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Genetic variation in parameters reflecting immune competence of swine

Genetic variation in total and differential white blood cell (WBC) counts, phagocytic capacity of polymorphonuclear leukocytes (PMNL), virus induced interferon-α (IFN-α) production, mitogen induced proliferation and interleukin 2 (IL-2) production of mononuclear cells (MNC) in vitro was studied in b...

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Autores principales: Edfors-Lilja, Inger, Wattrang, Eva, Magnusson, U., Fossum, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119906/
https://www.ncbi.nlm.nih.gov/pubmed/8128606
http://dx.doi.org/10.1016/0165-2427(94)90011-6
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author Edfors-Lilja, Inger
Wattrang, Eva
Magnusson, U.
Fossum, Caroline
author_facet Edfors-Lilja, Inger
Wattrang, Eva
Magnusson, U.
Fossum, Caroline
author_sort Edfors-Lilja, Inger
collection PubMed
description Genetic variation in total and differential white blood cell (WBC) counts, phagocytic capacity of polymorphonuclear leukocytes (PMNL), virus induced interferon-α (IFN-α) production, mitogen induced proliferation and interleukin 2 (IL-2) production of mononuclear cells (MNC) in vitro was studied in blood collected from 124 Yorkshire piglets, aged 8 weeks. The piglets were the offspring from 12 sires and 31 dams. Data from an earlier experiment, including 96 piglets of seven sires and 24 dams, were added when estimating heritabilities for Con A induced proliferation and IL-2 production. The highest heritability (h(2)=0.87±0.41) was estimated for the total number of PMNL. Medium high heritabilities (h(2)=0.3−0.4) were estimated for the phagocytic capacity of PMNL, Con A induced proliferation and IL-2 production and the total number of WBC, while the heritability estimates were lower (h(2)=0.00−0.08±0.12) for the total number of lymphocytes, serum concentrations of Ig and IFN-α production. Pronounced differences between litters from various dams were found for total number of lymphocytes, IFN-α production, Con A induced proliferation and IL-2 production. The Con A induced proliferation was positively correlated (r=0.48, P<0.001) with the IL-2 production and both these parameters were correlated (r=0.44 and 0.37, respectively, P<0.001) to the virus induced IFN-α production. Despite these positive correlations, no parental offspring group was uniformly superior across all traits measured. However, the heritabilities estimated for the immune parameters are sufficiently high to be used as genetic markers in selection for general immune competence of swine.
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spelling pubmed-71199062020-04-08 Genetic variation in parameters reflecting immune competence of swine Edfors-Lilja, Inger Wattrang, Eva Magnusson, U. Fossum, Caroline Vet Immunol Immunopathol Article Genetic variation in total and differential white blood cell (WBC) counts, phagocytic capacity of polymorphonuclear leukocytes (PMNL), virus induced interferon-α (IFN-α) production, mitogen induced proliferation and interleukin 2 (IL-2) production of mononuclear cells (MNC) in vitro was studied in blood collected from 124 Yorkshire piglets, aged 8 weeks. The piglets were the offspring from 12 sires and 31 dams. Data from an earlier experiment, including 96 piglets of seven sires and 24 dams, were added when estimating heritabilities for Con A induced proliferation and IL-2 production. The highest heritability (h(2)=0.87±0.41) was estimated for the total number of PMNL. Medium high heritabilities (h(2)=0.3−0.4) were estimated for the phagocytic capacity of PMNL, Con A induced proliferation and IL-2 production and the total number of WBC, while the heritability estimates were lower (h(2)=0.00−0.08±0.12) for the total number of lymphocytes, serum concentrations of Ig and IFN-α production. Pronounced differences between litters from various dams were found for total number of lymphocytes, IFN-α production, Con A induced proliferation and IL-2 production. The Con A induced proliferation was positively correlated (r=0.48, P<0.001) with the IL-2 production and both these parameters were correlated (r=0.44 and 0.37, respectively, P<0.001) to the virus induced IFN-α production. Despite these positive correlations, no parental offspring group was uniformly superior across all traits measured. However, the heritabilities estimated for the immune parameters are sufficiently high to be used as genetic markers in selection for general immune competence of swine. Published by Elsevier B.V. 1994-01 2002-12-20 /pmc/articles/PMC7119906/ /pubmed/8128606 http://dx.doi.org/10.1016/0165-2427(94)90011-6 Text en Copyright © 1994 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Edfors-Lilja, Inger
Wattrang, Eva
Magnusson, U.
Fossum, Caroline
Genetic variation in parameters reflecting immune competence of swine
title Genetic variation in parameters reflecting immune competence of swine
title_full Genetic variation in parameters reflecting immune competence of swine
title_fullStr Genetic variation in parameters reflecting immune competence of swine
title_full_unstemmed Genetic variation in parameters reflecting immune competence of swine
title_short Genetic variation in parameters reflecting immune competence of swine
title_sort genetic variation in parameters reflecting immune competence of swine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119906/
https://www.ncbi.nlm.nih.gov/pubmed/8128606
http://dx.doi.org/10.1016/0165-2427(94)90011-6
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