Sun Hongyan, Li Huan
1College of Animal Science and Technology, Yangzhou University, Yangzhou, 225009 Jiangsu China.
FAMSUN Co., Ltd., National Feed Processing Equipment Engineering Technology Research Center, Yangzhou, China.
3 Biotech. 2019 Sep;9(9):320. doi: 10.1007/s13205-019-1851-0. Epub 2019 Aug 5.
In this study, RNA-seq gene expression data were obtained for three different immune tissues (bone marrow, thymus, and bursa) at two time points from birds with three phenotypes (non-infected, resistant, and susceptible birds). A total of 380 significant differentially expressed genes (DEGs) were commonly expressed in each of the three tissues in the contrast of susceptible vs. non-infected birds at 5 days post-infection (dpi) and 106 significant DEGs were shared in susceptible vs. resistant birds at 5 dpi. For the co-expressed DEGs, a relatively high consistency in expression pattern was identified in the three tissues for the two contrasts. These co-expressed DEGs were involved in the biological process of response to stimulus, regulation of cell proliferation, signal transduction, and immune system. Moreover, three gene networks were identified for the co-expressed DEGs, showing the activation of the humoral immune response, cell survival, growth and death were the concordant response for the three lymphocyte tissues. Several potential biomarker genes, , , , , and were found, which may have critical functions in resistant birds to resist APEC infection. Taken together, this study provides a novel insight that may elucidate the molecular mechanisms underlying host response to systemic APEC infection, as well as enhances the probability of advancement in biomedical research.
在本研究中,从具有三种表型(未感染、抗性和易感)的鸟类中,在两个时间点获取了三种不同免疫组织(骨髓、胸腺和法氏囊)的RNA测序基因表达数据。在感染后5天(dpi),易感鸟类与未感染鸟类的对比中,三种组织中共有380个显著差异表达基因(DEG);在5 dpi时,易感鸟类与抗性鸟类共有106个显著DEG。对于共表达的DEG,在两种对比中,三种组织的表达模式具有相对较高的一致性。这些共表达的DEG参与了对刺激的反应、细胞增殖的调节、信号转导和免疫系统的生物学过程。此外,还为共表达的DEG鉴定了三个基因网络,表明体液免疫反应的激活、细胞存活、生长和死亡是三种淋巴细胞组织的一致反应。发现了几个潜在的生物标志物基因, 、 、 、 、 和 ,它们可能在抗性鸟类抵抗禽致病性大肠杆菌(APEC)感染中具有关键功能。综上所述,本研究提供了一个新的见解,可能阐明宿主对全身性APEC感染反应的分子机制,并提高生物医学研究取得进展的可能性。