Preliminary analysis on respiratory syncytial virus identified in children with acute respiratory infections in Tibet Autonomous Region, China.
- Author:
Jie DENG
1
;
Ru-Nan ZHU
;
Yuan QIAN
;
Yu SUN
;
Lin-Qing ZHAO
;
Fang WANG
;
Hong WU
;
Min-Na SHAN
;
Mei-Duo DEJI
Author Information
1. Laboratory of Virology, Beijing Municipal Laboratory of Infection and Immunity, Capital Institute of Pediatrics, Beijing 100020, China. jie_deng@sina.com
- Publication Type:Journal Article
- MeSH:
Acute Disease;
Amino Acid Sequence;
Female;
Humans;
Infant;
Male;
Molecular Sequence Data;
Phylogeny;
Respiratory Syncytial Virus Infections;
virology;
Respiratory Syncytial Viruses;
chemistry;
classification;
genetics;
isolation & purification;
Respiratory Tract Infections;
virology;
Sequence Alignment;
Tibet;
Viral Proteins;
chemistry;
genetics
- From:
Chinese Journal of Virology
2012;28(2):97-102
- CountryChina
- Language:Chinese
-
Abstract:
To understand the role of respiratory syncytial virus (RSV) in children with acute respiratory infections (ARI) in Tibet Autonomous Region and the contribution of two major groups of RSV, nasopharyngeal aspirates (NPA) were collected from hospitalized children with ARI in Department of Pediatrics, Tibet People's Hospital in Lasa, Tibet from April to July in 2011 and tested for seven common respiratory viruses and human metapneumovirus (hMPV) by direct immunofluorescence assay (DFA). Total RNAs were extracted from RSV positive samples by DFA and reverse transcripted to cDNA. Nested-PCR was employed to determine the genogroups of RSV, which were confirmed by real time-PCR and sequence analysis for G protein encoding gene. The Characteristics and variations of G genes from RSV in this project were identified by sequence comparison with those G genes in GenBank. Out of 167 samples, 65 were positive for respiratory viruses with a total positive rate of 38.9%, including 45 (69.2%, 45/65)positive samples for RSV. Among 42 samples that were positive for RSV and genotyped, 40 were identified as group A and 2 as group B. Sequence analysis of full-length G genes for 7 RSV of group A indicated that all of these belonged to subgroup GA2. The nucleotide identities between RSVs from Tibet and prototype A2 strain were 90.7%-91.8%, with 86.5%-87.2% identities of amino acid. The mutations of amino acids were mainly located in both ends of a highly conserved region in the ectodomain of the G proteins. The data indicated that RSV was the most important viral etiologic agent of ARI in spring of 2011 in Tibet and group A of RSV was predominant during the study period. High divergence existed in the ectodomain of G proteins of RSVs from Tibet.
