Title
Differences in viral load among human respiratory syncytial virus genotypes in hospitalized children with severe acute respiratory infections in the Philippines
Date Issued
27 June 2016
Access level
open access
Resource Type
journal article
Author(s)
Kadji F.M.N.
Okamoto M.
Furuse Y.
Tamaki R.
Suzuki A.
Lirio I.
Dapat C.
Malasao R.
Saito M.
Pedrera-Rico G.A.G.
Tallo V.
Lupisan S.
Oshitani H.
Tohoku University
Publisher(s)
BioMed Central Ltd.
Abstract
Background: Human respiratory syncytial virus (HRSV) is a leading viral etiologic agent of pediatric lower respiratory infections, including bronchiolitis and pneumonia. Two antigenic subgroups, HRSV-A and B, each contain several genotypes. While viral load may vary among HRSV genotypes and affect the clinical course of disease, data are scarce regarding the actual differences among genotypes. Therefore, this study estimated and compared viral load among NA1 and ON1 genotypes of HRSV-A and BA9 of HRSV-B. ON1 is a newly emerged genotype with a 72-nucleotide duplication in the G gene as observed previously with BA genotypes in HRSV-B. Findings: Children <5 years of age with an initial diagnosis of severe or very severe pneumonia at a hospital in the Philippines from September 2012 to December 2013 were enrolled. HRSV genotypes were determined and the viral load measured from nasopharyngeal swabs (NPS). The viral load of HRSV genotype NA1 were significantly higher than those of ON1 and BA9. Regression analysis showed that both genotype NA1 and younger age were significantly associated with high HRSV viral load. Conclusions: The viral load of NA1 was higher than that of ON1 and BA9 in NPS samples. HRSV genotypes may be associated with HRSV viral load. The reasons and clinical impacts of these differences in viral load among HRSV genotypes require further evaluation.
Volume
13
Issue
1
Language
English
OCDE Knowledge area
Virología
Sistema respiratorio
Subjects
Scopus EID
2-s2.0-84976602684
PubMed ID
Source
Virology Journal
ISSN of the container
1743422X
Sponsor(s)
We are grateful to the staff of Biliran Provincial Hospital and Tohoku-RITM Collaborating Research Center on Emerging and Reemerging Diseases. We also thank R. Kojima, S. Abe, M. Kishi, and M. Estanislao for their technical assistance. This work was supported by a grant-in-aid from the Japan Initiative for Global Research Network on Infectious Diseases (J-GRID) from Japan Agency for Medical Research and Development (AMED), Japan, Science and Technology Research Partnership for Sustainable Development (SATREPS) from Japan International Cooperation Agency (JICA) and AMED.
Sources of information:
Directorio de Producción Científica
Scopus