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作 者:许榜丰[1] 孟沙沙[1] 吴运谱[1] 陈艳[1] 杨焕良[1] 乔传玲[1] 陈化兰[1] XU Bangfeng MENG Shaha WU Yunpu CHEN Yan YANG Huanliang QIAO Chuanling* CHEN HuMan(Animal Influenza Laboratory of the Ministry of Agricultural, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China)
机构地区:[1]中国农业科学院哈尔滨兽医研究所农业部动物流感重点开放实验室/兽医生物技术国家重点实验室,黑龙江哈尔滨150001
出 处:《畜牧与兽医》2017年第1期61-64,共4页Animal Husbandry & Veterinary Medicine
基 金:哈尔滨市科技创新人才项目(2014RFXYJ116)
摘 要:为建立1株猪源2009/H1N1流感病毒A/swine/Heilongjiang/44/2009(HLJ44)的反向遗传系统,利用双向表达质粒p HW2000,分别构建了该病毒株8个基因节段的重组质粒,将其共转染于293T和MDCK混合培养的细胞,拯救出重组病毒R-HLJ44。测序结果表明,R-HLJ44与亲本病毒HLJ44的核苷酸序列完全一致;二者在细胞上具有相似的增殖特性;抗原性未发生变化;分别以106TCID50的剂量鼻腔感染BALB/c小鼠,结果显示R-HLJ44与亲本HLJ44在小鼠脏器中的复制滴度也基本一致。以上结果表明拯救的重组病毒保持了与亲本病毒一致的生物学特性。该病毒反向遗传系统的建立,为进一步研究H1N1亚型流感病毒的致病分子机制及新型疫苗研制等奠定了基础。To establish the reverse genetic system of a pandemic 2009 / H1N1 influenza virus,we firstly constructed the recombinant plasmids containing the eight gene segments of A / swine / Heilongjiang / 44 / 2009( HLJ44) based on the p HW2000 plasimds,respectively. Then the recombinant virus( designated R-HLJ44) was rescued by co-transfecting the eight recombinant plasmids into the cell mixtures of 293 T and MDCK. Whole genome sequence analysis indicated that the R-HLJ44 had the similar antigenic characteristics with the parental virus of HLJ44 and no nucleotides were changed compared with HLJ44. In addition,the virus replication titer of R-HLJ44 in BALB / c mice was similar to the parent virus by infecting mice with 106TCID50 of viruses. These results indicated the reverse genetic system of 2009 / H1N1 influenza virus was established,which lays the foundation for the further study on the pathogenicity mechanism and novel vaccine development of H1N1 subtype influenza viruses.
分 类 号:S852.65[农业科学—基础兽医学]
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