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Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge

Bacterial ghosts (BGs) have been applied through oral, aerogenic, intraocular or intranasal routes for mucosal immunization using a wide range of experimental animals. All these applications required a booster after primary immunization to achieve protective immunity against the lethal challenge. He...

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Autores principales: Mayr, Ulrike Beate, Kudela, Pavol, Atrasheuskaya, Alena, Bukin, Eugenij, Ignatyev, Georgy, Lubitz, Werner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815788/
https://www.ncbi.nlm.nih.gov/pubmed/22103353
http://dx.doi.org/10.1111/j.1751-7915.2011.00316.x
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author Mayr, Ulrike Beate
Kudela, Pavol
Atrasheuskaya, Alena
Bukin, Eugenij
Ignatyev, Georgy
Lubitz, Werner
author_facet Mayr, Ulrike Beate
Kudela, Pavol
Atrasheuskaya, Alena
Bukin, Eugenij
Ignatyev, Georgy
Lubitz, Werner
author_sort Mayr, Ulrike Beate
collection PubMed
description Bacterial ghosts (BGs) have been applied through oral, aerogenic, intraocular or intranasal routes for mucosal immunization using a wide range of experimental animals. All these applications required a booster after primary immunization to achieve protective immunity against the lethal challenge. Here we report for the first time that a single rectal dose of BGs produced from enterohaemorrhagic Escherichia coli (EHEC) O157:H7 fully protects mice against a 50% lethal challenge with a heterologous EHEC strain given at day 55. BGs from EHEC O157:H7 were prepared by a combination of protein E‐mediated cell lysis and expression of staphylococcal nuclease A guaranteeing the complete degradation of pathogen residual DNA. The lack of genetic material in the EHEC BGs vaccine abolished any potential hazard for horizontal gene transfer of plasmid encoded antibiotic resistance genes or pathogenic islands to the recipient's gut flora. Single rectal immunization using EHEC O157:H7 BGs without any addition of adjuvant significantly stimulated efficient humoral and cellular immune responses, and was equally protective as two immunizations, which indicates the possibility to develop a novel efficacious single dose mucosal EHEC O157:H7 BGs vaccine using a simplified immunization regimen.
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spelling pubmed-38157882014-02-12 Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge Mayr, Ulrike Beate Kudela, Pavol Atrasheuskaya, Alena Bukin, Eugenij Ignatyev, Georgy Lubitz, Werner Microb Biotechnol Research Articles Bacterial ghosts (BGs) have been applied through oral, aerogenic, intraocular or intranasal routes for mucosal immunization using a wide range of experimental animals. All these applications required a booster after primary immunization to achieve protective immunity against the lethal challenge. Here we report for the first time that a single rectal dose of BGs produced from enterohaemorrhagic Escherichia coli (EHEC) O157:H7 fully protects mice against a 50% lethal challenge with a heterologous EHEC strain given at day 55. BGs from EHEC O157:H7 were prepared by a combination of protein E‐mediated cell lysis and expression of staphylococcal nuclease A guaranteeing the complete degradation of pathogen residual DNA. The lack of genetic material in the EHEC BGs vaccine abolished any potential hazard for horizontal gene transfer of plasmid encoded antibiotic resistance genes or pathogenic islands to the recipient's gut flora. Single rectal immunization using EHEC O157:H7 BGs without any addition of adjuvant significantly stimulated efficient humoral and cellular immune responses, and was equally protective as two immunizations, which indicates the possibility to develop a novel efficacious single dose mucosal EHEC O157:H7 BGs vaccine using a simplified immunization regimen. Blackwell Publishing Ltd 2012-03 2012-02-20 /pmc/articles/PMC3815788/ /pubmed/22103353 http://dx.doi.org/10.1111/j.1751-7915.2011.00316.x Text en Copyright © 2011 The Authors. Microbial Biotechnology © 2011 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Research Articles
Mayr, Ulrike Beate
Kudela, Pavol
Atrasheuskaya, Alena
Bukin, Eugenij
Ignatyev, Georgy
Lubitz, Werner
Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge
title Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge
title_full Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge
title_fullStr Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge
title_full_unstemmed Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge
title_short Rectal single dose immunization of mice with Escherichia coli O157:H7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge
title_sort rectal single dose immunization of mice with escherichia coli o157:h7 bacterial ghosts induces efficient humoral and cellular immune responses and protects against the lethal heterologous challenge
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815788/
https://www.ncbi.nlm.nih.gov/pubmed/22103353
http://dx.doi.org/10.1111/j.1751-7915.2011.00316.x
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