Genistein treatment of cells inhibits arenavirus infection. (17/39)

Arenaviridae is a family of enveloped viruses some of which are capable of causing hemorrhagic fever syndromes in humans. In this report, we demonstrate that treatment of host cells with the tyrosine kinase inhibitor genistein inhibits infection of cells with the New World arenavirus Pichinde (PICV). The greatest degree of inhibition was observed in pre-treated target cells, but modest inhibition of infection was also seen when drug was added to cultures up to 48h after infection. We show that PICV-induced phosphorylation of the activating transcription factor-2 protein (ATF-2) and cyclic adenosine monophosphate response element binding protein (CREB) is inhibited following genistein treatment. Lastly, genistein treatment also inhibited transduction of cells with pseudotyped retrovirus particles expressing envelope proteins of the Old World arenavirus Lassa virus. These results demonstrate that kinase activity is required for arenavirus infection and that therapeutics designed to inhibit kinase activity should be explored.  (+info)

Genome comparison of virulent and avirulent strains of the Pichinde arenavirus. (18/39)

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Cytokine patterns in a comparative model of arenavirus haemorrhagic fever in guinea pigs. (19/39)

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Treatment of late stage disease in a model of arenaviral hemorrhagic fever: T-705 efficacy and reduced toxicity suggests an alternative to ribavirin. (20/39)

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Targeting inside-out phosphatidylserine as a therapeutic strategy for viral diseases. (21/39)

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Development of infectious clones for virulent and avirulent pichinde viruses: a model virus to study arenavirus-induced hemorrhagic fevers. (22/39)

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Molecular determinants of Pichinde virus infection of guinea pigs--a small animal model system for arenaviral hemorrhagic fevers. (23/39)

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Pichinde virus induces microvascular endothelial cell permeability through the production of nitric oxide. (24/39)

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