1 Food and Feed Immunology Group, Laboratory of Animal Products Chemistry, Graduate School of Agricultural Science, Tohoku University, 468-1, Aoba, Aramaki, Aoba-ku, Sendai, Miyagi, 980-0845, Japan.
2 Livestock Immunology Unit, International Education and Research Center for Food and Agricultural Immunology (CFAI), Graduate School of Agricultural Science, Tohoku University, 468-1, Aoba, Aramaki, Aoba-ku, Sendai, Miyagi, 980-0845, Japan.
Benef Microbes. 2017 Apr 26;8(2):309-321. doi: 10.3920/BM2016.0155. Epub 2017 Jan 2.
The bovine intestinal epithelial cell line (BIE cells) expresses the Toll-like receptor (TLR)3 and is able to mount an antiviral immune response after the stimulation with poly(I:C). In the present study, we aimed to further characterise the antiviral defence mechanisms in BIE cells by evaluating the innate immune response triggered by rotavirus (RV) infection. In addition, we attempted to determine whether immunobiotic bifidobacteria are able to confer protection of BIE cells against RV infection by beneficially modulating the antiviral immune response. RV OSU (porcine) and UK (bovine) effectively infected BIE cells, while a significant lower capacity to infect BIE cells was observed for human (Wa) and murine (EW) RV. We observed that viral infection in BIE cells triggered TLR3/RIG-I-mediated immune responses with activation of IRF3 and TRAF3, induction of interferon beta (IFN-β) and up-regulation of inflammatory cytokines. Our results also demonstrated that preventive treatments with Bifidobacterium infantis MCC12 or Bifidobacterium breve MCC1274 significantly reduced RV titres in infected BIE cells and differentially modulated the innate immune response. Of note, both strains significantly improved the production of the antiviral factor IFN-β in RV-infected BIE cells. In conclusion, this work provides comprehensive information on the antiviral immune response of BIE cells against RV, that can be further studied for the development of strategies aimed to improve antiviral defences in bovine intestinal epithelial cells. Our results also demonstrate that BIE cells could be used as a newly immunobiotic evaluation system against RV infection for application in the bovine host.
牛肠上皮细胞系(BIE 细胞)表达 Toll 样受体(TLR)3,在 poly(I:C)刺激后能够引发抗病毒免疫反应。在本研究中,我们旨在通过评估轮状病毒(RV)感染引发的先天免疫反应,进一步研究 BIE 细胞的抗病毒防御机制。此外,我们试图确定免疫生物双歧杆菌是否能够通过有益地调节抗病毒免疫反应来保护 BIE 细胞免受 RV 感染。OSU(猪)和 UK(牛)型 RV 有效地感染了 BIE 细胞,而 Wa(人)和 EW(鼠)型 RV 感染 BIE 细胞的能力明显较低。我们观察到,BIE 细胞中的病毒感染触发了 TLR3/RIG-I 介导的免疫反应,激活了 IRF3 和 TRAF3,诱导了干扰素β(IFN-β)的产生,并上调了炎症细胞因子。我们的结果还表明,双歧杆菌婴儿 MCC12 或短双歧杆菌 MCC1274 的预防性治疗显著降低了感染 BIE 细胞中的 RV 滴度,并差异调节了先天免疫反应。值得注意的是,两种菌株都显著提高了 RV 感染的 BIE 细胞中抗病毒因子 IFN-β的产生。总之,这项工作提供了 BIE 细胞针对 RV 的抗病毒免疫反应的全面信息,可进一步研究用于改善牛肠上皮细胞抗病毒防御的策略。我们的结果还表明,BIE 细胞可作为一种新的免疫生物评价系统,用于评估 RV 感染在牛宿主中的应用。