Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1983 Sep;46(3):673–682. doi: 10.1128/aem.46.3.673-682.1983

Adsorption of reovirus to clay minerals: effects of cation-exchange capacity, cation saturation, and surface area.

S M Lipson, G Stotzky
PMCID: PMC239333  PMID: 6639022

Abstract

The adsorption of reovirus to clay minerals has been reported by several investigators, but the mechanisms defining this association have been studied only minimally. The purpose of this investigation was to elucidate the mechanisms involved with this interaction. More reovirus type 3 was adsorbed, in both distilled and synthetic estuarine water, by low concentrations of montmorillonite than by comparable concentrations of kaolinite containing a mixed complement of cations on the exchange complex. Adsorption to the clays was essentially immediate and was correlated with the cation-exchange capacity of the clays, indicating that adsorption was primarily to negatively charged sites on the clays. Adsorption was greater with low concentrations of clays in estuarine water than in distilled water, as the higher ionic strength of the estuarine water reduced the electrokinetic potential of both clay and virus particles. The addition of cations (as chloride salts) to distilled water enhanced adsorption, with divalent cations being more effective than monovalent cations and 10(-2) M resulting in more adsorption than 10(-3) M. Potassium ions suppressed reovirus adsorption to montmorillonite, probably by collapsing the clay lattices and preventing the expression of the interlayer-derived cation-exchange capacity. More virus was adsorbed by montmorillonite made homoionic to various mono-, di-, and trivalent cations (except by montmorillonite homoionic to potassium) than by comparable concentrations of kaolinite homoionic to the same cations. The sequence of the amount of adsorption to homoionic montmorillonite was Al greater than Ca greater than Mg greater than Na greater than K; the sequence of adsorption to kaolinite was Na greater than Al greater than Ca greater than Mg greater than K. The constant partition-type adsorption isotherms obtained when the clay concentration was maintained constant and the virus concentration was varied indicated that a fixed proportion of the added virus population was adsorbed, regardless of the concentration of infectious particles. A heterogeneity within the reovirus population was indicated.

Full text

PDF
673

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ALLISON A. C., VALENTINE R. C. Virus particle adsorption, III. Adsorption of viruses by cell monolayers and effects of some variables on adsorption. Biochim Biophys Acta. 1960 Jun 3;40:400–410. doi: 10.1016/0006-3002(60)91380-9. [DOI] [PubMed] [Google Scholar]
  2. Adams D. J., Ridinger D. N., Spendlove R. S., Barnett B. B. Protamine precipitation of two reovirus particle types from polluted waters. Appl Environ Microbiol. 1982 Sep;44(3):589–596. doi: 10.1128/aem.44.3.589-596.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ahmed R., Fields B. N. Reassortment of genome segments between reovirus defective interfering particles and infectious virus: construction of temperature-sensitive and attenuated viruses by rescue of mutations from DI particles. Virology. 1981 Jun;111(2):351–363. doi: 10.1016/0042-6822(81)90339-1. [DOI] [PubMed] [Google Scholar]
  4. Browne J. E., Feldkamp J. R., White J. L., Hem S. L. Potential of organic cation-saturated montmorillonite as treatment for poisoning by weak bases. J Pharm Sci. 1980 Dec;69(12):1393–1395. doi: 10.1002/jps.2600691210. [DOI] [PubMed] [Google Scholar]
  5. Dahling D. R., Safferman R. S. Survival of enteric viruses under natural conditions in a subarctic river. Appl Environ Microbiol. 1979 Dec;38(6):1103–1110. doi: 10.1128/aem.38.6.1103-1110.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Drayna D., Fields B. N. Biochemical studies on the mechanism of chemical and physical inactivation of reovirus. J Gen Virol. 1982 Nov;63(Pt 1):161–170. doi: 10.1099/0022-1317-63-1-161. [DOI] [PubMed] [Google Scholar]
  7. Drewry W. A., Eliassen R. Virus movement in groundwater. J Water Pollut Control Fed. 1968 Aug;(Suppl):257–271. [PubMed] [Google Scholar]
  8. England B. Concentration of reovirus and adenovirus from sewage and effluents by protamine sulfate (salmine) treatment. Appl Microbiol. 1972 Sep;24(3):510–512. doi: 10.1128/am.24.3.510-512.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Floyd R., Sharp D. G. Viral aggregation: effects of salts on the aggregation of poliovirus and reovirus at low pH. Appl Environ Microbiol. 1978 Jun;35(6):1084–1094. doi: 10.1128/aem.35.6.1084-1094.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fraser D., Fleischmann C. Interaction of mycoplasma with viruses. I. Primary adsorption of virus is ionic in mechanism. J Virol. 1974 May;13(5):1067–1074. doi: 10.1128/jvi.13.5.1067-1074.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gerba C. P., Schaiberger G. E. Effect of particulates on virus survival in seawater. J Water Pollut Control Fed. 1975 Jan;47(1):93–103. [PubMed] [Google Scholar]
  12. Goyal S. M., Gerba C. P. Comparative adsorption of human enteroviruses, simian rotavirus, and selected bacteriophages to soils. Appl Environ Microbiol. 1979 Aug;38(2):241–247. doi: 10.1128/aem.38.2.241-247.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gunn R. A., Janowski H. T., Lieb S., Prather E. C., Greenberg H. B. Norwalk virus gastroenteritis following raw oyster consumption. Am J Epidemiol. 1982 Mar;115(3):348–351. doi: 10.1093/oxfordjournals.aje.a113311. [DOI] [PubMed] [Google Scholar]
  14. Irving L. G., Smith F. A. One-year survey of enteroviruses, adenoviruses, and reoviruses isolated from effluent at an activated-sludge purification plant. Appl Environ Microbiol. 1981 Jan;41(1):51–59. doi: 10.1128/aem.41.1.51-59.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. LaBelle R. L., Gerba C. P., Goyal S. M., Melnick J. L., Cech I., Bogdan G. F. Relationships between environmental factors, bacterial indicators, and the occurrence of enteric viruses in estuarine sediments. Appl Environ Microbiol. 1980 Mar;39(3):588–596. doi: 10.1128/aem.39.3.588-596.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Metcalf T. G., Stiles W. C. Enteroviruses within an estuarine environment. Am J Epidemiol. 1968 Nov;88(3):379–391. doi: 10.1093/oxfordjournals.aje.a120898. [DOI] [PubMed] [Google Scholar]
  17. Odom D. G., Rao M., Lawless J. G., Oro J. Association of nucleotides with homoionic clays. J Mol Evol. 1979 Apr 12;12(4):365–367. doi: 10.1007/BF01732031. [DOI] [PubMed] [Google Scholar]
  18. Ostle A. G., Holt J. G. Elution and inactivation of bacteriophages on soil and cation-exchange resin. Appl Environ Microbiol. 1979 Jul;38(1):59–65. doi: 10.1128/aem.38.1.59-65.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. PUCK T. T., GAREN A., CLINE J. The mechanism of virus attachment to host cells. I. The role of ions in the primary reaction. J Exp Med. 1951 Jan;93(1):65–88. doi: 10.1084/jem.93.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. PUCK T., SAGIK B. Virus and cell interaction with ion exchangers. J Exp Med. 1953 Jun;97(6):807–820. doi: 10.1084/jem.97.6.807. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pett D. M., Vanaman T. C., Joklik W. K. Studies on the amino and carboxyl terminal amino acid sequences of reovirus capsid polypeptides. Virology. 1973 Mar;52(1):174–186. doi: 10.1016/0042-6822(73)90407-8. [DOI] [PubMed] [Google Scholar]
  22. Portnoy B. L., Mackowiak P. A., Caraway C. T., Walker J. A., McKinley T. W., Klein C. A., Jr Oyster-associated hepatitis. Failure of shellfish certification programs to prevent outbreaks. JAMA. 1975 Sep 8;233(10):1065–1068. doi: 10.1001/jama.233.10.1065. [DOI] [PubMed] [Google Scholar]
  23. Rotmistrov M. N., Globa L. I., Nikovskaia G. N., Tarasevich Iu I. Sorbtsiia faga T2 E. coli B prirodnym Cherkasskim montmorrillonitom. Vopr Virusol. 1978 Jan-Feb;(1):108–111. [PubMed] [Google Scholar]
  24. Santoro T., Stotzky G. Sorption between microorganisms and clay minerals as determined by the electrical sensing zone particle analyser. Can J Microbiol. 1968 Apr;14(4):299–307. doi: 10.1139/m68-049. [DOI] [PubMed] [Google Scholar]
  25. Schaub S. A., Kenyon K. F., Bledsoe B., Thomas R. E. Evaluation of the overland runoff mode of land wastewater treatment for virus removal. Appl Environ Microbiol. 1980 Jan;39(1):127–134. doi: 10.1128/aem.39.1.127-134.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Schaub S. A., Sagik B. P. Association of enteroviruses with natural and artificially introduced colloidal solids in water and infectivity of solids-associated virions. Appl Microbiol. 1975 Aug;30(2):212–222. doi: 10.1128/am.30.2.212-222.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Schiffenbauer M., Stotzky G. Adsorption of coliphages T1 and T7 to clay minerals. Appl Environ Microbiol. 1982 Mar;43(3):590–596. doi: 10.1128/aem.43.3.590-596.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Shirobokov V. P. Ispol'zovanie bentonitovogo pokrytiia dlia titrovaniia énterovirusov metodom bliashek. Vopr Virusol. 1973 Sep-Oct;18(5):611–615. [PubMed] [Google Scholar]
  29. Sobsey M. D., Dean C. H., Knuckles M. E., Wagner R. A. Interactions and survival of enteric viruses in soil materials. Appl Environ Microbiol. 1980 Jul;40(1):92–101. doi: 10.1128/aem.40.1.92-101.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Stagg C. H., Wallis C., Ward C. H. Inactivation of clay-associated bacteriophage MS-2 by chlorine. Appl Environ Microbiol. 1977 Feb;33(2):385–391. doi: 10.1128/aem.33.2.385-391.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Stotzky G. Influence of clay minerals on microorganisms. II. Effect of various clay species, homoionic clays, and other particles on bacteria. Can J Microbiol. 1966 Aug;12(4):831–848. doi: 10.1139/m66-111. [DOI] [PubMed] [Google Scholar]
  32. Turk C. A., Moore B. E., Sagik B. P., Sorber C. A. Recovery of indigenous viruses from wastewater sludges, using a bentonite concentration procedure. Appl Environ Microbiol. 1980 Aug;40(2):423–425. doi: 10.1128/aem.40.2.423-425.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wilson R., Anderson L. J., Holman R. C., Gary G. W., Greenberg H. B. Waterborne gastroenteritis due to the Norwalk agent: clinical and epidemiologic investigation. Am J Public Health. 1982 Jan;72(1):72–74. doi: 10.2105/ajph.72.1.72. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES