Heritability and genome-wide association study of vaccine-induced immune response in Beagles: A pilot study

生物 遗传力 接种疫苗 免疫系统 病毒学 遗传变异 全基因组关联研究 抗原 免疫学 减毒疫苗 钩端螺旋体 犬瘟热 基因型 病毒 遗传学 单核苷酸多态性 毒力 钩端螺旋体病 基因
作者
Jeanna M. Blake,James P. Thompson,Harm HogenEsch,Kari J. Ekenstedt
出处
期刊:Vaccine [Elsevier BV]
卷期号:42 (12): 3099-3106
标识
DOI:10.1016/j.vaccine.2024.03.076
摘要

Both genetic and non-genetic factors contribute to individual variation in the immune response to vaccination. Understanding how genetic background influences variation in both magnitude and persistence of vaccine-induced immunity is vital for improving vaccine development and identifying possible causes of vaccine failure. Dogs provide a relevant biomedical model for investigating mammalian vaccine genetics; canine breed structure and long linkage disequilibrium simplify genetic studies in this species compared to humans. The objective of this study was to estimate the heritability of the antibody response to vaccination against viral and bacterial pathogens, and to identify genes driving variation of the immune response to vaccination in Beagles. Sixty puppies were immunized following a standard vaccination schedule with an attenuated combination vaccine containing antigens for canine adenovirus type 2, canine distemper virus, canine parainfluenza virus, canine parvovirus, and four strains of Leptospira bacteria. Serum antibody measurements for each viral and bacterial component were measured at multiple time points. Heritability estimations and GWAS were conducted using SNP genotypes at 279,902 markers together with serum antibody titer phenotypes. The heritability estimates were: (1) to Leptospira antigens, ranging from 0.178 to 0.628; and (2) to viral antigens, ranging from 0.199 to 0.588. There was not a significant difference between overall heritability of vaccine-induced immune response to Leptospira antigens compared to viral antigens. Genetic architecture indicates that SNPs of low to high effect contribute to immune response to vaccination. GWAS identified two genetic markers associated with vaccine-induced immune response phenotypes. Collectively, these findings indicate that genetic regulation of the immune response to vaccination is antigen-specific and influenced by multiple genes of small effect.
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