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Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains

An immunology-based in vivo screening regime was used to assess the potential pathogenicity of biotechnology-related microbes. Strains of Bacillus cereus (Bc), Bacillus subtilis (Bs), Bacillus thuringiensis (Bt), and Bt commercial products (CPs) were tested. Balb/c mice were endotracheally instilled...

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Detalles Bibliográficos
Autores principales: Tayabali, Azam F., Nguyen, Kathy C., Seligy, Verner L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3471316/
https://www.ncbi.nlm.nih.gov/pubmed/23087536
http://dx.doi.org/10.1080/02772248.2010.526784
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author Tayabali, Azam F.
Nguyen, Kathy C.
Seligy, Verner L.
author_facet Tayabali, Azam F.
Nguyen, Kathy C.
Seligy, Verner L.
author_sort Tayabali, Azam F.
collection PubMed
description An immunology-based in vivo screening regime was used to assess the potential pathogenicity of biotechnology-related microbes. Strains of Bacillus cereus (Bc), Bacillus subtilis (Bs), Bacillus thuringiensis (Bt), and Bt commercial products (CPs) were tested. Balb/c mice were endotracheally instilled with purified spores, diluted CP, or vegetative cells (VC) (live or dead). Exposed mice were evaluated for changes in behavioral and physical symptoms, bacterial clearance, pulmonary granulocytes, and pulmonary and circulatory pyrogenic cytokines (interleukins (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α), as well as acute phase biomarkers (fibrinogen and serum amyloid A). Except for some differences in clearance rates, no marked effects were observed in mice exposed to any spore at 10(6) or 10(7) colony forming units (cfu). In contrast, live Bc or Bt VCs (10(5) or 10(6) cfu) produced shock-like symptoms (lethargy, hunched appearance, ruffled fur, and respiratory distress), and 11–200-fold elevations in pyrogenic cytokines at 2-h post-exposure. In the study, 4-h effects included increased lethargy, ocular discharge, and 1.5–4-fold rise in circulatory acute phase markers, but no indications of recovery. Bs VC did not produce any changes in symptoms or biomarkers. After 2 or 4 h of exposure to dead VC, increases of only plasma IL-1? and TNF-α (4.6- and 12.4-fold, respectively) were observed. These findings demonstrate that purified spores produced no marked effects in mice compared to that of metabolically active bacteria. This early screening regime was successful in distinguishing the pathogenicity of the different Bacillus species, and might be useful for assessing the relative hazard potential of other biotechnology-related candidate strains.
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spelling pubmed-34713162012-10-18 Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains Tayabali, Azam F. Nguyen, Kathy C. Seligy, Verner L. Toxicol Environ Chem Research Article An immunology-based in vivo screening regime was used to assess the potential pathogenicity of biotechnology-related microbes. Strains of Bacillus cereus (Bc), Bacillus subtilis (Bs), Bacillus thuringiensis (Bt), and Bt commercial products (CPs) were tested. Balb/c mice were endotracheally instilled with purified spores, diluted CP, or vegetative cells (VC) (live or dead). Exposed mice were evaluated for changes in behavioral and physical symptoms, bacterial clearance, pulmonary granulocytes, and pulmonary and circulatory pyrogenic cytokines (interleukins (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α), as well as acute phase biomarkers (fibrinogen and serum amyloid A). Except for some differences in clearance rates, no marked effects were observed in mice exposed to any spore at 10(6) or 10(7) colony forming units (cfu). In contrast, live Bc or Bt VCs (10(5) or 10(6) cfu) produced shock-like symptoms (lethargy, hunched appearance, ruffled fur, and respiratory distress), and 11–200-fold elevations in pyrogenic cytokines at 2-h post-exposure. In the study, 4-h effects included increased lethargy, ocular discharge, and 1.5–4-fold rise in circulatory acute phase markers, but no indications of recovery. Bs VC did not produce any changes in symptoms or biomarkers. After 2 or 4 h of exposure to dead VC, increases of only plasma IL-1? and TNF-α (4.6- and 12.4-fold, respectively) were observed. These findings demonstrate that purified spores produced no marked effects in mice compared to that of metabolically active bacteria. This early screening regime was successful in distinguishing the pathogenicity of the different Bacillus species, and might be useful for assessing the relative hazard potential of other biotechnology-related candidate strains. Taylor & Francis 2010-11-10 2011-02 /pmc/articles/PMC3471316/ /pubmed/23087536 http://dx.doi.org/10.1080/02772248.2010.526784 Text en © 2011 Government of Canada http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Taylor & Francis journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tayabali, Azam F.
Nguyen, Kathy C.
Seligy, Verner L.
Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains
title Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains
title_full Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains
title_fullStr Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains
title_full_unstemmed Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains
title_short Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains
title_sort early murine immune responses from endotracheal exposures to biotechnology-related bacillus strains
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3471316/
https://www.ncbi.nlm.nih.gov/pubmed/23087536
http://dx.doi.org/10.1080/02772248.2010.526784
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