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Genetic variability of hepatitis A virus strain HAF-203 isolated in Brazil and expression of the VP1 gene in Escherichia coli
Baptista, Marcia L; Silva, Messias; Lima, Maria Amélia de; Yoshida, Clara F. T; Gaspar, Ana Maria C; Galler, Ricardo.
  • Baptista, Marcia L; Fundacao Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Virologia. Laboratório de Hepatites Virais. Rio de Janeiro. BR
  • Silva, Messias; Fundacao Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Virologia. Laboratório de Hepatites Virais. Rio de Janeiro. BR
  • Lima, Maria Amélia de; Fundacao Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Virologia. Laboratório de Hepatites Virais. Rio de Janeiro. BR
  • Yoshida, Clara F. T; Fundacao Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Virologia. Laboratório de Hepatites Virais. Rio de Janeiro. BR
  • Gaspar, Ana Maria C; Fundacao Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Virologia. Laboratório de Desenvolvimento Tecnológico. Rio de Janeiro. BR
  • Galler, Ricardo; Fundacao Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Bioquímica e Biologia Molecular. Laboratório de Biologia Molecular de Flavivírus. Rio de Janeiro. BR
Mem. Inst. Oswaldo Cruz ; 101(7): 759-766, Nov. 2006. ilus, tab
Article in English | LILACS | ID: lil-439460
ABSTRACT
The hepatitis A virus (HAV) HAF-203 strain was isolated from an acute case of HAV infection. The primary isolation of HAF-203 in Brazil and its adaptation to the FRhK-4 cell lineage allowed the production of large amounts of viral particles enabling molecular characterization of the first HAV isolate in Brazil. The aim of our study was to determine the nucleotide sequence of the HAF-203 strain genome, compare it to other HAV genomes and highlight its genetic variability. The complete nucleotide sequence of the HAF-203 strain (7472 nucleotides) was compared to those obtained earlier by others for other HAV isolates. These analyses revealed 19 HAF-specific nucleotide sequence differences with 10 amino acid substitutions. Most of the non-conservative changes were located at VP1, 2C, and 3D genes, but the 3B region was the most variable. The availability of HAF-203 complementary DNA was useful for the production of the recombinant VP1 protein, which is a major determinant of viral infectivity. This recombinant protein was shown by enzyme-linked immunoassay and blotting, to be immunogenic and resemble the native protein, therefore suggesting its value as a reagent for incorporation into diagnostic tests.
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Full text: Available Index: LILACS (Americas) Main subject: Genetic Variation / Viral Structural Proteins / Hepatitis A virus Limits: Animals / Humans Country/Region as subject: South America / Brazil Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2006 Type: Article Affiliation country: Brazil Institution/Affiliation country: Fundacao Oswaldo Cruz/BR

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Full text: Available Index: LILACS (Americas) Main subject: Genetic Variation / Viral Structural Proteins / Hepatitis A virus Limits: Animals / Humans Country/Region as subject: South America / Brazil Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2006 Type: Article Affiliation country: Brazil Institution/Affiliation country: Fundacao Oswaldo Cruz/BR