Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.

<h4>Background</h4>Antibiotic-resistant Salmonella enterica serovar Paratyphi A, the agent of paratyphoid A fever, poses an emerging public health dilemma in endemic areas of Asia and among travelers, as there is no licensed vaccine. Integral to our efforts to develop a S. Paratyphi A va...

Full description

Saved in:
Bibliographic Details
Main Authors: Orit Gat, James E Galen, Sharon Tennant, Raphael Simon, William C Blackwelder, David J Silverman, Marcela F Pasetti, Myron M Levine
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-11-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0001373&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850029463451992064
author Orit Gat
James E Galen
Sharon Tennant
Raphael Simon
William C Blackwelder
David J Silverman
Marcela F Pasetti
Myron M Levine
author_facet Orit Gat
James E Galen
Sharon Tennant
Raphael Simon
William C Blackwelder
David J Silverman
Marcela F Pasetti
Myron M Levine
author_sort Orit Gat
collection DOAJ
description <h4>Background</h4>Antibiotic-resistant Salmonella enterica serovar Paratyphi A, the agent of paratyphoid A fever, poses an emerging public health dilemma in endemic areas of Asia and among travelers, as there is no licensed vaccine. Integral to our efforts to develop a S. Paratyphi A vaccine, we addressed the role of flagella as a potential protective antigen by comparing cell-associated flagella with exported flagellin subunits expressed by attenuated strains.<h4>Methodology</h4>S. Paratyphi A strain ATCC 9150 was first deleted for the chromosomal guaBA locus, creating CVD 1901. Further chromosomal deletions in fliD (CVD 1901D) or flgK (CVD 1901K) were then engineered, resulting in the export of unpolymerized FliC, without impairing its overall expression. The virulence of the resulting isogenic strains was examined using a novel mouse LD(50) model to accommodate the human-host restricted S. Paratyphi A. The immunogenicity of the attenuated strains was then tested using a mouse intranasal model, followed by intraperitoneal challenge with wildtype ATCC 9150.<h4>Results</h4>Mucosal (intranasal) immunization of mice with strain CVD 1901 expressing cell-associated flagella conferred superior protection (vaccine efficacy [VE], 90%) against a lethal intraperitoneal challenge, compared with the flagellin monomer-exporting mutants CVD 1901K (30% VE) or CVD 1901D (47% VE). The superior protection induced by CVD 1901 with its cell-attached flagella was associated with an increased IgG2a:IgG1 ratio of FliC-specific antibodies with enhanced opsonophagocytic capacity.<h4>Conclusions</h4>Our results clearly suggest that enhanced anti-FliC antibody-mediated clearance of S. Paratyphi A by phagocytic cells, induced by vaccines expressing cell-associated rather than exported FliC, might be contributing to the vaccine-induced protection from S. Paratyphi A challenge in vivo. We speculate that an excess of IgG1 anti-FliC antibodies induced by the exported FliC may compete with the IgG2a subtype and block binding to specific phagocyte Fc receptors that are critical for clearing an S. Paratyphi A infection.
format Article
id doaj-art-7e29903c4ae5476fa2ba307b744af919
institution DOAJ
issn 1935-2727
1935-2735
language English
publishDate 2011-11-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Neglected Tropical Diseases
spelling doaj-art-7e29903c4ae5476fa2ba307b744af9192025-08-20T02:59:31ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352011-11-01511e137310.1371/journal.pntd.0001373Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.Orit GatJames E GalenSharon TennantRaphael SimonWilliam C BlackwelderDavid J SilvermanMarcela F PasettiMyron M Levine<h4>Background</h4>Antibiotic-resistant Salmonella enterica serovar Paratyphi A, the agent of paratyphoid A fever, poses an emerging public health dilemma in endemic areas of Asia and among travelers, as there is no licensed vaccine. Integral to our efforts to develop a S. Paratyphi A vaccine, we addressed the role of flagella as a potential protective antigen by comparing cell-associated flagella with exported flagellin subunits expressed by attenuated strains.<h4>Methodology</h4>S. Paratyphi A strain ATCC 9150 was first deleted for the chromosomal guaBA locus, creating CVD 1901. Further chromosomal deletions in fliD (CVD 1901D) or flgK (CVD 1901K) were then engineered, resulting in the export of unpolymerized FliC, without impairing its overall expression. The virulence of the resulting isogenic strains was examined using a novel mouse LD(50) model to accommodate the human-host restricted S. Paratyphi A. The immunogenicity of the attenuated strains was then tested using a mouse intranasal model, followed by intraperitoneal challenge with wildtype ATCC 9150.<h4>Results</h4>Mucosal (intranasal) immunization of mice with strain CVD 1901 expressing cell-associated flagella conferred superior protection (vaccine efficacy [VE], 90%) against a lethal intraperitoneal challenge, compared with the flagellin monomer-exporting mutants CVD 1901K (30% VE) or CVD 1901D (47% VE). The superior protection induced by CVD 1901 with its cell-attached flagella was associated with an increased IgG2a:IgG1 ratio of FliC-specific antibodies with enhanced opsonophagocytic capacity.<h4>Conclusions</h4>Our results clearly suggest that enhanced anti-FliC antibody-mediated clearance of S. Paratyphi A by phagocytic cells, induced by vaccines expressing cell-associated rather than exported FliC, might be contributing to the vaccine-induced protection from S. Paratyphi A challenge in vivo. We speculate that an excess of IgG1 anti-FliC antibodies induced by the exported FliC may compete with the IgG2a subtype and block binding to specific phagocyte Fc receptors that are critical for clearing an S. Paratyphi A infection.https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0001373&type=printable
spellingShingle Orit Gat
James E Galen
Sharon Tennant
Raphael Simon
William C Blackwelder
David J Silverman
Marcela F Pasetti
Myron M Levine
Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.
PLoS Neglected Tropical Diseases
title Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.
title_full Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.
title_fullStr Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.
title_full_unstemmed Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.
title_short Cell-associated flagella enhance the protection conferred by mucosally-administered attenuated Salmonella Paratyphi A vaccines.
title_sort cell associated flagella enhance the protection conferred by mucosally administered attenuated salmonella paratyphi a vaccines
url https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0001373&type=printable
work_keys_str_mv AT oritgat cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines
AT jamesegalen cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines
AT sharontennant cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines
AT raphaelsimon cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines
AT williamcblackwelder cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines
AT davidjsilverman cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines
AT marcelafpasetti cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines
AT myronmlevine cellassociatedflagellaenhancetheprotectionconferredbymucosallyadministeredattenuatedsalmonellaparatyphiavaccines