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Authordc.contributor.authorTapia Faúndes, Lorena 
Authordc.contributor.authorShaw, Chad A. es_CL
Authordc.contributor.authorAideyan, Letisha O. es_CL
Authordc.contributor.authorJewell, Alan M. es_CL
Authordc.contributor.authorDawson, Brian C. es_CL
Authordc.contributor.authorHaq, Taha R. es_CL
Authordc.contributor.authorPiedra, Pedro A. es_CL
Admission datedc.date.accessioned2014-12-30T20:33:13Z
Available datedc.date.available2014-12-30T20:33:13Z
Publication datedc.date.issued2014
Cita de ítemdc.identifier.citationPLOS One March 2014 | Volume 9 | Issue 3 | e90786en_US
Identifierdc.identifier.otherDOI: 10.1371/journal.pone.0090786
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/129519
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractHuman respiratory syncytial virus (HRSV) has three surface glycoproteins: small hydrophobic (SH), attachment (G) and fusion (F), encoded by three consecutive genes (SH-G-F). A 270-nt fragment of the G gene is used to genotype HRSV isolates. This study genotyped and investigated the variability of the gene and amino acid sequences of the three surface proteins of HRSV strains collected from 1987 to 2005 from one center. Sixty original clinical isolates and 5 prototype strains were analyzed. Sequences containing SH, F and G genes were generated, and multiple alignments and phylogenetic trees were analyzed. Genetic variability by protein domains comparing virus genotypes was assessed. Complete sequences of the SHG- F genes were obtained for all 65 samples: HRSV-A = 35; HRSV-B = 30. In group A strains, genotypes GA5 and GA2 were predominant. For HRSV-B strains, the genotype GB4 was predominant from 1992 to 1994 and only genotype BA viruses were detected in 2004–2005. Different genetic variability at nucleotide level was detected between the genes, with G gene being the most variable and the highest variability detected in the 270-nt G fragment that is frequently used to genotype the virus. High variability (.10%) was also detected in the signal peptide and transmembrane domains of the F gene of HRSV A strains. Variability among the HRSV strains resulting in non-synonymous changes was detected in hypervariable domains of G protein, the signal peptide of the F protein, a not previously defined domain in the F protein, and the antigenic site Ø in the pre-fusion F. Divergent trends were observed between HRSV -A and -B groups for some functional domains. A diverse population of HRSV -A and -B genotypes circulated in Houston during an 18 year period. We hypothesize that diverse sequence variation of the surface protein genes provide HRSV strains a survival advantage in a partially immune-protected community.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherPLOS Oneen_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Títulodc.titleGene Sequence Variability of the Three Surface Proteins of Human Respiratory Syncytial Virus (HRSV) in Texasen_US
Document typedc.typeArtículo de revista


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile