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Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity

The complement system is a part of the natural immune regulation mechanism against invading pathogens. Complement activation from three different pathways (classical, lectin, and alternative) leads to the formation of C5-convertase, an enzyme for cleavage of C5 into C5a and C5b, followed by C6, C7,...

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Autores principales: Khoa, D. V. A., Wimmers, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554877/
https://www.ncbi.nlm.nih.gov/pubmed/26194222
http://dx.doi.org/10.5713/ajas.14.0734
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author Khoa, D. V. A.
Wimmers, K.
author_facet Khoa, D. V. A.
Wimmers, K.
author_sort Khoa, D. V. A.
collection PubMed
description The complement system is a part of the natural immune regulation mechanism against invading pathogens. Complement activation from three different pathways (classical, lectin, and alternative) leads to the formation of C5-convertase, an enzyme for cleavage of C5 into C5a and C5b, followed by C6, C7, C8, and C9 in membrane attack complex. The C9 is the last complement component of the terminal lytic pathway, which plays an important role in lysis of the target cells depending on its self-polymerization to form transmembrane channels. To address the association of C9 with traits related to disease resistance, the complete porcine C9 cDNA was comparatively sequenced to detect single nucleotide polymorphisms (SNPs) in pigs of the breeds Hampshire (HS), Duroc (DU), Berlin miniature pig (BMP), German Landrace (LR), Pietrain (PIE), and Muong Khuong (Vietnamese potbelly pig). Genotyping was performed in 417 F(2) animals of a resource population (DUMI: DU×BMP) that were vaccinated with Mycoplasma hyopneumoniae, Aujeszky diseases virus and porcine respiratory and reproductive syndrome virus at 6, 14 and 16 weeks of age, respectively. Two SNPs were detected within the third exon. One of them has an amino acid substitution. The European porcine breeds (LR and PIE) show higher allele frequency of these SNPs than Vietnamese porcine breed (MK). Association of the substitution SNP with hemolytic complement activity indicated statistically significant differences between genotypes in the classical pathway but not in the alternative pathway. The interactions between eight time points of measurement of complement activity before and after vaccinations and genotypes were significantly different. The difference in hemolytic complement activity in the both pathways depends on genotype, kind of vaccine, age and the interaction to the other complement components. These results promote the porcine C9 (pC9) as a candidate gene to improve general animal health in the future.
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spelling pubmed-45548772015-09-01 Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity Khoa, D. V. A. Wimmers, K. Asian-Australas J Anim Sci Article The complement system is a part of the natural immune regulation mechanism against invading pathogens. Complement activation from three different pathways (classical, lectin, and alternative) leads to the formation of C5-convertase, an enzyme for cleavage of C5 into C5a and C5b, followed by C6, C7, C8, and C9 in membrane attack complex. The C9 is the last complement component of the terminal lytic pathway, which plays an important role in lysis of the target cells depending on its self-polymerization to form transmembrane channels. To address the association of C9 with traits related to disease resistance, the complete porcine C9 cDNA was comparatively sequenced to detect single nucleotide polymorphisms (SNPs) in pigs of the breeds Hampshire (HS), Duroc (DU), Berlin miniature pig (BMP), German Landrace (LR), Pietrain (PIE), and Muong Khuong (Vietnamese potbelly pig). Genotyping was performed in 417 F(2) animals of a resource population (DUMI: DU×BMP) that were vaccinated with Mycoplasma hyopneumoniae, Aujeszky diseases virus and porcine respiratory and reproductive syndrome virus at 6, 14 and 16 weeks of age, respectively. Two SNPs were detected within the third exon. One of them has an amino acid substitution. The European porcine breeds (LR and PIE) show higher allele frequency of these SNPs than Vietnamese porcine breed (MK). Association of the substitution SNP with hemolytic complement activity indicated statistically significant differences between genotypes in the classical pathway but not in the alternative pathway. The interactions between eight time points of measurement of complement activity before and after vaccinations and genotypes were significantly different. The difference in hemolytic complement activity in the both pathways depends on genotype, kind of vaccine, age and the interaction to the other complement components. These results promote the porcine C9 (pC9) as a candidate gene to improve general animal health in the future. Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2015-09 /pmc/articles/PMC4554877/ /pubmed/26194222 http://dx.doi.org/10.5713/ajas.14.0734 Text en Copyright © 2015 by Asian-Australasian Journal of Animal Sciences
spellingShingle Article
Khoa, D. V. A.
Wimmers, K.
Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity
title Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity
title_full Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity
title_fullStr Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity
title_full_unstemmed Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity
title_short Genetic Association of the Porcine C9 Complement Component with Hemolytic Complement Activity
title_sort genetic association of the porcine c9 complement component with hemolytic complement activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554877/
https://www.ncbi.nlm.nih.gov/pubmed/26194222
http://dx.doi.org/10.5713/ajas.14.0734
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