USDA, ARS, US Meat Animal Research Center, Clay Center, Nebraska, 68933, USA.
University of Nebraska-Lincoln, Great Plains Veterinary Educational Center, Clay Center, Nebraska, 68933, USA.
F1000Res. 2024 Mar 4;11:385. doi: 10.12688/f1000research.109488.2. eCollection 2022.
Bovine congestive heart failure (BCHF) has become increasingly prevalent among feedlot cattle in the Western Great Plains of North America with up to 7% mortality in affected herds. BCHF is an untreatable complex condition involving pulmonary hypertension that culminates in right ventricular failure and death. Genes associated with BCHF in feedlot cattle have not been previously identified. Our aim was to search for genomic regions associated with this disease.
A retrospective, matched case-control design with 102 clinical BCHF cases and their unaffected pen mates was used in a genome-wide association study. Paired nominal data from approximately 560,000 filtered single nucleotide polymorphisms (SNPs) were analyzed with McNemar's test.
Two independent genomic regions were identified as having the most significant association with BCHF: the arrestin domain-containing protein 3 gene ( ), and the nuclear factor IA gene ( , mid- -values, 1x10 and 2x10 , respectively). Animals with two copies of risk alleles at either gene were approximately eight-fold more likely to have BCHF than their matched pen mates with either one or zero risk alleles at both genes (CI = 3-17). Further, animals with two copies of risk alleles at both genes were 28-fold more likely to have BCHF than all others ( -value = 1×10 , CI = 4-206). A missense variant in (C182Y) represents a potential functional variant since the C182 codon is conserved among all other jawed vertebrate species observed. A two-SNP test with markers in both genes showed 29% of 273 BCHF cases had homozygous risk genotypes in both genes, compared to 2.5% in 198 similar unaffected feedlot cattle. This and other DNA tests may be useful for identifying feedlot animals with the highest risk for BCHF in the environments described here.
Although pathogenic roles for variants in the and genes are unknown, their discovery facilitates classifying animals by genetic risk and allows cattle producers to make informed decisions for selective breeding and animal health management.
北美大平原西部的牛饲养场中,牛充血性心力衰竭(BCHF)的发病率越来越高,患病牛群的死亡率高达 7%。BCHF 是一种无法治愈的复杂病症,涉及肺动脉高压,最终导致右心室衰竭和死亡。之前尚未确定与牛饲养场中的 BCHF 相关的基因。我们的目的是寻找与这种疾病相关的基因组区域。
采用回顾性、配对病例对照设计,对 102 例临床 BCHF 病例及其未受影响的同栏牛进行了全基因组关联研究。使用 McNemar 检验对来自约 560,000 个过滤单核苷酸多态性(SNP)的配对名义数据进行分析。
鉴定出两个与 BCHF 最显著相关的独立基因组区域: arrestin 结构域蛋白 3 基因()和核因子 IA 基因(),中间值分别为 1x10 和 2x10,在这两个基因中,每个基因具有两个风险等位基因的动物患 BCHF 的可能性是其匹配栏中具有两个或零个风险等位基因的动物的约 8 倍(CI = 3-17)。此外,两个基因都具有两个风险等位基因的动物患 BCHF 的可能性是所有其他动物的 28 倍(值= 1×10,CI = 4-206)。在(C182Y)中发现的错义变体是一个潜在的功能变体,因为 C182 密码子在所有观察到的有颌脊椎动物物种中都是保守的。在这两个基因中的两个标记物的双 SNP 检验显示,273 例 BCHF 病例中有 29%的动物在两个基因中均为纯合风险基因型,而在 198 例类似的未受影响的饲养场牛中,只有 2.5%的动物具有这种基因型。这种和其他 DNA 测试可能有助于在描述的环境中识别出 BCHF 风险最高的饲养场动物。
尽管在和基因中的变体的致病作用尚不清楚,但它们的发现促进了通过遗传风险对动物进行分类,并允许牛饲养者做出明智的决策,以进行选择性繁殖和动物健康管理。