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Simple protocol for population (Sanger) sequencing for Zika virus genomic regions
Cabral, Gabriela Bastos; Ferreira, João Leandro de Paula; Souza, Renato Pereira de; Cunha, Mariana Sequetin; Luchs, Adriana; Figueiredo, Cristina Adelaide; Brígido, Luís Fernando de Macedo.
Afiliación
  • Cabral, Gabriela Bastos; Instituto Adolfo Lutz. Centro de Virologia. Núcleo de Doenças Sanguíneas e Sexuais. São Paulo. BR
  • Ferreira, João Leandro de Paula; Instituto Adolfo Lutz. Centro de Virologia. Núcleo de Doenças Sanguíneas e Sexuais. São Paulo. BR
  • Souza, Renato Pereira de; Instituto Adolfo Lutz. Centro de Virologia. Núcleo de Doenças Sanguíneas e Sexuais. São Paulo. BR
  • Cunha, Mariana Sequetin; Instituto Adolfo Lutz. Centro de Virologia. Núcleo de Doenças Sanguíneas e Sexuais. São Paulo. BR
  • Luchs, Adriana; Instituto Adolfo Lutz. Centro de Virologia. Núcleo de Doenças Sanguíneas e Sexuais. São Paulo. BR
  • Figueiredo, Cristina Adelaide; Instituto Adolfo Lutz. Centro de Virologia. Núcleo de Doenças Sanguíneas e Sexuais. São Paulo. BR
  • Brígido, Luís Fernando de Macedo; Instituto Adolfo Lutz. Centro de Virologia. Núcleo de Doenças Sanguíneas e Sexuais. São Paulo. BR
Mem. Inst. Oswaldo Cruz ; 113(1): 38-44, Jan. 2018. tab, graf
Article en En | LILACS | ID: biblio-894888
Biblioteca responsable: BR1.1
ABSTRACT
BACKGROUND A number of Zika virus (ZIKV) sequences were obtained using Next-generation sequencing (NGS), a methodology widely applied in genetic diversity studies and virome discovery. However Sanger method is still a robust, affordable, rapid and specific tool to obtain valuable sequences. OBJECTIVE The aim of this study was to develop a simple and robust Sanger sequencing protocol targeting ZIKV relevant genetic regions, as envelope protein and nonstructural protein 5 (NS5). In addition, phylogenetic analysis of the ZIKV strains obtained using the present protocol and their comparison with previously published NGS sequences were also carried out. METHODS Six Vero cells isolates from serum and one urine sample were available to develop the procedure. Primer sets were designed in order to conduct a nested RT-PCR and a Sanger sequencing protocols. Bayesian analysis was used to infer phylogenetic relationships. FINDINGS Seven complete ZIKV envelope protein (1,571 kb) and six partial NS5 (0,798 Kb) were obtained using the protocol, with no amplification of NS5 gene from urine sample. Two NS5 sequences presented ambiguities at positions 495 and 196. Nucleotide analysis of a Sanger sequence and consensus sequence of previously NGS study revealed 100% identity. ZIKV strains described here clustered within the Asian lineage. MAIN CONCLUSIONS The present study provided a simple and low-cost Sanger protocol to sequence relevant genes of the ZIKV genome. The identity of Sanger generated sequences with published consensus NGS support the use of Sanger method for ZIKV population studies. The regions evaluated were able to provide robust phylogenetic signals and may be used to conduct molecular epidemiological studies and monitor viral evolution.
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Texto completo: 1 Colección: 01-internacional Base de datos: LILACS Asunto principal: ARN Viral / Genoma Viral / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Virus Zika Idioma: En Revista: Mem. Inst. Oswaldo Cruz Asunto de la revista: MEDICINA TROPICAL / PARASITOLOGIA Año: 2018 Tipo del documento: Article / Project document País de afiliación: Brasil Pais de publicación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: LILACS Asunto principal: ARN Viral / Genoma Viral / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Virus Zika Idioma: En Revista: Mem. Inst. Oswaldo Cruz Asunto de la revista: MEDICINA TROPICAL / PARASITOLOGIA Año: 2018 Tipo del documento: Article / Project document País de afiliación: Brasil Pais de publicación: Brasil