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1.
Biosens Bioelectron ; 91: 46-52, 2017 May 15.
Article in English | MEDLINE | ID: mdl-27987410

ABSTRACT

Accurate diagnosis of influenza viruses is difficult and generally requires a complex process because of viral diversity and rapid mutability. In this study, we report a simple and rapid strategy for the detection and differentiation of influenza viruses using glycan-functionalized gold nanoparticles (gGNPs). This method is based on the aggregation of gGNP probes on the viral surface, which is mediated by the specific binding of the virus to the glycans. Using a set of gGNPs bearing different glycan structures, fourteen influenza virus strains, including the major subtypes currently circulating in human and avian populations, were readily differentiated from each other and from a human respiratory syncytial virus in a single-step colorimetric procedure. The results presented here demonstrate the potential of this gGNP-based system in the development of convenient and portable sensors for the clinical diagnosis and surveillance of influenza viruses.


Subject(s)
Alphainfluenzavirus/isolation & purification , Betainfluenzavirus/isolation & purification , Colorimetry/methods , Gold/chemistry , Nanoparticles/chemistry , Orthomyxoviridae Infections/virology , Polysaccharides/chemistry , Animals , Biosensing Techniques/methods , Birds/virology , Humans , Influenza in Birds/virology , Influenza, Human/virology , Alphainfluenzavirus/classification , Betainfluenzavirus/classification , Point-of-Care Testing
2.
ACS Nano ; 8(5): 4600-7, 2014 May 27.
Article in English | MEDLINE | ID: mdl-24724848

ABSTRACT

Recent cases of human infection with avian influenza H5N1 and H7N9 viruses underscore an urgent need for techniques that can rapidly assess their potential threat to the humans. Determination of the receptor-binding property of influenza virus is crucial to direct viral control and prevention measures. Current methods to perform this analysis are dependent on immunoanalytical strategies that use unstable biological components and complex procedures. We have developed a facile colorimetric assay to determine the interaction of the viral hemagglutinin (HA) protein with host glycan receptors using glycan-functionalized gold nanoparticles (gGNPs). This method is based on the color and absorbance changes of gold probes when the solution is simply mixed with HAs or intact viruses. The resulting sensitivity and selectivity has enabled HA/virus binding to various glycan structures to be differentiated visually and rapidly. Using this system, we have screened, in parallel, the receptor specificity of eight representative human and avian viral HAs and three whole viruses including an emerging H7N9 strain. Our results reveal the detailed receptor-binding profiles of H7N9 virus and its HA and show that they effectively bind to human-type receptors. This gGNP-based assay represents a strategy that would be helpful for developing simple and sensitive systems to probe glycan-mediated biological processes.


Subject(s)
Gold/chemistry , Hemagglutinin Glycoproteins, Influenza Virus/chemistry , Metal Nanoparticles/chemistry , Orthomyxoviridae/chemistry , Polysaccharides/chemistry , Receptors, Virus/chemistry , Animals , Cell Line , Cloning, Molecular , Colorimetry , Humans , Influenza A Virus, H1N1 Subtype , Influenza A Virus, H3N2 Subtype , Influenza A Virus, H5N1 Subtype , Influenza A Virus, H7N9 Subtype , Light , Microscopy, Electron, Transmission , Recombinant Proteins/chemistry , Scattering, Radiation , Sialic Acids/chemistry , Viral Proteins/chemistry
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