Badia-Bringué Gerard, Canive María, Vázquez Patricia, Garrido Joseba M, Fernández Almudena, Juste Ramón A, Jiménez José Antonio, González-Recio Oscar, Alonso-Hearn Marta
Department of Animal Health, NEIKER-Basque Institute for Agricultural Research and Development, Basque Research and Technology Alliance (BRTA), 48160 Derio, Spain.
Doctoral Program in Molecular Biology and Biomedicine, Universidad del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU), 48940 Leioa, Spain.
Microorganisms. 2023 Jul 15;11(7):1817. doi: 10.3390/microorganisms11071817.
The mechanisms underlying host resistance to subsp. (MAP) infection are largely unknown. In the current study, we hypothesize that cows with an ability to produce higher levels of interferon-gamma (IFNɣ) might control MAP infection more successfully. To test this hypothesis, IFNɣ production was measured using a specific IFNɣ ELISA kit in avian purified protein derivative (aPPD)-stimulated blood samples collected from 152 Holstein cattle. DNA isolated from peripheral blood samples of the animals included in the study was genotyped with the EuroG Medium-Density Bead Chip, and the genotypes were imputed to whole-genome sequencing. A genome-wide association analysis (GWAS) revealed that high levels of IFNɣ in response to the aPPD were associated with a specific genetic profile (heritability = 0.64) and allowed the identification of 71 SNPs, 40 quantitative trait loci (QTL), and 104 candidate genes. A functional analysis using the 104 candidate genes revealed a significant enrichment of genes involved in the innate immune response and, more specifically, in necroptosis. Taken together, our results define a heritable and distinct immunogenetic profile associated with the production of high IFNɣ levels and with the capacity of the host to lyse MAP-infected macrophages by necroptosis.
宿主对副结核分枝杆菌亚种(MAP)感染的抗性机制在很大程度上尚不清楚。在当前研究中,我们假设能够产生更高水平干扰素-γ(IFNɣ)的奶牛可能更成功地控制MAP感染。为了验证这一假设,我们使用特定的IFNɣ ELISA试剂盒,对从152头荷斯坦奶牛采集的经禽纯化蛋白衍生物(aPPD)刺激的血样中的IFNɣ产生情况进行了测定。对纳入研究的动物外周血样本中分离的DNA,使用欧洲基因组中密度珠芯片进行基因分型,并将基因型推算至全基因组测序。全基因组关联分析(GWAS)显示,对aPPD产生的高水平IFNɣ与特定的遗传图谱相关(遗传力 = 0.64),并鉴定出71个单核苷酸多态性(SNP)、40个数量性状基因座(QTL)和104个候选基因。对这104个候选基因进行的功能分析表明,参与固有免疫反应,更具体地说是坏死性凋亡的基因有显著富集。综上所述,我们的结果定义了一种可遗传的独特免疫遗传图谱,其与高水平IFNɣ的产生以及宿主通过坏死性凋亡裂解MAP感染巨噬细胞的能力相关。