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...

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Main Authors: A. Darise Farris, Judith A. James, Igor Dozmorov, Mark Barton Frank, Michael Centola, Melissa Nguyen, Charles O’Connor Fullenwider, Philip M. Cox, Eric K. Dumas
Format: Article
Language:English
Published: MDPI AG 2011-09-01
Series:Toxins
Subjects:
Online Access:http://www.mdpi.com/2072-6651/3/9/1111/
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spelling doaj-7066541facb54d14b02774c38172cd692020-11-25T01:59:30ZengMDPI AGToxins2072-66512011-09-01391111113010.3390/toxins3091111Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse LungA. Darise FarrisJudith A. JamesIgor DozmorovMark Barton FrankMichael CentolaMelissa NguyenCharles O’Connor FullenwiderPhilip M. CoxEric K. DumasA 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.http://www.mdpi.com/2072-6651/3/9/1111/Lethal Toxinlunggene expression
collection DOAJ
language English
format Article
sources DOAJ
author A. Darise Farris
Judith A. James
Igor Dozmorov
Mark Barton Frank
Michael Centola
Melissa Nguyen
Charles O’Connor Fullenwider
Philip M. Cox
Eric K. Dumas
spellingShingle A. Darise Farris
Judith A. James
Igor Dozmorov
Mark Barton Frank
Michael Centola
Melissa Nguyen
Charles O’Connor Fullenwider
Philip M. Cox
Eric K. Dumas
Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
Toxins
Lethal Toxin
lung
gene expression
author_facet A. Darise Farris
Judith A. James
Igor Dozmorov
Mark Barton Frank
Michael Centola
Melissa Nguyen
Charles O’Connor Fullenwider
Philip M. Cox
Eric K. Dumas
author_sort A. Darise Farris
title Anthrax Lethal Toxin-Induced Gene Expression Changes in Mouse Lung
title_short 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_sort anthrax lethal toxin-induced gene expression changes in mouse lung
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2011-09-01
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.
topic Lethal Toxin
lung
gene expression
url http://www.mdpi.com/2072-6651/3/9/1111/
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