Evidence map›Paper›PMID 25401767›Full record

ArticlePloS one2014

Genomic selection for the improvement of antibody response to Newcastle disease and avian influenza virus in chickens.

Tianfei Liu, Hao Qu, Chenglong Luo, Xuewei Li, Dingming Shu, Mogens Sandø Lund, Guosheng Su

Abstract read
In one paragraph

Article in PloS one, 2014. 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
–field-weighted citation impact
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

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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.

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  11. Multiple-trait- and selection indices-genomic predictions for grain yield and protein content in rye for feeding purposes.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2016
    Article
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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.

Tianfei LiuCollege of Animal Science and Technology, Sichuan Agricultural University, Yaan, China; Institute of Animal Science, Guangdong Academy of Agricultural Sciences, Guangzhou, China; Center for Quantitative Genetics and Genomics, Department of Molecular Biology and Genetics, Aarhus University, Tjele, Denmark; State Key Laboratory of Livestock and Poultry Breeding, Guangzhou, China.
Hao QuInstitute of Animal Science, Guangdong Academy of Agricultural Sciences, Guangzhou, China; State Key Laboratory of Livestock and Poultry Breeding, Guangzhou, China.
Chenglong LuoInstitute of Animal Science, Guangdong Academy of Agricultural Sciences, Guangzhou, China; State Key Laboratory of Livestock and Poultry Breeding, Guangzhou, China.
Xuewei LiCollege of Animal Science and Technology, Sichuan Agricultural University, Yaan, China.
Dingming ShuInstitute of Animal Science, Guangdong Academy of Agricultural Sciences, Guangzhou, China; State Key Laboratory of Livestock and Poultry Breeding, Guangzhou, China.
Mogens Sandø LundCenter for Quantitative Genetics and Genomics, Department of Molecular Biology and Genetics, Aarhus University, Tjele, Denmark.
Guosheng SuCenter for Quantitative Genetics and Genomics, Department of Molecular Biology and Genetics, Aarhus University, Tjele, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Newcastle disease (ND) and avian influenza (AI) are the most feared diseases in the poultry industry worldwide. They can cause flock mortality up to 100%, resulting in a catastrophic economic loss. This is the first study to investigate the feasibility of genomic selection for antibody response to Newcastle disease virus (Ab-NDV) and antibody response to Avian Influenza virus (Ab-AIV) in chickens. The data were collected from a crossbred population. Breeding values for Ab-NDV and Ab-AIV were estimated using a pedigree-based best linear unbiased prediction model (BLUP) and a genomic best linear unbiased prediction model (GBLUP). Single-trait and multiple-trait analyses were implemented. According to the analysis using the pedigree-based model, the heritability for Ab-NDV estimated from the single-trait and multiple-trait models was 0.478 and 0.487, respectively. The heritability for Ab-AIV estimated from the two models was 0.301 and 0.291, respectively. The estimated genetic correlation between the two traits was 0.438. A four-fold cross-validation was used to assess the accuracy of the estimated breeding values (EBV) in the two validation scenarios. In the family sample scenario each half-sib family is randomly allocated to one of four subsets and in the random sample scenario the individuals are randomly divided into four subsets. In the family sample scenario, compared with the pedigree-based model, the accuracy of the genomic prediction increased from 0.086 to 0.237 for Ab-NDV and from 0.080 to 0.347 for Ab-AIV. In the random sample scenario, the accuracy was improved from 0.389 to 0.427 for Ab-NDV and from 0.281 to 0.367 for Ab-AIV. The multiple-trait GBLUP model led to a slightly higher accuracy of genomic prediction for both traits. These results indicate that genomic selection for antibody response to ND and AI in chickens is promising.

Indexed as

Selection, GeneticAnimalsAntibody FormationChickensGenetic Predisposition to DiseaseGenetic VariationHost-Pathogen InteractionsInfluenza A virusInfluenza in BirdsModels, BiologicalNewcastle DiseaseNewcastle disease virusQuantitative Trait, Heritable

Identifiers

PMID25401767
PMCPMC4234505

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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.