Evidence map›Paper›PMID 32321814›Full record

ArticleJournal of virology2020

Phylogeography and Antigenic Diversity of Low-Pathogenic Avian Influenza H13 and H16 Viruses.

Josanne H Verhagen, Marjolein Poen, David E Stallknecht, Stefan van der Vliet, Pascal Lexmond, Srinand Sreevatsan, Rebecca L Poulson, Ron A M Fouchier, Camille Lebarbenchon

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
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

9 authors at 5 institutions in 5 countries.

Josanne H VerhagenErasmus Medical Center, Department of Viroscience, Rotterdam, The Netherlands josanne.verhagen@lnu.se.
Marjolein PoenErasmus Medical Center, Department of Viroscience, Rotterdam, The Netherlands.
David E StallknechtSoutheastern Cooperative Wildlife Disease Study, College of Veterinary Medicine, Department of Population Health, University of Georgia, Athens, Georgia, USA.
Stefan van der VlietErasmus Medical Center, Department of Viroscience, Rotterdam, The Netherlands.
Pascal LexmondErasmus Medical Center, Department of Viroscience, Rotterdam, The Netherlands.
Srinand SreevatsanMichigan State University, College of Veterinary Medicine, Department of Pathobiology and Diagnostic Investigation, East Lansing, Michigan, USA.
Rebecca L PoulsonSoutheastern Cooperative Wildlife Disease Study, College of Veterinary Medicine, Department of Population Health, University of Georgia, Athens, Georgia, USA.
Ron A M FouchierErasmus Medical Center, Department of Viroscience, Rotterdam, The Netherlands.
Camille LebarbenchonSoutheastern Cooperative Wildlife Disease Study, College of Veterinary Medicine, Department of Population Health, University of Georgia, Athens, Georgia, USA.ORCID 0000-0002-0922-7573
Erasmus MC · NLUniversity of Georgia · USCentre National de la Recherche Scientifique · FRLinnaeus University · SEMichigan State University · US

Funding

NIAID NIH HHS HHSN266200700007CNIAID NIH HHS HHSN272201400008C
6 · The paper itself

Abstract

Low-pathogenic avian influenza viruses (LPAIVs) are genetically highly variable and have diversified into multiple evolutionary lineages that are primarily associated with wild-bird reservoirs. Antigenic variation has been described for mammalian influenza viruses and for highly pathogenic avian influenza viruses that circulate in poultry, but much less is known about antigenic variation of LPAIVs. In this study, we focused on H13 and H16 LPAIVs that circulate globally in gulls. We investigated the evolutionary history and intercontinental gene flow based on the hemagglutinin (HA) gene and used representative viruses from genetically distinct lineages to determine their antigenic properties by hemagglutination inhibition assays. For H13, at least three distinct genetic clades were evident, while for H16, at least two distinct genetic clades were evident. Twenty and ten events of intercontinental gene flow were identified for H13 and H16 viruses, respectively. At least two antigenic variants of H13 and at least one antigenic variant of H16 were identified. Amino acid positions in the HA protein that may be involved in the antigenic variation were inferred, and some of the positions were located near the receptor binding site of the HA protein, as they are in the HA protein of mammalian influenza A viruses. These findings suggest independent circulation of H13 and H16 subtypes in gull populations, as antigenic patterns do not overlap, and they contribute to the understanding of the genetic and antigenic variation of LPAIVs naturally circulating in wild birds.

Indexed as

AnimalsAnimals, WildAntigenic VariationBirdsCharadriiformesHemagglutination Inhibition TestsHemagglutinin Glycoproteins, Influenza VirusHemagglutininsHost SpecificityInfluenza A virusInfluenza in BirdsPhylogenyPhylogeographyHemagglutinin Glycoproteins, Influenza VirusHemagglutininsantigenic variationavian virusesecologyepidemiologyevolutiongullsinfluenzaseabirdwild birds

Identifiers

PMID32321814
PMCPMC7307148
OpenAlexW3020795228

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.