Evidence map›Paper›PMID 28282440›Full record

ArticlePLoS pathogens2017

H1N1 influenza viruses varying widely in hemagglutinin stability transmit efficiently from swine to swine and to ferrets.

Marion Russier, Guohua Yang, Atanaska Marinova-Petkova, Peter Vogel, Bryan S Kaplan, Richard J Webby, Charles J Russell

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 42 citations in OpenAlex.

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  20. An influenza A hemagglutinin small-molecule fusion inhibitor identified by a new high-throughput fluorescence polarization screen.Proceedings of the National Academy of Sciences of the United States of America · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Marion RussierDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States.ORCID 0000-0002-9633-9804
Guohua YangDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States.
Atanaska Marinova-PetkovaDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States.
Peter VogelDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, United States.ORCID 0000-0002-7535-0545
Bryan S KaplanDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States.
Richard J WebbyDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States.
Charles J RussellDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States.ORCID 0000-0001-5683-3990
St. Jude Children's Research Hospital · US

Funding

NIAID NIH HHS HHSN272201400006C
6 · The paper itself

Abstract

A pandemic-capable influenza virus requires a hemagglutinin (HA) surface glycoprotein that is immunologically unseen by most people and is capable of supporting replication and transmission in humans. HA stabilization has been linked to 2009 pH1N1 pandemic potential in humans and H5N1 airborne transmissibility in the ferret model. Swine have served as an intermediate host for zoonotic influenza viruses, yet the evolutionary pressure exerted by this host on HA stability was unknown. For over 70 contemporary swine H1 and H3 isolates, we measured HA activation pH to range from pH 5.1 to 5.9 for H1 viruses and pH 5.3 to 5.8 for H3 viruses. Thus, contemporary swine isolates vary widely in HA stability, having values favored by both avian (pH >5.5) and human and ferret (pH ≤5.5) species. Using an early 2009 pandemic H1N1 (pH1N1) virus backbone, we generated three viruses differing by one HA residue that only altered HA stability: WT (pH 5.5), HA1-Y17H (pH 6.0), and HA2-R106K (pH 5.3). All three replicated in pigs and transmitted from pig-to-pig and pig-to-ferret. WT and R106 viruses maintained HA genotype and phenotype after transmission. Y17H (pH 6.0) acquired HA mutations that stabilized the HA protein to pH 5.8 after transmission to pigs and 5.5 after transmission to ferrets. Overall, we found swine support a broad range of HA activation pH for contact transmission and many recent swine H1N1 and H3N2 isolates have stabilized (human-like) HA proteins. This constitutes a heightened pandemic risk and underscores the importance of ongoing surveillance and control efforts for swine viruses.

Indexed as

AnimalsFerretsHEK293 CellsHemagglutinin Glycoproteins, Influenza VirusHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryInfluenza A Virus, H1N1 SubtypeOrthomyxoviridae InfectionsProtein StabilityReal-Time Polymerase Chain ReactionSwineH1N1 virus hemagglutininHemagglutinin Glycoproteins, Influenza Virus

Identifiers

PMID28282440
PMCPMC5362248
OpenAlexW2593771697

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.