Literature detail

Functional balance of the hemagglutinin and neuraminidase activities accompanies the emergence of the 2009 H1N1 influenza pandemic.

Rui Xu1 Xueyong Zhu Ryan McBride Corwin M Nycholat Wenli Yu James C Paulson Ian A Wilson
Affiliations 1 institutions
  1. Department of Molecular Biology, Scripps Research Institute, La Jolla, California, USA.
PMID 22718832 2012 J Virol eng ppublish
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Article

Publication summary

The 2009 H1N1 influenza pandemic is the first human pandemic in decades and was of swine origin. Although swine are believed to be an intermediate host in the emergence of new human influenza viruses, there is still little known about the host barriers that keep swine influenza viruses from entering the human population. We surveyed swine progenitors and human viruses from the 2009 pandemic and measured the activities of the hemagglutinin (HA) and neuraminidase (NA), which are the two viral surface proteins that interact with host glycan receptors. A functional balance of these two activities (HA binding and NA cleavage) is found in human viruses but not in the swine progenitors. The human 2009 H1N1 pandemic virus exhibited both low HA avidity for glycan receptors as a result of mutations near the receptor binding site and weak NA enzymatic activity. Thus, a functional match between the hemagglutinin and neuraminidase appears to be necessary for efficient transmission between humans and may be an indicator of the pandemic potential of zoonotic viruses.

Animals Hemagglutinin Glycoproteins, Influenza Virus Humans Influenza A Virus, H1N1 Subtype Influenza, Human Kinetics Neuraminidase Orthomyxoviridae Infections Pandemics Polysaccharides Protein Binding Receptors, Virus Swine Swine Diseases Viral Proteins NA protein, influenza A virus

Structured evidence records

Evidence records

4 total
1 records
Extraction confidence 0.70
Key finding

Mutations near the HA receptor binding site in the 2009 H1N1 pandemic virus altered HA avidity and contributed to the functional balance between HA and NA activities during human adaptation.

Virus
Location
Not specified
Supporting text

The human 2009 H1N1 pandemic virus exhibited both low HA avidity for glycan receptors as a result of mutations near the receptor binding site and weak NA enzymatic activity.

Genes or proteins
hemagglutinin; neuraminidase
Analysis methods
comparative genomic analysis
1 records
Extraction confidence 0.95
Key finding

Mutations near the HA receptor binding site reduced receptor avidity and, coupled with weak NA activity, facilitated adaptation of the 2009 H1N1 influenza virus for efficient transmission in humans.

Virus
Host
Not specified
Location
Not specified
Supporting text

The human 2009 H1N1 pandemic virus exhibited both low HA avidity for glycan receptors as a result of mutations near the receptor binding site and weak NA enzymatic activity. Thus, a functional match between the hemagglutinin and neuraminidase appears to be necessary for efficient transmission between humans.

Genes or proteins
hemagglutinin; neuraminidase
Receptors
glycan receptors
Mechanism types
receptor_binding; replication_efficiency; transmission_fitness
1 records
Extraction confidence 0.90
Key finding

The 2009 H1N1 influenza virus showed reduced hemagglutinin binding affinity for glycan receptors due to mutations near the receptor binding site, indicating altered receptor usage relative to swine progenitors.

Virus
Location
Not specified
Supporting text

The human 2009 H1N1 pandemic virus exhibited both low HA avidity for glycan receptors as a result of mutations near the receptor binding site and weak NA enzymatic activity.

Method
binding assay; enzymatic activity assay
Receptors
glycan receptors
1 records
Extraction confidence 0.85
Key finding

The 2009 H1N1 influenza pandemic virus originated from swine, representing a swine-to-human spillover event.

Virus
Location
Not specified
Supporting text

The 2009 H1N1 influenza pandemic is the first human pandemic in decades and was of swine origin.

Transmission direction
animal-to-human