首页> 美国卫生研究院文献>other >Sequence-Based Genotyping of Expressed Swine Leukocyte Antigen Class I Alleles by Next-Generation Sequencing Reveal Novel Swine Leukocyte Antigen Class I Haplotypes and Alleles in Belgian Danish and Kenyan Fattening Pigs and Göttingen Minipigs
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Sequence-Based Genotyping of Expressed Swine Leukocyte Antigen Class I Alleles by Next-Generation Sequencing Reveal Novel Swine Leukocyte Antigen Class I Haplotypes and Alleles in Belgian Danish and Kenyan Fattening Pigs and Göttingen Minipigs

机译:通过下一代测序对表达的猪白细胞抗原I类等位基因进行基于序列的基因分型揭示了比利时丹麦和肯尼亚育肥猪和哥廷根小型猪的新型猪白细胞抗原I类单倍型和等位基因

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摘要

The need for typing of the swine leukocyte antigen (SLA) is increasing with the expanded use of pigs as models for human diseases and organ-transplantation experiments, their use in infection studies, and for design of veterinary vaccines. Knowledge of SLA sequences is furthermore a prerequisite for the prediction of epitope binding in pigs. The low number of known SLA class I alleles and the limited knowledge of their prevalence in different pig breeds emphasizes the need for efficient SLA typing methods. This study utilizes an SLA class I-typing method based on next-generation sequencing of barcoded PCR amplicons. The amplicons were generated with universal primers and predicted to resolve 68–88% of all known SLA class I alleles dependent on amplicon size. We analyzed the SLA profiles of 72 pigs from four different pig populations; Göttingen minipigs and Belgian, Kenyan, and Danish fattening pigs. We identified 67 alleles, nine previously described haplotypes and 15 novel haplotypes. The highest variation in SLA class I profiles was observed in the Danish pigs and the lowest among the Göttingen minipig population, which also have the highest percentage of homozygote individuals. Highlighting the fact that there are still numerous unknown SLA class I alleles to be discovered, a total of 12 novel SLA class I alleles were identified. Overall, we present new information about known and novel alleles and haplotypes and their prevalence in the tested pig populations.
机译:随着人们越来越多地将猪用作人类疾病和器官移植实验的模型,它们在感染研究中的应用以及兽医疫苗的设计,对猪白细胞抗原(SLA)进行分型的需求日益增加。此外,了解SLA序列是预测猪中表位结合的先决条件。已知的SLA I类等位基因数量很少,并且在不同猪种中其流行程度的知识有限,这表明需要有效的SLA分型方法。这项研究利用基于条形码PCR扩增子的下一代测序的SLA I类分型方法。扩增子是由通用引物产生的,并预计可解析所有已知SLA I类等位基因的68–88%,具体取决于扩增子的大小。我们分析了来自四个不同猪群的72头猪的SLA谱;哥廷根小型猪和比利时,肯尼亚和丹麦的育肥猪。我们确定了67个等位基因,9个先前描述的单倍型和15个新的单倍型。在丹麦猪中观察到SLA I类谱的最高变异,在哥廷根小型猪种群中最低,这也是纯合子个体百分比最高。突出表明仍有许多未知的SLA I类等位基因被发现的事实,总共鉴定出12种新的SLA I类等位基因。总体而言,我们提供了有关已知和新型等位基因和单倍型及其在测试猪群中的流行情况的新信息。

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