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      Promotion of vesicular stomatitis virus nucleocapsid protein production by arthopod saliva.

      Acta virologica
      Animals, Arachnid Vectors, physiology, Cell Line, Dermacentor, Mice, Nucleocapsid, biosynthesis, Nucleocapsid Proteins, Phosphoproteins, Saliva, Salivary Glands, chemistry, metabolism, Vesicular stomatitis Indiana virus, Viral Structural Proteins, Virus Replication

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          Abstract

          In a previous study (Hajnicka, V. et al., Parasitology 116, 533-538, 1998), the infectivity titer of vesicular stomatitis virus (VSV) was shown to increase up to 10,000-fold when mouse L cells were treated with tick salivary gland extract (SGE) prior to infection. To examine this effect at the level of viral protein production, radiolabeled VSV-infected cells were analyzed by double-dimensional gel electrophoresis. A pre-treatment of cells with SGE from partially fed ticks in amounts corresponding to 1 or 3 salivary glands increased the level of both viral nucleocapsid (N) protein and phosphoprotein (P) in a dose-dependent manner. The effect was more pronounced for N protein and could account for the dramatic increase in infectious virus yield. Promotion of viral infectivity by arthropod saliva may support the arthropode-borne transmission cycle of VSV.

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