Cargando…

Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle

Individuals often respond differently to the same vaccine; some of this variation may be caused by genetic differences among animals. Our objective was to estimate heritability and identify genomic regions associated with humoral response to an Escherichia coli O157:H7 vaccine in beef cattle. Crossb...

Descripción completa

Detalles Bibliográficos
Autores principales: Marley, Kara B., Kuehn, Larry A., Keele, John W., Wileman, Benjamin W., Gonda, Michael G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951538/
https://www.ncbi.nlm.nih.gov/pubmed/29758060
http://dx.doi.org/10.1371/journal.pone.0197347
_version_ 1783323044679254016
author Marley, Kara B.
Kuehn, Larry A.
Keele, John W.
Wileman, Benjamin W.
Gonda, Michael G.
author_facet Marley, Kara B.
Kuehn, Larry A.
Keele, John W.
Wileman, Benjamin W.
Gonda, Michael G.
author_sort Marley, Kara B.
collection PubMed
description Individuals often respond differently to the same vaccine; some of this variation may be caused by genetic differences among animals. Our objective was to estimate heritability and identify genomic regions associated with humoral response to an Escherichia coli O157:H7 vaccine in beef cattle. Crossbred beef cattle (n = 651) were vaccinated with a commercially available E. coli O157:H7 vaccine. Serum was collected at time of initial vaccination (d 0), booster (d 21), and d 56 after initial vaccination. Total antibodies specific to siderophore receptor and porin proteins in the vaccine were quantified by enzyme-linked immunosorbent assay. Genomic DNA was isolated from whole blood and genotyped with the bovine GeneSeek Genomic Profiler-High Density 78K or 26K Single Nucleotide Polymorphism BeadChip and imputed to 777,000 SNP genotypes. Heritability was estimated by restricted maximum likelihood (REML) using both 1) pedigree and 2) genomic relationships among individuals. Fixed effects were contemporary group, calf age, sex, principal components from SNP genotype data, and pedigree-derived heterozygosity effects. Additive and dominance effects of SNPs were estimated individually while accounting for contemporary group, sex, and the top 20 principal components calculated from the genomic relationship matrix. Heritability of initial response to vaccination (d 21 –d 0) was 0.10 ± 0.175 using pedigree relationships and 0.14 ± 0.149 using genomic relationships, but neither estimate was statistically different from zero. Heritability of booster (d 56 –d 21) and overall (d 56 –d 0) responses were low and not statistically significant from zero. There were no clusters of linked SNP associated with vaccine response, but eight regionally isolated SNPs were significantly associated with initial or overall response to vaccination. Regional genetic variation for initial response to an E. coli O157:H7 vaccine was observed, although overall heritability of this response was not statistically significant from zero.
format Online
Article
Text
id pubmed-5951538
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-59515382018-05-25 Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle Marley, Kara B. Kuehn, Larry A. Keele, John W. Wileman, Benjamin W. Gonda, Michael G. PLoS One Research Article Individuals often respond differently to the same vaccine; some of this variation may be caused by genetic differences among animals. Our objective was to estimate heritability and identify genomic regions associated with humoral response to an Escherichia coli O157:H7 vaccine in beef cattle. Crossbred beef cattle (n = 651) were vaccinated with a commercially available E. coli O157:H7 vaccine. Serum was collected at time of initial vaccination (d 0), booster (d 21), and d 56 after initial vaccination. Total antibodies specific to siderophore receptor and porin proteins in the vaccine were quantified by enzyme-linked immunosorbent assay. Genomic DNA was isolated from whole blood and genotyped with the bovine GeneSeek Genomic Profiler-High Density 78K or 26K Single Nucleotide Polymorphism BeadChip and imputed to 777,000 SNP genotypes. Heritability was estimated by restricted maximum likelihood (REML) using both 1) pedigree and 2) genomic relationships among individuals. Fixed effects were contemporary group, calf age, sex, principal components from SNP genotype data, and pedigree-derived heterozygosity effects. Additive and dominance effects of SNPs were estimated individually while accounting for contemporary group, sex, and the top 20 principal components calculated from the genomic relationship matrix. Heritability of initial response to vaccination (d 21 –d 0) was 0.10 ± 0.175 using pedigree relationships and 0.14 ± 0.149 using genomic relationships, but neither estimate was statistically different from zero. Heritability of booster (d 56 –d 21) and overall (d 56 –d 0) responses were low and not statistically significant from zero. There were no clusters of linked SNP associated with vaccine response, but eight regionally isolated SNPs were significantly associated with initial or overall response to vaccination. Regional genetic variation for initial response to an E. coli O157:H7 vaccine was observed, although overall heritability of this response was not statistically significant from zero. Public Library of Science 2018-05-14 /pmc/articles/PMC5951538/ /pubmed/29758060 http://dx.doi.org/10.1371/journal.pone.0197347 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Marley, Kara B.
Kuehn, Larry A.
Keele, John W.
Wileman, Benjamin W.
Gonda, Michael G.
Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle
title Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle
title_full Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle
title_fullStr Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle
title_full_unstemmed Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle
title_short Genetic variation in humoral response to an Escherichia coli O157:H7 vaccine in beef cattle
title_sort genetic variation in humoral response to an escherichia coli o157:h7 vaccine in beef cattle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951538/
https://www.ncbi.nlm.nih.gov/pubmed/29758060
http://dx.doi.org/10.1371/journal.pone.0197347
work_keys_str_mv AT marleykarab geneticvariationinhumoralresponsetoanescherichiacolio157h7vaccineinbeefcattle
AT kuehnlarrya geneticvariationinhumoralresponsetoanescherichiacolio157h7vaccineinbeefcattle
AT keelejohnw geneticvariationinhumoralresponsetoanescherichiacolio157h7vaccineinbeefcattle
AT wilemanbenjaminw geneticvariationinhumoralresponsetoanescherichiacolio157h7vaccineinbeefcattle
AT gondamichaelg geneticvariationinhumoralresponsetoanescherichiacolio157h7vaccineinbeefcattle