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Impact of the H274Y Substitution on N1, N4, N5, and N8 Neuraminidase Enzymatic Properties and Expression in Reverse Genetic Influenza A Viruses
by
Escuret, Vanessa
, Lina, Bruno
, Barthelemy, Mendy
, Picard, Caroline
, Frobert, Emilie
, Gaymard, Alexandre
, Vazzoler, Guilhem
, Massin, Pascale
, Sabatier, Murielle
, Casalegno, Jean-Sébastien
, Valette, Martine
, Ottmann, Michèle
in
Acids
/ Affinity
/ Amino Acid Substitution
/ Amino Acid Substitution Antiviral Agents / pharmacology Drug Resistance, Viral / genetics Enzyme Inhibitors / pharmacology Humans Influenza A Virus, H1N1 Subtype / genetics Influenza A virus / genetics Influenza, Human Neuraminidase / genetics Neuraminidase / metabolism Oseltamivir / pharmacology Reverse Genetics
/ Analysis
/ Antiviral activity
/ Antiviral Agents - pharmacology
/ Antiviral drugs
/ birds
/ Cloning
/ Communication
/ Drug Resistance, Viral - genetics
/ Enzymatic analysis
/ Enzyme Inhibitors - pharmacology
/ Exo-a-sialidase
/ Genetic aspects
/ Genetics
/ group-1 neuraminidases
/ H274Y-NA substitution
/ H275Y-NA substitution
/ Humans
/ Identification and classification
/ Influenza
/ Influenza A
/ Influenza A virus - genetics
/ Influenza A Virus, H1N1 Subtype - genetics
/ influenza A viruses
/ Influenza viruses
/ Influenza, Human
/ Life Sciences
/ Mass spectrometry
/ Mass spectroscopy
/ Methods
/ Mutagenesis
/ Mutation
/ Neuraminidase - genetics
/ Neuraminidase - metabolism
/ Oseltamivir
/ Oseltamivir - pharmacology
/ oseltamivir resistance
/ Plasmids
/ Proteins
/ Reverse Genetics
/ Scientific imaging
/ sialidase
/ Software
/ Viral genetics
/ Viruses
/ Zanamivir
2024
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Impact of the H274Y Substitution on N1, N4, N5, and N8 Neuraminidase Enzymatic Properties and Expression in Reverse Genetic Influenza A Viruses
by
Escuret, Vanessa
, Lina, Bruno
, Barthelemy, Mendy
, Picard, Caroline
, Frobert, Emilie
, Gaymard, Alexandre
, Vazzoler, Guilhem
, Massin, Pascale
, Sabatier, Murielle
, Casalegno, Jean-Sébastien
, Valette, Martine
, Ottmann, Michèle
in
Acids
/ Affinity
/ Amino Acid Substitution
/ Amino Acid Substitution Antiviral Agents / pharmacology Drug Resistance, Viral / genetics Enzyme Inhibitors / pharmacology Humans Influenza A Virus, H1N1 Subtype / genetics Influenza A virus / genetics Influenza, Human Neuraminidase / genetics Neuraminidase / metabolism Oseltamivir / pharmacology Reverse Genetics
/ Analysis
/ Antiviral activity
/ Antiviral Agents - pharmacology
/ Antiviral drugs
/ birds
/ Cloning
/ Communication
/ Drug Resistance, Viral - genetics
/ Enzymatic analysis
/ Enzyme Inhibitors - pharmacology
/ Exo-a-sialidase
/ Genetic aspects
/ Genetics
/ group-1 neuraminidases
/ H274Y-NA substitution
/ H275Y-NA substitution
/ Humans
/ Identification and classification
/ Influenza
/ Influenza A
/ Influenza A virus - genetics
/ Influenza A Virus, H1N1 Subtype - genetics
/ influenza A viruses
/ Influenza viruses
/ Influenza, Human
/ Life Sciences
/ Mass spectrometry
/ Mass spectroscopy
/ Methods
/ Mutagenesis
/ Mutation
/ Neuraminidase - genetics
/ Neuraminidase - metabolism
/ Oseltamivir
/ Oseltamivir - pharmacology
/ oseltamivir resistance
/ Plasmids
/ Proteins
/ Reverse Genetics
/ Scientific imaging
/ sialidase
/ Software
/ Viral genetics
/ Viruses
/ Zanamivir
2024
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Impact of the H274Y Substitution on N1, N4, N5, and N8 Neuraminidase Enzymatic Properties and Expression in Reverse Genetic Influenza A Viruses
by
Escuret, Vanessa
, Lina, Bruno
, Barthelemy, Mendy
, Picard, Caroline
, Frobert, Emilie
, Gaymard, Alexandre
, Vazzoler, Guilhem
, Massin, Pascale
, Sabatier, Murielle
, Casalegno, Jean-Sébastien
, Valette, Martine
, Ottmann, Michèle
in
Acids
/ Affinity
/ Amino Acid Substitution
/ Amino Acid Substitution Antiviral Agents / pharmacology Drug Resistance, Viral / genetics Enzyme Inhibitors / pharmacology Humans Influenza A Virus, H1N1 Subtype / genetics Influenza A virus / genetics Influenza, Human Neuraminidase / genetics Neuraminidase / metabolism Oseltamivir / pharmacology Reverse Genetics
/ Analysis
/ Antiviral activity
/ Antiviral Agents - pharmacology
/ Antiviral drugs
/ birds
/ Cloning
/ Communication
/ Drug Resistance, Viral - genetics
/ Enzymatic analysis
/ Enzyme Inhibitors - pharmacology
/ Exo-a-sialidase
/ Genetic aspects
/ Genetics
/ group-1 neuraminidases
/ H274Y-NA substitution
/ H275Y-NA substitution
/ Humans
/ Identification and classification
/ Influenza
/ Influenza A
/ Influenza A virus - genetics
/ Influenza A Virus, H1N1 Subtype - genetics
/ influenza A viruses
/ Influenza viruses
/ Influenza, Human
/ Life Sciences
/ Mass spectrometry
/ Mass spectroscopy
/ Methods
/ Mutagenesis
/ Mutation
/ Neuraminidase - genetics
/ Neuraminidase - metabolism
/ Oseltamivir
/ Oseltamivir - pharmacology
/ oseltamivir resistance
/ Plasmids
/ Proteins
/ Reverse Genetics
/ Scientific imaging
/ sialidase
/ Software
/ Viral genetics
/ Viruses
/ Zanamivir
2024
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Impact of the H274Y Substitution on N1, N4, N5, and N8 Neuraminidase Enzymatic Properties and Expression in Reverse Genetic Influenza A Viruses
Journal Article
Impact of the H274Y Substitution on N1, N4, N5, and N8 Neuraminidase Enzymatic Properties and Expression in Reverse Genetic Influenza A Viruses
2024
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Overview
The H274Y substitution (N2 numbering) in neuraminidase (NA) N1 confers oseltamivir resistance to A(H1N1) influenza viruses. This resistance has been associated with reduced N1 expression using transfected cells, but the effect of this substitution on the enzymatic properties and on the expression of other group-1-NA subtypes is unknown. The aim of the present study was to evaluate the antiviral resistance, enzymatic properties, and expression of wild-type (WT) and H274Y-substituted NA for each group-1-NA. To this end, viruses with WT or H274Y-substituted NA (N1pdm09 or avian N4, N5 or N8) were generated by reverse genetics, and for each reverse-genetic virus, antiviral susceptibility, NA affinity (Km), and maximum velocity (Vm) were measured. The enzymatic properties were coupled with NA quantification on concentrated reverse genetic viruses using mass spectrometry. The H274Y-NA substitution resulted in highly reduced inhibition by oseltamivir and normal inhibition by zanamivir and laninamivir. This resistance was associated with a reduced affinity for MUNANA substrate and a conserved Vm in all viruses. NA quantification was not significantly different between viruses carrying WT or H274Y-N1, N4 or N8, but was lower for viruses carrying H274Y-N5 compared to those carrying a WT-N5. In conclusion, the H274Y-NA substitution of different group-1-NAs systematically reduced their affinity for MUNANA substrate without a significant impact on NA Vm. The impact of the H274Y-NA substitution on viral NA expression was different according to the studied NA.
Publisher
MDPI AG,MDPI
Subject
/ Affinity
/ Analysis
/ Antiviral Agents - pharmacology
/ birds
/ Cloning
/ Drug Resistance, Viral - genetics
/ Enzyme Inhibitors - pharmacology
/ Genetics
/ Humans
/ Identification and classification
/ Influenza A virus - genetics
/ Influenza A Virus, H1N1 Subtype - genetics
/ Methods
/ Mutation
/ Plasmids
/ Proteins
/ Software
/ Viruses
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