TY - JOUR
T1 - Biogenesis of poxviruses
T2 - Transitory expression of Molluscum contagiosum early functions
AU - McFadden, Grant
AU - Pace, William E.
AU - Purres, Jack
AU - Dales, Samuel
N1 - Funding Information:
1 Supported by grants from USPHS and Medical Research Council of Canada. * With assistance by Sharon Wilton. 3 To whom reprint requests should be addressed.
PY - 1979/4/30
Y1 - 1979/4/30
N2 - Inoculation of primate cells with Molluscum contagiosum (MC) produces extreme cell rounding, aggregation, and surface convolutions termed cytopathic effect (CPE). The CPE is transitory, completely reversible, and temporally connected with formation of virus-specified RNA and antigen. The early functions are expressed from the inoculum virus cores which are released into the host cytoplasm but never become uncoated. Although cores persist for at least 10 days, the cells are completely viable, regain their normal form, and remain susceptible to reinfection with MC. Attempts at rescuing MC uncoating by means of coinfection with vaccinia, Yaba, and Shope fibroma viruses or inoculation of differentiating keratinocytes from explants of human epidermis, were unsuccessful. It is, therefore, most likely that MC replication is blocked in vitro because the agent is unable to pass through the uncoating phase.
AB - Inoculation of primate cells with Molluscum contagiosum (MC) produces extreme cell rounding, aggregation, and surface convolutions termed cytopathic effect (CPE). The CPE is transitory, completely reversible, and temporally connected with formation of virus-specified RNA and antigen. The early functions are expressed from the inoculum virus cores which are released into the host cytoplasm but never become uncoated. Although cores persist for at least 10 days, the cells are completely viable, regain their normal form, and remain susceptible to reinfection with MC. Attempts at rescuing MC uncoating by means of coinfection with vaccinia, Yaba, and Shope fibroma viruses or inoculation of differentiating keratinocytes from explants of human epidermis, were unsuccessful. It is, therefore, most likely that MC replication is blocked in vitro because the agent is unable to pass through the uncoating phase.
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U2 - 10.1016/0042-6822(79)90463-X
DO - 10.1016/0042-6822(79)90463-X
M3 - Article
C2 - 452419
AN - SCOPUS:0018397104
SN - 0042-6822
VL - 94
SP - 297
EP - 313
JO - Virology
JF - Virology
IS - 2
ER -