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Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection

Salmonella enterica, a Gram-negative pathogen, has over 2500 serovars that infect a wide range of hosts. In humans, S. enterica causes typhoid or gastroenteritis and is a major public health concern. In this study, SseB (the tip protein of the Salmonella pathogenicity island 2 type III secretion sys...

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Autores principales: Das, Sayan, Howlader, Debaki R., Lu, Ti, Whittier, Sean K., Hu, Gang, Sharma, Simran, Dietz, Zackary K., Ratnakaram, Siva S. K., Varisco, David J., Ernst, Robert K., Picking, William D., Picking, Wendy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347375/
https://www.ncbi.nlm.nih.gov/pubmed/37457702
http://dx.doi.org/10.3389/fimmu.2023.1208848
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author Das, Sayan
Howlader, Debaki R.
Lu, Ti
Whittier, Sean K.
Hu, Gang
Sharma, Simran
Dietz, Zackary K.
Ratnakaram, Siva S. K.
Varisco, David J.
Ernst, Robert K.
Picking, William D.
Picking, Wendy L.
author_facet Das, Sayan
Howlader, Debaki R.
Lu, Ti
Whittier, Sean K.
Hu, Gang
Sharma, Simran
Dietz, Zackary K.
Ratnakaram, Siva S. K.
Varisco, David J.
Ernst, Robert K.
Picking, William D.
Picking, Wendy L.
author_sort Das, Sayan
collection PubMed
description Salmonella enterica, a Gram-negative pathogen, has over 2500 serovars that infect a wide range of hosts. In humans, S. enterica causes typhoid or gastroenteritis and is a major public health concern. In this study, SseB (the tip protein of the Salmonella pathogenicity island 2 type III secretion system) was fused with the LTA1 subunit of labile-toxin from enterotoxigenic E. coli to make the self-adjuvanting antigen L-SseB. Two unique nanoparticle formulations were developed to allow multimeric presentation of L-SseB. Mice were vaccinated with these formulations and protective efficacy determined via challenging the mice with S. enterica serovars. The polysaccharide (chitosan) formulation was found to elicit better protection when compared to the squalene nanoemulsion. When the polysaccharide formulation was used to vaccinate rabbits, protection from S. enterica challenge was elicited. In summary, L-SseB in a particulate polysaccharide formulation appears to be an attractive candidate vaccine capable of broad protection against S. enterica.
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spelling pubmed-103473752023-07-15 Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection Das, Sayan Howlader, Debaki R. Lu, Ti Whittier, Sean K. Hu, Gang Sharma, Simran Dietz, Zackary K. Ratnakaram, Siva S. K. Varisco, David J. Ernst, Robert K. Picking, William D. Picking, Wendy L. Front Immunol Immunology Salmonella enterica, a Gram-negative pathogen, has over 2500 serovars that infect a wide range of hosts. In humans, S. enterica causes typhoid or gastroenteritis and is a major public health concern. In this study, SseB (the tip protein of the Salmonella pathogenicity island 2 type III secretion system) was fused with the LTA1 subunit of labile-toxin from enterotoxigenic E. coli to make the self-adjuvanting antigen L-SseB. Two unique nanoparticle formulations were developed to allow multimeric presentation of L-SseB. Mice were vaccinated with these formulations and protective efficacy determined via challenging the mice with S. enterica serovars. The polysaccharide (chitosan) formulation was found to elicit better protection when compared to the squalene nanoemulsion. When the polysaccharide formulation was used to vaccinate rabbits, protection from S. enterica challenge was elicited. In summary, L-SseB in a particulate polysaccharide formulation appears to be an attractive candidate vaccine capable of broad protection against S. enterica. Frontiers Media S.A. 2023-06-30 /pmc/articles/PMC10347375/ /pubmed/37457702 http://dx.doi.org/10.3389/fimmu.2023.1208848 Text en Copyright © 2023 Das, Howlader, Lu, Whittier, Hu, Sharma, Dietz, Ratnakaram, Varisco, Ernst, Picking and Picking https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Das, Sayan
Howlader, Debaki R.
Lu, Ti
Whittier, Sean K.
Hu, Gang
Sharma, Simran
Dietz, Zackary K.
Ratnakaram, Siva S. K.
Varisco, David J.
Ernst, Robert K.
Picking, William D.
Picking, Wendy L.
Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection
title Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection
title_full Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection
title_fullStr Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection
title_full_unstemmed Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection
title_short Immunogenicity and protective efficacy of nanoparticle formulations of L-SseB against Salmonella infection
title_sort immunogenicity and protective efficacy of nanoparticle formulations of l-sseb against salmonella infection
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347375/
https://www.ncbi.nlm.nih.gov/pubmed/37457702
http://dx.doi.org/10.3389/fimmu.2023.1208848
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