.
Santos, Claudia N. D.
Carvalho, Ricardo
Lopes, Oscar S.
Galler, Ricardo
Resumen
The Oswaldo Cruz Foundation produces most of the yellow fever (YF) vaccine prepared world wide. As part of a broader approach to determine the genetic variability in YF l7D seeds and vaccines and its relevance to viral attenuation the 17DD virus was purifed directly from chick embryo homogenates which is the source of virus used for vaccination of millions of people in Brazil and other countries for half a century. Neutralization and hemagglutination tests showed that the purified virus is similar to the original stock. Furthermore, radioimmune precipitation of 35S-methionine-labeled viral proteins using mouse hyperimmune ascitic fluid revealed identical patterns for the purified 17DD virus and the YF l7D-204 strain except for the 17DD E protein which migrated slower on SDS-PAGE. This difference is likely to be due to N-linked glycosylation. Finally, comparison by northern blot nybridization of virion RNAs of purified 17DD with two other strains of YF virus only fenome-sized molecules for all three viruses. These observations suggest that vaccine phenotype is primarily associated with the accumulation of mutations.