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In Vitro Survey of Autographa californica Nuclear Polyhedrosis Virus Interaction with Nontarget Vertebrate Host Cells

机译:与非靶点脊椎动物宿主细胞相互作用的自体苜蓿核多角体病毒相互作用的体外调查

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Thirty-five nontarget host cell lines, 23 of human and 12 of nonhuman vertebrate origin, were exposed to Autographa californica nuclear polyhedrosis virus preparations derived from four different sources: polyhedra, hemolymph, cell culture medium, and cultured cells. The virus and cells were incubated together at two different temperatures, 28 or 37°C, for four different lengths of time, 16, 40, 64, or 168 h, and the cells were assayed for the presence of virus by a peroxidase-antiperoxidase detection method. The estimated sensitivity of the assay as routinely conducted was 0.98 ng of alkali-liberated viral protein and 1.95 ng of budded viral protein per mm2. No evidence of frank replication was obtained in any of the 35 cell lines tested, although virus uptake appeared to be quite common. Virus uptake was confirmed in some cases by electron microscopy. The degree of virus uptake appeared to be dependent on cell type, time and temperature of incubation, and viral phenotype. Virus purified from polyhedra was generally taken up more readily than were the other forms tested.
机译:将35种非靶标宿主细胞系(人类的23种和非人类脊椎动物的12种)暴露于衍生自四种不同来源的多形Autocalia californica核多角体病毒制剂:多面体,血淋巴,细胞培养基和培养的细胞。病毒和细胞在两个不同的温度(28或37°C)下一起孵育四个不同的时间长度(16、40、64或168小时),并通过过氧化物酶-抗过氧化物酶检测细胞中病毒的存在检测方法。按常规进行的测定估计灵敏度为每平方毫米0.98 ng碱性释放的病毒蛋白和1.95 ng萌芽的病毒蛋白。尽管似乎很普遍地吸收了病毒,但在测试的35个细胞系中,没有获得坦率复制的证据。在某些情况下,通过电子显微镜确认了病毒吸收。病毒的摄取程度似乎取决于细胞类型,孵育时间和温度以及病毒表型。与其他测试形式相比,从多面体纯化的病毒通常更易于吸收。

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