An enterobacterial common antigen mutant of Salmonella enterica serovar Typhimurium as a vaccine candidate
Abstract Due to increasing rates of invasive Salmonella enterica serovar Typhimurium infection, there is a need for an effective vaccine to prevent this disease. Previous studies showed that a mutation in the first gene of the Enterobacterial common antigen biosynthetic pathway, wecA , resulted in a...
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Veröffentlicht in: | International journal of medical microbiology 2015-09, Vol.305 (6), p.511-522 |
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description | Abstract Due to increasing rates of invasive Salmonella enterica serovar Typhimurium infection, there is a need for an effective vaccine to prevent this disease. Previous studies showed that a mutation in the first gene of the Enterobacterial common antigen biosynthetic pathway, wecA , resulted in attenuation of S . Typhimurium in a murine model of salmonellosis. Furthermore, immunization with a wecA − strain protected against lethal challenge with the parental wild type S . Typhimurium strain. Herein, we examined whether the S . Typhimurium wecA− strain could also provide cross-protection against non-parental strains of S. Typhimurium and S. Enteritidis. We found that intraperitoneal immunization (IP) with S . Typhimurium SL1344 wecA− resulted in a significant increase in survival compared to control mice for all Salmonella challenge strains tested. Oral immunization with SL1344 wecA− also resulted in increased survival; however, protection was less significant than with intraperitoneal immunization. The increase in survival of SL1344 wecA − immunized mice was associated with a Salmonella -specific IgG antibody response. Furthermore, analysis of sera from IP and orally immunized animals revealed cross-reactive antibodies to numerous Salmonella isolates. Functional analysis of antibodies found within the sera from IP immunized animals revealed agglutination and opsonophagocytic activity against all tested O:4 Salmonella serovars. Together these results indicate that immunization with a S . Typhimurium wecA− strain confers protection against lethal challenge with wild type S. Typhimurium and S . Enteritidis and that immunization correlates with functional antibody production. |
doi_str_mv | 10.1016/j.ijmm.2015.05.004 |
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Scott</creator><creatorcontrib>Bridge, Dacie R ; Whitmire, Jeannette M ; Gilbreath, Jeremy J ; Metcalf, Eleanor S ; Merrell, D. Scott</creatorcontrib><description>Abstract Due to increasing rates of invasive Salmonella enterica serovar Typhimurium infection, there is a need for an effective vaccine to prevent this disease. Previous studies showed that a mutation in the first gene of the Enterobacterial common antigen biosynthetic pathway, wecA , resulted in attenuation of S . Typhimurium in a murine model of salmonellosis. Furthermore, immunization with a wecA − strain protected against lethal challenge with the parental wild type S . Typhimurium strain. Herein, we examined whether the S . Typhimurium wecA− strain could also provide cross-protection against non-parental strains of S. Typhimurium and S. Enteritidis. We found that intraperitoneal immunization (IP) with S . Typhimurium SL1344 wecA− resulted in a significant increase in survival compared to control mice for all Salmonella challenge strains tested. Oral immunization with SL1344 wecA− also resulted in increased survival; however, protection was less significant than with intraperitoneal immunization. The increase in survival of SL1344 wecA − immunized mice was associated with a Salmonella -specific IgG antibody response. Furthermore, analysis of sera from IP and orally immunized animals revealed cross-reactive antibodies to numerous Salmonella isolates. Functional analysis of antibodies found within the sera from IP immunized animals revealed agglutination and opsonophagocytic activity against all tested O:4 Salmonella serovars. Together these results indicate that immunization with a S . Typhimurium wecA− strain confers protection against lethal challenge with wild type S. Typhimurium and S . Enteritidis and that immunization correlates with functional antibody production.</description><identifier>ISSN: 1438-4221</identifier><identifier>EISSN: 1618-0607</identifier><identifier>DOI: 10.1016/j.ijmm.2015.05.004</identifier><identifier>PMID: 26070977</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Administration, Oral ; Animals ; Antibody ; Antigens, Bacterial - genetics ; Antigens, Bacterial - immunology ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacterial Vaccines - administration & dosage ; Bacterial Vaccines - immunology ; Cross Protection ; Disease Models, Animal ; Female ; Immunoglobulin G - blood ; Infectious Disease ; Live-attenuated ; Medical Education ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Salmonella Enteritidis ; Salmonella Infections - immunology ; Salmonella Infections - prevention & control ; Salmonella Typhimurium ; Salmonella typhimurium - genetics ; Salmonella typhimurium - immunology ; Serogroup ; Vaccination ; Vaccine ; Vaccines, Attenuated - immunology ; wecA</subject><ispartof>International journal of medical microbiology, 2015-09, Vol.305 (6), p.511-522</ispartof><rights>2015</rights><rights>Published by Elsevier GmbH.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c591t-8d7657bdc9d7c7e35b8049e98307765d56c6ae2800a9d8266761937a174555c93</citedby><cites>FETCH-LOGICAL-c591t-8d7657bdc9d7c7e35b8049e98307765d56c6ae2800a9d8266761937a174555c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijmm.2015.05.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26070977$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bridge, Dacie R</creatorcontrib><creatorcontrib>Whitmire, Jeannette M</creatorcontrib><creatorcontrib>Gilbreath, Jeremy J</creatorcontrib><creatorcontrib>Metcalf, Eleanor S</creatorcontrib><creatorcontrib>Merrell, D. Scott</creatorcontrib><title>An enterobacterial common antigen mutant of Salmonella enterica serovar Typhimurium as a vaccine candidate</title><title>International journal of medical microbiology</title><addtitle>Int J Med Microbiol</addtitle><description>Abstract Due to increasing rates of invasive Salmonella enterica serovar Typhimurium infection, there is a need for an effective vaccine to prevent this disease. Previous studies showed that a mutation in the first gene of the Enterobacterial common antigen biosynthetic pathway, wecA , resulted in attenuation of S . Typhimurium in a murine model of salmonellosis. Furthermore, immunization with a wecA − strain protected against lethal challenge with the parental wild type S . Typhimurium strain. Herein, we examined whether the S . Typhimurium wecA− strain could also provide cross-protection against non-parental strains of S. Typhimurium and S. Enteritidis. We found that intraperitoneal immunization (IP) with S . Typhimurium SL1344 wecA− resulted in a significant increase in survival compared to control mice for all Salmonella challenge strains tested. Oral immunization with SL1344 wecA− also resulted in increased survival; however, protection was less significant than with intraperitoneal immunization. The increase in survival of SL1344 wecA − immunized mice was associated with a Salmonella -specific IgG antibody response. Furthermore, analysis of sera from IP and orally immunized animals revealed cross-reactive antibodies to numerous Salmonella isolates. Functional analysis of antibodies found within the sera from IP immunized animals revealed agglutination and opsonophagocytic activity against all tested O:4 Salmonella serovars. Together these results indicate that immunization with a S . Typhimurium wecA− strain confers protection against lethal challenge with wild type S. Typhimurium and S . Enteritidis and that immunization correlates with functional antibody production.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antibody</subject><subject>Antigens, Bacterial - genetics</subject><subject>Antigens, Bacterial - immunology</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacterial Vaccines - administration & dosage</subject><subject>Bacterial Vaccines - immunology</subject><subject>Cross Protection</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Immunoglobulin G - blood</subject><subject>Infectious Disease</subject><subject>Live-attenuated</subject><subject>Medical Education</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Salmonella Enteritidis</subject><subject>Salmonella Infections - immunology</subject><subject>Salmonella Infections - prevention & control</subject><subject>Salmonella Typhimurium</subject><subject>Salmonella typhimurium - genetics</subject><subject>Salmonella typhimurium - immunology</subject><subject>Serogroup</subject><subject>Vaccination</subject><subject>Vaccine</subject><subject>Vaccines, Attenuated - immunology</subject><subject>wecA</subject><issn>1438-4221</issn><issn>1618-0607</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1r3DAQNaEhSdP-gR6Kjr14O5ItyYJSCKFfEOghyVlopdlWriVtJXth_31kNu2hh8LADLwPpPea5g2FDQUq3o8bP4awYUD5BupAf9ZcUUGHFgTIF_Xuu6HtGaOXzctSRgBgqhMXzSWrOCgpr5rxJhKMM-a0NbYubyZiUwgpEhNn_wMjCctcT5J25N5MFcBpMieNt4aUKj2YTB6O-58-LNkvgZhCDDkYa31EYk103pkZXzXnOzMVfP28r5vHz58ebr-2d9-_fLu9uWstV3RuBycFl1tnlZNWYse3A_QK1dCBrIjjwgqDbAAwyg1MCCmo6qShsuecW9VdN-9Ovvucfi9YZh18seurI6alaCphGJSomkplJ6rNqZSMO73PPph81BT0mrEe9ZqxXjPWUAf6Knr77L9sA7q_kj-hVsKHEwHrLw8esy7WY7TofEY7a5f8__0__iO3k4816-kXHrGMacmx5qepLkyDvl9bXkumvBbMGe2eAHOOomw</recordid><startdate>20150901</startdate><enddate>20150901</enddate><creator>Bridge, Dacie R</creator><creator>Whitmire, Jeannette M</creator><creator>Gilbreath, Jeremy J</creator><creator>Metcalf, Eleanor S</creator><creator>Merrell, D. Scott</creator><general>Elsevier GmbH</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150901</creationdate><title>An enterobacterial common antigen mutant of Salmonella enterica serovar Typhimurium as a vaccine candidate</title><author>Bridge, Dacie R ; Whitmire, Jeannette M ; Gilbreath, Jeremy J ; Metcalf, Eleanor S ; Merrell, D. Scott</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c591t-8d7657bdc9d7c7e35b8049e98307765d56c6ae2800a9d8266761937a174555c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antibody</topic><topic>Antigens, Bacterial - genetics</topic><topic>Antigens, Bacterial - immunology</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacterial Vaccines - administration & dosage</topic><topic>Bacterial Vaccines - immunology</topic><topic>Cross Protection</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Immunoglobulin G - blood</topic><topic>Infectious Disease</topic><topic>Live-attenuated</topic><topic>Medical Education</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Salmonella Enteritidis</topic><topic>Salmonella Infections - immunology</topic><topic>Salmonella Infections - prevention & control</topic><topic>Salmonella Typhimurium</topic><topic>Salmonella typhimurium - genetics</topic><topic>Salmonella typhimurium - immunology</topic><topic>Serogroup</topic><topic>Vaccination</topic><topic>Vaccine</topic><topic>Vaccines, Attenuated - immunology</topic><topic>wecA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bridge, Dacie R</creatorcontrib><creatorcontrib>Whitmire, Jeannette M</creatorcontrib><creatorcontrib>Gilbreath, Jeremy J</creatorcontrib><creatorcontrib>Metcalf, Eleanor S</creatorcontrib><creatorcontrib>Merrell, D. Scott</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of medical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bridge, Dacie R</au><au>Whitmire, Jeannette M</au><au>Gilbreath, Jeremy J</au><au>Metcalf, Eleanor S</au><au>Merrell, D. Scott</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An enterobacterial common antigen mutant of Salmonella enterica serovar Typhimurium as a vaccine candidate</atitle><jtitle>International journal of medical microbiology</jtitle><addtitle>Int J Med Microbiol</addtitle><date>2015-09-01</date><risdate>2015</risdate><volume>305</volume><issue>6</issue><spage>511</spage><epage>522</epage><pages>511-522</pages><issn>1438-4221</issn><eissn>1618-0607</eissn><abstract>Abstract Due to increasing rates of invasive Salmonella enterica serovar Typhimurium infection, there is a need for an effective vaccine to prevent this disease. Previous studies showed that a mutation in the first gene of the Enterobacterial common antigen biosynthetic pathway, wecA , resulted in attenuation of S . Typhimurium in a murine model of salmonellosis. Furthermore, immunization with a wecA − strain protected against lethal challenge with the parental wild type S . Typhimurium strain. Herein, we examined whether the S . Typhimurium wecA− strain could also provide cross-protection against non-parental strains of S. Typhimurium and S. Enteritidis. We found that intraperitoneal immunization (IP) with S . Typhimurium SL1344 wecA− resulted in a significant increase in survival compared to control mice for all Salmonella challenge strains tested. Oral immunization with SL1344 wecA− also resulted in increased survival; however, protection was less significant than with intraperitoneal immunization. The increase in survival of SL1344 wecA − immunized mice was associated with a Salmonella -specific IgG antibody response. Furthermore, analysis of sera from IP and orally immunized animals revealed cross-reactive antibodies to numerous Salmonella isolates. Functional analysis of antibodies found within the sera from IP immunized animals revealed agglutination and opsonophagocytic activity against all tested O:4 Salmonella serovars. Together these results indicate that immunization with a S . Typhimurium wecA− strain confers protection against lethal challenge with wild type S. Typhimurium and S . Enteritidis and that immunization correlates with functional antibody production.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>26070977</pmid><doi>10.1016/j.ijmm.2015.05.004</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals Antibody Antigens, Bacterial - genetics Antigens, Bacterial - immunology Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacterial Vaccines - administration & dosage Bacterial Vaccines - immunology Cross Protection Disease Models, Animal Female Immunoglobulin G - blood Infectious Disease Live-attenuated Medical Education Mice Mice, Inbred BALB C Mice, Inbred C57BL Salmonella Enteritidis Salmonella Infections - immunology Salmonella Infections - prevention & control Salmonella Typhimurium Salmonella typhimurium - genetics Salmonella typhimurium - immunology Serogroup Vaccination Vaccine Vaccines, Attenuated - immunology wecA |
title | An enterobacterial common antigen mutant of Salmonella enterica serovar Typhimurium as a vaccine candidate |
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