Leibniz Institute for Farm Animal Biology (FBN), Institute for Genome Biology, Functional Genome Analysis Research Unit, Wilhelm-Stahl-Allee 2, D-18196, Dummerstorf, Germany.
Leibniz Institute for Farm Animal Biology (FBN), Institute for Genome Biology, Genomics Research Unit, Wilhelm-Stahl-Allee 2, D-18196, Dummerstorf, Germany.
BMC Genomics. 2019 Jul 31;20(1):623. doi: 10.1186/s12864-019-5976-7.
Epigenetic changes such as cytosine (CpG) DNA methylations regulate gene expression patterns in response to environmental cues including infections. Microbial infections induce DNA methylations that play a potential role in modulating host-immune response. In the present study, we sought to determine DNA methylation changes induced by the mastitis causing Escherichia coli (E. coli) in porcine mammary epithelial cells (PMEC). Two time points (3 h and 24 h) were selected based on specific transcriptomic changes during the early and late immune responses, respectively.
DNA methylation analysis revealed 561 and 898 significant (P < 0.01) differentially methylated CpG sites at 3 h and 24 h after E. coli challenge in PMEC respectively. These CpG sites mapped to genes that have functional roles in innate and adaptive immune responses. Significantly, hypomethylated CpG sites were found in the promoter regions of immune response genes such as SDF4, SRXN1, CSF1 and CXCL14. The quantitative transcript estimation indicated higher expression associated with the DNA CpG methylation observed in these immune response genes. Further, E. coli challenge significantly reduced the expression levels of DNMT3a, a subtype of de novo DNA methylation enzyme, in PMEC indicating the probable reason for the hypomethylation observed in the immune response genes.
Our study revealed E. coli infection induced DNA methylation loci in the porcine genome. The differentially methylated CpGs were identified in the regulatory regions of genes that play important role in immune response. These results will help to understand epigenetic mechanisms for immune regulation during coliform mastitis in pigs.
表观遗传变化,如胞嘧啶(CpG)DNA 甲基化,可调节基因表达模式,以响应包括感染在内的环境线索。微生物感染诱导的 DNA 甲基化可能在调节宿主免疫反应中发挥作用。在本研究中,我们试图确定乳腺炎大肠杆菌(E. coli)在猪乳腺上皮细胞(PMEC)中诱导的 DNA 甲基化变化。根据早期和晚期免疫反应中特定转录组变化,分别选择了两个时间点(3 h 和 24 h)。
DNA 甲基化分析显示,在大肠杆菌挑战后 3 h 和 24 h,PMEC 分别有 561 个和 898 个显著(P < 0.01)差异甲基化 CpG 位点。这些 CpG 位点映射到在先天和适应性免疫反应中具有功能作用的基因。值得注意的是,免疫反应基因如 SDF4、SRXN1、CSF1 和 CXCL14 的启动子区域发现了低甲基化 CpG 位点。定量转录估计表明,与这些免疫反应基因中观察到的 DNA CpG 甲基化相关的表达更高。此外,大肠杆菌挑战显著降低了 PMEC 中从头 DNA 甲基化酶亚类 DNMT3a 的表达水平,这表明观察到的免疫反应基因低甲基化的可能原因。
我们的研究揭示了大肠杆菌感染诱导猪基因组中的 DNA 甲基化位点。差异甲基化 CpG 位于在免疫反应中起重要作用的基因的调控区域。这些结果将有助于了解大肠杆菌乳腺炎中免疫调节的表观遗传机制。