Tizioto Polyana C, Kim JaeWoo, Seabury Christopher M, Schnabel Robert D, Gershwin Laurel J, Van Eenennaam Alison L, Toaff-Rosenstein Rachel, Neibergs Holly L, Taylor Jeremy F
Embrapa Southeast Livestock, São Carlos, São Paulo, Brazil; Division of Animal Sciences, University of Missouri, Columbia, Missouri, United States of America.
Division of Animal Sciences, University of Missouri, Columbia, Missouri, United States of America.
PLoS One. 2015 Jun 29;10(6):e0131459. doi: 10.1371/journal.pone.0131459. eCollection 2015.
Susceptibility to bovine respiratory disease (BRD) is multi-factorial and is influenced by stress in conjunction with infection by both bacterial and viral pathogens. While vaccination is broadly used in an effort to prevent BRD, it is far from being fully protective and cases diagnosed from a combination of observed clinical signs without any attempt at identifying the causal pathogens are usually treated with antibiotics. Dairy and beef cattle losses from BRD are profound worldwide and genetic studies have now been initiated to elucidate host loci which underlie susceptibility with the objective of enabling molecular breeding to reduce disease prevalence. In this study, we employed RNA sequencing to examine the bronchial lymph node transcriptomes of controls and beef cattle which had individually been experimentally challenged with bovine respiratory syncytial virus, infectious bovine rhinotracheitis, bovine viral diarrhea virus, Pasteurella multocida, Mannheimia haemolytica or Mycoplasma bovis to identify the genes that are involved in the bovine immune response to infection. We found that 142 differentially expressed genes were located in previously described quantitative trait locus regions associated with risk of BRD. Mutations affecting the expression or amino acid composition of these genes may affect disease susceptibility and could be incorporated into molecular breeding programs. Genes involved in innate immunity were generally found to be differentially expressed between the control and pathogen-challenged animals suggesting that variation in these genes may lead to a heritability of susceptibility that is pathogen independent. However, we also found pathogen-specific expression profiles which suggest that host genetic variation for BRD susceptibility is pathogen dependent.
牛呼吸道疾病(BRD)的易感性是多因素的,受应激以及细菌和病毒病原体感染的共同影响。虽然疫苗接种广泛用于预防BRD,但远未达到完全保护的效果,并且通常对仅根据观察到的临床症状诊断出的病例(未尝试鉴定致病病原体)使用抗生素进行治疗。BRD给全球奶牛和肉牛造成的损失巨大,目前已启动基因研究以阐明易感性背后的宿主基因座,目的是通过分子育种降低疾病发生率。在本研究中,我们采用RNA测序技术检测对照牛以及分别经牛呼吸道合胞病毒、传染性牛鼻气管炎病毒、牛病毒性腹泻病毒、多杀性巴氏杆菌、溶血曼氏杆菌或牛支原体实验性攻毒的肉牛的支气管淋巴结转录组,以鉴定参与牛对感染免疫反应的基因。我们发现142个差异表达基因位于先前描述的与BRD风险相关的数量性状基因座区域。影响这些基因表达或氨基酸组成的突变可能影响疾病易感性,并可纳入分子育种计划。通常发现参与先天免疫的基因在对照动物和受病原体攻击的动物之间存在差异表达,这表明这些基因的变异可能导致与病原体无关的易感性遗传。然而,我们也发现了病原体特异性的表达谱,这表明BRD易感性的宿主基因变异是病原体依赖性的。