Polyribosomes of cells abortively or productively infected with adenovirus, papovavirus, or their hybrid
- 19 Downloads
- 1 Citations
Summary
The polyribosomes of African green monkey kidney (GMK) cells have been characterized during productive and abortive infections with adenovirus type 2, simian papovavirus SV40, and the PARA (defective SV40)-adenovirus type 2 hybrid. An early increase in uptake of H3-uridine was followed by a progressive decrease in both the amount of polyribosomes and in uptake of the label in all three systems that involved an adenovirus. Thus, the polyribosome distribution patterns obtained from GMK cells abortively infected with adenovirus type 2 did not differ significantly in optical density profile or incorporation of H3-uridine from the distributions obtained from GMK cells productively infected with either adenovirus 2 and SV40 or PARA-adenovirus type 2.
A decrease in the amount of polyribosomes was not evident when GMK cells were infected with SV40. During the productive cycle of SV40 in GMK cells, the fifth (pentamer) polysome peak enlarged as the infection progressed. This increase was reflected both in increased optical density and incorporated H3-uridine. Material from this peak reacted with antibody to SV40 capsid antigen in the complement-fixation test. Arabinofurano-sylcytosine, a DNA inhibitor that blocks SV40 replication at a step prior to capsid formation, inhibited the formation of this peak. Treatment of the cellular extracts with EDTA or ribonuclease did not shift this peak to a lighter part of the gradient, along with the other polyribosomes. Virus particles, some of which proved to be infective for monkey cells, were present in electron micrographs of the pentamer peak.
Keywords
Density Profile Productive Cycle Early Increase African Green Monkey Cellular ExtractPreview
Unable to display preview. Download preview PDF.
References
- 1.Anderer, F. A., H. D. Schlumberger, M. A. Koch, H. Frank, andH. J. Eggers: Structure of simian virus 40. II. Symmetry and components of the virus particle. Virology32, 511 (1967).Google Scholar
- 2.Baum, S. G., W. H. Wiese, andP. R. Reich: Studies on the mechanism of enhancement of adenovirus 7 infection in African green monkey cells by simian virus 40: Formation of adenovirus-specific RNA. Virology34, 373 (1968).Google Scholar
- 3.Boeyé, A., J. L. Melnick, andF. Rapp: Adenovirus-SV40 “hybrids”: Plaque purification into lines in which the determinant for the SV40 tumor antigen is lost or retained. Virology26, 511 (1965).Google Scholar
- 4.Boeyé, A., J. L. Melnick, andF. Rapp: SV40-adenovirus “hybrids”: Presence of two genotypes and the requirement of their complementation for viral replication. Virology28, 56 (1966).Google Scholar
- 5.Bresnick, E., andF. Rapp: Thymidine kinase activity in cells abortively and productively infected with human adenoviruses. Virology34, 799 (1968).Google Scholar
- 6.Butel, J. S., andF. Rapp: Replication in simian cells of defective viruses in an SV40-adenovirus “hybrid” population. J. Bact.91, 278 (1966).Google Scholar
- 7.Butel, J. S., andF. Rapp: Complementation between a defective monkey cell-adapting component and human adenoviruses in simian cells. Virology31, 573 (1967).Google Scholar
- 8.Feldman, L. A., J. S. Butel, andF. Rapp: Interaction of a simian papovavirus and adenoviruses. I. Induction of adenovirus tumor antigen during abortive infection of simian cells. J. Bact.91, 813 (1966).Google Scholar
- 9.Fujiwara, S., andA. S. Kaplan: Site of protein synthesis in cells infected with pseudorabies virus. Virology32, 60 (1967).Google Scholar
- 10.Hatanaka, M., andR. Dulbecco: Induction of DNA synthesis by SV40. Proc. nat. Acad. Sci. (Wash.)56, 736 (1966).Google Scholar
- 11.Kit, S.: Enzyme inductions in cell cultures during productive and abortive infections by papovavirus SV40. In: Symposium on the Molecular Biology of Viruses.J. S. Colter andW. Paranchych (eds.). New York: Academic Press, Inc., 1967.Google Scholar
- 12.Levine, A. J., andH. S. Ginsberg: Mechanism by which fiber antigen inhibits multiplication of type 5 adenovirus. J. Virol.1, 747 (1967).Google Scholar
- 13.Malmgren, R. A., A. S. Rabson, P. G. Carney, andF. J. Paul: Immunofluorescence of green monkey kidney cells infected with adenovirus 12 and with adenovirus 12 plus simian virus 40. J. Bact.91, 262 (1966).Google Scholar
- 14.Melnick, J. L.: Analytical serology of animal viruses. In: Analytical Serology of Microorganisms.J. G. B. Kwapinski (ed.). New York: John Wiley and Sons, 1969.Google Scholar
- 15.Naegele, R. F., andF. Rapp: Enhancement of the replication of human adenoviruses in simian cells by simian adenovirus SV15. J. Virol.1, 838 (1967).Google Scholar
- 16.Oda, K., andR. Dulbecco: Induction of cellular mRNA synthesis in BSC-1 cells infected by SV40. Virology35, 439 (1968).Google Scholar
- 17.Penman, S., C. Vesco, andM. Penman: Localization and kinetics of formation of nuclear heterodisperse RNA, cytoplasmic heterodisperse RNA and polyribosome-associated messenger RNA in HeLa cells. J. molec. Biol.34, 49 (1968).Google Scholar
- 18.Rapp, F.: Dependence and complementation among animal viruses containing deoxyribonucleic acid. In: The Molecular Biology of Viruses.L. V. Crawford andM. G. P. Stoker (eds.). London: Cambridge Univ. Press, 1968.Google Scholar
- 19.Rapp, F. J., S. Butel, L. A. Feldman, T. Kitahara, andJ. L. Melnick: Differential effects of inhibitors on the steps leading to the formation of SV40 tumor and virus antigens. J. exp. Med.121, 935 (1965).Google Scholar
- 20.Rapp, F. J., S. Butel, andJ. L. Melnick: SV40-adenovirus “hybrid” populations: Transfer of SV40 determinants from one type of adenovirus to another. Proc. nat. Acad. Sci. (Wash.)54, 717 (1965).Google Scholar
- 21.Rapp, F. L., A. Feldman, andM. Mandel: Synthesis of virus deoxyribonucleic acid during abortive infection of simian cells by human adenoviruses. J. Bact.92, 931 (1966).Google Scholar
- 22.Rapp, F., M. Jerkofsky, andD. Vanderslice: Characterization of defectiveness of human adenoviruses in green monkey kidney cells. Proc. Soc. exp. Biol. (N.Y.)126, 782 (1967).Google Scholar
- 23.Rapp, F., andJ. L. Melnick: Papovavirus SV40, adenovirus and their hybrids: Transformation, complementation, and transcapsidation. Progr. med. Virol.8, 349 (1966).Google Scholar
- 24.Rowe, W. P., andS. G. Baum: Studies of adenovirus SV40 hybrid viruses. II. Defectiveness of the hybrid particles. J. exp. Med.122, 955 (1965).Google Scholar
- 25.Summers, D. F., J. V. Maizel, andJ. E. Darnell: The decrease in size and synthetic activity of poliovirus polysomes late in the infectious cycle. Virology31, 427 (1967).Google Scholar
- 26.Sydiskis, R. J., andB. Roizman: Polysomes and protein synthesis in cells infected with a DNA virus. Science153, 76 (1966).Google Scholar
- 27.Sydiskis, R. J., andB. Roizman: The sedimentation profiles of cytoplasmic polyribosomes in mammalian cells productively and abortively infected with herpes simplex virus. Virology34, 562 (1968).Google Scholar
- 28.Thomas, D. C., andM. Green: Biochemical studies on adenovirus multiplication. XI. Evidence of a cytoplasmic site for the synthesis of viralcoded proteins. Proc. nat. Acad. Sci. (Wash.)56, 243 (1966).Google Scholar