Gene Sequence Variability of the Three Surface Proteins of Human Respiratory Syncytial Virus (HRSV) in Texas
Author
dc.contributor.author
Tapia Faúndes, Lorena
Author
dc.contributor.author
Shaw, Chad A.
es_CL
Author
dc.contributor.author
Aideyan, Letisha O.
es_CL
Author
dc.contributor.author
Jewell, Alan M.
es_CL
Author
dc.contributor.author
Dawson, Brian C.
es_CL
Author
dc.contributor.author
Haq, Taha R.
es_CL
Author
dc.contributor.author
Piedra, Pedro A.
es_CL
Admission date
dc.date.accessioned
2014-12-30T20:33:13Z
Available date
dc.date.available
2014-12-30T20:33:13Z
Publication date
dc.date.issued
2014
Cita de ítem
dc.identifier.citation
PLOS One March 2014 | Volume 9 | Issue 3 | e90786
en_US
Identifier
dc.identifier.other
DOI: 10.1371/journal.pone.0090786
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/129519
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
Human 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.