Wikström Frida Hasslung, Meehan Brian M, Berg Mikael, Timmusk Sirje, Elving Josefine, Fuxler Lisbeth, Magnusson Mattias, Allan Gordon M, McNeilly Francis, Fossum Caroline
Department of Molecular Bioscience, Section for Veterinary Immunology and Virology, Swedish University of Agricultural Sciences, SE-751 23 Uppsala, Sweden.
J Virol. 2007 May;81(10):4919-27. doi: 10.1128/JVI.02797-06. Epub 2007 Feb 28.
DNA sequences containing CpG motifs are recognized as immunomodulators in several species. Phosphodiester oligodeoxyribonucleotides (ODNs) representing sequences from the genome of porcine circovirus type 2 (PCV2) have been identified as potent inducers (ODN PCV2/5) or inhibitors (ODN PCV2/1) of alpha interferon (IFN-alpha) production by porcine peripheral blood mononuclear cells (poPBMCs) in vitro. In this study, the IFN-alpha-inducing or -inhibitory activities of specific phosphodiester ODNs were demonstrated to be dependent on their ability to form secondary structures. When a poly(G) sequence was added to a stimulatory self-complementary ODN, high levels of IFN-alpha were elicited, and the induction was not dependent on pretreatment with the transfecting agent Lipofectin. In addition, the IFN-alpha-inducing ODN required the presence of an intact CpG dinucleotide, whereas the inhibitory activity of ODN PCV2/1 was not affected by methylation or removal of the central CpG dinucleotide. Of particular significance, the IFN-alpha inhibition elicited by ODN PCV2/1 was only effective against induction stimulated by DNA control inducers and not RNA control inducers, indicating activity directed to TLR9 signaling. The PCV2 genome as a whole was demonstrated to induce IFN-alpha in cultures of poPBMCs, and the presence of immune modulatory sequences within the genome of PCV2 may, therefore, have implications with regard to the immune evasion mechanisms utilized by PCV2.
含有CpG基序的DNA序列在多个物种中被识别为免疫调节剂。代表猪圆环病毒2型(PCV2)基因组序列的磷酸二酯寡脱氧核糖核苷酸(ODN)已被确定为猪外周血单个核细胞(poPBMCs)体外产生α干扰素(IFN-α)的强效诱导剂(ODN PCV2/5)或抑制剂(ODN PCV2/1)。在本研究中,特定磷酸二酯ODN的IFN-α诱导或抑制活性被证明取决于它们形成二级结构的能力。当在一个刺激性的自我互补ODN中添加一个聚(G)序列时,会引发高水平的IFN-α,并且这种诱导不依赖于用转染剂Lipofectin进行预处理。此外,诱导IFN-α的ODN需要完整的CpG二核苷酸存在,而ODN PCV2/1的抑制活性不受中央CpG二核苷酸甲基化或去除的影响。特别重要的是,ODN PCV2/1引起的IFN-α抑制仅对DNA对照诱导剂刺激的诱导有效,而对RNA对照诱导剂无效,表明其活性针对TLR9信号传导。整个PCV2基因组在poPBMCs培养物中被证明可诱导IFN-α因此,PCV2基因组中免疫调节序列的存在可能与PCV2利用的免疫逃避机制有关。