Hepatitis C virus (HCV) circulating in patients' blood acquired cytopa
thogenic properties after infection of suckling mouse brain cells. HCV
infection of PS cells was studied for 11 months. Three stages of infe
ction were distinguished: noncytocidal infection, poorly manifest dest
ruction of PS cells, and intensive cytodestruction and cell repopulati
on. Persistent HCV was steadily released in PS culture and caused dest
ruction of BHK-21, Vero, PS, HAK, sad chick embryo cells. Infective ti
ters of HCV in culture fluid collected from these cultures were 10.0 =
11.0 lg TCD50/0.2 ml. Cytopathogenic activity of HCV regularly confir
med by the polymerase chain reaction was neutralized by anti-HCV-posit
ive sera of patients with hepatitis C. Persistent HCV formed heterogen
eous plaques in chick embryo fibroblast cultures and agglutinated goos
e erythrocytes. Indirect immunofluorescence demonstrated that 25 to 45
% of infected cells contained virus-specific antigens. The PS-HCV syst
em holds the best promise for theoretical and practical studies of hep
atitis C.