Evidence map›Paper›PMID 26819311›Full record

ArticleJournal of virology2016

Spatiotemporal Analysis of the Genetic Diversity of Seal Influenza A(H10N7) Virus, Northwestern Europe.

Rogier Bodewes, Siamak Zohari, Jesper S Krog, Matthew D Hall, Timm C Harder, Theo M Bestebroer, Marco W G van de Bildt, Monique I Spronken, Lars E Larsen, Ursula Siebert and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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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

21 authors at 8 institutions in 5 countries.

Rogier BodewesDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands rogier.bodewes@gmail.com.
Siamak ZohariDepartment of Virology, Immunobiology and Parasitology, National Veterinary Institute, Uppsala, Sweden.
Jesper S KrogNational Veterinary Institute, Technical University of Denmark, Frederiksberg, Denmark.
Matthew D HallCentre for Immunity, Infection and Evolution, University of Edinburgh, Edinburgh, United Kingdom.
Timm C HarderFederal Research Institute for Animal Health, Friedrich-Loeffler-Institut, Greifswald Insel-Riems, Germany.
Theo M BestebroerDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Marco W G van de BildtDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Monique I SpronkenDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Lars E LarsenNational Veterinary Institute, Technical University of Denmark, Frederiksberg, Denmark.
Ursula SiebertInstitute for Terrestrial and Aquatic Wildlife Research, University of Veterinary Medicine Hannover, Büsum, Germany.
Peter WohlseinDepartment of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany.
Christina PuffDepartment of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany.
Frauke SeehusenDepartment of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany.
Wolfgang BaumgärtnerDepartment of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany.
Tero HärkönenDepartment of Environmental Research and Monitoring, Swedish Museum of Natural History, Stockholm, Sweden.
Saskia L SmitsDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Sander HerfstDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Albert D M E OsterhausDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Ron A M FouchierDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Marion P KoopmansDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Thijs KuikenDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Erasmus MC · NLUniversity of Veterinary Medicine Hannover, Foundation · DEErasmus University Rotterdam · NLTechnical University of Denmark · DKCentre for Immunity, Infection and Evolution · GBFriedrich-Loeffler-Institut · DESwedish Museum of Natural History · SESwedish Veterinary Agency · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledInfluenza A viruses are major pathogens for humans, domestic animals, and wildlife, and these viruses occasionally cross the species barrier. In spring 2014, increased mortality of harbor seals (Phoca vitulina), associated with infection with an influenza A(H10N7) virus, was reported in Sweden and Denmark. Within a few months, this virus spread to seals of the coastal waters of Germany and the Netherlands, causing the death of thousands of animals. Genetic analysis of the hemagglutinin (HA) and neuraminidase (NA) genes of this seal influenza A(H10N7) virus revealed that it was most closely related to various avian influenza A(H10N7) viruses. The collection of samples from infected seals during the course of the outbreak provided a unique opportunity to follow the adaptation of the avian virus to its new seal host. Sequence data for samples collected from 41 different seals from four different countries between April 2014 and January 2015 were obtained by Sanger sequencing and next-generation sequencing to describe the molecular epidemiology of the seal influenza A(H10N7) virus. The majority of sequence variation occurred in the HA gene, and some mutations corresponded to amino acid changes not found in H10 viruses isolated from Eurasian birds. Also, sequence variation in the HA gene was greater at the beginning than at the end of the epidemic, when a number of the mutations observed earlier had been fixed. These results imply that when an avian influenza virus jumps the species barrier from birds to seals, amino acid changes in HA may occur rapidly and are important for virus adaptation to its new mammalian host. IMPORTANCE: Influenza A viruses are major pathogens for humans, domestic animals, and wildlife. In addition to the continuous circulation of influenza A viruses among various host species, cross-species transmission of influenza A viruses occurs occasionally. Wild waterfowl and shorebirds are the main reservoir for most influenza A virus subtypes, and spillover of influenza A viruses from birds to humans or other mammalian species may result in major outbreaks. In the present study, various sequencing methods were used to elucidate the genetic changes that occurred after the introduction and subsequent spread of an avian influenza A(H10N7) virus among harbor seals of northwestern Europe by use of various samples collected during the outbreak. Such detailed knowledge of genetic changes necessary for introduction and adaptation of avian influenza A viruses to mammalian hosts is important for a rapid risk assessment of such viruses soon after they cross the species barrier.

Indexed as

Genetic VariationSpatio-Temporal AnalysisAmino Acid SubstitutionAnimalsComputational BiologyEuropeGenome, ViralHemagglutinin Glycoproteins, Influenza VirusHigh-Throughput Nucleotide SequencingInfluenza A Virus, H10N7 SubtypeOrthomyxoviridae InfectionsPhocaPhylogenyPhylogeographyHemagglutinin Glycoproteins, Influenza Virus

Identifiers

PMID26819311
PMCPMC4836327
OpenAlexW2263654205

What OpenQuestion holds

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Registered trials

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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.