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Activity of the Bacillus anthracis 20 kDa protective antigen component
BACKGROUND: Anthrax is caused by Bacillus anthracis that produce two exotoxins, lethal toxin and edema toxin. The lethal toxin is composed of the lethal factor (LF) complexed with the cell binding protective antigen (PA(83), 83 kDa). Likewise, the edema factor (EF) binds to the PA(83 )to form the ed...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2564935/ https://www.ncbi.nlm.nih.gov/pubmed/18808698 http://dx.doi.org/10.1186/1471-2334-8-124 |
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author | Hammamieh, Rasha Ribot, Wilson J Abshire, Terry G Jett, Marti Ezzell, John |
author_facet | Hammamieh, Rasha Ribot, Wilson J Abshire, Terry G Jett, Marti Ezzell, John |
author_sort | Hammamieh, Rasha |
collection | PubMed |
description | BACKGROUND: Anthrax is caused by Bacillus anthracis that produce two exotoxins, lethal toxin and edema toxin. The lethal toxin is composed of the lethal factor (LF) complexed with the cell binding protective antigen (PA(83), 83 kDa). Likewise, the edema factor (EF) binds to the PA(83 )to form the edema toxin. Once PA83 is bound to the host cell surface, a furin-like protease cleaves the full-length, inactive protein into 63 kDa and 20 kDa antigens (PA(63 )and PA(20)). PA(63 )forms a heptamer and is internalized via receptor mediated endocytosis forming a protease-stable pore, which allows EF and LF to enter the cell and exert their toxic effects. Both proteolytically cleaved protective antigens (PA(63 )and PA(20 )fragments) are found in the blood of infected animals. The 63 kDa protective antigen PA(63 )fragment has been thoroughly studied while little is known about the PA(20). METHODS: In this study we examined the role of PA(20 )using high throughput gene expression analysis of human peripheral blood mononuclear cells (PBMC) exposed to the PA(20). We constructed a PA mutant in which a Factor Xa proteolytic recognition site was genetically engineered into the protective antigen PA(83 )to obtain PA(20 )using limited digestion of this recombinant PA(83 )with trypsin. RESULTS: Global gene expression response studies indicated modulation of various immune functions and showed gene patterns indicative of apoptosis via the Fas pathway in a subset of the lymphoid cells. This finding was extended to include observations of increased Caspase-3 enzymatic activity and the identification of increases in the population of apoptotic, but not necrotic cells, based on differential staining methods. We identified a list of ~40 inflammatory mediators and heat-shock proteins that were altered similarly upon exposure of PBMC to either rPA(20 )or B. anthracis spores/vegetative cells. CONCLUSION: This study shows that the PA(20 )has an effect on human peripheral blood leukocytes and can induce apoptosis in the absence of other PA components. |
format | Text |
id | pubmed-2564935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25649352008-10-09 Activity of the Bacillus anthracis 20 kDa protective antigen component Hammamieh, Rasha Ribot, Wilson J Abshire, Terry G Jett, Marti Ezzell, John BMC Infect Dis Research Article BACKGROUND: Anthrax is caused by Bacillus anthracis that produce two exotoxins, lethal toxin and edema toxin. The lethal toxin is composed of the lethal factor (LF) complexed with the cell binding protective antigen (PA(83), 83 kDa). Likewise, the edema factor (EF) binds to the PA(83 )to form the edema toxin. Once PA83 is bound to the host cell surface, a furin-like protease cleaves the full-length, inactive protein into 63 kDa and 20 kDa antigens (PA(63 )and PA(20)). PA(63 )forms a heptamer and is internalized via receptor mediated endocytosis forming a protease-stable pore, which allows EF and LF to enter the cell and exert their toxic effects. Both proteolytically cleaved protective antigens (PA(63 )and PA(20 )fragments) are found in the blood of infected animals. The 63 kDa protective antigen PA(63 )fragment has been thoroughly studied while little is known about the PA(20). METHODS: In this study we examined the role of PA(20 )using high throughput gene expression analysis of human peripheral blood mononuclear cells (PBMC) exposed to the PA(20). We constructed a PA mutant in which a Factor Xa proteolytic recognition site was genetically engineered into the protective antigen PA(83 )to obtain PA(20 )using limited digestion of this recombinant PA(83 )with trypsin. RESULTS: Global gene expression response studies indicated modulation of various immune functions and showed gene patterns indicative of apoptosis via the Fas pathway in a subset of the lymphoid cells. This finding was extended to include observations of increased Caspase-3 enzymatic activity and the identification of increases in the population of apoptotic, but not necrotic cells, based on differential staining methods. We identified a list of ~40 inflammatory mediators and heat-shock proteins that were altered similarly upon exposure of PBMC to either rPA(20 )or B. anthracis spores/vegetative cells. CONCLUSION: This study shows that the PA(20 )has an effect on human peripheral blood leukocytes and can induce apoptosis in the absence of other PA components. BioMed Central 2008-09-22 /pmc/articles/PMC2564935/ /pubmed/18808698 http://dx.doi.org/10.1186/1471-2334-8-124 Text en Copyright © 2008 Hammamieh 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 Hammamieh, Rasha Ribot, Wilson J Abshire, Terry G Jett, Marti Ezzell, John Activity of the Bacillus anthracis 20 kDa protective antigen component |
title | Activity of the Bacillus anthracis 20 kDa protective antigen component |
title_full | Activity of the Bacillus anthracis 20 kDa protective antigen component |
title_fullStr | Activity of the Bacillus anthracis 20 kDa protective antigen component |
title_full_unstemmed | Activity of the Bacillus anthracis 20 kDa protective antigen component |
title_short | Activity of the Bacillus anthracis 20 kDa protective antigen component |
title_sort | activity of the bacillus anthracis 20 kda protective antigen component |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2564935/ https://www.ncbi.nlm.nih.gov/pubmed/18808698 http://dx.doi.org/10.1186/1471-2334-8-124 |
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