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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...

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Autores principales: Manafi, Ali, Kohanteb, Jamshid, Mehrabani, Davood, Japoni, Aziz, Amini, Masoud, Naghmachi, Mohsen, Zaghi, Ahmad Hosseinzadeh, Khalili, Nazanin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
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.
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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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