Cargando…

Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung

A major virulence factor of Bacillus anthracis is the anthrax Lethal Toxin (LeTx), a bipartite toxin composed of Protective Antigen and Lethal Factor. Systemic administration of LeTx to laboratory animals leads to death associated with vascular leakage and pulmonary edema. In this study, we investig...

Descripción completa

Detalles Bibliográficos
Autores principales: Dumas, Eric K., Cox, Philip M., Fullenwider, Charles O’Connor, Nguyen, Melissa, Centola, Michael, Frank, Mark Barton, Dozmorov, Igor, James, Judith A., Farris, A. Darise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202878/
https://www.ncbi.nlm.nih.gov/pubmed/22039574
http://dx.doi.org/10.3390/toxins3091111
_version_ 1782215052817858560
author Dumas, Eric K.
Cox, Philip M.
Fullenwider, Charles O’Connor
Nguyen, Melissa
Centola, Michael
Frank, Mark Barton
Dozmorov, Igor
James, Judith A.
Farris, A. Darise
author_facet Dumas, Eric K.
Cox, Philip M.
Fullenwider, Charles O’Connor
Nguyen, Melissa
Centola, Michael
Frank, Mark Barton
Dozmorov, Igor
James, Judith A.
Farris, A. Darise
author_sort Dumas, Eric K.
collection PubMed
description A major virulence factor of Bacillus anthracis is the anthrax Lethal Toxin (LeTx), a bipartite toxin composed of Protective Antigen and Lethal Factor. Systemic administration of LeTx to laboratory animals leads to death associated with vascular leakage and pulmonary edema. In this study, we investigated whether systemic exposure of mice to LeTx would induce gene expression changes associated with vascular/capillary leakage in lung tissue. We observed enhanced susceptibility of A/J mice to death by systemic LeTx administration compared to the C57BL/6 strain. LeTx-induced groups of both up- and down-regulated genes were observed in mouse lungs 6 h after systemic administration of wild type toxin compared to lungs of mice exposed to an inactive mutant form of the toxin. Lungs of the less susceptible C57BL/6 strain showed 80% fewer differentially expressed genes compared to lungs of the more sensitive A/J strain. Expression of genes known to regulate vascular permeability was modulated by LeTx in the lungs of the more susceptible A/J strain. Unexpectedly, the largest set of genes with altered expression was immune specific, characterized by the up-regulation of lymphoid genes and the down-regulation of myeloid genes. Transcripts encoding neutrophil chemoattractants, modulators of tumor regulation and angiogenesis were also differentially expressed in both mouse strains. These studies provide new directions for the investigation of vascular leakage and pulmonary edema induced by anthrax LeTx.
format Online
Article
Text
id pubmed-3202878
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-32028782011-10-27 Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung Dumas, Eric K. Cox, Philip M. Fullenwider, Charles O’Connor Nguyen, Melissa Centola, Michael Frank, Mark Barton Dozmorov, Igor James, Judith A. Farris, A. Darise Toxins (Basel) Article A major virulence factor of Bacillus anthracis is the anthrax Lethal Toxin (LeTx), a bipartite toxin composed of Protective Antigen and Lethal Factor. Systemic administration of LeTx to laboratory animals leads to death associated with vascular leakage and pulmonary edema. In this study, we investigated whether systemic exposure of mice to LeTx would induce gene expression changes associated with vascular/capillary leakage in lung tissue. We observed enhanced susceptibility of A/J mice to death by systemic LeTx administration compared to the C57BL/6 strain. LeTx-induced groups of both up- and down-regulated genes were observed in mouse lungs 6 h after systemic administration of wild type toxin compared to lungs of mice exposed to an inactive mutant form of the toxin. Lungs of the less susceptible C57BL/6 strain showed 80% fewer differentially expressed genes compared to lungs of the more sensitive A/J strain. Expression of genes known to regulate vascular permeability was modulated by LeTx in the lungs of the more susceptible A/J strain. Unexpectedly, the largest set of genes with altered expression was immune specific, characterized by the up-regulation of lymphoid genes and the down-regulation of myeloid genes. Transcripts encoding neutrophil chemoattractants, modulators of tumor regulation and angiogenesis were also differentially expressed in both mouse strains. These studies provide new directions for the investigation of vascular leakage and pulmonary edema induced by anthrax LeTx. MDPI 2011-09-07 /pmc/articles/PMC3202878/ /pubmed/22039574 http://dx.doi.org/10.3390/toxins3091111 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Dumas, Eric K.
Cox, Philip M.
Fullenwider, Charles O’Connor
Nguyen, Melissa
Centola, Michael
Frank, Mark Barton
Dozmorov, Igor
James, Judith A.
Farris, A. Darise
Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
title Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
title_full Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
title_fullStr Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
title_full_unstemmed Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
title_short Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
title_sort anthrax lethal toxin-induced gene expression changes in mouse lung
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202878/
https://www.ncbi.nlm.nih.gov/pubmed/22039574
http://dx.doi.org/10.3390/toxins3091111
work_keys_str_mv AT dumaserick anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT coxphilipm anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT fullenwidercharlesoconnor anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT nguyenmelissa anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT centolamichael anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT frankmarkbarton anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT dozmorovigor anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT jamesjuditha anthraxlethaltoxininducedgeneexpressionchangesinmouselung
AT farrisadarise anthraxlethaltoxininducedgeneexpressionchangesinmouselung