Moen Thomas, Torgersen Jacob, Santi Nina, Davidson William S, Baranski Matthew, Ødegård Jørgen, Kjøglum Sissel, Velle Bente, Kent Matthew, Lubieniecki Krzysztof P, Isdal Eivind, Lien Sigbjørn
AquaGen, 7462 Trondheim, Norway
AquaGen, 7462 Trondheim, Norway.
Genetics. 2015 Aug;200(4):1313-26. doi: 10.1534/genetics.115.175406. Epub 2015 Jun 2.
Infectious pancreatic necrosis virus (IPNV) is the cause of one of the most prevalent diseases in farmed Atlantic salmon (Salmo salar). A quantitative trait locus (QTL) has been found to be responsible for most of the genetic variation in resistance to the virus. Here we describe how a linkage disequilibrium-based test for deducing the QTL allele was developed, and how it was used to produce IPN-resistant salmon, leading to a 75% decrease in the number of IPN outbreaks in the salmon farming industry. Furthermore, we describe how whole-genome sequencing of individuals with deduced QTL genotypes was used to map the QTL down to a region containing an epithelial cadherin (cdh1) gene. In a coimmunoprecipitation assay, the Cdh1 protein was found to bind to IPNV virions, strongly indicating that the protein is part of the machinery used by the virus for internalization. Immunofluorescence revealed that the virus colocalizes with IPNV in the endosomes of homozygous susceptible individuals but not in the endosomes of homozygous resistant individuals. A putative causal single nucleotide polymorphism was found within the full-length cdh1 gene, in phase with the QTL in all observed haplotypes except one; the absence of a single, all-explaining DNA polymorphism indicates that an additional causative polymorphism may contribute to the observed QTL genotype patterns. Cdh1 has earlier been shown to be necessary for the internalization of certain bacteria and fungi, but this is the first time the protein is implicated in internalization of a virus.
传染性胰腺坏死病毒(IPNV)是养殖大西洋鲑(Salmo salar)中最常见疾病之一的病因。已发现一个数量性状位点(QTL)是对该病毒抗性的大部分遗传变异的原因。在此,我们描述了如何开发一种基于连锁不平衡的测试来推导QTL等位基因,以及如何将其用于培育抗IPN的鲑鱼,从而使鲑鱼养殖行业中IPN爆发的数量减少了75%。此外,我们描述了如何利用推导的QTL基因型个体的全基因组测序将QTL定位到一个包含上皮钙黏蛋白(cdh1)基因的区域。在共免疫沉淀试验中,发现Cdh1蛋白与IPNV病毒粒子结合,强烈表明该蛋白是病毒用于内化的机制的一部分。免疫荧光显示,在纯合易感个体的内体中病毒与IPNV共定位,但在纯合抗性个体的内体中则不共定位。在全长cdh1基因内发现了一个推定的因果单核苷酸多态性,除一种单倍型外,在所有观察到的单倍型中均与QTL处于同一相位;缺乏一个能解释所有情况的单一DNA多态性表明,可能还有一个致病多态性导致了观察到的QTL基因型模式。先前已表明Cdh1对某些细菌和真菌的内化是必需的,但这是该蛋白首次与病毒内化有关。