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Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007

Global dengue virus spread in tropical and sub-tropical regions has become a major international public health concern. It is evident that DENV genetic diversity plays a significant role in the immunopathology of the disease and that the identification of polymorphisms associated with adaptive respo...

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Autores principales: Villabona-Arenas, Christian Julian, Mondini, Adriano, Bosch, Irene, Schimitt, Diane, Calzavara-Silva, Carlos E., de A Zanotto, Paolo M., Nogueira, Maurício L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646734/
https://www.ncbi.nlm.nih.gov/pubmed/23667626
http://dx.doi.org/10.1371/journal.pone.0063496
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author Villabona-Arenas, Christian Julian
Mondini, Adriano
Bosch, Irene
Schimitt, Diane
Calzavara-Silva, Carlos E.
de A Zanotto, Paolo M.
Nogueira, Maurício L.
author_facet Villabona-Arenas, Christian Julian
Mondini, Adriano
Bosch, Irene
Schimitt, Diane
Calzavara-Silva, Carlos E.
de A Zanotto, Paolo M.
Nogueira, Maurício L.
author_sort Villabona-Arenas, Christian Julian
collection PubMed
description Global dengue virus spread in tropical and sub-tropical regions has become a major international public health concern. It is evident that DENV genetic diversity plays a significant role in the immunopathology of the disease and that the identification of polymorphisms associated with adaptive responses is important for vaccine development. The investigation of naturally occurring genomic variants may play an important role in the comprehension of different adaptive strategies used by these mutants to evade the human immune system. In order to elucidate this role we sequenced the complete polyprotein-coding region of thirty-three DENV-3 isolates to characterize variants circulating under high endemicity in the city of São José de Rio Preto, Brazil, during the onset of the 2006-07 epidemic. By inferring the evolutionary history on a local-scale and estimating rates of synonymous (dS) and nonsynonimous (dN) substitutions, we have documented at least two different introductions of DENV-3 into the city and detected 10 polymorphic codon sites under significant positive selection (dN/dS > 1) and 8 under significant purifying selection (dN/dS < 1). We found several polymorphic amino acid coding sites in the envelope (15), NS1 (17), NS2A (11), and NS5 (24) genes, which suggests that these genes may be experiencing relatively recent adaptive changes. Furthermore, some polymorphisms correlated with changes in the immunogenicity of several epitopes. Our study highlights the existence of significant and informative DENV variability at the spatio-temporal scale of an urban outbreak.
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spelling pubmed-36467342013-05-10 Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007 Villabona-Arenas, Christian Julian Mondini, Adriano Bosch, Irene Schimitt, Diane Calzavara-Silva, Carlos E. de A Zanotto, Paolo M. Nogueira, Maurício L. PLoS One Research Article Global dengue virus spread in tropical and sub-tropical regions has become a major international public health concern. It is evident that DENV genetic diversity plays a significant role in the immunopathology of the disease and that the identification of polymorphisms associated with adaptive responses is important for vaccine development. The investigation of naturally occurring genomic variants may play an important role in the comprehension of different adaptive strategies used by these mutants to evade the human immune system. In order to elucidate this role we sequenced the complete polyprotein-coding region of thirty-three DENV-3 isolates to characterize variants circulating under high endemicity in the city of São José de Rio Preto, Brazil, during the onset of the 2006-07 epidemic. By inferring the evolutionary history on a local-scale and estimating rates of synonymous (dS) and nonsynonimous (dN) substitutions, we have documented at least two different introductions of DENV-3 into the city and detected 10 polymorphic codon sites under significant positive selection (dN/dS > 1) and 8 under significant purifying selection (dN/dS < 1). We found several polymorphic amino acid coding sites in the envelope (15), NS1 (17), NS2A (11), and NS5 (24) genes, which suggests that these genes may be experiencing relatively recent adaptive changes. Furthermore, some polymorphisms correlated with changes in the immunogenicity of several epitopes. Our study highlights the existence of significant and informative DENV variability at the spatio-temporal scale of an urban outbreak. Public Library of Science 2013-05-07 /pmc/articles/PMC3646734/ /pubmed/23667626 http://dx.doi.org/10.1371/journal.pone.0063496 Text en © 2013 Villabona-Arenas et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Villabona-Arenas, Christian Julian
Mondini, Adriano
Bosch, Irene
Schimitt, Diane
Calzavara-Silva, Carlos E.
de A Zanotto, Paolo M.
Nogueira, Maurício L.
Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007
title Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007
title_full Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007
title_fullStr Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007
title_full_unstemmed Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007
title_short Dengue Virus Type 3 Adaptive Changes during Epidemics in São Jose de Rio Preto, Brazil, 2006–2007
title_sort dengue virus type 3 adaptive changes during epidemics in são jose de rio preto, brazil, 2006–2007
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646734/
https://www.ncbi.nlm.nih.gov/pubmed/23667626
http://dx.doi.org/10.1371/journal.pone.0063496
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