Premium
Enhancement of hepatitis A propagation in tissue culture with 5,6‐dichloro‐1‐β‐D‐ribofuranosylbenzimidazole
Author(s) -
Widell Anders,
Hansson Bengt Göran,
Nordenfelt Erik,
Öberg Bo
Publication year - 1988
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.1890240403
Subject(s) - vero cell , virology , infectivity , cell culture , biology , virus , tissue culture , antigen , hepatitis a virus , hepatitis a , microbiology and biotechnology , hepatitis , in vitro , immunology , biochemistry , genetics
Abstract The adenosine analog 5,6‐dichloro‐1‐β‐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 μM 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 10 log or more. DRB thus seems to be a useful enhancer of HAV growth in tissue culture.