Cargando…

Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice

BACKGROUND: The aim of the present study was to assess possible health effects of airway exposures to Bacillus thuringiensis (Bt) based biopesticides in mice. Endpoints were lung inflammation evaluated by presence of inflammatory cells in bronchoalveolar lavage fluid (BALF), clearance of bacteria fr...

Descripción completa

Detalles Bibliográficos
Autores principales: Barfod, Kenneth K, Poulsen, Steen S, Hammer, Maria, Larsen, Søren T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940858/
https://www.ncbi.nlm.nih.gov/pubmed/20815884
http://dx.doi.org/10.1186/1471-2180-10-233
_version_ 1782186855176863744
author Barfod, Kenneth K
Poulsen, Steen S
Hammer, Maria
Larsen, Søren T
author_facet Barfod, Kenneth K
Poulsen, Steen S
Hammer, Maria
Larsen, Søren T
author_sort Barfod, Kenneth K
collection PubMed
description BACKGROUND: The aim of the present study was to assess possible health effects of airway exposures to Bacillus thuringiensis (Bt) based biopesticides in mice. Endpoints were lung inflammation evaluated by presence of inflammatory cells in bronchoalveolar lavage fluid (BALF), clearance of bacteria from the lung lumen and histological alterations of the lungs. Hazard identifications of the biopesticides were carried out using intratracheal (i.t.) instillation, followed by an inhalation study. The two commercial biopesticides used were based on the Bt. subspecies kurstaki and israelensis, respectively. Groups of BALB/c mice were i.t instilled with one bolus (3.5 × 10(5 )or 3.4 × 10(6 )colony forming units (CFU) per mouse) of either biopesticide. Control mice were instilled with sterile water. BALFs were collected and the inflammatory cells were counted and differentiated. The BALFs were also subjected to CFU counts. RESULTS: BALF cytology showed an acute inflammatory response dominated by neutrophils 24 hours after instillation of biopesticide. Four days after instillation, the neutrophil number was normalised and inflammation was dominated by lymphocytes and eosinophils, whereas 70 days after instillation, the inflammation was interstitially located with few inflammatory cells present in the lung lumen. Half of the instilled mice had remaining CFU recovered from BALF 70 days after exposure. To gain further knowledge with relevance for risk assessment, mice were exposed to aerosols of biopesticide one hour per day for 2 × 5 days. Each mouse received 1.9 × 10(4 )CFU Bt israelensis or 2.3 × 10(3 )CFU Bt kurstaki per exposure. Seventy days after end of the aerosol exposures, 3 out of 17 mice had interstitial lung inflammation. CFU could be recovered from 1 out of 10 mice 70 days after exposure to aerosolised Bt kurstaki. Plethysmography showed that inhalation of Bt aerosol did not induce airway irritation. CONCLUSIONS: Repeated low dose aerosol exposures to commercial Bt based biopesticides can induce sub-chronic lung inflammation in mice, which may be the first step in the development of chronic lung diseases. Inhalation of Bt aerosols does not induce airway irritation, which could explain why workers may be less inclined to use a filter mask during the application process, and are thereby less protected from exposure to Bt spores.
format Text
id pubmed-2940858
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-29408582010-09-17 Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice Barfod, Kenneth K Poulsen, Steen S Hammer, Maria Larsen, Søren T BMC Microbiol Research Article BACKGROUND: The aim of the present study was to assess possible health effects of airway exposures to Bacillus thuringiensis (Bt) based biopesticides in mice. Endpoints were lung inflammation evaluated by presence of inflammatory cells in bronchoalveolar lavage fluid (BALF), clearance of bacteria from the lung lumen and histological alterations of the lungs. Hazard identifications of the biopesticides were carried out using intratracheal (i.t.) instillation, followed by an inhalation study. The two commercial biopesticides used were based on the Bt. subspecies kurstaki and israelensis, respectively. Groups of BALB/c mice were i.t instilled with one bolus (3.5 × 10(5 )or 3.4 × 10(6 )colony forming units (CFU) per mouse) of either biopesticide. Control mice were instilled with sterile water. BALFs were collected and the inflammatory cells were counted and differentiated. The BALFs were also subjected to CFU counts. RESULTS: BALF cytology showed an acute inflammatory response dominated by neutrophils 24 hours after instillation of biopesticide. Four days after instillation, the neutrophil number was normalised and inflammation was dominated by lymphocytes and eosinophils, whereas 70 days after instillation, the inflammation was interstitially located with few inflammatory cells present in the lung lumen. Half of the instilled mice had remaining CFU recovered from BALF 70 days after exposure. To gain further knowledge with relevance for risk assessment, mice were exposed to aerosols of biopesticide one hour per day for 2 × 5 days. Each mouse received 1.9 × 10(4 )CFU Bt israelensis or 2.3 × 10(3 )CFU Bt kurstaki per exposure. Seventy days after end of the aerosol exposures, 3 out of 17 mice had interstitial lung inflammation. CFU could be recovered from 1 out of 10 mice 70 days after exposure to aerosolised Bt kurstaki. Plethysmography showed that inhalation of Bt aerosol did not induce airway irritation. CONCLUSIONS: Repeated low dose aerosol exposures to commercial Bt based biopesticides can induce sub-chronic lung inflammation in mice, which may be the first step in the development of chronic lung diseases. Inhalation of Bt aerosols does not induce airway irritation, which could explain why workers may be less inclined to use a filter mask during the application process, and are thereby less protected from exposure to Bt spores. BioMed Central 2010-09-03 /pmc/articles/PMC2940858/ /pubmed/20815884 http://dx.doi.org/10.1186/1471-2180-10-233 Text en Copyright ©2010 Barfod et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Barfod, Kenneth K
Poulsen, Steen S
Hammer, Maria
Larsen, Søren T
Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice
title Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice
title_full Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice
title_fullStr Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice
title_full_unstemmed Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice
title_short Sub-chronic lung inflammation after airway exposures to Bacillus thuringiensis biopesticides in mice
title_sort sub-chronic lung inflammation after airway exposures to bacillus thuringiensis biopesticides in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940858/
https://www.ncbi.nlm.nih.gov/pubmed/20815884
http://dx.doi.org/10.1186/1471-2180-10-233
work_keys_str_mv AT barfodkennethk subchroniclunginflammationafterairwayexposurestobacillusthuringiensisbiopesticidesinmice
AT poulsensteens subchroniclunginflammationafterairwayexposurestobacillusthuringiensisbiopesticidesinmice
AT hammermaria subchroniclunginflammationafterairwayexposurestobacillusthuringiensisbiopesticidesinmice
AT larsensørent subchroniclunginflammationafterairwayexposurestobacillusthuringiensisbiopesticidesinmice