Evidence map›Paper›PMID 35880574›Full record

ArticleMolecular biology and evolution2022

Comparative Genomics of the Waterfowl Innate Immune System.

Elinor Jax, Paolo Franchini, Vaishnovi Sekar, Jente Ottenburghs, Daniel Monné Parera, Roman T Kellenberger, Katharine E Magor, Inge Müller, Martin Wikelski, Robert H S Kraus

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

10 authors at 5 institutions in 6 countries.

Elinor JaxDepartment of Migration, Max Planck Institute of Animal Behavior, Radolfzell, Germany.ORCID 0000-0001-5225-8634
Paolo FranchiniDepartment of Biology, University of Konstanz, Konstanz, Germany.ORCID 0000-0002-8184-1463
Vaishnovi SekarDepartment of Biology, Lund University, Lund, Sweden.ORCID 0000-0002-6810-1591
Jente OttenburghsWildlife Ecology and Conservation Group, Wageningen University, Wageningen, The Netherlands.ORCID 0000-0002-0335-9655
Daniel Monné PareraDepartment of Biology, University of Konstanz, Konstanz, Germany.
Roman T KellenbergerDepartment of Plant Sciences, University of Cambridge, Cambridge, United Kingdom.
Katharine E MagorDepartment of Biological Sciences and Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Canada.
Inge MüllerDepartment of Migration, Max Planck Institute of Animal Behavior, Radolfzell, Germany.
Martin WikelskiDepartment of Migration, Max Planck Institute of Animal Behavior, Radolfzell, Germany.
Robert H S KrausDepartment of Migration, Max Planck Institute of Animal Behavior, Radolfzell, Germany.
University of Konstanz · DEStockholm University · SEUniversity of Alberta · CAUniversity of Cambridge · GBWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animal species differ considerably in their ability to fight off infections. Finding the genetic basis of these differences is not easy, as the immune response is comprised of a complex network of proteins that interact with one another to defend the body against infection. Here, we used population- and comparative genomics to study the evolutionary forces acting on the innate immune system in natural hosts of the avian influenza virus (AIV). For this purpose, we used a combination of hybrid capture, next- generation sequencing and published genomes to examine genetic diversity, divergence, and signatures of selection in 127 innate immune genes at a micro- and macroevolutionary time scale in 26 species of waterfowl. We show across multiple immune pathways (AIV-, toll-like-, and RIG-I -like receptors signalling pathways) that genes involved genes in pathogen detection (i.e., toll-like receptors) and direct pathogen inhibition (i.e., antimicrobial peptides and interferon-stimulated genes), as well as host proteins targeted by viral antagonist proteins (i.e., mitochondrial antiviral-signaling protein, [MAVS]) are more likely to be polymorphic, genetically divergent, and under positive selection than other innate immune genes. Our results demonstrate that selective forces vary across innate immune signaling signalling pathways in waterfowl, and we present candidate genes that may contribute to differences in susceptibility and resistance to infectious diseases in wild birds, and that may be manipulated by viruses. Our findings improve our understanding of the interplay between host genetics and pathogens, and offer the opportunity for new insights into pathogenesis and potential drug targets.

Indexed as

Immunity, InnateInfluenza A virusAnimalsBirdsGenomicsImmune SystemAnatidaeDNA polymorphismgenetic divergencemallardnatural selection

Identifiers

PMID35880574
PMCPMC9356732
OpenAlexW4287958392

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.