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Viral immunogenicity determines epidemiological fitness in a cohort of DENV-1 infection in Brazil.

Tauyne Menegaldo Pinheiro | Mânlio Tasso de Oliveira Mota | Aripuanã Sakurada Aranha Watanabe | Joice Matos Biselli-Périco | Betânia Paiva Drumond | Milene Rocha Ribeiro | Danila Vedovello | João Pessoa Araújo | Paulo Filemon Paolucci Pimenta | Bárbara Aparecida Chaves | Mayara Marques Carneiro da Silva | Izabella Cristina Andrade Batista | Michelle Premazzi Papa | Lana Monteiro Meuren | Carolina Gonçalves de Oliveira Lucas | Flavio Lemos Matassoli | Laura Helena Vega Gonzales Gil | Adriana Bozzi | Carlos Eduardo Calzavara-Silva | Luciana Barros de Arruda | Danielle da Glória de Souza | Mauro Martins Teixeira | Nikos Vasilakis | Maurício Lacerda Nogueira
PLoS neglected tropical diseases | 2018

The dynamics of dengue virus (DENV) circulation depends on serotype, genotype and lineage replacement and turnover. In São José do Rio Preto, Brazil, we observed that the L6 lineage of DENV-1 (genotype V) remained the dominant circulating lineage even after the introduction of the L1 lineage. We investigated viral fitness and immunogenicity of the L1 and L6 lineages and which factors interfered with the dynamics of DENV epidemics. The results showed a more efficient replicative fitness of L1 over L6 in mosquitoes and in human and non-human primate cell lines. Infections by the L6 lineage were associated with reduced antigenicity, weak B and T cell stimulation and weak host immune system interactions, which were associated with higher viremia. Our data, therefore, demonstrate that reduced viral immunogenicity and consequent greater viremia determined the increased epidemiological fitness of DENV-1 L6 lineage in São José do Rio Preto.

Pubmed ID: 29813061

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ATCC (tool)

RRID:SCR_001672

Global nonprofit biological resource center (BRC) and research organization that provides biological products, technical services and educational programs to private industry, government and academic organizations. Its mission is to acquire, authenticate, preserve, develop and distribute biological materials, information, technology, intellectual property and standards for the advancement and application of scientific knowledge. The primary purpose of ATCC is to use its resources and experience as a BRC to become the world leader in standard biological reference materials management, intellectual property resource management and translational research as applied to biomaterial development, standardization and certification. ATCC characterizes cell lines, bacteria, viruses, fungi and protozoa, as well as develops and evaluates assays and techniques for validating research resources and preserving and distributing biological materials to the public and private sector research communities.

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RRID:SCR_002760

NIH genetic sequence database that provides annotated collection of all publicly available DNA sequences for almost 280 000 formally described species (Jan 2014) .These sequences are obtained primarily through submissions from individual laboratories and batch submissions from large-scale sequencing projects, including whole-genome shotgun (WGS) and environmental sampling projects. Most submissions are made using web-based BankIt or standalone Sequin programs, and GenBank staff assigns accession numbers upon data receipt. It is part of International Nucleotide Sequence Database Collaboration and daily data exchange with European Nucleotide Archive (ENA) and DNA Data Bank of Japan (DDBJ) ensures worldwide coverage. GenBank is accessible through NCBI Entrez retrieval system, which integrates data from major DNA and protein sequence databases along with taxonomy, genome, mapping, protein structure and domain information, and biomedical journal literature via PubMed. BLAST provides sequence similarity searches of GenBank and other sequence databases. Complete bimonthly releases and daily updates of GenBank database are available by FTP.

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Bio-Rad Laboratories (tool)

RRID:SCR_008426

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Clustal W2 (tool)

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THIS RESOURCE IS NO LONGER IN SERVICE, documented on January 19, 2022. Command line version of multiple sequence alignment program Clustal for DNA or proteins. Alignment is progressive and considers sequence redundancy. No longer being maintained. Please consider using Clustal Omega instead which accepts nucleic acid or protein sequences in multiple sequence formats NBRF/PIR, EMBL/UniProt, Pearson (FASTA), GDE, ALN/ClustalW, GCG/MSF, RSF.

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BEAST (tool)

RRID:SCR_010228

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RRID:SCR_010519

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Hep-G2 (tool)

RRID:CVCL_0027

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RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

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