Semliki Forest Virus in HEp-2 Cell Cultures
- 1 October 1967
- journal article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 1 (5) , 996-1009
- https://doi.org/10.1128/jvi.1.5.996-1009.1967
Abstract
The growth and development of Semliki Forest virus (SFV), an arbovirus of serological group A, in HEp-2 cells in tissue culture was examined by various techniques at frequent intervals. Infectivity and fluorescent-antibody studies demonstrated the presence of infective virus and viral antigens within the cells at 8 hr after infection. The antigen was particulate and distributed throughout the cytoplasm. Thereafter, there was rapid progression of virus production and cell destruction. By electron microscopy, tubular structures bounded by a fine membrane were observed in cytoplasm at 12 hr. Rows of small (25 mμ) virus particles were often present on the outer surface of these membranes, and at later times they became progressively more encrusted with the small virus particles. These structures subsequently increased rapidly in number, size, and complexity, and the space between the membrane and the tubules increased, thus forming vacuoles which contained tubules and were covered with the small particles. At later times (24 hr and later) larger (42 to 50 mμ) particles were observed, usually inside of the vacuoles. These larger particles (and occasionally the smaller ones) were also seen at the cell periphery and in the extracellular space. The large SFV particles appear to form by three distinct processes: (i) from the smaller particles, (ii) by development on an intravacuolar membrane, and (iii) at the ends of the tubules. The mode of development of SFV is unique among viruses studied to date, but in some characteristics it resembles that of other group A arboviruses. Its development differs from that of most arboviruses of group B and other serological groups.Keywords
This publication has 23 references indexed in Scilit:
- MORPHOLOGICAL DEVELOPMENT OF CHIKUNGUNYA VIRUSCanadian Journal of Microbiology, 1966
- Analysis of the development of Japanese B encephalitis (JBE) virusJournal of Ultrastructure Research, 1965
- A NEW MARAGLAS, D.E.R.® 732, EMBEDMENT FOR ELECTRON MICROSCOPYThe Journal of cell biology, 1964
- Electron microscopic study of spinal cord of mice infected with yellow fever virusJournal of Ultrastructure Research, 1963
- THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPYThe Journal of cell biology, 1963
- Electron microscopic and biological studies on the growth of Venezuelan equine encephalitis virus in KB cellsVirology, 1962
- STRUCTURE AND DEVELOPMENT OF VIRUSES AS OBSERVED IN THE ELECTRON MICROSCOPEThe Journal of Experimental Medicine, 1961
- Amino Acid Metabolism in Mammalian Cell CulturesScience, 1959
- Staining of Tissue Sections for Electron Microscopy with Heavy MetalsThe Journal of cell biology, 1958
- STUDIES WITH THE ELECTRON MICROSCOPE OF VIRUS-HOST RELATIONSHIPS IN EHRLICH ASCITES TUMOR CELLSThe Journal of Experimental Medicine, 1955