INRA, UMR 1348 PEGASE, Domaine de la Prise, F-35590 Saint-Gilles, France.
Genet Sel Evol. 2014 Feb 19;46(1):14. doi: 10.1186/1297-9686-46-14.
Coccidiosis is a major parasitic disease that causes huge economic losses to the poultry industry. Its pathogenicity leads to depression of body weight gain, lesions and, in the most serious cases, death in affected animals. Genetic variability for resistance to coccidiosis in the chicken has been demonstrated and if this natural resistance could be exploited, it would reduce the costs of the disease. Previously, a design to characterize the genetic regulation of Eimeria tenella resistance was set up in a Fayoumi × Leghorn F2 cross. The 860 F2 animals of this design were phenotyped for weight gain, plasma coloration, hematocrit level, intestinal lesion score and body temperature. In the work reported here, the 860 animals were genotyped for a panel of 1393 (157 microsatellites and 1236 single nucleotide polymorphism (SNP) markers that cover the sequenced genome (i.e. the 28 first autosomes and the Z chromosome). In addition, with the aim of finding an index capable of explaining a large amount of the variance associated with resistance to coccidiosis, a composite factor was derived by combining the variables of all these traits in a single variable. QTL detection was performed by linkage analysis using GridQTL and QTLMap. Single and multi-QTL models were applied.
Thirty-one QTL were identified i.e. 27 with the single-QTL model and four with the multi-QTL model and the average confidence interval was 5.9 cM. Only a few QTL were common with the previous study that used the same design but focused on the 260 more extreme animals that were genotyped with the 157 microsatellites only. Major differences were also found between results obtained with QTLMap and GridQTL.
The medium-density SNP panel made it possible to genotype new regions of the chicken genome (including micro-chromosomes) that were involved in the genetic control of the traits investigated. This study also highlights the strong variations in QTL detection between different models and marker densities.
球虫病是一种主要的寄生虫病,给家禽养殖业造成了巨大的经济损失。其致病性导致受感染动物体重增长下降、出现病变,在最严重的情况下,甚至死亡。鸡对球虫病的抗性存在遗传可变性,如果能够利用这种天然抗性,就可以降低疾病的成本。此前,在法尤姆鸡与来航鸡的 F2 杂交中设计了一个方案,用于鉴定艾美耳球虫抗性的遗传调控。该设计中的 860 只 F2 动物被表型分析体重增加、血浆着色、血细胞比容水平、肠道病变评分和体温。在本报告中,这 860 只动物被 1393 个(157 个微卫星和 1236 个单核苷酸多态性(SNP)标记)的面板进行了基因型分析,这些标记覆盖了测序基因组(即 28 条第一染色体和 Z 染色体)。此外,为了找到一个能够解释与球虫病抗性相关的大量变异的指标,通过将所有这些性状的变量组合成一个单一变量,衍生出一个复合因子。通过 GridQTL 和 QTLMap 进行连锁分析进行 QTL 检测。应用了单 QTL 和多 QTL 模型。
鉴定出 31 个 QTL,即 27 个单 QTL 模型和 4 个多 QTL 模型,平均置信区间为 5.9cM。与使用相同设计但重点关注仅用 157 个微卫星进行基因分型的 260 只更极端动物的先前研究相比,只有少数 QTL 是共同的。与 QTLMap 和 GridQTL 获得的结果之间也存在显著差异。
中密度 SNP 面板使得对涉及所研究性状遗传控制的鸡基因组新区域(包括微染色体)进行基因分型成为可能。本研究还强调了不同模型和标记密度之间 QTL 检测的强烈变化。