4.6 Article

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

期刊

PEERJ
卷 5, 期 -, 页码 -

出版社

PEERJ INC
DOI: 10.7717/peerj.3970

关键词

Prevalence; Respiratory syncytial virus; Thailand; G glycoprotein

资金

  1. National Research Council of Thailand
  2. National Research University Project, Office of Higher Education Commission [NRU-59-002-HR]
  3. National Science and Technology Development Agency [P-15-50004]
  4. Outstanding Professor of Thailand Research Fund [DPG5480002]
  5. Chulalongkorn University Ratchadaphiseksomphot Endowment Fund [RES560530093]
  6. Centenary Academic Development Project [CU56-HR01]
  7. Center of Excellence in Clinical Virology [GCE 58-014-30-004]
  8. King Chulalongkorn Memorial Hospital
  9. Chulalongkorn University
  10. 100th Anniversary Chulalongkorn University Fund
  11. Overseas Research Experience Scholarship for Graduate Student

向作者/读者索取更多资源

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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