The rapidly turning over phosphorylation of specific nuclear nonhistone proteins, especially 42-, 33-, and 30-kDa polypeptides, and its relation to the transcriptional activity of hnRNA genes was investigated in isolated nuclei from salivary gland cells of Chironornus tentuns. Incubation conditions
Enhancement of hepatitis A propagation in tissue culture with 5,6-dichloro-1-β-D-ribofuranosylbenzimidazole
✍ Scribed by Dr. Anders Widell; Bengt Göran Hansson; Erik Nordenfelt; Bo Öberg
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 429 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
The adenosine analog 5,6-dichloro-l-~-D-ribofuranosylbenzimidazole (DRB) was found to increase the production of hepatitis A (HAV) antigen in two monkey kidney cell lines (Frhk-4 and Vero cells). DRB, a known inhibitor of the synthesis of messenger RNA, caused moderate changes in cell morphology. However, Frhk-4 cells could be maintained for several weeks at 80 FM of DRB, the concentration that caused maximal enhancement on HAV. DRB should be present from about the time of virus inoculation and its strongest effect was seen at low multiplicities of infection. Using radioimmunofocus assay it could be shown that DRB increased the amount of infectious virus. DRB treatment was applied in primary isolation of HAV from feces. In nine of ten strains HAV antigen expression was strongly increased and in six of the ten strains infectivity of harvested material increased by one 'Tog or more. DRB thus seems to be a useful enhancer of HAV growth in tissue culture.
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