Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn model
<p>Abstract</p> <p>Background</p> <p><it>Pseudomonas aeruginosa </it>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.<...
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doaj-83504033f7d244b8aabb7b96964ee9432020-11-24T21:19:07ZengBMCBMC Microbiology1471-21802009-02-01912310.1186/1471-2180-9-23Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn modelNaghmachi MohsenAmini MasoudJaponi AzizMehrabani DavoodKohanteb JamshidManafi AliZaghi Ahmad HosseinzadehKhalili Nazanin<p>Abstract</p> <p>Background</p> <p><it>Pseudomonas aeruginosa </it>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.</p> <p>Methods</p> <p>The toxoid was prepared from exotoxin A taken from toxigenic strains of <it>P. aeruginosa </it>(PA 103). 50 mice were immunized with the toxoid, burned with hot metal and infected with 1 × 10<sup>8 </sup>CFU of toxigenic strains of <it>P. aeruginosa </it>(experimental group); 25 non-immunized mice were also burned and infected (control group). The mortality rate and presence of any exotoxin and <it>P. aeruginosa </it>in the sera, liver and spleen were determined.</p> <p>Results</p> <p>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 <it>P. aeruginosa </it>and followed for 70 days. 3 of these mice died. Neither <it>P. aeruginosa </it>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 <it>P. aeruginosa </it>and exotoxin A were isolated from sera, spleen and liver.</p> <p>Conclusion</p> <p>Active immunization of mice using a semi-purified exotoxin A derived from <it>P. aeruginosa </it>was 93.8% effective at protecting mice from subsequent <it>P. aeruginosa </it>infections in a mouse burn model.</p> http://www.biomedcentral.com/1471-2180/9/23 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Naghmachi Mohsen Amini Masoud Japoni Aziz Mehrabani Davood Kohanteb Jamshid Manafi Ali Zaghi Ahmad Hosseinzadeh Khalili Nazanin |
spellingShingle |
Naghmachi Mohsen Amini Masoud Japoni Aziz Mehrabani Davood Kohanteb Jamshid Manafi Ali Zaghi Ahmad Hosseinzadeh Khalili Nazanin Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn model BMC Microbiology |
author_facet |
Naghmachi Mohsen Amini Masoud Japoni Aziz Mehrabani Davood Kohanteb Jamshid Manafi Ali Zaghi Ahmad Hosseinzadeh Khalili Nazanin |
author_sort |
Naghmachi Mohsen |
title |
Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn model |
title_short |
Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn model |
title_full |
Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn model |
title_fullStr |
Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn model |
title_full_unstemmed |
Active immunization using exotoxin A confers protection against <it>Pseudomonas aeruginosa </it>infection in a mouse burn model |
title_sort |
active immunization using exotoxin a confers protection against <it>pseudomonas aeruginosa </it>infection in a mouse burn model |
publisher |
BMC |
series |
BMC Microbiology |
issn |
1471-2180 |
publishDate |
2009-02-01 |
description |
<p>Abstract</p> <p>Background</p> <p><it>Pseudomonas aeruginosa </it>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.</p> <p>Methods</p> <p>The toxoid was prepared from exotoxin A taken from toxigenic strains of <it>P. aeruginosa </it>(PA 103). 50 mice were immunized with the toxoid, burned with hot metal and infected with 1 × 10<sup>8 </sup>CFU of toxigenic strains of <it>P. aeruginosa </it>(experimental group); 25 non-immunized mice were also burned and infected (control group). The mortality rate and presence of any exotoxin and <it>P. aeruginosa </it>in the sera, liver and spleen were determined.</p> <p>Results</p> <p>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 <it>P. aeruginosa </it>and followed for 70 days. 3 of these mice died. Neither <it>P. aeruginosa </it>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 <it>P. aeruginosa </it>and exotoxin A were isolated from sera, spleen and liver.</p> <p>Conclusion</p> <p>Active immunization of mice using a semi-purified exotoxin A derived from <it>P. aeruginosa </it>was 93.8% effective at protecting mice from subsequent <it>P. aeruginosa </it>infections in a mouse burn model.</p> |
url |
http://www.biomedcentral.com/1471-2180/9/23 |
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