YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].

Plague, initiated by Yersinia pestis infection, is a rapidly progressing disease with a high mortality rate if not quickly treated. The existence of antibiotic-resistant Y. pestis strains emphasizes the need for the development of novel countermeasures against plague. We previously reported the gene...

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Main Authors: Ayelet Zauberman, Yehuda Flashner, Yinon Levy, Yaron Vagima, Avital Tidhar, Ofer Cohen, Erez Bar-Haim, David Gur, Moshe Aftalion, Gideon Halperin, Avigdor Shafferman, Emanuelle Mamroud
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3865221?pdf=render
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author Ayelet Zauberman
Yehuda Flashner
Yinon Levy
Yaron Vagima
Avital Tidhar
Ofer Cohen
Erez Bar-Haim
David Gur
Moshe Aftalion
Gideon Halperin
Avigdor Shafferman
Emanuelle Mamroud
author_facet Ayelet Zauberman
Yehuda Flashner
Yinon Levy
Yaron Vagima
Avital Tidhar
Ofer Cohen
Erez Bar-Haim
David Gur
Moshe Aftalion
Gideon Halperin
Avigdor Shafferman
Emanuelle Mamroud
author_sort Ayelet Zauberman
collection DOAJ
description Plague, initiated by Yersinia pestis infection, is a rapidly progressing disease with a high mortality rate if not quickly treated. The existence of antibiotic-resistant Y. pestis strains emphasizes the need for the development of novel countermeasures against plague. We previously reported the generation of a recombinant Y. pestis strain (Kim53ΔJ+P) that over-expresses Y. enterocolitica YopP. When this strain was administered subcutaneously to mice, it elicited a fast and effective protective immune response in models of bubonic, pneumonic and septicemic plague. In the present study, we further characterized the immune response induced by the Kim53ΔJ+P recombinant strain. Using a panel of mouse strains defective in specific immune functions, we observed the induction of a prompt protective innate immune response that was interferon-γ dependent. Moreover, inoculation of mice with Y. pestis Kim53ΔJ+P elicited a rapid protective response against secondary infection by other bacterial pathogens, including the enteropathogen Y. enterocolitica and the respiratory pathogen Francisella tularensis. Thus, the development of new therapies to enhance the innate immune response may provide an initial critical delay in disease progression following the exposure to highly virulent bacterial pathogens, extending the time window for successful treatment.
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spelling doaj.art-61b2332f79954324bc5c8bbf9fa915532022-12-21T18:41:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8356010.1371/journal.pone.0083560YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].Ayelet ZaubermanYehuda FlashnerYinon LevyYaron VagimaAvital TidharOfer CohenErez Bar-HaimDavid GurMoshe AftalionGideon HalperinAvigdor ShaffermanEmanuelle MamroudPlague, initiated by Yersinia pestis infection, is a rapidly progressing disease with a high mortality rate if not quickly treated. The existence of antibiotic-resistant Y. pestis strains emphasizes the need for the development of novel countermeasures against plague. We previously reported the generation of a recombinant Y. pestis strain (Kim53ΔJ+P) that over-expresses Y. enterocolitica YopP. When this strain was administered subcutaneously to mice, it elicited a fast and effective protective immune response in models of bubonic, pneumonic and septicemic plague. In the present study, we further characterized the immune response induced by the Kim53ΔJ+P recombinant strain. Using a panel of mouse strains defective in specific immune functions, we observed the induction of a prompt protective innate immune response that was interferon-γ dependent. Moreover, inoculation of mice with Y. pestis Kim53ΔJ+P elicited a rapid protective response against secondary infection by other bacterial pathogens, including the enteropathogen Y. enterocolitica and the respiratory pathogen Francisella tularensis. Thus, the development of new therapies to enhance the innate immune response may provide an initial critical delay in disease progression following the exposure to highly virulent bacterial pathogens, extending the time window for successful treatment.http://europepmc.org/articles/PMC3865221?pdf=render
spellingShingle Ayelet Zauberman
Yehuda Flashner
Yinon Levy
Yaron Vagima
Avital Tidhar
Ofer Cohen
Erez Bar-Haim
David Gur
Moshe Aftalion
Gideon Halperin
Avigdor Shafferman
Emanuelle Mamroud
YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].
PLoS ONE
title YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].
title_full YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].
title_fullStr YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].
title_full_unstemmed YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].
title_short YopP-expressing variant of Y. pestis activates a potent innate immune response affording cross-protection against yersiniosis and tularemia [corrected].
title_sort yopp expressing variant of y pestis activates a potent innate immune response affording cross protection against yersiniosis and tularemia corrected
url http://europepmc.org/articles/PMC3865221?pdf=render
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