Analysis of genetic variability and mapping of point mutations in influenza virus by the RNase A mismatch cleavage method

We have applied the RNase A mismatch cleavage method to analyze genetic variability in RNA viruses by using influenza virus as a model system. Uniformly labeled RNA probes synthesized from a cloned hemagglutinin gene of a given viral strain were hybridized to RNA isolated from other strains of chara...

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Detalhes bibliográficos
Autores: Lopez-Galindez, Luis Cecilio; Lopez, Juan Antonio; Melero, Jose Antonio; Fuente, Luis de la; Martínez, Concepción; Ortin, Juan; Perucho, Manuel
Tipo de documento: Artigo
Data de publicação:1988
País:España
Recursos:Instituto de Salud Carlos III (ISCIII)
Repositório:Repisalud
Idioma:Inglês
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/7734
Acesso em linha:http://hdl.handle.net/20.500.12105/7734
Nível de acesso:Acesso aberto
Palavra-chave:Animals
Cell Line
Chick Embryo
Influenza A virus
Nucleic Acid Hybridization
Plasmids
Ribonuclease, Pancreatic
Genes, Viral
Genetic Variation
Mutation
Descrição
Resumo:We have applied the RNase A mismatch cleavage method to analyze genetic variability in RNA viruses by using influenza virus as a model system. Uniformly labeled RNA probes synthesized from a cloned hemagglutinin gene of a given viral strain were hybridized to RNA isolated from other strains of characterized or uncharacterized genetic composition. The RNA.RNA heteroduplexes containing a variable number of base mismatches were digested with RNase A, and the resistant products were analyzed by denaturing polyacrylamide gel electrophoresis. We show that many of these single base mismatches are cleaved by RNase A, generating unique and characteristic patterns of resistant RNA fragments specific for each of the different viral strains. Comparative analysis of the cleavage patterns allows a qualitative estimation of the genetic relatedness and evolution of field strains. We also show that cleavage by RNase A at single base mismatches can readily detect and localize point mutations present in monoclonal antibody-resistant variants. This method should have wide applications in the study of RNA viruses, not only for epidemiological analysis but also in some diagnostic problems, such as characterization of phenotypic mutants.