Evidence map›Paper›PMID 29132293›Full record

ArticleBMC genomics2017

Genomic regions associated with host response to porcine reproductive and respiratory syndrome vaccination and co-infection in nursery pigs.

Jenelle R Dunkelberger, Nick V L Serão, Ziqing Weng, Emily H Waide, Megan C Niederwerder, Maureen A Kerrigan, Joan K Lunney, Raymond R R Rowland, Jack C M Dekkers

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review: innovation through research in the North American pork industry.Animal : an international journal of animal bioscience · 2019
    Review
  10. Article
  11. Analysis of Effect ofFrontiers in pharmacology · 2019
    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

9 authors at 5 institutions in 2 countries.

Jenelle R DunkelbergerDepartment of Animal Science, Iowa State University, Ames, IA, 50011, USA.
Nick V L SerãoDepartment of Animal Science, Iowa State University, Ames, IA, 50011, USA.
Ziqing WengDepartment of Animal Science, Iowa State University, Ames, IA, 50011, USA.
Emily H WaideDepartment of Animal Science, Iowa State University, Ames, IA, 50011, USA.
Megan C NiederwerderDepartment of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, 66506, USA.
Maureen A KerriganDepartment of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, 66506, USA.
Joan K LunneyUSDA, ARS, BARC, APDL, Beltsville, MD, 20705, USA.
Raymond R R RowlandDepartment of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, 66506, USA.
Jack C M DekkersDepartment of Animal Science, Iowa State University, Ames, IA, 50011, USA. jdekkers@iastate.edu.
Iowa State University · USKansas State University · USABS Consulting (United States) · USAgricultural Research Service · USMorristown Medical Center · US

Funding

USDA National Needs Training Grant 2012-38420-19286USDA NIFA 2013-68004-20362
6 · The paper itself

Abstract

backgroundThe WUR1000125 (WUR) single nucleotide polymorphism (SNP) can be used as a genetic marker for host response to porcine reproductive and respiratory syndrome (PRRS), PRRS vaccination, and co-infection with porcine circovirus type 2b (PCV2b). Objectives of this study were to identify genomic regions other than WUR associated with host response to PRRS vaccination and PRRSV/PCV2b co-infection and regions with a different effect on host response to co-infection, depending on previous vaccination for PRRS.

methodsCommercial crossbred nursery pigs were pre-selected for WUR genotype (n = 171 AA and 198 AB pigs) where B is the dominant and favorable allele. Half of the pigs were vaccinated for PRRS and 4 weeks later, all pigs were co-infected with PRRS virus and PCV2b. Average daily gain (ADG) and viral load (VL) were quantified post vaccination (Post Vx) and post co-infection (Post Co-X). Single-SNP genome-wide association analyses were then conducted to identify genomic regions associated with response to vaccination and co-infection.

resultsMultiple SNPs near the major histocompatibility complex were significantly associated with PCV2b VL (-log

conclusionsMultiple genomic regions were associated with PCV2b VL and ADG Post Vx and Post Co-X. Different SNPs were associated with ADG, depending on previous vaccination for PRRS. Results of functional annotation analyses and novel approaches of using previously-reported QTL support the identified regions.

Indexed as

GenomicsVaccinationAnimalsCoinfectionFemaleGenome-Wide Association StudyHost-Pathogen InteractionsMalePolymorphism, Single NucleotidePorcine Reproductive and Respiratory SyndromePorcine respiratory and reproductive syndrome virusQuantitative Trait LociSwineViral LoadFunctional annotationGenome-wide association studyPCV2PRRSQuantitative trait locusSwineWUR10000125

Identifiers

PMID29132293
PMCPMC5682865
OpenAlexW2768428218

What OpenQuestion holds

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LicenceCC BY
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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.