Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-26T04:53:52.179Z Has data issue: false hasContentIssue false

Effects of oxygen on aerosol survival of radiation sensitive and resistant strains of Escherichia coli B

Published online by Cambridge University Press:  15 May 2009

C. S. Cox
Affiliation:
Naval Biomedical Research Laboratory, Naval Supply Center, Oakland, California 94625
M. C. Bondurant
Affiliation:
Naval Biomedical Research Laboratory, Naval Supply Center, Oakland, California 94625
M. T. Hatch
Affiliation:
Naval Biomedical Research Laboratory, Naval Supply Center, Oakland, California 94625
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The aerosol survivals in air and nitrogen of radiation sensitive and resistant mutants of Escherichia coli B have been determined with logarithmic and resting phase bacteria. No consistent correlation was found between radiation sensitivity and aerosol sensitivity in the strains tested. Hence, the phenotypes Fil Her Exr, which determine sensitivity to radiation, do not influence aerosol survival, i.e. these known mechanisms which repair radiation-induced damage do not operate in aerosol stressed E. coli. In all cases the survival in air was less than that in nitrogen particularly so for E. coli Bs-1. The effect is explained in terms of a toxic action of oxygen. Comparison of survival of log and resting phase bacteria show that log phase cells are less aerosol stable than are resting phase cells. The ability to synthesize DNA in bacteria collected from the aerosol was less than in control unstressed bacteria, and this effect was independent of the presence of oxygen. Reduced ability to synthesize DNA could have been caused by reduced metabolic activity. It is shown that two different death mechanisms occur simultaneously in aerosols at low relative humidity. One mechanism is oxygen dependent and the other oxygen independent. The former was not through a decrease in metabolic activity, whereas the latter could be.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1971

References

REFERENCES

Anderson, J. D. & Cox, C. S. (1967). Microbial Survival. Symposium of the Society of General Microbiology 17, 203.Google Scholar
Benbough, J. E. (1967). Death mechanisms in airborne Escherichia coli. Journal of General Microbiology 47, 325.CrossRefGoogle ScholarPubMed
Benbough, J. E. (1969). Factors affecting the toxicity of oxygen toward airborne coliform bacteria. Journal of General Microbiology 56, 241.CrossRefGoogle Scholar
Cox, C. S. (1965). The mode of action of protecting agents. First International Symposium on Aerobiology, p. 345.Google Scholar
Cox, C. S. (1966 a). The survival of Escherichia coli atomized into air and into nitrogen from distilled water and from solutions of protecting agents, as a function of relative humidity. Journal of General Microbiology 43, 383.CrossRefGoogle Scholar
Cox, C. S. (1966 b). The survival of Escherichia coli in nitrogen under changing conditions of relative humidity. Journal of General Microbiology 45, 283.CrossRefGoogle ScholarPubMed
Cox, C. S. (1967). The aerosol survival of Escherichia coli Jepp sprayed from protecting agents into nitrogen atmospheres under shifting conditions of relative humidity. Journal of General Microbiology 49, 109.CrossRefGoogle Scholar
Cox, C. S. (1968 a). The aerosol survival of Escherichia coli B in nitrogen, argon and helium atmospheres and the influence of relative humidity. Journal of General Microbiology 50, 139.CrossRefGoogle ScholarPubMed
Cox, C. S. (1968 b). The aerosol survival and cause of death of Escherichia coli K 12. Journal of General Microbiology 54, 169.CrossRefGoogle Scholar
Cox, C. S. (1969). The cause of loss of viability of airborne Escherichia coli K 12. Journal of General Microbiology 57, 77.CrossRefGoogle Scholar
Cox, C. S. (1970). Aerosol survival of Escherichia coli B disseminated from the dry state. Applied Microbiology 19, 604.CrossRefGoogle ScholarPubMed
Cox, C. S. (1971). Aerosol survival of Pasteurella tularensis disseminated from the wet and dry state. Applied Microbiology 21, 482.CrossRefGoogle Scholar
Cox, C. S. & Baldwin, F. (1966). The use of phage to study causes of loss of viability of Escherichia coli B in aerosols. Journal of General Microbiology 44, 15.CrossRefGoogle Scholar
Cox, C. S. & Baldwin, F. (1967). The toxic effect of oxygen upon aerosol survival of Escherichia coli B. Journal of General Microbiology 49, 115.CrossRefGoogle ScholarPubMed
Cox, C. S. & Heckly, R. J. (1972). Kinetics and mechanism of action of oxygen in oxygen-induced death of dried bacteria. To be published.Google Scholar
Ferry, R. M., Brown, W. F. & Damon, E. B. (1958). Studies of the loss of viability of bacterial aerosols. III. Factors affecting death rates of certain non-pathogens. Journal of Hygiene 56, 389.CrossRefGoogle ScholarPubMed
Hatch, M. T. & Dimmick, R. L. (1965). A study of dynamic aerosols of bacteria subjected to rapid changes in relative humidity, first International Symposium on Aerobiology, p. 265.Google Scholar
Hatch, M. T. & Dimmick, R. L. (1966). Physiological responses of airborne bacteria to shifts in relative humidity. Bacteriological Reviews 30, 597.CrossRefGoogle ScholarPubMed
Hatch, M. T. & Warren, J. C. (1969). Enhanced recovery of airborne T3 eoliphage and Pasteurella pestis bacteriophage by means of a pre-sampling humidiflcation technique. Applied Microbiology 17, 685.CrossRefGoogle Scholar
Hatch, M. T. & Wolochow, H. (1969). Bacterial survival: consequences of the airborne state. An Introduction to Experimental Aerobiology, p. 267. Ed. Dimmick, R. L. and Akers, Ann B.. New York, London, Sydney, Toronto: Wiley Interscience.Google Scholar
Hatch, M. T., Wright, D. N. & Bailey, G. D. (1970). Response of airborne Mycoplasma pneumoniae to abrupt changes in relative humidity. Applied Microbiology 19, 232.CrossRefGoogle ScholarPubMed
Hess, G. E. (1965). Effects of oxygen on aerosolized Serratia marcescens. Applied Microbiology 13, 781.CrossRefGoogle ScholarPubMed
Lieb, M. (1964). Dark repair of UV induction in K 12 (γ). Virology 23, 381.CrossRefGoogle Scholar
Webb, S. J. (1965). Bound water in Biological Integrity. Springfield, Illinois, U.S.A.: Charles C. Thomas.Google Scholar
Webb, S. J. (1967). The influence of oxygen and inositol on survival of semi-dried organisms. Canadian Journal of Microbiology 13, 733.CrossRefGoogle Scholar
Webb, S. J. (1969). The effects of oxygen on the possible repair of dehydration damage by Escherichia coli. Journal of General Microbiology 58, 317.CrossRefGoogle ScholarPubMed
Witkin, E. M. (1963). The effect of acriflavin on photoreversal of lethal and mutagenic damage produced in bacteria by ultra-violet light. Proceedings of the National Academy of Sciences U.S.A. 50, 425.CrossRefGoogle Scholar