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Clinical Research Centre Watford Road Harrow, Middlesex HA1 3UJ
Samples taken from either rhinovirus- or poliovirus-infected suspensions of L132 cells at various times during the growth cycle were assayed for intra- and extracellular virus infectivity, trypan blue uptake and release of acid phosphatase from lysosomes. At similar times infected L132 cell monolayers were observed for cell rounding (virus c.p.e.). At 16 h after infection with rhinovirus 2, cells showed no change in the distribution of acid phosphatase activity but had undergone extreme cytopathogenic changes; at this time 99% of the virus was intracellular and few cells took up trypan blue. Poliovirus-infected cells showed no change in the distribution of acid phosphatase at 6 h after infection when cytopathogenic changes were extreme, but 2 h later when cells began to take up trypan blue and release virus, acid phosphatase was released from the lysosomes.
It is suggested that lysosomal enzymes have no role in the induction of virus c.p.e. but are involved at a later stage of degeneration of the cell.
* Present address: Department of Microbiology, University of Leeds, Leeds LS2 9JT.
Present address: Department of Surgery, University of Otago Medical School, P.O. Box 913, Dunedin, New Zealand.
Present address: Institute for Research on Animal Diseases, Compton, Newbury, Berks.
Present address: Developmental Biochemistry Section, National Institute for Medical Research, Mill Hill, London NW7 1AA.
Received 12 July 1973;
accepted 1 November 1973.
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