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A cell clone strain from <Emphasis Type="Italic">Mythimna separata</Emphasis> (Lepidoptera: Noctuidae) highly susceptible to <Emphasis Type="Italic">Autographa californica</Emphasis> multiple nucleopolyhedrovirus (AcMNPV) and <Emphasis Type="Italic">M. separata</Emphasis> NPV (MsNPV)
Authors:Xiang-Qian Meng  Gui-Ling Zheng  Chuan-De Zhao  Fang-Hao Wan  Chang-You Li
Institution:1.Key Lab of Integrated Crop Pest Management of Shandong Province, College of Agronomy and Plant Protection,Qingdao Agricultural University,Qingdao,China;2.State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology,Chinese Academy of Sciences,Beijing,China;3.State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection,Chinese Academy of Agricultural Sciences,Beijing,China
Abstract:In this study, we describe a cell line, Ms-10C, cloned from the line QAU-Ms-E-10 (simplified Ms-10), an embryonic line from Mythimna separata. The cloned cell line was significantly more sensitive to nucleopolyhedrovirus (NPV). Ms-10C cells were mainly spherical with a diameter of 14.42 ± 2.23 μm. DNA amplification fingerprinting (DAF) confirmed the profile of PCR-amplified bands of the cloned cell line was consistent with those of the parental cell line, Ms-10. The sequencing result of the mitochondrial cytochrome c oxidase I (mtCO I) fragment confirmed that the amplified 636-bps mtCOI fragment was 100% identical to that of M. separata. Its chromosomes exhibited the typical characters of lepidopteran cell lines. Its population doubling time was 42.2 h at 27°C. Ms-10C was more sensitive than Ms-10 to both Autographa californica multiple nucleopolyhedrovirus (AcMNPV) and M. separata nucleopolyhedrovirus (MsNPV). At 4 d post infection, the infection rates of two viruses reached 94.2 and 92.3%, respectively. The availability of this cell clone strain will provide a useful tool for the basic research on nucleopolyhedrovirus and for potential application in expression of recombinant proteins with baculovirus expression vector system.
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