Osmiophilic Globules and Myelinic Bodies in Cells Infected with Two Comoviruses Free

Abstract

Summary

Bean leaf cells infected with bean pod mottle virus or cowpea mosaic virus contain osmiophilic globules (OG) in the cytoplasm. OG and myelinic bodies (MB) occurred between the plasmalemma and cell wall, and also embedded in the cell wall. Tubules containing virus particles were associated with OG and MB outside the cytoplasm, and membranes of some tubules were associated with MB. It is suggested that OG move from the cytoplasm through the plasmalemma, remain near the cell wall and become transformed into MB.

Loading

Article metrics loading...

/content/journal/jgv/10.1099/0022-1317-25-3-445
1974-12-01
2024-03-28
Loading full text...

Full text loading...

/deliver/fulltext/jgv/25/3/JV0250030445.html?itemId=/content/journal/jgv/10.1099/0022-1317-25-3-445&mimeType=html&fmt=ahah

References

  1. Caliguiri L. A., Tamm I. 1970; The role of cytoplasmic membranes in poliovirus biosynthesis. Virology 42:100–111
    [Google Scholar]
  2. Dales S., Eggers H. J., Tamm I., Palade G. E. 1965; Electron microscopic study of the formation of poliovirus. Virology 26:379–389
    [Google Scholar]
  3. De Zoeten G. A., Gaard G., Diez F. B. 1972; Nuclear vesiculation associated with pea enation mosaic virus-infected plant tissue. Virology 48:638–647
    [Google Scholar]
  4. Esau K., Hoefert L. L. 1971; Composition and fine structure of minor veins in Tetragonia leaf. Protoplasma 72:237–253
    [Google Scholar]
  5. Esau K., Hoefert L. L. 1972; Development of infection with beet western yellows virus in the sugarbeet. Virology 48:724–738
    [Google Scholar]
  6. Hooper G. G., Wiese M. V. 1972; Cytoplasmic inclusions in wheat affected by wheat spindle streak mosaic. Virology 47:664–672
    [Google Scholar]
  7. Jones A. T., Kinninmonth A. M., Roberts I. M. 1973; Ultra-structural changes in differentiated leaf cells infected with cherry leaf roll virus. Journal of General Virology 18:61–64
    [Google Scholar]
  8. Kim K. S., Fulton J. P. 1971; Tubules with viruslike particles in leaf cells infected with bean pod mottle virus. Virology 43:329–337
    [Google Scholar]
  9. Kim K. S., Fulton J. P. 1972; Fine structure of plant cells infected with bean pod mottle virus. Virology 49:112–121
    [Google Scholar]
  10. Kim K. S., Fulton J. P. 1973; Plant virus-induced cell wall overgrowth and associated membrane elaboration. Journal of Ultrastructure Research 45:328–342
    [Google Scholar]
  11. Milne R. G. 1970; An electron microscope study of tomato spotted wilt virus in sections of infected cells and in negative stain preparations. Journal of General Virology 6:267–276
    [Google Scholar]
  12. Mosser A. G., Caliguiri A., Tamm I. 1972; Incorporation of lipid precursors into cytoplasmic membranes of poliovirus-infected HeLa cells. Virology 47:39–47
    [Google Scholar]
  13. Murant A. F., Roberts I. M., Goold R. A. 1973; Cytopathological changes and extractable infectivity in Nicotiana clevelandii leaves infected with carrot mottle virus. Journal of General Virology 21:269–283
    [Google Scholar]
  14. O’brien T. P. 1967; Observations on the fine structure of the oat coleoptile. i. The epidermal cells of the extreme apex. Protoplasma 63:385–416
    [Google Scholar]
  15. Peterson J. F. 1970; Electron microscopy of soil-borne wheat mosaic virus in host cells. Virology 42:304–310
    [Google Scholar]
  16. Robards A. W. 1968; On the ultrastructure of differentiating secondary xylem in willow. Protoplasma 65:449–464
    [Google Scholar]
  17. Robards A. W., Kidwaii P. 1969; Vesicular involvement in differentiating plant vascular cells. New Phytologist 68:343–349
    [Google Scholar]
  18. Roberts I. M., Harrison B. D. 1970; Inclusion bodies and tubular structures in Chenopodium amaranticolor plants infected with strawberry latent ringspot virus. Journal of General Virology 7:47–54
    [Google Scholar]
  19. Sahambi H. S., Milne R. G., Cook S. M., Gibbs A. J., Woods R. D. 1973; Broad bean wilt and nasturtium ringspot viruses are related. Phytopathologische Zeitschrift 76:158–165
    [Google Scholar]
  20. Scott F. M., Hammer K. C., Baker E., Bowler E. 1958; Electron microscope studies of the epidermis of Allium cepa. American Journal of Botany 45:449–461
    [Google Scholar]
  21. Smith D. G., Marchant R. 1968; Lipid inclusions in the vacuoles of Saccharomyces cerevisiae. Archiv fur Mikrobiologie 60:340–347
    [Google Scholar]
  22. Spencer D. F., Kimmins W. C. 1971; Ultrastructure of tobacco mosaic virus lesions and surrounding tissue in Phaseolus vulgaris var. Pinto. Canadian Journal of Botany 49:417–421
    [Google Scholar]
  23. Szubinska B. 1971; ‘New membrane’ formation in Amoebaproteus upon injury of individual cells. Journal of Cell Biology 49:747–772
    [Google Scholar]
  24. Tu J. D., Hiruki C. 1971; Electron microscopy of cell wall thickening in local lesions of potato virus M-infected red kidney bean. Phytopathology 61:862–868
    [Google Scholar]
  25. Van Der Scheer C., Groenewegen J. 1971; Structures in cells of Vigna unguiculata infected with cowpea mosaic virus. Virology 46:493–497
    [Google Scholar]
  26. Walkey D. G. A., Webb M. J. W. 1970; Tubular inclusion bodies in plants infected with viruses of the NEPO type. Journal of General Virology 7:159–166
    [Google Scholar]
  27. Weintraub M., Ragetli H. W. J. 1970; Electron microscopy of the bean and cowpea strains of southern bean mosaic virus within leaf cells. Journal of Ultrastructure Research 32:167–189
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jgv/10.1099/0022-1317-25-3-445
Loading
/content/journal/jgv/10.1099/0022-1317-25-3-445
Loading

Data & Media loading...

Most cited Most Cited RSS feed