河北师范大学生命科学学院,中国科学院动物研究所,国家野生动物疫病研究中心,北京市野生动物救护中心,中国科学院动物研究所, 国家野生动物疫病研究中心,中国科学院动物研究所, 国家野生动物疫病研究中心,中国科学院动物研究所, 国家野生动物疫病研究中心,河北省实验动物中心,河北省实验动物学重点实验室,河北师范大学生命学院,中国科学院动物研究所, 国家野生动物疫病研究中心
北京市家禽产业技术体系创新团队, 中国科学院知识创新工程(KSCX2-YW-N-063), USDA-IOZ CAS中美合作项目(O760621234), 国家“十一五”科技支撑计划(2009BAI83B01)和国家自然科学基金(31072126/C1804, 31101806/C1804)资助项目
College of Life Science, Hebei Normal University,National Research Center for Wildlife Borne Diseases, Institute of Zoology; Chinese Academy of Sciences,Bei jing Wildlife Rescue and Rehabilitation Center,National Research Center for Wildlife Borne Diseases, Institute of Zoology; Chinese Academy of Sciences,National Research Center for Wildlife Borne Diseases, Institute of Zoology; Chinese Academy of Sciences,National Research Center for Wildlife Borne Diseases, Institute of Zoology; Chinese Academy of Sciences,Hebei Key Lab of Laboratory Animal Science, Hebei Province Center for Laboratory animal Sciences,College of Life Science, Hebei Normal University,National Research Center for Wildlife Borne Diseases, Institute of Zoology; Chinese Academy of Sciences
This work was supported by grants from Beijing Research Group for Poultry Production Technology System, Knowledge Innovation Program of the Chinese Academy of Sciences (KSCX2-EW-J-2), The USDA-IOZ CAS joint project (O760621234), Science & Technology support project of the eleventh-five-year plan of China (2009BAI83B01) and The National Natural Science Foundation of China (31072126/C1804, 31101806/C1804)
对高致病性禽流感病毒感染最为有效的治疗应采用抗病毒和抗炎症的联合治疗.本试验用流感病毒H5N1感染不同细胞株(A549细胞和MDCK细胞),采用不同浓度格尔德霉素对病毒感染细胞培养物作用不同时长,检测流感病毒滴度;ELISA检测格尔德霉素作用于流感病毒H5N1感染A549细胞12 h、24 h促炎性细胞因子IFN-α、TNF-α和IL-6水平.结果显示,流感病毒H5N1感染A549细胞和MDCK细胞,格尔德霉素极显著地抑制了流感病毒H5N1在细胞培养物的增殖(P < 0.01),而在病毒感染36 h和48 h,格尔德霉素并没有显著抑制流感病毒在MDCK细胞上的增殖(P > 0.05).促炎性细胞因子分析结果显示,格尔德霉素在流感病毒感染A549细胞12 h和24 h均显著降低了促炎性细胞因子IFN-α、TNF-α和IL-6的分泌(P < 0.05).上述实验结果显示,格尔德霉素具有抑制流感病毒H5N1增殖及其所介导的炎性反应的双重效应,为格尔德霉素成为应对流感病毒流行的备选药物提供基础科学依据.
Better effective therapy for highly pathogenic influenza virus infection should consist of combinations of an effective antiviral agent and immunomodulatory agents to control viral replication and pulmonary injury, respectively. Here we evaluated the virus titres in different cells (A549 cells and MDCK cells) infected with influenza virus H5N1 by plaque assay with the various concentrations of Geldanamycin at different time points. The levels of proinflammatory cytokines from A549 cell infected with influenza virus H5N1were detected by ELISA in the absence or presence of Geldanamycin. Our findings showed that Geldanamycin significantly inhibited influenza virus growth in MDCK cells and A549 cells(P < 0.01). However, influenza virus growth were not inhibited with Geldanamycin on 36 h and 48 h(P > 0.05)after infection with influenza virus H5N1. Analysis of proinflammatory cytokines in Geldanamycin-treated A549 cells revealed significant reductions in IFN-α,TNF-α or IL-6 on 12 h and 24 h after infection with influenza virus H5N1(P < 0.05). All the results indicated that Geldanamycin have the dual effect of combine antivirus with anti-inflammation, which provided the science data for the potential use of Geldanamycin as a novel, highly effective anti-influenza virus drug.
胡奕,刘朋朋,张志明,卢鹤真,罗静,王承民,刘军须,赵宝华,何宏轩.格尔德霉素抑制高致病性禽流感病毒增殖及其所介导炎性反应研究[J].生物化学与生物物理进展,2013,40(11):1132-1139
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