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Intra-host diversities of the receptor-binding domain of stork faeces-derived avian H5N1 viruses and its significance as predicted by molecular dynamic simulation
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Metadata
Document Title
Intra-host diversities of the receptor-binding domain of stork faeces-derived avian H5N1 viruses and its significance as predicted by molecular dynamic simulation
Author
Ubol S, Suksatu A, Modhiran N, Sangma C, Thitithanyanont A, Fukuda M, Juthayothin T
Name from Authors Collection
Scopus Author ID
56874822000
Affiliations
Mahidol University; Kasetsart University; United States Department of Defense; United States Army; Walter Reed Army Institute of Research (WRAIR); Armed Forces Research Institute of Medical Science (AFRIMS); National Science & Technology Development Agency - Thailand; National Center Genetic Engineering & Biotechnology (BIOTEC)
Type
Article
Source Title
JOURNAL OF GENERAL VIROLOGY
Year
2011
Volume
92
Page
307-314
Open Access
Green Published, Bronze
Publisher
MICROBIOLOGY SOC
DOI
10.1099/vir.0.025973-0
Format
Abstract
Virus evolution facilitates the emergence of viruses with unpredictable impacts on human health. This study investigated intra-host variations of the receptor-binding domain (RBD) of the haemagglutinin (HA) gene of the avian H5N1 viruses obtained from the 2004 and 2005 epidemics. The results showed that the mutation frequency of the RBD ranged from 0.3 to 0.6 %. The mutations generated one consensus and several minor populations. The consensus population of the 2004 epidemic was transmitted to the 2005 outbreak with increased frequency (39 and 45%, respectively). Molecular dynamics simulation was applied to predict the significance of the variants. The results revealed that the consensus sequence (E218K/V248I) interacted unstably with sialic acid (SA) with an alpha 2,6 linkage (SA alpha 2,6Gal). Although the mutated K140R/E218K1V2481 and Y191C/E218K/V2481 sequences decreased the HA binding capacity to alpha 2,3-linked SA, they were shown to bind a2,6-linked SA with increased affinity. Moreover, the substitutions at aa 140 and 191 were positive-selection sites. These data suggest that the K140R and Y191C mutations may represent a step towards human adaptation of the avian H5N1 virus.
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
Funding Sponsor
National Science and Technology Development Agency [BT-B-01-MG-14-50092]; National Institute of Health; National Institute of Allergy and Infectious Diseases [YI-AI-5026-01]; Thailand Graduate Institute of Science and Technology (TGIST)
License
Copyright
Rights
SGM
Publication Source
WOS