Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784867248881532928 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9828334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT gaziehsan doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination AT baylissmarc doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination AT osullivanchristine doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination AT butlerellisclare doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination AT francebrian doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination AT clappertonrichardm doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination AT paynedean doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination AT govannorman doseresponseanalysisofbacillusthuringiensishd1crysporereductiononsurfacesusingformaldehydewithpregermination |