» Articles » PMID: 33193739

Genomic Analysis of IgG Antibody Response to Common Pathogens in Commercial Sows in Health-Challenged Herds

Overview
Journal Front Genet
Date 2020 Nov 16
PMID 33193739
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Losses due to infectious diseases are one of the main factors affecting productivity in the swine industry, motivating the investigation of disease resilience-related traits for genetic selection. However, these traits are not expected to be expressed in the nucleus herds, where selection is performed. One alternative is to use information from the commercial level to identify and select nucleus animals genetically superior for coping with pathogen challenges. In this study, we analyzed the genetic basis of antibody (Ab) response to common infectious pathogens in health-challenged commercial swine herds as potential indicator traits for disease resilience, including Ab response to influenza A virus of swine (IAV), (MH), porcine circovirus (PCV2), and (APP; different serotypes). Ab response was measured in blood at entry into gilt rearing, post-acclimation (∼40 days after entering the commercial herd), and parities 1 and 2. Heritability estimates for Ab response to IAV, MH, and PCV2 ranged from 0 to 0.76. Ab response to APP ranged from 0 to 0.40. The genetic correlation (r ) of Ab response to IAV with MH, PCV2, PRRSV, and APP (average Ab responses for all serotypes of APP) were positive (>0.29) at entry. APP was negatively correlated with PCV2 and MH at entry and parity 2 but positively correlated with MH at post-acclimation and parity 1. Genomic regions associated with Ab response to different APP serotypes were identified on 13 chromosomes. The region on chromosome 14 (2 Mb) was associated with several serotypes of APP, explaining up to 4.3% of the genetic variance of Ab to APP7 at entry. In general, genomic prediction accuracies for Ab response were low to moderate, except average Ab response to all infectious pathogens evaluated. These results suggest that genetic selection of Ab response in commercial sows is possible, but with variable success depending on the trait and the time-point of collection. Future work is needed to determine genetic correlations of Ab response with disease resilience, reproductive performance, and other production traits.

Citing Articles

A genome-wide screen for resilient responses in growing pigs.

Laghouaouta H, Fraile L, Suarez-Mesa R, Ros-Freixedes R, Estany J, Pena R Genet Sel Evol. 2022; 54(1):50.

PMID: 35787790 PMC: 9251948. DOI: 10.1186/s12711-022-00739-1.


Assessing the statistical training in animal science graduate programs in the United States: survey on statistical training.

Serao N, Petry A, Sanglard L, Rossoni-Serao M, Bundy J J Anim Sci. 2021; 99(5).

PMID: 33738494 PMC: 8280918. DOI: 10.1093/jas/skab086.

References
1.
Lee Y, Alam M, Choi B, Kim K, Kim J . A Whole Genome Association Study to Detect Single Nucleotide Polymorphisms for Blood Components (Immunity) in a Cross between Korean Native Pig and Yorkshire. Asian-Australas J Anim Sci. 2014; 25(12):1674-80. PMC: 4094150. DOI: 10.5713/ajas.2012.12503. View

2.
Sato T, Okamura T, Kojima-Shibata C, Kadowaki H, Suzuki E, Uenishi H . Correlated response of peripheral blood cytokines with selection for reduced mycoplasma pneumonia of swine lesions in Landrace pigs. Anim Sci J. 2015; 87(4):477-83. DOI: 10.1111/asj.12462. View

3.
Thacker E, Halbur P, Ross R, Thanawongnuwech R, Thacker B . Mycoplasma hyopneumoniae potentiation of porcine reproductive and respiratory syndrome virus-induced pneumonia. J Clin Microbiol. 1999; 37(3):620-7. PMC: 84495. DOI: 10.1128/JCM.37.3.620-627.1999. View

4.
Dempsey P, Allison M, Akkaraju S, Goodnow C, Fearon D . C3d of complement as a molecular adjuvant: bridging innate and acquired immunity. Science. 1996; 271(5247):348-50. DOI: 10.1126/science.271.5247.348. View

5.
Serao N, Matika O, Kemp R, Harding J, Bishop S, Plastow G . Genetic analysis of reproductive traits and antibody response in a PRRS outbreak herd. J Anim Sci. 2014; 92(7):2905-21. DOI: 10.2527/jas.2014-7821. View