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Saliva of blood-feeding arthropods promotes infection by the vector-borne pathogens they transmit. To investigate this phenomenon in vitro, cultures of mouse L cells were treated with a salivary gland extract (SGE) prepared from feeding ticks and then infected with vesicular stomatitis virus (VSV). At low input doses of VSV, viral yield was increased 100-fold to 10,000-fold by 16-23 h post-infection compared with untreated cultures, and depending on the SGE concentration. SGE-mediated acceleration of viral yield corresponded with the earlier appearance of VSV nucleocapsid protein as detected by 2-dimensional electrophoresis of infected cells. The observation that physiological doses of virus (i.e. doses likely to be inoculated by an infected arthropod vector into its vertebrate host during blood-feeding) respond to SGE treatment in vitro provides a new opportunity for identifying the factors in tick saliva that promote virus transmission in vivo.

Type

Journal article

Journal

Parasitology

Publication Date

06/1998

Volume

116 ( Pt 6)

Pages

533 - 538

Keywords

Animals, Connective Tissue Cells, Electrophoresis, Polyacrylamide Gel, In Vitro Techniques, L Cells (Cell Line), Mice, Salivary Glands, Ticks, Time Factors, Tissue Extracts, Vesicular stomatitis Indiana virus, Viral Core Proteins