Literature DB >> 35439920

Using egg production longitudinal recording to study the genetic background of resilience in purebred and crossbred laying hens.

Nicolas Bedere1, Tom V L Berghof2,3, Katrijn Peeters4, Marie-Hélène Pinard-van der Laan5, Jeroen Visscher4, Ingrid David6, Han A Mulder2.   

Abstract

BACKGROUND: There is growing interest in using genetic selection to obtain more resilient farm animals (i.e. that are minimally affected by disturbances or rapidly recover from them). The aims of this study were to: (i) estimate the genetic parameters of resilience indicator traits based on egg production data, (ii) assess whether these traits are genetically correlated in purebreds and crossbreds, and (iii) assess the genetic correlations of these traits with egg production (EP) as total number of eggs between 25 and 83 weeks. Purebred hens (33,825 from a White Leghorn (WA) line and 34,397 from a Rhode Island (BD) line were housed in individual cages, while crossbred hens were housed in collective cages of 6 to 8 paternal half-sibs (12,852 WA and 3898 BD crossbred groups, where the name of the group refers to the line used as the sire). Deviations of a hen's weekly egg production from the average of the corresponding batch were calculated. Resilience indicator traits investigated were the natural logarithm of the variance (LNVAR), the skewness (SKEW), and the lag-one autocorrelation (AUTO-R) of these deviations.
RESULTS: In both purebred lines, EP was estimated to be lowly heritable (WA: 0.11 and BD: 0.12). Resilience indicators were also estimated to be lowly heritable in both lines (LNVAR: 0.10 and 0.12, SKEW: 0.04 and 0.02, AUTO-R: 0.06 and 0.08 in WA and BD, respectively). In both crossbred groups, EP, AUTO-R, and SKEW were estimated to be less heritable than in purebreds (EP: [Formula: see text] ≤ 0.07; and resilience indicator traits: [Formula: see text] ≤ 0.03), while LNVAR had an [Formula: see text] estimate that was similar to or higher in crossbreds ([Formula: see text] ranged from 0.13 to 0.21) than in purebreds. In both purebreds and crossbreds, resilience indicator traits were estimated to have favorable genetic correlations with EP and between each other. For all traits and in both lines, estimates of genetic correlations between purebreds and crossbreds ([Formula: see text]) differed from 1 and ranged from 0.16 to 0.63.
CONCLUSIONS: These results show that selection for resilience based on EP data can be considered in breeding programs for layers. Genetic improvement of resilience in crossbreds can be achieved by using information on purebreds, but would be greatly enhanced by the integration of information on crossbreds in breeding programs.
© 2022. The Author(s).

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Year:  2022        PMID: 35439920      PMCID: PMC9020098          DOI: 10.1186/s12711-022-00716-8

Source DB:  PubMed          Journal:  Genet Sel Evol        ISSN: 0999-193X            Impact factor:   5.100


  36 in total

1.  Evaluation of egg production in layers using random regression models.

Authors:  A Wolc; J Arango; P Settar; N P O'Sullivan; J C M Dekkers
Journal:  Poult Sci       Date:  2011-01       Impact factor: 3.352

2.  Marker-assisted selection for commercial crossbred performance.

Authors:  J C M Dekkers
Journal:  J Anim Sci       Date:  2007-05-15       Impact factor: 3.159

3.  Genetic variability in residual variation of body weight and conformation scores in broiler chickens.

Authors:  A Wolc; I M S White; S Avendano; W G Hill
Journal:  Poult Sci       Date:  2009-06       Impact factor: 3.352

4.  Genetic control of residual variance of yearling weight in Nellore beef cattle.

Authors:  L H S Iung; H H R Neves; H A Mulder; R Carvalheiro
Journal:  J Anim Sci       Date:  2017-04       Impact factor: 3.159

5.  Variance component and breeding value estimation for genetic heterogeneity of residual variance in Swedish Holstein dairy cattle.

Authors:  L Rönnegård; M Felleki; W F Fikse; H A Mulder; E Strandberg
Journal:  J Dairy Sci       Date:  2013-02-15       Impact factor: 4.034

6.  Genetic heterogeneity of residual variance in broiler chickens.

Authors:  Suzanne J Rowe; Ian M S White; Santiago Avendaño; William G Hill
Journal:  Genet Sel Evol       Date:  2006-11-28       Impact factor: 4.297

7.  Genetic variance in micro-environmental sensitivity for milk and milk quality in Walloon Holstein cattle.

Authors:  J Vandenplas; C Bastin; N Gengler; H A Mulder
Journal:  J Dairy Sci       Date:  2013-07-17       Impact factor: 4.034

8.  Exploration of variance, autocorrelation, and skewness of deviations from lactation curves as resilience indicators for breeding.

Authors:  M Poppe; R F Veerkamp; M L van Pelt; H A Mulder
Journal:  J Dairy Sci       Date:  2019-11-20       Impact factor: 4.034

9.  Novel Resilience Phenotypes Using Feed Intake Data From a Natural Disease Challenge Model in Wean-to-Finish Pigs.

Authors:  Austin M Putz; John C S Harding; Michael K Dyck; F Fortin; Graham S Plastow; Jack C M Dekkers
Journal:  Front Genet       Date:  2019-01-08       Impact factor: 4.599

10.  Quantifying resilience of humans and other animals.

Authors:  Marten Scheffer; J Elizabeth Bolhuis; Denny Borsboom; Timothy G Buchman; Sanne M W Gijzel; Dave Goulson; Jan E Kammenga; Bas Kemp; Ingrid A van de Leemput; Simon Levin; Carmel Mary Martin; René J F Melis; Egbert H van Nes; L Michael Romero; Marcel G M Olde Rikkert
Journal:  Proc Natl Acad Sci U S A       Date:  2018-10-29       Impact factor: 11.205

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