A Standard Method To Inactivate Bacillus anthracis Spores to Sterility via Gamma Irradiation
| Autor: | Casey B. Bernhards, Susan L. Welkos, Henry S. Gibbons, T.L. Buhr, Bryan A. Rivers, Avery V. Quirk, Jerry W. Pfarr, Christopher P. Klimko, Augustus W. Fountain, Todd Sickler, Joel A. Bozue, Alena M Calm, Josephine S. Esteban-Trexler, Z.A. Minter, Neil L. Kennihan, Matthew D. Bohmke, A.A. Young, David P. Fetterer, D.C. McPherson, Melissa C. Hunter, Jeremy A. Miller, Christopher K. Cote, April A. Shea, Sarah E. Katoski, Jennifer L. Shoe, Amber Prugh |
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| Rok vydání: | 2018 |
| Předmět: |
Microbiological Techniques
0301 basic medicine Sterility 030106 microbiology Select agent Biology Applied Microbiology and Biotechnology Microbiology 03 medical and health sciences Methods Sterility assurance level Retrospective Studies Spores Bacterial Colony-forming unit Microbial Viability Ecology fungi Sterilization Sterilization (microbiology) biology.organism_classification Bacillus anthracis Spore Gamma Rays Food Science Biotechnology Gamma irradiation |
| Zdroj: | Applied and Environmental Microbiology. 84 |
| ISSN: | 1098-5336 0099-2240 |
| DOI: | 10.1128/aem.00106-18 |
| Popis: | In 2015, a laboratory of the United States Department of Defense (DoD) inadvertently shipped preparations of gamma-irradiated spores of Bacillus anthracis that contained live spores. In response, a systematic evidence-based method for preparing, concentrating, irradiating, and verifying the inactivation of spore materials was developed. We demonstrate the consistency of spore preparations across multiple biological replicates and show that two different DoD institutions independently obtained comparable dose-inactivation curves for a monodisperse suspension of B. anthracis spores containing 3 × 10 10 CFU. Spore preparations from three different institutions and three strain backgrounds yielded similar decimal reduction (D 10 ) values and irradiation doses required to ensure sterility (D SAL ) to the point at which the probability of detecting a viable spore is 10 −6 . Furthermore, spores of a genetically tagged strain of B. anthracis strain Sterne were used to show that high densities of dead spores suppress the recovery of viable spores. Together, we present an integrated method for preparing, irradiating, and verifying the inactivation of spores of B. anthracis for use as standard reagents for testing and evaluating detection and diagnostic devices and techniques. IMPORTANCE The inadvertent shipment by a U.S. Department of Defense (DoD) laboratory of live Bacillus anthracis (anthrax) spores to U.S. and international destinations revealed the need to standardize inactivation methods for materials derived from biological select agents and toxins (BSAT) and for the development of evidence-based methods to prevent the recurrence of such an event. Following a retrospective analysis of the procedures previously employed to generate inactivated B. anthracis spores, a study was commissioned by the DoD to provide data required to support the production of inactivated spores for the biodefense community. The results of this work are presented in this publication, which details the method by which spores can be prepared, irradiated, and tested, such that the chance of finding residual living spores in any given preparation is 1/1,000,000. These irradiated spores are used to test equipment and methods for the detection of agents of biological warfare and bioterrorism. |
| Databáze: | OpenAIRE |
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