[1]丁芳艺,宋海鑫,梁荣,等.猪流行性腹泻病毒感染对猪小肠上皮细胞I型干扰素产生通路的影响[J].江苏农业学报,2021,(01):99-105.[doi:doi:10.3969/j.issn.1000-4440.2021.01.013]
 DING Fang-yi,SONG Hai-xin,LIANG Rong,et al.Effects of porcine epidemic diarrhea virus infection on IFN-β production pathway in porcine intestinal epithelial cells[J].,2021,(01):99-105.[doi:doi:10.3969/j.issn.1000-4440.2021.01.013]
点击复制

猪流行性腹泻病毒感染对猪小肠上皮细胞I型干扰素产生通路的影响()
分享到:

江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2021年01期
页码:
99-105
栏目:
畜牧兽医·水产养殖
出版日期:
2021-02-28

文章信息/Info

Title:
Effects of porcine epidemic diarrhea virus infection on IFN-β production pathway in porcine intestinal epithelial cells
作者:
丁芳艺123宋海鑫123梁荣123苗晋锋2费荣梅2刘永杰2余祖功2张金秋1345
(1.江苏省农业科学院动物免疫工程研究所,江苏南京210014;2.南京农业大学动物医学院,江苏南京210095;3.省部共建国家重点实验室培育基地——江苏省食品质量安全重点实验室,江苏南京210014;4.江苏省动物重要疫病与人兽共患病防控协同创新中心,江苏扬州225009;5.江苏大学药学院,江苏镇江212013)
Author(s):
DING Fang-yi123SONG Hai-xin123LIANG Rong123MIAO Jin-feng2FEI Rong-mei2LIU Yong-jie2YU Zu-gong2ZHANG Jin-qiu1345
(1.Institute of Veterinary Immunology and Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China;2.College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China;3.Jiangsu Key Laboratory for Food Quality and Safety——State Key Laboratory Cultivation Base, Nanjing 210014, China;4.Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China;5.College of Pharmacy, Jiangsu University, Zhenjiang 212013, China)
关键词:
天然免疫猪流行性腹泻病毒猪小肠上皮细胞I型干扰素
Keywords:
innate immunityporcine epidemic diarrhea virusporcine intestinal epithelial cellstype I interferon
分类号:
S828.7
DOI:
doi:10.3969/j.issn.1000-4440.2021.01.013
文献标志码:
A
摘要:
猪流行性腹泻病毒(Porcine epidemic diarrhea virus, PEDV)是严重危害仔猪肠道健康的病原之一。用病毒感染复数(MOI)=1.0的PEDV感染猪小肠上皮细胞,通过间接免疫荧光试验,证实PEDV能在猪小肠上皮细胞中增殖。通过实时荧光定量PCR(RT-qPCR)检测,发现Toll 样受体3(TLR3)编码基因、视黄醇诱导基因 I/黑色素瘤分化相关基因5(RIG-I/MDA5)的mRNA表达水平分别从感染后2 h、4 h开始显著升高(P<0.05),分别在感染后12 h、24 h达到最高值;线粒体抗病毒信号蛋白(MAVS)编码基因的mRNA相对表达量从感染后6 h开始显著升高(P<0.05),随后基本保持不变。下游接头蛋白质β干扰素TIR结构域衔接蛋白质(TRIF)、肿瘤坏死因子相关因子3(TRAF3)、IκB 激酶ε(IKK-ε)和TANK结合激酶1(TBK1)编码基因的mRNA相对表达量在感染后4 h出现显著上升(P<0.05),随后IKK-ε编码基因的mRNA相对表达量在感染后8 h达到最高值,TRIF、TRAF3和TBK1编码基因的mRNA相对表达量均在感染后12 h达到最高值。干扰素调节因子3(IRF3)编码基因的mRNA相对表达量在感染早期无显著变化,在感染后24 h达到最高值(P<0.05)。与对照组相比,PEDV感染无法诱导猪小肠上皮细胞(IPEC-J2)IFN-β编码基因的mRNA相对表达量显著升高,但能有效抑制Poly(I:C)(聚肌胞苷酸)诱导的IFN-β产生。结果表明,PEDV能够在感染早期激活TLRs、RLRs介导的I型IFN产生通路中相关受体及接头蛋白质的基因表达,但最终能抑制干扰素产生,并能在猪小肠上皮细胞中有效增殖。
Abstract:
Porcine epidemic diarrhea virus (PEDV) is one of the pathogens that seriously endanger the intestinal health of piglets. Porcine intestinal epithelial cells (IPEC-J2) were infected with PEDV at a multiplicity of infection MOI of 1.0. Virus proliferation in IPEC-J2 was observed by indirect immunofluorescence assay (IFA). Through real-time fluorescent quantitative PCR (RT-PCR) detection, it was found that the mRNA levels of TLR3 encoding gene and RIG-I/MDA5 significantly increased from 2 hours post infection (hpi) and 4 hpi, respectively (P<0.05), and peaked at 12 hpi and 24 hpi. The relative mRNA expression of mitochondrial antiviral signaling protein (MAVS) coding gene significantly increased at 6 hpi (P<0.05), and then remained unchanged. The mRNA levels of TRIF, TRAF3, IKK-ε and TBK1 coding genes significantly increased from 4 hpi (P<0.05), and then the relative mRNA expression of IKK-ε encoding genes reached the highest level at 8 hpi while TRIF, TRAF3 and TBK1 encoding genes at 24 hpi. The relative mRNA expression of interferon regulatory factor 3 (IRF3) encoding gene showed no significant change at the early stage after infection, and reached the highest level at 12 hpi. Compared with control group, there was no significant difference of IFN mRNA expression in IPEC-J2 infected with PEDV. However, PEDV infection could inhibit the production of IFN-β induced by Poly(I:C). The results suggested that PEDV could activate TLRs and RLRs signaling pathway in the early stage after infection, and effectively proliferate in IPEC-J2 by inhibiting IFN-β.

参考文献/References:

[1]CAVANAGH D. Nidovirales: a new order comprising Coronaviridae and Arteriviridae[J]. Archives of Virology, 1997, 142(3): 629-633.
[2]SUN R Q, CAI R J, CHEN Y Q, et al. Outbreak of porcine epidemic diarrhea in suckling piglets, China[J]. Emerging Infectious Diseases, 2012, 18(1): 161-163.
[3]KOCHERHANS R, BRIDGEN A, ACKERMANN M, et al. Completion of the porcine epidemic diarrhoea coronavirus (PEDV) genome sequence[J]. Virus Genes, 2001, 23(2): 137-144.
[4]XING Y L, CHEN J F, TU J, et al. The papain-like protease of porcine epidemic diarrhea virus negatively regulates type I interferon pathway by acting as a viral deubiquitinase[J]. The Journal of General Virology, 2013, 94(7): 1554-1567.
[5]DING Z, FANG L R, JING H Y, et al. Porcine epidemic diarrhea virus nucleocapsid protein antagonizes beta interferon production by sequestering the interaction between IRF3 and TBK1[J]. Journal of Virology, 2014, 88(16): 8936-8945.
[6]HOFMANN M, WYLER R. Propagation of the virus of porcine epidemic diarrhea in cell culture[J]. Journal of Clinical Microbiology, 1988, 26(11):2235-2239.
[7]THOMPSON M R, KAMINSKI J J, KURT-JONES E A, et al. Pattern recognition receptors and the innate immune response to viral infection[J]. Viruses, 2011, 3(6): 920-940.
[8]ZHANG J Q, MIAO J F, HOU J B, et al. The effects of H3N2 swine influenza virus infection on TLRs and RLRs signaling pathways in porcine alveolar macrophages[J]. Virol Journal, 2015, 12: 61.
[9]KAWAI T, TAKAHASHI K, SATO S, et al. IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction[J]. Nature Immunology, 2005, 6(10): 981-988.
[10]XU L G, WANG Y Y, HAN K J, et al. VISA is an adapter protein required for virus-triggered IFN-β signaling[J]. Molecular Cell, 2005, 19(6): 727-740.
[11]CAO L Y, GE X Y, GAO Y, et al. Porcine epidemic diarrhea virus infection induces NF-κB activation through the TLR2, TLR3 and TLR9 pathways in porcine intestinal epithelial cells[J]. Journal of General Virology, 2015, 96(7): 1757-1767.
[12]MIAN M F, AHMED A N, RAD M, et al. Length of dsRNA (poly I:C) drives distinct innate immune responses, depending on the cell type[J]. Journal of Leukocyte Biology, 2013, 94(5): 1025-1036.
[13]孙敏. 猪流行性腹泻病毒遗传变异规律与Ⅰ型干扰素逃避机制[D]. 南京:南京农业大学, 2017.
[14]李亮. 猪肠类器官模型的建立及干扰素λ在肠道黏膜免疫中抗猪流行性腹泻病毒(PEDV)作用机制的研究[D]. 北京: 中国农业大学, 2019.
[15]CAO L Y, GE X Y, GAO Y, et al. Porcine epidemic diarrhea virus inhibits dsRNA-induced interferon-β production in porcine intestinal epithelial cells by blockade of the RIG-I-mediated pathway[J]. Virology Journal, 2015, 12: 127.
[16]DING Z, FANG L, JING H, et al. Porcine epidemic diarrhea virus nucleocapsid protein antagonizes beta interferon production by sequestering the interaction between IRF3 and TBK1[J]. Journal of Virology, 2014, 88(16): 8936-8945.
[17]XING Y L, CHEN J F, TU J, et al. The papain-like protease of porcine epidemic diarrhea virus negatively regulates type Ⅰ interferon pathway by acting as a viral deubiquitinase[J]. Journal of General Virology, 2013, 94(7): 1554-1567.
[18]ZHANG Q Z, SHI K C, YOO D W. Suppression of type Ⅰ interferon production by porcine epidemic diarrhea virus and degradation of CREB-binding protein by nsp1[J]. Virology, 2016, 489: 252-268.
[19]ZHU X Y, FANG L R, WANG D, et al. Porcine deltacoronavirus nsp5 inhibits interferon-β production through the cleavage of NEMO[J]. Virology, 2017, 502: 33-38.
[20]李红杰,王晓雪,高冬生,等. 猪流行性腹泻病毒Nsp7的亚细胞定位和对Ⅰ型干扰素应答的影响[J]. 畜牧兽医学报, 2017, 48(3): 501-507.

相似文献/References:

[1]祁光宇,刘斌,赵兴绪.猪流行性腹泻病毒HB2015分离株N基因表达及单克隆抗体的制备[J].江苏农业学报,2018,(01):76.[doi:doi:10.3969/j.issn.1000-4440.2018.01.011]
 QI Guang-yu,LIU Bin,ZHAO Xing-xu.Expression of N gene of porcine epidemic diarrhea virus(PEDV) HB2015 strain and preparation of monoclonal antibodies against PEDV[J].,2018,(01):76.[doi:doi:10.3969/j.issn.1000-4440.2018.01.011]
[2]杨晓宇,徐雷,殷鑫欢,等.猪非典型性瘟病毒与猪流行性腹泻病毒双重PCR方法的建立与应用[J].江苏农业学报,2018,(05):1081.[doi:doi:10.3969/j.issn.1000-4440.2018.05.016]
 YANG Xiao-yu,XU Lei,YIN Xin-huan,et al.Establishment and application of double PCR method between atypical porcine pestivirus and porcine epidemic diarrhea virus[J].,2018,(01):1081.[doi:doi:10.3969/j.issn.1000-4440.2018.05.016]

备注/Memo

备注/Memo:
收稿日期:2020-09-15基金项目:国家自然科学基金项目(31772701);江苏省农业科技自主创新基金项目[CX(17)3027]作者简介:丁芳艺(1995-),男,江西上饶人,硕士,主要从事畜禽疫病防控方向的研究。(E-mail)dingfy0526@163.com。宋海鑫为共同第一作者。通讯作者:张金秋,(E-mail)jqzh03@126.com
更新日期/Last Update: 2021-03-15