Skip to main content
Log in

Ebola virus infection in guinea pigs: presumable role of granulomatous inflammation in pathogenesis

  • Originals Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

An approach combining virology with light and electron microscopy was used to study the organs of guinea pigs during nine serial passages of Ebola virus, strain Zaire. It was observed that the wild type of Ebola virus causes severe granulomatous inflammation in the liver and reproduces in the cells of the mononuclear phagocyte system (MPS). Based on morphological characterization, two types of virus-cell interactions were demonstrated. The obtained data evidenced for heterogeneity of the population of wild type of Ebola virus. The virus accumulated in the liver of the infected animals, and the lesions became more pronounced with passage. Degenerative changes appeared, and their severity was increased with passage in the other organs as well. The set of target cells diversified and, as a result, not only the MPS cells, but also hepatocytes, spongiocytes, endotheliocytes and fibroblasts became involved in the reproduction of Ebola virus. The possible role of granulomatous inflammation in the development of the adaptive mechanism of Ebola virus to guinea pigs is discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Allison AC (1984) Role of macrophage activation in the pathogenesis of chronic inflammation and its pharmacological control. Adv Inflam Res 7: 201–203

    Google Scholar 

  2. Baskerville A, Fisher-Hoch SP, Neild GH, Dowsett AB (1985) Ultrastructural pathology of experimental Ebola haemorrhagic fever virus infection. J Pathol 147: 199–209

    Google Scholar 

  3. Bown ETW, Platt GS, Lloyd G, Harris WI, Platt GS, Baskerville A, Vella EE (1977) Viral haemorrhagic fever in Southern Sudan and Northern Zaire. Preliminary studies on the aethiological agent. Lancet 1: 571–573

    Google Scholar 

  4. Bowen ETW, Platt GS, Simpson DIH, McArdell GB, Raymon RT (1978) Ebola haemorrahagic fever: experimental infection in monkeys. Trans Roy Soc Trop Med Hyg 72: 188–191

    Google Scholar 

  5. Bowen ETW, Platt GS, Lloyd G, Raymond RT, Simpson DIH (1980) A comparative study of strains of Ebola virus isolated from Southern Sudan and Northern Zaire in 1976. J Med Virol 6: 129–138

    Google Scholar 

  6. Brown BW (1961) Some properties of the Spearman estimator in bioassay. Biometrika 48: 293–302

    Google Scholar 

  7. Coleman D (1986) Regulation of macrophage phagocytosis. Eur J Clin Microbiol 5: 1–6

    Google Scholar 

  8. Cosgrif ThM, Morril JC, Jennings GB, Hodgson LA, Slayter MV, Gibbs PH, Peters CJ (1989) Hemostatic derangement produced by Rifr Valley Fever virus in rhesus monkeys. Rev Infect Dis 11: Suppl 4: S807–814

    Google Scholar 

  9. Ellis DS, Bowen ETW, Simpson DIH, Stamford S (1978) Ebola virus: a comparison, at ultrastructural level, of the behaviour of the Sudan and Zaire strains in monkeys. Br J Exp Pathol 59: 584–593

    Google Scholar 

  10. Ellis DS, Simpson DIH, Francis DP, Knobloch I, Bowen ETW, Lolik P, Deng IM (1978) Ultrastructure of Ebola virus particles in human liver. J Clin Pathol 31: 201–208

    Google Scholar 

  11. Gut JP, Anton M, Bingen A, Vetter JM, Kirn A (1981) Frog virus 3 induces a fatal hepatitis in rats. Lab Invest 45: 218–228

    Google Scholar 

  12. Hume D, Gordon S (1982) Macrophage biochemistry. Life Chem Rep 1: 1–47

    Google Scholar 

  13. Hunt RD, Carlton WW, King NW (1978) Viral diseases. In: Benirschke K, Garner FM, Jones TC (eds) pathology of laboratory animals vol. 2. Berlin Heidelberg New York, pp 1285–1365

  14. Hurley JV (1983) Acute inflammation, 2nd ed. Churchill Livingstone, Edinburgh

    Google Scholar 

  15. Johnstone R, Chadwick D, Cohn Z (1981) Priming of macrophages for enhanced oxidative metabolism by exposure to proteolytic enzymes. J Exp Med 153: 1678–1683

    Google Scholar 

  16. Kaplan A, Silverberg M (1988) Mediators of inflammation: an overview. Method Enzymol 163: 1–23

    Google Scholar 

  17. Korb G, Slenczka W (1971) Histologic findings in liver and spleens of guinea pigs after infection by the Marburg virus. In: Martini GA, Siegert R (eds) Marburg virus disease. Springer, Berlin Heidelberg New York, pp 123–124

    Google Scholar 

  18. Lefkowith JH, Goldstein H, Yatto R, Gerber MA (1987) Cytopathic liver injury in acute delta virus hepatitis. Gastroenterology 92: 1262–1266

    Google Scholar 

  19. Movat H (1985) Inflammatory reactions. Elsevier, Amsterdam

    Google Scholar 

  20. Pereboeva LA, Tkachev VK, Kolesnikova LV, Krendeleva LYa, Ryabchikova EI, Smolina MP (1993) Ultrastructural changes of guinea pig organs in sequential passages of Ebola virus. Probl Virol 4: 179–182 (in Russian)

    Google Scholar 

  21. Reynoilds RJ, Penn RL, Grafton WD (1984) Tissue morphology of Histoplasma capsulatum in acute histoplasmosis. Am Rev Resp Dis 130: 317–320

    Google Scholar 

  22. Riches D, Stanworth D (1981) Studies on the possible involvement of complement component C3 in the initiation of acid hydrolase secretion by macrophages. Immunology 44: 29–39

    Google Scholar 

  23. Robin J, Bres P, Camain R (1971) Passage of Marburg virus in guinea pigs. In: Martini GA, Siegert R (eds) Marburg virus disease. Springer, Berlin Heidelberg New York, pp 117–122

    Google Scholar 

  24. Rogoff T, Lipsky P (1981) Role of the Kupffer cells in local and systemic immune response. Gastroenterology 80: 854–860

    Google Scholar 

  25. Ryabchikova EI, Baranova SG, Tkachev VK, Grazhdantseva AA (1993) Morphological changes in Ebola virus infection of guinea pigs. Probl Virol 4: 176–179 (in Russian)

    Google Scholar 

  26. Siegert R (1972) Marburg virus. Virol Monogr 11: 113–118

    Google Scholar 

  27. Truden J, Boros D (1985) Collagenase, elastase and nonspecific protease production by vigorous or immunomodulatted liver granulomas and granuloma macrophage/eosonophils of S. mansoni-infected mice. Am J Pathol 121: 166–175

    Google Scholar 

  28. Wahl S, Hunt D, Allen J (1986) Bacterial cell wall-induced hepatic granulomas. An in vivo model of T-cell dependent fibrosis. J Exp Med 163: 884–903

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ryabchikova, E., Kolesnikova, L., Smolina, M. et al. Ebola virus infection in guinea pigs: presumable role of granulomatous inflammation in pathogenesis. Archives of Virology 141, 909–921 (1996). https://doi.org/10.1007/BF01718165

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01718165

Keywords

Navigation