检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:郭志军 谢慧凡 吴其文 陈洪博[1,3] 邱龙新 GUO Zhijun;XIE Huifan;WU Qiwen;CHEN Hongbo;QIU Longxin(School of Life Science,Longyan University,Longyan,Fujian 364012,China;Fujian Longyan Minxiong Biotechnology Co.,Ltd,Longyan,Fujian 364012,China;Fujian Provincial Universities Key Laboratory of Preventive Veterinary Medicine and Biotechnology,Longyan,Fujian 364012,China)
机构地区:[1]龙岩学院生命科学学院,福建龙岩364012 [2]福建龙岩闽雄生物科技股份有限公司,福建龙岩364012 [3]预防兽医学与生物技术福建省高等学校重点实验室,福建龙岩364012
出 处:《西北农林科技大学学报(自然科学版)》2022年第5期18-24,35,共8页Journal of Northwest A&F University(Natural Science Edition)
基 金:中央引导地方科技发展专项(2019L3011);龙岩市奇迈基金项目(2018LYQM0201);预防兽医学与生物技术福建省高等学校重点实验室开放课题(2019KF01)。
摘 要:【目的】研究鬼针草水提物(BPE)的体外抗伪狂犬病毒(Pseudorabies virus,PrV)作用。【方法】制备640 mg/mL(以生药计)的BPE,检测其对仓鼠肾上皮细胞(BHK-21)的毒性(半数中毒浓度(TC_(50)))及对PrV体外抗性(半数抑制浓度(EC_(50)))和治疗指数(TI)。采用CCK-8法检测BPE抗PrV的机制。采用间接免疫荧光法检测BPE对gB蛋白表达和PrV所致细胞凋亡的影响,采用实时荧光定量PCR方法检测BPE对PrV gB基因表达的影响。【结果】BPE对BHK-21细胞的TC_(50)为28.7 mg/mL,对PrV的EC_(50)为5.16 mg/mL,TI为5.56。BPE抗PrV的机制为抑制PrV增殖和灭活PrV。BPE可抑制PrV诱导的BHK-21细胞凋亡,抑制PrV gB基因和蛋白的表达。【结论】BPE具有明显的体外抗PrV活性。【Objective】This study aimed to investigate the protective effect of aqueous extract of Bidens pilosa L.(BPE)on Pseudorabies virus(PrV)in vitro.【Method】The cytotoxicity and anti-PrV activity of BPE at concentration of 640 mg/mL on BHK-21 cells were detected by CCK-8,and the anti-PrV mechanism of BPE was investigated by CCK-8.The TC_(50),EC_(50) and TI were determined.The indirect immunofluorescence was used to detect the effect of BPE on PrV-induced apoptosis and expression of PrV gB protein,and the real-time fluorescence quantitative PCR was used to detect the expression of PrV gB gene.【Result】The TC_(50) of BPE in BHK-21 cells was 28.7 mg/mL,the IC_(50) of PrV was 5.16 mg/mL,and the TI was 5.56.The mechanism of anti-PrV was based on inhibiting PrV proliferation and inactivating PrV.BPE might protect PrV-infected BHK-21 cells through suppressing expression of PrV gB gene and protein(P<0.01)and inhibiting PrV-induced apoptosis of BHK-21 cells.【Conclusion】BPE had significant anti-PrV activity in vitro.
分 类 号:S853.7[农业科学—临床兽医学] S852.659.1[农业科学—兽医学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:13.59.111.209