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Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever

Salmonella Typhi and Salmonella Paratyphi A are the leading causative agents of enteric fever which cause morbidity and mortality worldwide. Currently, there is no combination vaccine which could protect infection from both the strains. In this paper, we are focusing on the development of a novel bi...

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Autores principales: Howlader, Debaki R., Koley, Hemanta, Sinha, Ritam, Maiti, Suhrid, Bhaumik, Ushasi, Mukherjee, Priyadarshini, Dutta, Shanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138408/
https://www.ncbi.nlm.nih.gov/pubmed/30216367
http://dx.doi.org/10.1371/journal.pone.0203631
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author Howlader, Debaki R.
Koley, Hemanta
Sinha, Ritam
Maiti, Suhrid
Bhaumik, Ushasi
Mukherjee, Priyadarshini
Dutta, Shanta
author_facet Howlader, Debaki R.
Koley, Hemanta
Sinha, Ritam
Maiti, Suhrid
Bhaumik, Ushasi
Mukherjee, Priyadarshini
Dutta, Shanta
author_sort Howlader, Debaki R.
collection PubMed
description Salmonella Typhi and Salmonella Paratyphi A are the leading causative agents of enteric fever which cause morbidity and mortality worldwide. Currently, there is no combination vaccine which could protect infection from both the strains. In this paper, we are focusing on the development of a novel bivalent typhoidal Outer Membrane Vesicles (OMVs) based immunogen against enteric fever. We have isolated Salmonella Typhi and Paratyphi A OMVs and also characterized OMVs associated antigens. Then we immunized adult mice with three doses of our newly formulated bivalent immunogen orally (25 μg/200 μl). After three doses of oral immunization, we found our immunogen could significantly induce humoral response. We have also found serum IgG against LPS, Vi-polysaccharide etc. OMV immunization induces CD4, CD8 and CD19 population in immunized mice spleen. It also induces Th1 and Th17-cell mediated immunity. We also found bivalent OMVs immunization can prevent more than lethal dose of heterologous Salmonella strains mediated systemic infection in adult mice model. We determined that, the protective immune responses depend on the humoral and cell-mediated immune response. Furthermore, we have evaluated the mode of protective immune response carried out by anti-OMVs antibody by significantly inhibiting bacterial motility and mucin penetration ability. Taken together, these findings suggest that our bivalent immunogen could be used as a novel candidate vaccine against enteric fever.
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spelling pubmed-61384082018-09-27 Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever Howlader, Debaki R. Koley, Hemanta Sinha, Ritam Maiti, Suhrid Bhaumik, Ushasi Mukherjee, Priyadarshini Dutta, Shanta PLoS One Research Article Salmonella Typhi and Salmonella Paratyphi A are the leading causative agents of enteric fever which cause morbidity and mortality worldwide. Currently, there is no combination vaccine which could protect infection from both the strains. In this paper, we are focusing on the development of a novel bivalent typhoidal Outer Membrane Vesicles (OMVs) based immunogen against enteric fever. We have isolated Salmonella Typhi and Paratyphi A OMVs and also characterized OMVs associated antigens. Then we immunized adult mice with three doses of our newly formulated bivalent immunogen orally (25 μg/200 μl). After three doses of oral immunization, we found our immunogen could significantly induce humoral response. We have also found serum IgG against LPS, Vi-polysaccharide etc. OMV immunization induces CD4, CD8 and CD19 population in immunized mice spleen. It also induces Th1 and Th17-cell mediated immunity. We also found bivalent OMVs immunization can prevent more than lethal dose of heterologous Salmonella strains mediated systemic infection in adult mice model. We determined that, the protective immune responses depend on the humoral and cell-mediated immune response. Furthermore, we have evaluated the mode of protective immune response carried out by anti-OMVs antibody by significantly inhibiting bacterial motility and mucin penetration ability. Taken together, these findings suggest that our bivalent immunogen could be used as a novel candidate vaccine against enteric fever. Public Library of Science 2018-09-14 /pmc/articles/PMC6138408/ /pubmed/30216367 http://dx.doi.org/10.1371/journal.pone.0203631 Text en © 2018 Howlader et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Howlader, Debaki R.
Koley, Hemanta
Sinha, Ritam
Maiti, Suhrid
Bhaumik, Ushasi
Mukherjee, Priyadarshini
Dutta, Shanta
Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever
title Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever
title_full Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever
title_fullStr Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever
title_full_unstemmed Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever
title_short Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever
title_sort development of a novel s. typhi and paratyphi a outer membrane vesicles based bivalent vaccine against enteric fever
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138408/
https://www.ncbi.nlm.nih.gov/pubmed/30216367
http://dx.doi.org/10.1371/journal.pone.0203631
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