A Standard Method To Inactivate Bacillus anthracis Spores to Sterility via Gamma Irradiation

Author:

Cote Christopher K.1,Buhr Tony2,Bernhards Casey B.34,Bohmke Matthew D.2,Calm Alena M.3,Esteban-Trexler Josephine S.1,Hunter Melissa1,Katoski Sarah E.3,Kennihan Neil2,Klimko Christopher P.1,Miller Jeremy A.1,Minter Zachary A.2,Pfarr Jerry W.3,Prugh Amber M.3,Quirk Avery V.1,Rivers Bryan A.3,Shea April A.1,Shoe Jennifer L.1,Sickler Todd M.3,Young Alice A.2,Fetterer David P.5,Welkos Susan L.1,Bozue Joel A.1ORCID,McPherson Derrell2,Fountain Augustus W.3,Gibbons Henry S.3

Affiliation:

1. Bacteriology Division, United States Army Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA

2. Naval Surface Warfare Center, Dahlgren Division, Dahlgren, Virginia, USA

3. United States Army Edgewood Chemical Biological Center, Aberdeen Proving Ground, Maryland, USA

4. Defense Threat Reduction Agency/National Research Council Research Associate Program, Aberdeen Proving Ground, Maryland, USA

5. Biostatistics Division, United States Army Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA

Abstract

ABSTRACT 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.

Funder

Office of the Deputy Assistant Secretary of Defense for Chemical and Biological Defense

DOD | Defense Threat Reduction Agency

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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