The Tohoku Journal of Experimental Medicine
Online ISSN : 1349-3329
Print ISSN : 0040-8727
ISSN-L : 0040-8727
Influence of Various Experimental Conditions on the Inhibitory Effects of (E)-5-(2-Bromovinyl)-2'-Deoxyuridine on Varicella-Zoster Virus Replication in Cell Culture
MASANORI BABASHIRO SHIGETAERIK DE CLERCQ
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1984 Volume 143 Issue 4 Pages 441-449

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Abstract

BABA, M., SHIGETA, S. and DE CLERCQ, E. Influence of Various Experimental Conditions on the Inhibitory Effects of (E)-5-(2-Bromovinyl)-2'-Deoxy-uridine on Varicella-Zoster Virus Replication in Cell Culture. Tohoku J. exp. Med., 1984, 143(4), 441-449 - Inhibition of varicella-zoster virus (VZV) replica-tion by (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) has been examined in vitro under various experimental conditions. The 50% inhibitory dose (ID50) of BVDU for VZV replication in human embryonal fibroblast (HEF) cultures was 0.016μg/ml, if the assay was based on the reduction of visible foci. If the assay was based on the reduction of immunofluorescent foci, the ID50 was 3 times higher. There was no significant difference in ID50, whether the HEF cultures were infected with cell-free or cell-associated VZV. When the HEF cells were infected with VZV at different multiplicities of infection (MOI), the ID50 of BVDU increased in parallel with the increase of MOI. BVDU was normally added immediately after virus infection. However, the addition of BVDU could be delayed until 8hr after infection without substantial decrease of activity. On the other hand, BVDU did not cause any inhibition of focus formation when it was removed within 8hr after VZV infection. If removed at 24 or 48hr after infection, BVDU caused a significant reduction in focus formation. BVDU had no effect on focus formation if added to the HEF cells before virus infection. BVDU was also found to inhibit VZV focus formation in Vero cells, but only at an ID50 that was 5-10 times higher than the ID50 noted in HEF cells.

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