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Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil

BACKGROUND: HBV genotype F is primarily found in indigenous populations from South America and is classified in four subgenotypes (F1 to F4). Subgenotype F2a is the most common in Brazil among genotype F cases. The aim of this study was to characterize HBV genotype F2a circulating in 16 patients fro...

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Autores principales: Alvarado-Mora, Mónica V, Botelho-Lima, Livia S, Santana, Rubia A, Sitnik, Roberta, Ferreira, Paulo Abrão, do Amaral Mello, Francisco, Mangueira, Cristovão P, Carrilho, Flair J, R Rebello Pinho, João
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015599/
https://www.ncbi.nlm.nih.gov/pubmed/24139701
http://dx.doi.org/10.1186/1756-0500-6-423
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author Alvarado-Mora, Mónica V
Botelho-Lima, Livia S
Santana, Rubia A
Sitnik, Roberta
Ferreira, Paulo Abrão
do Amaral Mello, Francisco
Mangueira, Cristovão P
Carrilho, Flair J
R Rebello Pinho, João
author_facet Alvarado-Mora, Mónica V
Botelho-Lima, Livia S
Santana, Rubia A
Sitnik, Roberta
Ferreira, Paulo Abrão
do Amaral Mello, Francisco
Mangueira, Cristovão P
Carrilho, Flair J
R Rebello Pinho, João
author_sort Alvarado-Mora, Mónica V
collection PubMed
description BACKGROUND: HBV genotype F is primarily found in indigenous populations from South America and is classified in four subgenotypes (F1 to F4). Subgenotype F2a is the most common in Brazil among genotype F cases. The aim of this study was to characterize HBV genotype F2a circulating in 16 patients from São Paulo, Brazil. Samples were collected between 2006 and 2012 and sent to Hospital Israelita Albert Einstein. A fragment of 1306 bp partially comprising HBsAg and DNA polymerase coding regions was amplified and sequenced. Viral sequences were genotyped by phylogenetic analysis using reference sequences from GenBank (n=198), including 80 classified as subgenotype F2a. Bayesian Markov chain Monte Carlo simulation implemented in BEAST v.1.5.4 was applied to obtain the best possible estimates using the model of nucleotide substitutions GTR+G+I. FINDINGS: It were identified three groups of sequences of subgenotype F2a: 1) 10 sequences from São Paulo state; 2) 3 sequences from Rio de Janeiro and one from São Paulo states; 3) 8 sequences from the West Amazon Basin. CONCLUSIONS: These results showing for the first time the distribution of F2a subgenotype in Brazil. The spreading and the dynamic of subgenotype F2a in Brazil requires the study of a higher number of samples from different regions as it is unfold in almost all Brazilian populations studied so far. We cannot infer with certainty the origin of these different groups due to the lack of available sequences. Nevertheless, our data suggest that the common origin of these groups probably occurred a long time ago.
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spelling pubmed-40155992014-05-10 Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil Alvarado-Mora, Mónica V Botelho-Lima, Livia S Santana, Rubia A Sitnik, Roberta Ferreira, Paulo Abrão do Amaral Mello, Francisco Mangueira, Cristovão P Carrilho, Flair J R Rebello Pinho, João BMC Res Notes Short Report BACKGROUND: HBV genotype F is primarily found in indigenous populations from South America and is classified in four subgenotypes (F1 to F4). Subgenotype F2a is the most common in Brazil among genotype F cases. The aim of this study was to characterize HBV genotype F2a circulating in 16 patients from São Paulo, Brazil. Samples were collected between 2006 and 2012 and sent to Hospital Israelita Albert Einstein. A fragment of 1306 bp partially comprising HBsAg and DNA polymerase coding regions was amplified and sequenced. Viral sequences were genotyped by phylogenetic analysis using reference sequences from GenBank (n=198), including 80 classified as subgenotype F2a. Bayesian Markov chain Monte Carlo simulation implemented in BEAST v.1.5.4 was applied to obtain the best possible estimates using the model of nucleotide substitutions GTR+G+I. FINDINGS: It were identified three groups of sequences of subgenotype F2a: 1) 10 sequences from São Paulo state; 2) 3 sequences from Rio de Janeiro and one from São Paulo states; 3) 8 sequences from the West Amazon Basin. CONCLUSIONS: These results showing for the first time the distribution of F2a subgenotype in Brazil. The spreading and the dynamic of subgenotype F2a in Brazil requires the study of a higher number of samples from different regions as it is unfold in almost all Brazilian populations studied so far. We cannot infer with certainty the origin of these different groups due to the lack of available sequences. Nevertheless, our data suggest that the common origin of these groups probably occurred a long time ago. BioMed Central 2013-10-21 /pmc/articles/PMC4015599/ /pubmed/24139701 http://dx.doi.org/10.1186/1756-0500-6-423 Text en Copyright © 2013 Alvarado-Mora et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Alvarado-Mora, Mónica V
Botelho-Lima, Livia S
Santana, Rubia A
Sitnik, Roberta
Ferreira, Paulo Abrão
do Amaral Mello, Francisco
Mangueira, Cristovão P
Carrilho, Flair J
R Rebello Pinho, João
Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil
title Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil
title_full Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil
title_fullStr Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil
title_full_unstemmed Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil
title_short Distribution of hepatitis B virus subgenotype F2a in São Paulo, Brazil
title_sort distribution of hepatitis b virus subgenotype f2a in são paulo, brazil
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015599/
https://www.ncbi.nlm.nih.gov/pubmed/24139701
http://dx.doi.org/10.1186/1756-0500-6-423
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