[瑞士Fleckvieh牛已知和新的遗传缺陷及其流行概况]。

IF 0.8 4区 农林科学 Q3 VETERINARY SCIENCES
B A Weber, T Leuenberger, M Hauser, J C F Bousmar, C Gurtner, F R Seefried, C Drögemüller, J G P Jacinto
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引用次数: 0

摘要

简介:在瑞士的Fleckvieh (SF)牛品种中,由荷尔斯坦(HO)和西蒙塔尔(SI)品种杂交而来,迄今为止已经描述了两种遗传性疾病,血小板病变(TP)和牛扩张性心肌病(BDCMP),以及四种所谓的生育单倍型,Fleckvieh单倍型1,2,4,5 (FH1,2,4,5)。此外,自2015年发现与apob相关的遗传性疾病胆固醇缺乏症(CD)后,已在密切相关的HO品种中得到了全面的描述,但迄今尚未在SF品种中报道。遗传性色素性视网膜炎(RP)导致RP1基因致病性变异的纯合子携带者进行性视网膜变性,已被证明发生在几个欧洲牛品种中,但尚未在SF人群中描述。本研究的目的是确定SF和两个密切相关的品种HO和SI中已知遗传缺陷和生育单倍型以及CD的患病率。我们还调查了RP在SF人群中的患病率,并通过一系列病例描述了这种遗传疾病。为了确定患病率,我们分析了来自瑞士育种协会数据库的65000多头牛的SNP阵列基因分型数据,并基于这些结果对4头RP1纯合子动物进行了临床评估。SF中引起RP的等位基因频率为13%,而以前只在HO中描述的引起CD的等位基因在SF中发现,等位基因频率为1.17%。其余6个遗传缺陷发生在SF中,或者等位基因频率较低(TP 0.24%, BDCMP 1.93%, FH2 0.03%, FH5 0.02%),或者根本不存在(FH1, FH4)。4只RP1纯合子动物平均年龄为7.5岁,表现出不同程度的视力障碍。总的来说,临床和病理结果与rp1相关的RP一致。在疑似病例中,通过基因检测进行RP1基因分型可以确认RP的诊断。由于常规使用SNP基因分型来估计育种值,遗传缺陷的基因型是已知的,至少在活跃的育种群体中是已知的,因此可以在交配前进行考虑。避免冒险交配将改善动物的健康和福利,防止动物损失,从而防止经济损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Overview of known and new genetic defects and their prevalence in Swiss Fleckvieh cattle].

Introduction: In the Swiss Fleckvieh (SF) cattle breed, derived from crosses between the Holstein (HO) and Simmental (SI) breeds, two inherited diseases, thrombocytopathy (TP) and bovine dilated cardiomyopathy (BDCMP), and four so-called fertility haplotypes, Fleckvieh haplotype 1,2,4,5 (FH1,2,4,5), have been described so far. In addition, the APOB-related hereditary disease cholesterol deficiency (CD) has been thoroughly described in the closely related HO breed after its discovery in 2015, but to date it has not been reported in the SF breed. The hereditary disease retinitis pigmentosa (RP), which leads to progressive retinal degeneration in homozygous carriers of a pathogenic variant of the RP1 gene, has been shown to occur in several European cattle breeds, but has not been described in the SF population. The aim of this study was to determine the prevalence of the known genetic defects and fertility haplotypes, as well as CD, in SF and the two closely related breeds, HO and SI. We also investigated the prevalence of RP in the SF population and characterised the genetic disease through a case series. To determine the prevalence, the SNP array genotyping data of over 65 000 cattle from the Swiss breeding association database were analyzed and based on those results, four RP1 homozygous animals were clinically evaluated. The allele frequency of the RP causing allele in SF was 13 % and the CD causing allele, previously described only in HO, was found in SF with an allele frequency of 1,17 %. The remaining six genetic defects occurred in SF either with a low allele frequency (TP 0,24 %, BDCMP 1,93 %, FH2 0,03 %, FH5 0,02 %) or not at all (FH1, FH4). The four RP1 homozygous animals with a mean age of 7,5 years old Showed varying degrees of visual impairment. Overall, the clinical and pathological findings were consistent with RP1-associated RP. In a suspected case, RP1 genotyping by genetic testing can confirm the diagnosis of RP. Due to the routine use of SNP genotyping to estimate breeding values, the genotypes of genetic defects are known, at least in the active breeding population, and can therefore be considered before matings. Avoiding risk mating will improve animal health and welfare and prevent animal losses, and therefore economic losses.

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来源期刊
Schweizer Archiv fur Tierheilkunde
Schweizer Archiv fur Tierheilkunde 农林科学-兽医学
CiteScore
1.50
自引率
14.30%
发文量
46
审稿时长
18-36 weeks
期刊介绍: Das Schweizer Archiv für Tierheilkunde ist die älteste veterinärmedizinische Zeitschrift der Welt (gegründet 1816). Es ist das wissenschaftliche und praxisbezogene offizielle Publikationsorgan der Gesellschaft Schweizer Tierärztinnen und Tierärzte.
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