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Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice

Yersinia Pestis outer proteins, plasminogen activator protease and Yop secretion protein F are necessary for the full virulence of Yesinia pestis and have been proposed as potential protective antigens for vaccines against plague. In the current study, we used DNA immunization as a tool to study the...

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Autores principales: Wang, Shixia, Joshi, Swati, Mboudjeka, Innocent, Liu, Fangjun, Ling, Tzufan, Goguen, Jon D., Lu, Shan
Formato: Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2288748/
https://www.ncbi.nlm.nih.gov/pubmed/18291562
http://dx.doi.org/10.1016/j.vaccine.2008.01.024
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author Wang, Shixia
Joshi, Swati
Mboudjeka, Innocent
Liu, Fangjun
Ling, Tzufan
Goguen, Jon D.
Lu, Shan
author_facet Wang, Shixia
Joshi, Swati
Mboudjeka, Innocent
Liu, Fangjun
Ling, Tzufan
Goguen, Jon D.
Lu, Shan
author_sort Wang, Shixia
collection PubMed
description Yersinia Pestis outer proteins, plasminogen activator protease and Yop secretion protein F are necessary for the full virulence of Yesinia pestis and have been proposed as potential protective antigens for vaccines against plague. In the current study, we used DNA immunization as a tool to study the relative protective immunity of these proteins with a standardized intranasal challenge system in mice. While the natural full-length gene sequences for most of these Y. pestis proteins did not display a good level of protein expression in vitro when delivered by a DNA vaccine vector, the overall immunogenicity of these wild type gene DNA vaccines was low in eliciting antigen-specific antibody responses and gene sequence modifications improved both of these parameters. However, even modified YopD, YopO and YscF antigens were only able to partially protect immunized mice at various levels against lethal challenge with Y. pestis KIM 1001 strain while no protection was observed with either the YopB or Pla antigens. These results demonstrate that DNA immunization is effective in screening, optimizing and comparing optimal antigen designs and immunogenicity of candidate antigens for the development of a subunit-based plague vaccine.
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spelling pubmed-22887482009-03-20 Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice Wang, Shixia Joshi, Swati Mboudjeka, Innocent Liu, Fangjun Ling, Tzufan Goguen, Jon D. Lu, Shan Vaccine Article Yersinia Pestis outer proteins, plasminogen activator protease and Yop secretion protein F are necessary for the full virulence of Yesinia pestis and have been proposed as potential protective antigens for vaccines against plague. In the current study, we used DNA immunization as a tool to study the relative protective immunity of these proteins with a standardized intranasal challenge system in mice. While the natural full-length gene sequences for most of these Y. pestis proteins did not display a good level of protein expression in vitro when delivered by a DNA vaccine vector, the overall immunogenicity of these wild type gene DNA vaccines was low in eliciting antigen-specific antibody responses and gene sequence modifications improved both of these parameters. However, even modified YopD, YopO and YscF antigens were only able to partially protect immunized mice at various levels against lethal challenge with Y. pestis KIM 1001 strain while no protection was observed with either the YopB or Pla antigens. These results demonstrate that DNA immunization is effective in screening, optimizing and comparing optimal antigen designs and immunogenicity of candidate antigens for the development of a subunit-based plague vaccine. Elsevier Ltd. 2008-03-20 2008-02-04 /pmc/articles/PMC2288748/ /pubmed/18291562 http://dx.doi.org/10.1016/j.vaccine.2008.01.024 Text en Copyright © 2008 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wang, Shixia
Joshi, Swati
Mboudjeka, Innocent
Liu, Fangjun
Ling, Tzufan
Goguen, Jon D.
Lu, Shan
Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice
title Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice
title_full Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice
title_fullStr Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice
title_full_unstemmed Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice
title_short Relative immunogenicity and protection potential of candidate Yersinia Pestis antigens against lethal mucosal plague challenge in Balb/C mice
title_sort relative immunogenicity and protection potential of candidate yersinia pestis antigens against lethal mucosal plague challenge in balb/c mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2288748/
https://www.ncbi.nlm.nih.gov/pubmed/18291562
http://dx.doi.org/10.1016/j.vaccine.2008.01.024
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