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作 者:张瑞永[1,2] 管宇 吴信明 梅建国 姚春阳 沈志强 雷连成[1]
机构地区:[1]吉林大学动物医学学院,吉林长春130062 [2]山东绿都生物科技有限公司,山东滨州256600
出 处:《动物医学进展》2016年第9期16-20,共5页Progress In Veterinary Medicine
基 金:山东省重点研发计划项目(2015GSF121027)
摘 要:依次采用含60、30、20、10mL/L血清浓度的低血清培养基驯化PK-15细胞,并给驯化好的细胞上接种猪圆环病毒2型(PCV-2),以确定PCV-2在该培养体系下的生长情况。结果用含60、30、20mL/L血清浓度的低血清培养基各进行3代次驯化,PK-15细胞能完全适应且生长状态良好;当血清浓度降至10mL/L时,传代1次细胞无法保持良好状态,细胞出现贴壁较差、生长停滞等现象。各血清浓度培养体系中细胞生长曲线测定结果显示,在细胞培养的0、24、48、72、96h各组细胞密度与常规培养的对照组差别不明显。因此用该低血清培养体系培养PK-15细胞时,血清最低添加量为20mL/L。用该体系培养的PK-15细胞接种PCV-2后,通过荧光抗体染色测定病毒滴度。结果显示,低血清培养的PCV-2病毒滴度为10^(6.5)TCID_(50)/mL,与常规条件培养的PCV-2对照(病毒滴度为10^(6.375 )TCID_(50)/mL)差别不明显,表明该体系可用于PCV-2的增殖。表明研究建立了PK-15细胞低血清培养PCV-2体系,为PCV-2的相关研究奠定了基础。In this study,the low serum media containing 6% 3% 2%and 1% sera, respectively, were used to culture PK-15 cells and to proliferate the porcine circovirus type 2. The results showed that PK-15 ceils were in good growth state in concentrations of 6%, 3% and 2% sera culture medium, respectively, but when the concentration of the serum was decreased to 1%,the cells were in poor attachment and growth. Meanwhile,the densities of PK-15 cells at 0 h,24 h,48 h and 72 h time point in concentrations of 6% ,3% and 2% serum culture medium was not significantly different with the control. Thereby,the culture media containing 2 ~ serum were selected for cell cultivation and virus yield,and the virus titers were determined by indirect immunofluorescent assay. The results showed that the PCV-2 titer of the low serum culture was 10^6.5TCID50/mL,a little bit higher than that of the control (106'375TCID50/mL),but the difference was not significant. In this study,the PK-15 cell culture aging system with low serum culture medium for PCV-2 proliferation was established, which laid the foundation for the research of PCV-2.
关 键 词:PK-15细胞 低血清培养基 猪圆环病毒2型 增殖 间接免疫荧光
分 类 号:S852.659.2[农业科学—基础兽医学]
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