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Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015

Respiratory syncytial virus (RSV) causes acute lower respiratory tract infection in infants and young children worldwide. To investigate the RSV burden in Thailand over four consecutive years (January 2012 to December 2015), we screened 3,306 samples obtained from children ≤5 years old with acute re...

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Autores principales: Thongpan, Ilada, Mauleekoonphairoj, John, Vichiwattana, Preeyaporn, Korkong, Sumeth, Wasitthankasem, Rujipat, Vongpunsawad, Sompong, Poovorawan, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661434/
https://www.ncbi.nlm.nih.gov/pubmed/29085762
http://dx.doi.org/10.7717/peerj.3970
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author Thongpan, Ilada
Mauleekoonphairoj, John
Vichiwattana, Preeyaporn
Korkong, Sumeth
Wasitthankasem, Rujipat
Vongpunsawad, Sompong
Poovorawan, Yong
author_facet Thongpan, Ilada
Mauleekoonphairoj, John
Vichiwattana, Preeyaporn
Korkong, Sumeth
Wasitthankasem, Rujipat
Vongpunsawad, Sompong
Poovorawan, Yong
author_sort Thongpan, Ilada
collection PubMed
description Respiratory syncytial virus (RSV) causes acute lower respiratory tract infection in infants and young children worldwide. To investigate the RSV burden in Thailand over four consecutive years (January 2012 to December 2015), we screened 3,306 samples obtained from children ≤5 years old with acute respiratory tract infection using semi-nested reverse-transcription polymerase chain reaction (RT-PCR). In all, 8.4% (277/3,306) of the specimens tested positive for RSV, most of which appeared in the rainy months of July to November. We then genotyped RSV by sequencing the G glycoprotein gene and performed phylogenetic analysis to determine the RSV antigenic subgroup. The majority (57.4%, 159/277) of the RSV belonged to subgroup A (RSV-A), of which NA1 genotype was the most common in 2012 while ON1 genotype became prevalent the following year. Among samples tested positive for RSV-B subgroup B (RSV-B) (42.6%, 118/277), most were genotype BA9 (92.6%, 87/94) with some BA10 and BA-C. Predicted amino acid sequence from the partial G region showed highly conserved N-linked glycosylation site at residue N237 among all RSV-A ON1 strains (68/68), and at residues N296 (86/87) and N310 (87/87) among RSV-B BA9 strains. Positive selection of key residues combined with notable sequence variations on the G gene contributed to the continued circulation of this rapidly evolving virus.
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spelling pubmed-56614342017-10-30 Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015 Thongpan, Ilada Mauleekoonphairoj, John Vichiwattana, Preeyaporn Korkong, Sumeth Wasitthankasem, Rujipat Vongpunsawad, Sompong Poovorawan, Yong PeerJ Virology Respiratory syncytial virus (RSV) causes acute lower respiratory tract infection in infants and young children worldwide. To investigate the RSV burden in Thailand over four consecutive years (January 2012 to December 2015), we screened 3,306 samples obtained from children ≤5 years old with acute respiratory tract infection using semi-nested reverse-transcription polymerase chain reaction (RT-PCR). In all, 8.4% (277/3,306) of the specimens tested positive for RSV, most of which appeared in the rainy months of July to November. We then genotyped RSV by sequencing the G glycoprotein gene and performed phylogenetic analysis to determine the RSV antigenic subgroup. The majority (57.4%, 159/277) of the RSV belonged to subgroup A (RSV-A), of which NA1 genotype was the most common in 2012 while ON1 genotype became prevalent the following year. Among samples tested positive for RSV-B subgroup B (RSV-B) (42.6%, 118/277), most were genotype BA9 (92.6%, 87/94) with some BA10 and BA-C. Predicted amino acid sequence from the partial G region showed highly conserved N-linked glycosylation site at residue N237 among all RSV-A ON1 strains (68/68), and at residues N296 (86/87) and N310 (87/87) among RSV-B BA9 strains. Positive selection of key residues combined with notable sequence variations on the G gene contributed to the continued circulation of this rapidly evolving virus. PeerJ Inc. 2017-10-27 /pmc/articles/PMC5661434/ /pubmed/29085762 http://dx.doi.org/10.7717/peerj.3970 Text en ©2017 Thongpan 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Virology
Thongpan, Ilada
Mauleekoonphairoj, John
Vichiwattana, Preeyaporn
Korkong, Sumeth
Wasitthankasem, Rujipat
Vongpunsawad, Sompong
Poovorawan, Yong
Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015
title Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015
title_full Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015
title_fullStr Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015
title_full_unstemmed Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015
title_short Respiratory syncytial virus genotypes NA1, ON1, and BA9 are prevalent in Thailand, 2012–2015
title_sort respiratory syncytial virus genotypes na1, on1, and ba9 are prevalent in thailand, 2012–2015
topic Virology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661434/
https://www.ncbi.nlm.nih.gov/pubmed/29085762
http://dx.doi.org/10.7717/peerj.3970
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