Department of Animal Science, The University of Tennessee, 2506 River Drive, Knoxville, TN, 37996, USA.
Department of Entomology and Plant Pathology, The University of Tennessee, 2431 Joe Johnson Drive, Knoxville, TN, 37996, USA.
Immunogenetics. 2018 Sep;70(9):553-562. doi: 10.1007/s00251-018-1065-3. Epub 2018 Jun 3.
Mastitis is a detrimental disease in the dairy industry that decreases milk quality and costs upwards of $2 billion annually. Often, mastitis results from bacteria entering the gland through the teat opening. Streptococcus uberis is responsible for a high percentage of subclinical and clinical mastitis. Following an intramammary experimental challenge with S. uberis on Holstein cows (n = 40), milk samples were collected and somatic cell counts (SCC) were determined by the Dairy Herd Improvement Association Laboratory. Traditional genome-wide association studies (GWAS) have utilized test day SCC or SCC lactation averages to identify loci of interest. Our approach utilizes SCC collected following a S. uberis experimental challenge to generate three novel phenotypes: (1) area under the curve (AUC) of SCC for 0-7 days and (2) 0-28 days post-challenge; and (3) when SCC returned to below 200,000 cells/mL post-challenge (< 21 days, 21-28 days, or > 28 days). Polymorphisms were identified using Illumina's BovineSNP50 v2 DNA BeadChip. Associations were tested using Plink software and identified 16 significant (p < 1.0 × 10) single-nucleotide polymorphisms (SNPs) across the phenotypes. Most significant SNPs were in genes linked to cell signaling, migration, and apoptosis. Several have been recognized in relation to infectious processes (ATF7, SGK1, and PACRG), but others less so (TRIO, GLRA1, CELSR2, TIAM2, CPE). Further investigation of these genes and their roles in inflammation (e.g., SCC) can provide potential targets that influence resolution of mammary gland infection. Likewise, further investigation of the identified SNP with mastitis and other disease phenotypes can provide greater insight to the potential of these SNP as genetic markers.
乳腺炎是乳制品行业的一种有害疾病,会降低牛奶质量,每年造成的损失超过 20 亿美元。乳腺炎通常是由于细菌通过乳头开口进入乳腺。停乳链球菌是引起亚临床和临床乳腺炎的主要原因之一。在荷斯坦奶牛(n=40)中进行了停乳链球菌的实验性乳腺内挑战后,收集了奶样,并通过乳业 herd improvement association(DHI)实验室确定了体细胞计数(SCC)。传统的全基因组关联研究(GWAS)已经利用了测试日 SCC 或 SCC 泌乳平均值来确定感兴趣的基因座。我们的方法利用停乳链球菌实验性挑战后收集的 SCC 生成了三个新的表型:(1)0-7 天 SCC 的曲线下面积(AUC)和(2)0-28 天;以及(3)SCC 恢复到挑战后低于 200,000 个细胞/ml 以下(<21 天,21-28 天或>28 天)。使用 Illumina 的 BovineSNP50 v2 DNA BeadChip 鉴定了多态性。使用 Plink 软件测试了关联,并在表型中鉴定了 16 个显著(p<1.0×10)的单核苷酸多态性(SNP)。最显著的 SNP 位于与细胞信号转导、迁移和凋亡相关的基因中。其中一些与感染过程有关(ATF7、SGK1 和 PACRG),但其他则较少(TRIO、GLRA1、CELSR2、TIAM2 和 CPE)。进一步研究这些基因及其在炎症(如 SCC)中的作用,可以为影响乳腺感染消退的潜在靶点提供参考。同样,进一步研究与乳腺炎和其他疾病表型相关的鉴定 SNP,可以为这些 SNP 作为遗传标记的潜力提供更深入的了解。