Adaptation of the receptor-binding preference from alpha2,3- to alpha2,6-linked sialic acid is an essential step for an avian influenza virus to transmit efficiently in human population and become a pandemic virus. The currently available assays for receptor-binding preference are complex and not widely available. A simple high-throughput screening assay will facilitate early detection of a potential pandemic virus, which is crucial for the prevention and control of the possible pandemic. We wanted to develop a simple assay to differentiate influenza viruses with alpha2,3- or alpha2,6-linked receptor-binding preference. The assay employs a specific sialidase (from Salmonella thyphimurium) that can eliminate alpha2,3-linked sialic acid from red blood cells. A reduction of hemagglutination titer indicates alpha2,3-linked receptor preference in this assay. Using a panel of H5N1 avian influenza isolates and H1/H3 human influenza isolates, as well as mutated H5 reverse genetics virus, the assay could accurately differentiate the viruses according to their receptor-binding preference. Furthermore, the assay was sufficiently sensitive to detect a minor variant with alpha2,6-linkage-specificity in a background of alpha2,3-linkage-specific virus. We have developed a simple screening assay capable of detecting avian influenza viruses that have switched their receptor-binding preference.
AnimalsErythrocytesGeeseHemagglutination TestsHemagglutinin Glycoproteins, Influenza VirusHumansInfluenza A virusInfluenza A Virus, H5N1 SubtypeReceptors, VirusSialic Acids
Structured evidence records
Evidence records
3 total
Receptor Usage2 records
Receptor UsageExtraction confidence 0.95
Key finding
H5N1 avian influenza viruses bind preferentially to alpha2,3-linked sialic acid receptors, while human H1/H3 influenza viruses show preference for alpha2,6-linked sialic acid, and the developed assay detects these receptor-binding differences.
Adaptation of the receptor-binding preference from alpha2,3- to alpha2,6-linked sialic acid is an essential step for an avian influenza virus to transmit efficiently in human population and become a pandemic virus. Using a panel of H5N1 avian influenza isolates and H1/H3 human influenza isolates, as well as mutated H5 reverse genetics virus, the assay could accurately differentiate the viruses according to their receptor-binding preference.
A minor variant with alpha2,6-linkage receptor specificity was detected within an alpha2,3-linkage-specific avian influenza virus population, indicating receptor-binding heterogeneity.
Furthermore, the assay was sufficiently sensitive to detect a minor variant with alpha2,6-linkage-specificity in a background of alpha2,3-linkage-specific virus.
Method
receptor-binding assay
Receptors
alpha2,6-linked sialic acid
Molecular Adaptation1 records
Molecular AdaptationExtraction confidence 0.95
Key finding
H5N1 avian influenza viruses showed molecular adaptation through receptor-binding preference switching from alpha2,3- to alpha2,6-linked sialic acid, a key mechanism underlying avian-to-human host adaptation.
Adaptation of the receptor-binding preference from alpha2,3- to alpha2,6-linked sialic acid is an essential step for an avian influenza virus to transmit efficiently in human population and become a pandemic virus. Using a panel of H5N1 avian influenza isolates and H1/H3 human influenza isolates, as well as mutated H5 reverse genetics virus, the assay could accurately differentiate the viruses according to their receptor-binding preference.