Skip to main content
Log in

Ecology of bacterial communities in the schistosomiasis vector snailBiomphalaria glabrata

  • Published:
Microbial Ecology Aims and scope Submit manuscript

Abstract

The internal colony-forming bacterial flora of the schistosome intermediate host snailBiomphalaria glabrata (Say) has been characterized in ca. 500 individual snails from Puerto Rico, Guadeloupe, and St. Lucia, and from laboratory aquaria. Freshly captured wild snails harbor 2–40×106 CFU·g−1, and healthy aquarium snails harbor 4–16×107 CFU·g−1, whereas moribund individuals have 4–10 times as many bacteria as healthy individuals from the same habitats.Pseudomonas spp. are the most common predominant bacteria in normal snails, whereasAcinetobacter, Aeromonas, andMoraxella spp. predominate in moribund snails. External bacterial populations in water appear to have little effect on the composition and size of the flora in any snail. In addition to normal (healthy) and moribund snails, a third group of snails has been distinguished on the basis of internal bacterial density and predominating genera. These “high-density” snails may have undergone stresses and may harbor opportunistic pathogens. The microfloras of wild and laboratory-reared snails can be altered and stimulated to increase in density by crowding the snails or treating them with antibiotics.

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.

Similar content being viewed by others

References

  1. Bucher, G. E.: Bacteria of grasshoppers of western Canada: III. Frequency of occurrence, pathogenicity. J. Insect Pathol.1, 391–405 (1959)

    Google Scholar 

  2. Campbell, R. W., and J. D. Podgewaite: The disease complex of the gypsy moth. 1. Major components. J. Invert. Pathol.18, 101–107 (1971)

    Google Scholar 

  3. Chernin, E.: A method of securing bacteriologically sterile snails (Australorbis glabratus). Proc. Soc. Exp. Biol. Med.96, 204–210 (1957)

    PubMed  Google Scholar 

  4. Coelho, P. M. Z., Y. P. Figuerredo, J. Pellegrino, and G. R. Melo:Biomphalaria glabrata: The crowding effect related to aquarium water components. J. Parasitol.63, 284 (1977)

    PubMed  Google Scholar 

  5. Cohen, J.: Mathematical models of schistosomiasis. Annu. Rev. Ecol. Sys.8, 209–233 (1977)

    Google Scholar 

  6. Cole, R. M., C. S. Richards, and T. J. Popkin: Novel bacterium infecting an African snail. J. Bacteriol.132, 950–966 (1977)

    PubMed  Google Scholar 

  7. Connell, J. M.: The influence of interspecific competition and other factors on the distribution of the barnacle,Chthamatus stellatus. Ecology42, 133–146 (1961)

    Google Scholar 

  8. Dean, W. W., A. R. Mead, and W. T. Northey:Aeromonas liquefaciens in the giant African snail,Achatina fulica. J. Invert. Pathol.16, 346–351 (1970)

    Google Scholar 

  9. Ducklow, H. W., P. J. Boyle, P. W. Maugel, C. Strong, and R. Mitchell: Bacterial flora of the schistosome vector snailBiomphalaria glabrata. Appl. Environ. Microbiol.38, 667–672 (1979)

    PubMed  Google Scholar 

  10. Ducklow, H. W., and R. Mitchell: Observations on naturally and artificially diseased tropical corals: a scanning electron microscope study. Microb. Ecol.5, 215–233 (1979)

    Google Scholar 

  11. Ferguson, F. F.: Role of Biological Agents in the Control of Schistosome-Bearing Snails. U.S. Public Health Service: Center for Disease Control, Atlanta, GA (1977)

    Google Scholar 

  12. Fisher, W. S.: Relationships of epibiotic fouling and mortalities of eggs of the dungeness crab (Cancer magister). J. Fish. Res. Board Can.33, 2849–2853 (1976)

    Google Scholar 

  13. Geesey, G. G., R. Mutch, J. W. Costerton, and R. B. Green: Sessile bacteria: an important component of the microbial population in small mountain streams. Limnol. Oceanogr.23, 1214–1223 (1978)

    Google Scholar 

  14. Greany, P. D., G. E. Allen, J. C. Webb, J. L. Sharp, and D. L. Chambers: Stress-induced septicemia as an impediment to lab-rearing of the fruit fly parasitoidBiosteres (Opius) logicaudatus (Hymenoptera: braconidae) and the Caribbean fruit flyAnastrepha suspensa (Diptera: tephritidae). J. Invert. Pathol.29, 153–161 (1977)

    Google Scholar 

  15. Harper, J. L.: Approaches to the study of plant competition. In: Mechanisms in Biological Competition. Symp. Soc. Exp. Biol.XV, 1–268 (1961)

    Google Scholar 

  16. Jobin, W. R.: Population dynamics of aquatic snails in three farm ponds of Puerto Rico. Am. J. Trop. Med. Hyg.19, 1038–1048 (1970)

    PubMed  Google Scholar 

  17. Jordan, P., and G. Webbe: Human Schistosomiasis. Charles C. Thomas, Springfield. Ill. (1969)

    Google Scholar 

  18. Michelson, E. H.: An acid-fast pathogen of freshwater snails. Am. J. Trop. Med. Hyg.10, 423–427 (1961)

    PubMed  Google Scholar 

  19. Michelson, E.H., and L. Dubois: Agglutinins and lysins in the molluscan family planorbidae: a survey of hemolymph, egg masses, and albumin gland extracts. Biol. Bull.153, 219–227 (1977)

    PubMed  Google Scholar 

  20. Mitchell, R., and I. Chet: Indirect ecological effects of pollution. In R. Mitchell (ed.): Water Pollution Microbiology, Vol. 2. John Wiley & Sons, New York (1978)

    Google Scholar 

  21. Pointier, J. P., B. Salvat, A. Delplanque, and Y. Glovan: Principal factors involved in the settlement ofBiomphalaria glabrata (Say, 1818), snail intermediate of schistosomiasis in Guadeloupe. Ann. Parasitol. (Paris)52, 277–323 (1977)

    Google Scholar 

  22. Ramsay, A. J., J. C. Fry: Response of epiphytic bacteria to the treatment of two aquatic macrophytes with the herbicide paraquat. Water Res.10, 453–459 (1976)

    Google Scholar 

  23. Richards, C. S.: Variations in infectivity forBiomphalaria glabrata in strains ofSchistosoma mansoni from the same geographical area. Bull. WHO54, 706–707 (1976)

    PubMed  Google Scholar 

  24. Richards, C.S.: Spirochaetes in planorbid molluscs. Trans. Am. Microsc. Soc.97, 191–199 (1978)

    PubMed  Google Scholar 

  25. deSouza, C. P., M. das G. Vilela, M. A. R. deCarvalho, and E. C. Viera: Rearing of the snailBiomphalaria glabrata under axenic conditions in isolators. Am. J. Trop. Med. Hyg.26, 1013–1017 (1977)

    PubMed  Google Scholar 

  26. Sturrock, R. F.: Ecological notes on the habitats of the freshwater snailBiomphalaria glabrata, intermediate host ofSchistosoma mansoni on St. Lucia West Indies. Carib. J. Sci.14, 149–162 (1974)

    Google Scholar 

  27. Tripp, M. R.: The fate of foreign materials experimentally introduced into the snailAustralorbis glabratus. J. Parasitol.47, 745–749 (1961)

    PubMed  Google Scholar 

  28. Viera, E. C.: Influence of vitamin E on reproduction ofBiomphalaria glabrata under axenic conditions. Am. J. Trop. Med. Hyg.16, 792–796 (1967)

    PubMed  Google Scholar 

  29. Von Graevenitz, A.: The role of opportunistic bacteria in human disease. Annu. Rev. Microbiol.31, 447–471 (1977)

    PubMed  Google Scholar 

  30. Warren, K. S., and V. A. Newill: Schistosomiasis—A Bibliography of the World's Literature from 1852 to 1962. Western Reserve University Press, Cleveland (1967)

    Google Scholar 

  31. Warren, K. S., and D. B. Hoffman: Schistosomiasis III: Abstracts of the Complete Literature 1963–1974, 2 vols. Hemisphere Publishing Co., Washington, D.C. (1976)

    Google Scholar 

  32. Wright, C.A.: The crowding phenomenon in laboratory colonies of freshwater snails. Ann. Trop. Med. Parasitol.54, 224–232 (1960)

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ducklow, H.W., Clausen, K. & Mitchell, R. Ecology of bacterial communities in the schistosomiasis vector snailBiomphalaria glabrata . Microb Ecol 7, 253–274 (1981). https://doi.org/10.1007/BF02010308

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02010308

Keywords

Navigation