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Inactivation and Ultrastructure Analysis of Bacillus spp. and Clostridium perfringens Spores

Published online by Cambridge University Press:  04 February 2014

Christine A. Brantner
Affiliation:
National Bioforensic Analysis Center, National Biodefense Analysis and Countermeasures Center, Fort Detrick, MD, 21702, USA
Ryan M. Hannah
Affiliation:
National Bioforensic Analysis Center, National Biodefense Analysis and Countermeasures Center, Fort Detrick, MD, 21702, USA
James P. Burans
Affiliation:
National Bioforensic Analysis Center, National Biodefense Analysis and Countermeasures Center, Fort Detrick, MD, 21702, USA
Robert K. Pope*
Affiliation:
National Bioforensic Analysis Center, National Biodefense Analysis and Countermeasures Center, Fort Detrick, MD, 21702, USA
*
*Corresponding author. E-mail: [email protected]
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Abstract

Bacterial endospores are resistant to many environmental factors from temperature extremes to ultraviolet irradiation and are generally more difficult to inactivate or kill than vegetative bacterial cells. It is often considered necessary to treat spores or samples containing spores with chemical fixative solutions for prolonged periods of time (e.g., 1–21 days) to achieve fixation/inactivation to enable electron microscopy (EM) examination outside of containment laboratories. Prolonged exposure to chemical fixatives, however, can alter the ultrastructure of spores for EM analyses. This study was undertaken to determine the minimum amount of time required to inactivate/sterilize and fix spore preparations from several bacterial species using a universal fixative solution for EM that maintains the ultrastructural integrity of the spores. We show that a solution of 4% paraformaldehyde with 1% glutaraldehyde inactivated spore preparations of Bacillus anthracis, Bacillus cereus, Bacillus megaterium, Bacillus thuringiensis, and Clostridium perfringens in 30 min, and Bacillus subtilis in 240 min. These results suggest that this fixative solution can be used to inactivate and fix spores from several major groups of bacterial spore formers after 240 min, enabling the fixed preparations to be removed from biocontainment and safely analyzed by EM outside of biocontainment.

Type
Biological Applications
Copyright
Copyright © Microscopy Society of America 2014 

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References

Ball, D.A., Taylor, R., Todd, S.J., Redmond, C., Couture-Tosi, E., Sylvestre, P., Moir, A. & Bullough, P.A. (2008). Structure of the exosporium and sublayers of spores of the Bacillus cereus family revealed by electron crystallography. Mol Microbiol 68(4), 947958.Google Scholar
Bozue, J., Moody, K.L., Cote, C.K., Stiles, B.G., Friedlander, A.M., Welkos, S.L. & Hale, M.L. (2007). Bacillus anthracis spores of the bclA mutant exhibit increased adherence to epithelial cells, fibroblasts, and endothelial cells but not to macrophages. Infect Immun 75(9), 44984505.Google Scholar
Bozzolla, J.J. & Russell, L.D. (1999). Electron Microscopy: Principles and Techniques for Biologists, 2nd ed. Sudbury, MA: Jones and Bartlett Publishers.Google Scholar
Cano, R.J. & Borucki, M.K. (1995). Revival and identification of bacterial spores in 25- to 40-million-year-old Dominican amber. Science 268(5213), 10601064.CrossRefGoogle ScholarPubMed
Dauphin, L.A., Newton, B.R., Rasmussen, M.V., Meyer, R.F. & Bowen, M.D. (2008). Gamma irradiation can be used to inactivate Bacillus anthracis spores without compromising the sensitivity of diagnostic assays. Appl Environ Microbiol 74(14), 44274433.CrossRefGoogle ScholarPubMed
Duncan, C.L. & Strong, D.H. (1968). Improved medium for sporulation of Clostridium perfringens . Appl Microbiol 16, 8289.Google Scholar
Dykstra, M.J. (2010). Why 4F:1G fixative works for me. Microsc Today 18, 5053.Google Scholar
Friedlander, A.M. (2000). Anthrax: Clinical features, pathogenesis, and potential biological warfare threat. Curr Clin Top Infect Dis 20, 335349.Google Scholar
Gerhardt, P. & Black, S.H. (1961). Permeability of bacterial spores. J Bacteriol 82, 750760.Google Scholar
Gerhardt, P., Scherrer, R. & Black, S.H. (1972). Molecular sieving by dormant spore structures. In Spores V, Halvorson, H.O., Hanson, R. & Campbell, L.L. (Eds.), pp. 6874. Washington, DC: American Society for Microbiology.Google Scholar
Hazelton, P.R. & Gelderblom, H.R. (2003). Electron microscopy for rapid diagnosis of infectious agents in emergent situations. Emerging Infect Dis 9(3), 294303.Google Scholar
Horne, T., Turner, G.C. & Willis, A.T. (1959). Inactivation of spores of Bacillus anthracis by γ-radiation. Nature 4659, 475476.Google Scholar
Inglesby, T.V., Henderson, D.A., Bartlett, J.G., Ascher, M.S., Eitzen, E., Friedlander, A.M., Hauer, J., McDade, J., Osterholm, M.T., O'Toole, T., Parker, G., Perl, T.M., Russell, P.K. & Tonat, K. (1999). Anthrax as a biological weapon: Medical and public health management. J Am Med Assoc 281(18), 17351745.Google Scholar
Kailas, L., Terry, C., Abbott, N., Taylor, R., Mullin, N., Tzokov, S.B., Todd, S.J., Wallace, B.A., Hobbs, J.K., Moir, A. & Bullough, P.A. (2011). Surface architecture of endospores of the Bacillus cereus/anthracis/thuringiensis family at the subnanometer scale. Proc Natl Acad Sci USA 108(38), 1601416019.Google Scholar
Khadre, M.A. & Yousef, A.E. (2001). Sporicidal action of ozone and hydrogen peroxide: A comparative study. Int J Food Microbiol 71, 131138.Google Scholar
Koch, C., Jensen, S.S., Oster, A. & Houen, G. (1996). A comparison of the immunogenicity of the native and denatured forms of a protein. Acta Pathol, Microbiol Im Scand 104, 115125.Google Scholar
Madeley, C.R. & Biel, S.S. (2006). For debate: Is disinfection of specimens, which may contain unknown or bio-terrorist organisms, essential before electron microscopic examination? J Infect 53, 7074.Google Scholar
McDonnell, G. & Russell, A.D. (1999). Antiseptics and disinfectants: Activity, action, and resistance. Clin Microbiol Rev 12(1), 147179.CrossRefGoogle ScholarPubMed
Mock, M. & Fouet, A. (2001). Anthrax. Annu Rev Microbiol 55, 647671.Google Scholar
Nicholson, W.L., Munakata, N., Horneck, G., Melosh, H.J. & Setlow, P. (2000). Resistance of Bacillus endospores to extreme terrestrial and extraterrestrial environments. Microbiol Mol Biol Rev 64(3), 548572.Google Scholar
Reynolds, E.S. (1963). The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol 17, 208212.Google Scholar
Rikimaru, T., Kondo, M., Kajimura, K., Hashimoto, K., Oyamada, K., Miyazaki, S., Sagawa, K., Aizawa, H. & Oizumi, K. (2002). Efficacy of common antiseptics against multidrug-resistant Mycobacterium tuberculosis . Int J Tuberc Lung Dis 6(9), 763770.Google Scholar
Rotz, L.D., Khan, A.S., Lillibridge, S.R., Ostroff, S.M. & Hughes, J.M. (2002). Public health assessment of potential biological terrorism agents. Emerging Infect Dis 8(2), 225230.Google Scholar
Russell, A.D. (1994). Glutaraldehyde: Current status and uses. Infect Control Hosp Epidemiol 15, 724733.Google Scholar
Rutala, W.A., Weber, D.J. & Healthcare Infection Control Practices Advisory Committee (HICPAC) (2008). Guideline for Disinfection and Sterilization in Healthcare Facilities, 2008. CDC Bulletin, pp. 42–47. Available at http://www.cdc.gov/hicpac/Disinfection_Sterilization/acknowledg.html.Google Scholar
Sagripanti, J.L. (1992). Metal-based formulations with high microbicidal activity. Appl Environ Microbiol 58(9), 31573162.Google Scholar
Schwebach, J.R., Jacobs, W.R. Jr. & Casadevall, A. (2001). Sterilization of Mycobacterium tuberculosis Erdman samples by antimicrobial fixation in a biosafety level 3 laboratory. J Clin Microbiol 39(2), 769771.Google Scholar
Setlow, P. (2006). Spores of Bacillus subtilis: Their resistance to and killing by radiation, heat, and chemicals. J Appl Microbiol 101, 514525.Google Scholar
Talaro, K.P. (2009). Foundations in Microbiology, 7th ed. New York: McGraw-Hill Publishers.Google Scholar