Evidence map›Paper›PMID 28666475›Full record

ArticleGenetics, selection, evolution : GSE2017

A model to estimate effects of SNPs on host susceptibility and infectivity for an endemic infectious disease.

Floor Biemans, Mart C M de Jong, Piter Bijma

Abstract read
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Article in Genetics, selection, evolution : GSE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review: Livestock disease resilience: from individual to herd level.Animal : an international journal of animal bioscience · 2021
    Review
  4. Article
  5. Article
  6. The economic value of RGenetics, selection, evolution : GSE · 2020
    Article
  7. Review
  8. Article
  9. Article
  10. Derivation of the economic value of RGenetics, selection, evolution : GSE · 2018
    Article
  11. Can We Breed Cattle for Lower Bovine TB Infectivity?Frontiers in veterinary science · 2018
    Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Floor BiemansQuantitative Veterinary Epidemiology Group, Wageningen University and Research, Wageningen, The Netherlands. floor.biemans@wur.nl.ORCID 0000-0002-0303-8448
Mart C M de JongQuantitative Veterinary Epidemiology Group, Wageningen University and Research, Wageningen, The Netherlands.
Piter BijmaAnimal Breeding and Genomics Centre, Wageningen University and Research, Wageningen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfectious diseases in farm animals affect animal health, decrease animal welfare and can affect human health. Selection and breeding of host individuals with desirable traits regarding infectious diseases can help to fight disease transmission, which is affected by two types of (genetic) traits: host susceptibility and host infectivity. Quantitative genetic studies on infectious diseases generally connect an individual's disease status to its own genotype, and therefore capture genetic effects on susceptibility only. However, they usually ignore variation in exposure to infectious herd mates, which may limit the accuracy of estimates of genetic effects on susceptibility. Moreover, genetic effects on infectivity will exist as well. Thus, to design optimal breeding strategies, it is essential that genetic effects on infectivity are quantified. Given the potential importance of genetic effects on infectivity, we set out to develop a model to estimate the effect of single nucleotide polymorphisms (SNPs) on both host susceptibility and host infectivity. To evaluate the quality of the resulting SNP effect estimates, we simulated an endemic disease in 10 groups of 100 individuals, and recorded time-series data on individual disease status. We quantified bias and precision of the estimates for different sizes of SNP effects, and identified the optimum recording interval when the number of records is limited.

resultsWe present a generalized linear mixed model to estimate the effect of SNPs on both host susceptibility and host infectivity. SNP effects were on average slightly underestimated, i.e. estimates were conservative. Estimates were less precise for infectivity than for susceptibility. Given our sample size, the power to estimate SNP effects for susceptibility was 100% for differences between genotypes of a factor 1.56 or more, and was higher than 60% for infectivity for differences between genotypes of a factor 4 or more. When disease status was recorded 11 times on each animal, the optimal recording interval was 25 to 50% of the average infectious period.

conclusionsOur model was able to estimate genetic effects on susceptibility and infectivity. In future genome-wide association studies, it may serve as a starting point to identify genes that affect disease transmission and disease prevalence.

Indexed as

Genetic Predisposition to DiseaseModels, GeneticAnimalsBreedingCommunicable DiseasesComputer SimulationGenome-Wide Association StudyGenotypeHost-Pathogen InteractionsLinear ModelsPolymorphism, Single Nucleotide

Identifiers

PMID28666475
PMCPMC5492932

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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.