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Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain

Anthrax is a lethal disease caused by the gram-positive spore-producing bacterium Bacillus anthracis. Live attenuated vaccines, such as the nonencapsulated Sterne strain, do not meet the safety standards mandated for human use in the Western world and are approved for veterinary purposes only. Here...

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Autores principales: Chitlaru, Theodor, Israeli, Ma’ayan, Bar-Haim, Erez, Elia, Uri, Rotem, Shahar, Ehrlich, Sharon, Cohen, Ofer, Shafferman, Avigdor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702213/
https://www.ncbi.nlm.nih.gov/pubmed/26732659
http://dx.doi.org/10.1038/srep18908
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author Chitlaru, Theodor
Israeli, Ma’ayan
Bar-Haim, Erez
Elia, Uri
Rotem, Shahar
Ehrlich, Sharon
Cohen, Ofer
Shafferman, Avigdor
author_facet Chitlaru, Theodor
Israeli, Ma’ayan
Bar-Haim, Erez
Elia, Uri
Rotem, Shahar
Ehrlich, Sharon
Cohen, Ofer
Shafferman, Avigdor
author_sort Chitlaru, Theodor
collection PubMed
description Anthrax is a lethal disease caused by the gram-positive spore-producing bacterium Bacillus anthracis. Live attenuated vaccines, such as the nonencapsulated Sterne strain, do not meet the safety standards mandated for human use in the Western world and are approved for veterinary purposes only. Here we demonstrate that disrupting the htrA gene, encoding the chaperone/protease HtrA (High Temperature Requirement A), in the virulent Bacillus anthracis Vollum strain results in significant virulence attenuation in guinea pigs, rabbits and mice, underlying the universality of the attenuated phenotype associated with htrA knockout. Accordingly, htrA disruption was implemented for the development of a Sterne-derived safe live vaccine compatible with human use. The novel B. anthracis SterneΔhtrA strain secretes functional anthrax toxins but is 10–10(4)-fold less virulent than the Sterne vaccine strain depending on animal model (mice, guinea pigs, or rabbits). In spite of this attenuation, double or even single immunization with SterneΔhtrA spores elicits immune responses which target toxaemia and bacteremia resulting in protection from subcutaneous or respiratory lethal challenge with a virulent strain in guinea pigs and rabbits. The efficacy of the immune-protective response in guinea pigs was maintained for at least 50 weeks after a single immunization.
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spelling pubmed-47022132016-01-19 Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain Chitlaru, Theodor Israeli, Ma’ayan Bar-Haim, Erez Elia, Uri Rotem, Shahar Ehrlich, Sharon Cohen, Ofer Shafferman, Avigdor Sci Rep Article Anthrax is a lethal disease caused by the gram-positive spore-producing bacterium Bacillus anthracis. Live attenuated vaccines, such as the nonencapsulated Sterne strain, do not meet the safety standards mandated for human use in the Western world and are approved for veterinary purposes only. Here we demonstrate that disrupting the htrA gene, encoding the chaperone/protease HtrA (High Temperature Requirement A), in the virulent Bacillus anthracis Vollum strain results in significant virulence attenuation in guinea pigs, rabbits and mice, underlying the universality of the attenuated phenotype associated with htrA knockout. Accordingly, htrA disruption was implemented for the development of a Sterne-derived safe live vaccine compatible with human use. The novel B. anthracis SterneΔhtrA strain secretes functional anthrax toxins but is 10–10(4)-fold less virulent than the Sterne vaccine strain depending on animal model (mice, guinea pigs, or rabbits). In spite of this attenuation, double or even single immunization with SterneΔhtrA spores elicits immune responses which target toxaemia and bacteremia resulting in protection from subcutaneous or respiratory lethal challenge with a virulent strain in guinea pigs and rabbits. The efficacy of the immune-protective response in guinea pigs was maintained for at least 50 weeks after a single immunization. Nature Publishing Group 2016-01-06 /pmc/articles/PMC4702213/ /pubmed/26732659 http://dx.doi.org/10.1038/srep18908 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chitlaru, Theodor
Israeli, Ma’ayan
Bar-Haim, Erez
Elia, Uri
Rotem, Shahar
Ehrlich, Sharon
Cohen, Ofer
Shafferman, Avigdor
Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain
title Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain
title_full Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain
title_fullStr Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain
title_full_unstemmed Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain
title_short Next-Generation Bacillus anthracis Live Attenuated Spore Vaccine Based on the htrA(-) (High Temperature Requirement A) Sterne Strain
title_sort next-generation bacillus anthracis live attenuated spore vaccine based on the htra(-) (high temperature requirement a) sterne strain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702213/
https://www.ncbi.nlm.nih.gov/pubmed/26732659
http://dx.doi.org/10.1038/srep18908
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