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Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination

AIM: To establish a basis for rapid remediation of large areas contaminated with Bacillus anthracis spores. METHODS AND RESULTS: Representative surfaces of wood, steel and cement were coated by nebulization with B. thuringiensis HD‐1 cry‐ (a simulant for B. anthracis) at 5.9 ± 0.2, 6.3 ± 0.2 and 5.8...

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Autores principales: Gazi, Ehsan, Bayliss, Marc, O'Sullivan, Christine, Butler‐Ellis, Clare, France, Brian, Clapperton, Richard M., Payne, Dean, Govan, Norman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828334/
https://www.ncbi.nlm.nih.gov/pubmed/35945896
http://dx.doi.org/10.1111/jam.15767
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author Gazi, Ehsan
Bayliss, Marc
O'Sullivan, Christine
Butler‐Ellis, Clare
France, Brian
Clapperton, Richard M.
Payne, Dean
Govan, Norman
author_facet Gazi, Ehsan
Bayliss, Marc
O'Sullivan, Christine
Butler‐Ellis, Clare
France, Brian
Clapperton, Richard M.
Payne, Dean
Govan, Norman
author_sort Gazi, Ehsan
collection PubMed
description AIM: To establish a basis for rapid remediation of large areas contaminated with Bacillus anthracis spores. METHODS AND RESULTS: Representative surfaces of wood, steel and cement were coated by nebulization with B. thuringiensis HD‐1 cry‐ (a simulant for B. anthracis) at 5.9 ± 0.2, 6.3 ± 0.2 and 5.8 ± 0.2 log10 CFU per cm(2), respectively. These were sprayed with formaldehyde, either with or without pre‐germination. Low volume (equivalent to ≤2500 L ha(−1)) applications of formaldehyde at 30 g l(−1) to steel or cement surfaces resulted in ≥4 or ≤2 log10 CFU per cm(2) reductions respectively, after 2 h exposure. Pre‐germinating spores (500 mmol l(−1) l‐alanine and 25 mmol l(−1) inosine, pH 7) followed by formaldehyde application showed higher levels of spore inactivation than formaldehyde alone with gains of up to 3.4 log10 CFU per cm(2) for a given dose. No loss in B. thuringiensis cry‐ viability was measured after the 2 h germination period, however, a pre‐heat shock log10 reduction was seen for B. anthracis strains: LSU149 (1.7 log10), Vollum and LSU465 (both 0.9 log10), LSU442 (0.2 log10), Sterne (0.8 log10) and Ames (0.6 log10). CONCLUSIONS: A methodology was developed to produce representative spore contamination of surfaces along with a laboratory‐based technique to measure the efficacy of decontamination. Dose–response analysis was used to optimize decontamination. Pre‐germinating spores was found to increase effectiveness of decontamination but requires careful consideration of total volume used (germinant and decontaminant) by surface type. SIGNIFICANCE AND IMPACT OF THE STUDY: To be practically achievable, decontamination of a wide area contaminated with B. anthracis spores must be effective, timely and minimize the amount of materials required. This study uses systematic dose–response methodology to demonstrate that such an approach is feasible.
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spelling pubmed-98283342023-01-10 Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination Gazi, Ehsan Bayliss, Marc O'Sullivan, Christine Butler‐Ellis, Clare France, Brian Clapperton, Richard M. Payne, Dean Govan, Norman J Appl Microbiol Regular Issue AIM: To establish a basis for rapid remediation of large areas contaminated with Bacillus anthracis spores. METHODS AND RESULTS: Representative surfaces of wood, steel and cement were coated by nebulization with B. thuringiensis HD‐1 cry‐ (a simulant for B. anthracis) at 5.9 ± 0.2, 6.3 ± 0.2 and 5.8 ± 0.2 log10 CFU per cm(2), respectively. These were sprayed with formaldehyde, either with or without pre‐germination. Low volume (equivalent to ≤2500 L ha(−1)) applications of formaldehyde at 30 g l(−1) to steel or cement surfaces resulted in ≥4 or ≤2 log10 CFU per cm(2) reductions respectively, after 2 h exposure. Pre‐germinating spores (500 mmol l(−1) l‐alanine and 25 mmol l(−1) inosine, pH 7) followed by formaldehyde application showed higher levels of spore inactivation than formaldehyde alone with gains of up to 3.4 log10 CFU per cm(2) for a given dose. No loss in B. thuringiensis cry‐ viability was measured after the 2 h germination period, however, a pre‐heat shock log10 reduction was seen for B. anthracis strains: LSU149 (1.7 log10), Vollum and LSU465 (both 0.9 log10), LSU442 (0.2 log10), Sterne (0.8 log10) and Ames (0.6 log10). CONCLUSIONS: A methodology was developed to produce representative spore contamination of surfaces along with a laboratory‐based technique to measure the efficacy of decontamination. Dose–response analysis was used to optimize decontamination. Pre‐germinating spores was found to increase effectiveness of decontamination but requires careful consideration of total volume used (germinant and decontaminant) by surface type. SIGNIFICANCE AND IMPACT OF THE STUDY: To be practically achievable, decontamination of a wide area contaminated with B. anthracis spores must be effective, timely and minimize the amount of materials required. This study uses systematic dose–response methodology to demonstrate that such an approach is feasible. John Wiley and Sons Inc. 2022-10-24 2022-12 /pmc/articles/PMC9828334/ /pubmed/35945896 http://dx.doi.org/10.1111/jam.15767 Text en © 2022 Crown copyright and The Authors. Journal of Applied Microbiology published by John Wiley & Sons Ltd on behalf of Society for Applied Microbiology. This article is published with the permission of the Controller of HMSO and the King's Printer for Scotland. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Issue
Gazi, Ehsan
Bayliss, Marc
O'Sullivan, Christine
Butler‐Ellis, Clare
France, Brian
Clapperton, Richard M.
Payne, Dean
Govan, Norman
Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination
title Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination
title_full Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination
title_fullStr Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination
title_full_unstemmed Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination
title_short Dose–response analysis of Bacillus thuringiensis HD‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination
title_sort dose–response analysis of bacillus thuringiensis hd‐1 cry‐ spore reduction on surfaces using formaldehyde with pre‐germination
topic Regular Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828334/
https://www.ncbi.nlm.nih.gov/pubmed/35945896
http://dx.doi.org/10.1111/jam.15767
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