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Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model
BACKGROUND: Pseudomonas aeruginosa is an important cause of nosocomial infection and may lead to septicemia and death. We evaluated the immunogenicity of semi-purified exotoxin A from the bacterium in a mouse burn model. METHODS: The toxoid was prepared from exotoxin A taken from toxigenic strains o...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2644702/ https://www.ncbi.nlm.nih.gov/pubmed/19183501 http://dx.doi.org/10.1186/1471-2180-9-23 |
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author | Manafi, Ali Kohanteb, Jamshid Mehrabani, Davood Japoni, Aziz Amini, Masoud Naghmachi, Mohsen Zaghi, Ahmad Hosseinzadeh Khalili, Nazanin |
author_facet | Manafi, Ali Kohanteb, Jamshid Mehrabani, Davood Japoni, Aziz Amini, Masoud Naghmachi, Mohsen Zaghi, Ahmad Hosseinzadeh Khalili, Nazanin |
author_sort | Manafi, Ali |
collection | PubMed |
description | BACKGROUND: Pseudomonas aeruginosa is an important cause of nosocomial infection and may lead to septicemia and death. We evaluated the immunogenicity of semi-purified exotoxin A from the bacterium in a mouse burn model. METHODS: The toxoid was prepared from exotoxin A taken from toxigenic strains of P. aeruginosa (PA 103). 50 mice were immunized with the toxoid, burned with hot metal and infected with 1 × 10(8 )CFU of toxigenic strains of P. aeruginosa (experimental group); 25 non-immunized mice were also burned and infected (control group). The mortality rate and presence of any exotoxin and P. aeruginosa in the sera, liver and spleen were determined. RESULTS: In the experimental group, 2 mice died before the burns were administered and were excluded from the study. The remainder (48 mice) were challenged with a lethal dose of P. aeruginosa and followed for 70 days. 3 of these mice died. Neither P. aeruginosa nor exotoxin A was not detected in the liver, spleen or sera of the surviving mice. The protective efficacy of toxoid vaccination was therefore 93.8%. In the control group, all mice died from bacteremia and septicemia, most (80%) within 6 days, and P. aeruginosa and exotoxin A were isolated from sera, spleen and liver. CONCLUSION: Active immunization of mice using a semi-purified exotoxin A derived from P. aeruginosa was 93.8% effective at protecting mice from subsequent P. aeruginosa infections in a mouse burn model. |
format | Text |
id | pubmed-2644702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26447022009-02-19 Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model Manafi, Ali Kohanteb, Jamshid Mehrabani, Davood Japoni, Aziz Amini, Masoud Naghmachi, Mohsen Zaghi, Ahmad Hosseinzadeh Khalili, Nazanin BMC Microbiol Research article BACKGROUND: Pseudomonas aeruginosa is an important cause of nosocomial infection and may lead to septicemia and death. We evaluated the immunogenicity of semi-purified exotoxin A from the bacterium in a mouse burn model. METHODS: The toxoid was prepared from exotoxin A taken from toxigenic strains of P. aeruginosa (PA 103). 50 mice were immunized with the toxoid, burned with hot metal and infected with 1 × 10(8 )CFU of toxigenic strains of P. aeruginosa (experimental group); 25 non-immunized mice were also burned and infected (control group). The mortality rate and presence of any exotoxin and P. aeruginosa in the sera, liver and spleen were determined. RESULTS: In the experimental group, 2 mice died before the burns were administered and were excluded from the study. The remainder (48 mice) were challenged with a lethal dose of P. aeruginosa and followed for 70 days. 3 of these mice died. Neither P. aeruginosa nor exotoxin A was not detected in the liver, spleen or sera of the surviving mice. The protective efficacy of toxoid vaccination was therefore 93.8%. In the control group, all mice died from bacteremia and septicemia, most (80%) within 6 days, and P. aeruginosa and exotoxin A were isolated from sera, spleen and liver. CONCLUSION: Active immunization of mice using a semi-purified exotoxin A derived from P. aeruginosa was 93.8% effective at protecting mice from subsequent P. aeruginosa infections in a mouse burn model. BioMed Central 2009-02-01 /pmc/articles/PMC2644702/ /pubmed/19183501 http://dx.doi.org/10.1186/1471-2180-9-23 Text en Copyright ©2009 Manafi 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 Manafi, Ali Kohanteb, Jamshid Mehrabani, Davood Japoni, Aziz Amini, Masoud Naghmachi, Mohsen Zaghi, Ahmad Hosseinzadeh Khalili, Nazanin Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model |
title | Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model |
title_full | Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model |
title_fullStr | Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model |
title_full_unstemmed | Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model |
title_short | Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model |
title_sort | active immunization using exotoxin a confers protection against pseudomonas aeruginosa infection in a mouse burn model |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2644702/ https://www.ncbi.nlm.nih.gov/pubmed/19183501 http://dx.doi.org/10.1186/1471-2180-9-23 |
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