SalmoBreed AS, Bergen, Norway.
J Hered. 2019 Oct 10;110(6):720-726. doi: 10.1093/jhered/esz040.
Cardiomyopathy syndrome is a severe, viral disease of Atlantic salmon that mostly affects farmed animals during their late production stage at sea. Caused by piscine myocarditis virus (PMCV), over the past few years outbreaks due to this disease have resulted in significant losses to the aquaculture industry. However, there is currently no vaccine that has proven effective against this virus. In this study, using a challenge model, we investigated the genetic variation for resistance to PMCV, by screening a large number of animals using a 55 K SNP array. In particular, we aimed to identify genetic markers that are tightly linked to higher disease resistance and can potentially be used in breeding programs. Using genomic information, we estimated a heritability of 0.51 ± 0.06, suggesting that resistance against this virus, to a great extent, is controlled by genetic factors. Through association analysis, we identified a significant quantitative trait locus (QTL) on chromosome 27, explaining approximately 57% of the total additive genetic variation. The region harboring this QTL contains various immune-related candidate genes, many of which have previously been shown to have a different expression profile between the naïve and infected animals. We also identified a suggestive association on chromosome 12, with the QTL linked markers located in 2 putatively immune-related genes. These results are of particular interest, as they can readily be implemented into breeding programs, can further assist in fine-mapping the causative mutations, and help in better understanding the biology of the disease and the immunological mechanisms underlying resistance against PMCV.
心肌病综合征是一种严重的病毒性疾病,主要影响养殖大西洋鲑鱼在海上养殖后期。该病由鱼类心肌炎病毒(PMCV)引起,近年来,由于这种疾病的爆发,给水产养殖业造成了重大损失。然而,目前还没有针对这种病毒的有效疫苗。在这项研究中,我们使用了一种挑战模型,通过使用 55 K SNP 阵列对大量动物进行筛选,来研究对 PMCV 的抗性的遗传变异。特别是,我们旨在确定与更高疾病抗性紧密相关的遗传标记,这些标记有可能被用于选育计划。利用基因组信息,我们估计出了 0.51±0.06 的遗传力,表明对这种病毒的抗性在很大程度上受遗传因素控制。通过关联分析,我们在第 27 号染色体上确定了一个显著的数量性状位点(QTL),该 QTL 解释了大约 57%的总加性遗传变异。包含该 QTL 的区域含有各种与免疫相关的候选基因,其中许多基因在未感染和感染动物之间的表达谱存在差异。我们还在第 12 号染色体上发现了一个提示性关联,QTL 连锁标记位于 2 个推测的免疫相关基因中。这些结果特别有趣,因为它们可以很容易地被应用于选育计划,可以进一步协助对致病突变进行精细定位,并有助于更好地了解疾病的生物学和对 PMCV 的免疫机制。