Improvement of Biological Indicators by Uniformly Distributing Bacillus subtilis Spores in Monolayers To Evaluate Enhanced Spore Decontamination Technologies

Author:

Raguse Marina1,Fiebrandt Marcel2,Stapelmann Katharina3,Madela Kazimierz4,Laue Michael4,Lackmann Jan-Wilm23,Thwaite Joanne E.5,Setlow Peter6,Awakowicz Peter2,Moeller Ralf1

Affiliation:

1. German Aerospace Center (DLR e.V.), Institute of Aerospace Medicine, Radiation Biology Department, Space Microbiology Research Group, Cologne, Germany

2. Ruhr University Bochum, Institute of Electrical Engineering and Plasma Technology, Faculty of Electrical Engineering and Information Technology, Bochum, Germany

3. Ruhr University Bochum, Institute of Electrical Engineering and Plasma Technology, Biomedical Applications of Plasma Technology, Bochum, Germany

4. Robert Koch Institute, Advanced Light and Electron Microscopy, Berlin, Germany

5. Defence Science and Technology Laboratory, Chemical, Biological and Radiological Division, Salisbury, United Kingdom

6. University of Connecticut Health Center, Department of Molecular Biology and Biophysics, Farmington, Connecticut, USA

Abstract

ABSTRACT Novel decontamination technologies, including cold low-pressure plasma and blue light (400 nm), are promising alternatives to conventional surface decontamination methods. However, the standardization of the assessment of such sterilization processes remains to be accomplished. Bacterial endospores of the genera Bacillus and Geobacillus are frequently used as biological indicators (BIs) of sterility. Ensuring standardized and reproducible BIs for reliable testing procedures is a significant problem in industrial settings. In this study, an electrically driven spray deposition device was developed, allowing fast, reproducible, and homogeneous preparation of Bacillus subtilis 168 spore monolayers on glass surfaces. A detailed description of the structural design as well as the operating principle of the spraying device is given. The reproducible formation of spore monolayers of up to 5 × 10 7 spores per sample was verified by scanning electron microscopy. Surface inactivation studies revealed that monolayered spores were inactivated by UV-C (254 nm), low-pressure argon plasma (500 W, 10 Pa, 100 standard cubic cm per min), and blue light (400 nm) significantly faster than multilayered spores were. We have thus succeeded in the uniform preparation of reproducible, highly concentrated spore monolayers with the potential to generate BIs for a variety of nonpenetrating surface decontamination techniques.

Funder

Deutsche Forschungsgemeinschaft

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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