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The 16MΔvjbR as an ideal live attenuated vaccine candidate for differentiation between Brucella vaccination and infection
Brucellosis brings great economic burdens for developing countries. Live attenuated vaccines are the most efficient means for prevention and control of animal Brucellosis. However, the difficulties of differentiating of infection from vaccine immunization, which is essential for eradication programs...
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Published in: | Veterinary microbiology 2011-08, Vol.151 (3), p.354-362 |
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creator | Wang, Yufei Bai, Yaoxia Qu, Qing Xu, Jie Chen, Yanfen Zhong, Zhijun Qiu, Yefeng Wang, Tongkun Du, Xinying Wang, Zhoujia Yu, Shuang Fu, Simei Yuan, Jing Zhen, Qing Yu, Yaqing Chen, Zeliang Huang, Liuyu |
description | Brucellosis brings great economic burdens for developing countries. Live attenuated vaccines are the most efficient means for prevention and control of animal
Brucellosis. However, the difficulties of differentiating of infection from vaccine immunization, which is essential for eradication programs, limit their applications. Therefore, the development of a vaccine that could differentiate infection from immunization will overcome the limitations and get extensive application. VjbR is a quorum sensing regulator involving in
Brucella's intracellular survival. The vjbR∷Tn5 mutants have been proven effective against wild type strain challenge, implying its possibility of use in vaccine candidate development. To further evaluate this candidate gene, in the present study, the antigenicity of purified recombinant VjbR protein was analyzed. Antibodies to
Brucella melitensis VjbR could be detected in sera from patients and animals with brucellosis but not in control ones, implying the potential use of this protein as a diagnostic antigen. Then a
vjbR mutant of
B. melitensis 16M was constructed by replacing the
vjbR with kanamycin gene. The mutant showed reduced survival in macrophage and mice. Vaccination of BALB/c mice with 16MΔvjbR conferred significant protective immunity against
B. melitensis strain 16M challenges, being equivalent to which induced by the license vaccine Rev.1. The
vjbR deletion mutant elicited an anti-
Brucella-specific immunoglobulin G response and induced the secretion of gamma interferon and interleukin-10. The most importance is that, the use of
vjbR mutants as vaccines in association with diagnostic tests based on the VjbR antigen would allow the serological differentiation between infected and vaccinated animals. These results suggest that 16MΔvjbR is an ideal live attenuated vaccine candidate against
B. melitensis and deserves further evaluation for vaccine development. |
doi_str_mv | 10.1016/j.vetmic.2011.03.031 |
format | article |
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Brucellosis. However, the difficulties of differentiating of infection from vaccine immunization, which is essential for eradication programs, limit their applications. Therefore, the development of a vaccine that could differentiate infection from immunization will overcome the limitations and get extensive application. VjbR is a quorum sensing regulator involving in
Brucella's intracellular survival. The vjbR∷Tn5 mutants have been proven effective against wild type strain challenge, implying its possibility of use in vaccine candidate development. To further evaluate this candidate gene, in the present study, the antigenicity of purified recombinant VjbR protein was analyzed. Antibodies to
Brucella melitensis VjbR could be detected in sera from patients and animals with brucellosis but not in control ones, implying the potential use of this protein as a diagnostic antigen. Then a
vjbR mutant of
B. melitensis 16M was constructed by replacing the
vjbR with kanamycin gene. The mutant showed reduced survival in macrophage and mice. Vaccination of BALB/c mice with 16MΔvjbR conferred significant protective immunity against
B. melitensis strain 16M challenges, being equivalent to which induced by the license vaccine Rev.1. The
vjbR deletion mutant elicited an anti-
Brucella-specific immunoglobulin G response and induced the secretion of gamma interferon and interleukin-10. The most importance is that, the use of
vjbR mutants as vaccines in association with diagnostic tests based on the VjbR antigen would allow the serological differentiation between infected and vaccinated animals. These results suggest that 16MΔvjbR is an ideal live attenuated vaccine candidate against
B. melitensis and deserves further evaluation for vaccine development.</description><identifier>ISSN: 0378-1135</identifier><identifier>EISSN: 1873-2542</identifier><identifier>DOI: 10.1016/j.vetmic.2011.03.031</identifier><identifier>PMID: 21530111</identifier><identifier>CODEN: VMICDQ</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; antibodies ; Antibody Formation ; antigens ; Applied microbiology ; Bacterial Proteins - blood ; Bacterial Proteins - genetics ; Bacterial Proteins - immunology ; Bacteriology ; Biological and medical sciences ; Brucella ; Brucella melitensis ; Brucella melitensis - genetics ; Brucella melitensis - immunology ; Brucella Vaccine - genetics ; Brucella Vaccine - immunology ; brucellosis ; Brucellosis - immunology ; Brucellosis - prevention & control ; Cell Line ; developing countries ; diagnostic techniques ; Female ; Fundamental and applied biological sciences. Psychology ; Gene Deletion ; genes ; Humans ; immunity ; immunoglobulin G ; Immunoglobulin G - immunology ; Interferon-gamma - immunology ; interferons ; interleukin-10 ; Interleukin-10 - immunology ; kanamycin ; Live attenuated vaccines ; live vaccines ; Macrophages - immunology ; Macrophages - microbiology ; Mice ; Mice, Inbred BALB C ; Microbiology ; Miscellaneous ; mutants ; patients ; quorum sensing ; recombinant proteins ; secretion ; Sequence Deletion ; vaccination ; vaccine development ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) ; Vaccines, Attenuated - genetics ; Vaccines, Attenuated - immunology ; VjbR</subject><ispartof>Veterinary microbiology, 2011-08, Vol.151 (3), p.354-362</ispartof><rights>2011 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-c701d26516779df9ecbc190091bd61ffc478a591676a244a11625b6fe2a081f23</citedby><cites>FETCH-LOGICAL-c447t-c701d26516779df9ecbc190091bd61ffc478a591676a244a11625b6fe2a081f23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24391764$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21530111$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yufei</creatorcontrib><creatorcontrib>Bai, Yaoxia</creatorcontrib><creatorcontrib>Qu, Qing</creatorcontrib><creatorcontrib>Xu, Jie</creatorcontrib><creatorcontrib>Chen, Yanfen</creatorcontrib><creatorcontrib>Zhong, Zhijun</creatorcontrib><creatorcontrib>Qiu, Yefeng</creatorcontrib><creatorcontrib>Wang, Tongkun</creatorcontrib><creatorcontrib>Du, Xinying</creatorcontrib><creatorcontrib>Wang, Zhoujia</creatorcontrib><creatorcontrib>Yu, Shuang</creatorcontrib><creatorcontrib>Fu, Simei</creatorcontrib><creatorcontrib>Yuan, Jing</creatorcontrib><creatorcontrib>Zhen, Qing</creatorcontrib><creatorcontrib>Yu, Yaqing</creatorcontrib><creatorcontrib>Chen, Zeliang</creatorcontrib><creatorcontrib>Huang, Liuyu</creatorcontrib><title>The 16MΔvjbR as an ideal live attenuated vaccine candidate for differentiation between Brucella vaccination and infection</title><title>Veterinary microbiology</title><addtitle>Vet Microbiol</addtitle><description>Brucellosis brings great economic burdens for developing countries. Live attenuated vaccines are the most efficient means for prevention and control of animal
Brucellosis. However, the difficulties of differentiating of infection from vaccine immunization, which is essential for eradication programs, limit their applications. Therefore, the development of a vaccine that could differentiate infection from immunization will overcome the limitations and get extensive application. VjbR is a quorum sensing regulator involving in
Brucella's intracellular survival. The vjbR∷Tn5 mutants have been proven effective against wild type strain challenge, implying its possibility of use in vaccine candidate development. To further evaluate this candidate gene, in the present study, the antigenicity of purified recombinant VjbR protein was analyzed. Antibodies to
Brucella melitensis VjbR could be detected in sera from patients and animals with brucellosis but not in control ones, implying the potential use of this protein as a diagnostic antigen. Then a
vjbR mutant of
B. melitensis 16M was constructed by replacing the
vjbR with kanamycin gene. The mutant showed reduced survival in macrophage and mice. Vaccination of BALB/c mice with 16MΔvjbR conferred significant protective immunity against
B. melitensis strain 16M challenges, being equivalent to which induced by the license vaccine Rev.1. The
vjbR deletion mutant elicited an anti-
Brucella-specific immunoglobulin G response and induced the secretion of gamma interferon and interleukin-10. The most importance is that, the use of
vjbR mutants as vaccines in association with diagnostic tests based on the VjbR antigen would allow the serological differentiation between infected and vaccinated animals. These results suggest that 16MΔvjbR is an ideal live attenuated vaccine candidate against
B. melitensis and deserves further evaluation for vaccine development.</description><subject>Animals</subject><subject>antibodies</subject><subject>Antibody Formation</subject><subject>antigens</subject><subject>Applied microbiology</subject><subject>Bacterial Proteins - blood</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - immunology</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Brucella</subject><subject>Brucella melitensis</subject><subject>Brucella melitensis - genetics</subject><subject>Brucella melitensis - immunology</subject><subject>Brucella Vaccine - genetics</subject><subject>Brucella Vaccine - immunology</subject><subject>brucellosis</subject><subject>Brucellosis - immunology</subject><subject>Brucellosis - prevention & control</subject><subject>Cell Line</subject><subject>developing countries</subject><subject>diagnostic techniques</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Deletion</subject><subject>genes</subject><subject>Humans</subject><subject>immunity</subject><subject>immunoglobulin G</subject><subject>Immunoglobulin G - immunology</subject><subject>Interferon-gamma - immunology</subject><subject>interferons</subject><subject>interleukin-10</subject><subject>Interleukin-10 - immunology</subject><subject>kanamycin</subject><subject>Live attenuated vaccines</subject><subject>live vaccines</subject><subject>Macrophages - immunology</subject><subject>Macrophages - microbiology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>mutants</subject><subject>patients</subject><subject>quorum sensing</subject><subject>recombinant proteins</subject><subject>secretion</subject><subject>Sequence Deletion</subject><subject>vaccination</subject><subject>vaccine development</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><subject>Vaccines, Attenuated - genetics</subject><subject>Vaccines, Attenuated - immunology</subject><subject>VjbR</subject><issn>0378-1135</issn><issn>1873-2542</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkdGK1TAQhoMo7tnVNxDNjXjVY6ZJk_ZG0MVVYUXQ3euQJhPNoSddk7aiz-Fz-Uzm2KPeKQyEzHz_zDA_IQ-AbYGBfLrbLjjtg93WDGDLeAm4RTbQKl7Vjahvkw3jqq0AeHNCTnPeMcZEJ9ldclJDw4sKNuTb1SekIN_--L7s-vfUZGoiDQ7NQIewIDXThHE2Ezq6GGtDRGpNdMGVFPVjoi54jwnjFMwUxkh7nL4gRvoizRaHwRxla7EoaYge7eF3j9zxZsh4__iekeuLl1fnr6vLd6_enD-_rKwQaqqsYuBq2YBUqnO-Q9tb6BjroHcSvLdCtabpSlmaWggDIOumlx5rw1rwNT8jT9a-N2n8PGOe9D7kX7tFHOes266Dhqmm-T-plADG5aGnWEmbxpwTen2Twt6krxqYPtijd3q1Rx_s0YyXgCJ7eBww93t0f0S__SjA4yNgsjWDTybakP9ygnegpCjco5XzZtTmYyrM9YcySTAGhah5IZ6tBJbTLgGTzjZgtOhCKvfXbgz_3vUneKi5fQ</recordid><startdate>20110805</startdate><enddate>20110805</enddate><creator>Wang, Yufei</creator><creator>Bai, Yaoxia</creator><creator>Qu, Qing</creator><creator>Xu, Jie</creator><creator>Chen, Yanfen</creator><creator>Zhong, Zhijun</creator><creator>Qiu, Yefeng</creator><creator>Wang, Tongkun</creator><creator>Du, Xinying</creator><creator>Wang, Zhoujia</creator><creator>Yu, Shuang</creator><creator>Fu, Simei</creator><creator>Yuan, Jing</creator><creator>Zhen, Qing</creator><creator>Yu, Yaqing</creator><creator>Chen, Zeliang</creator><creator>Huang, Liuyu</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><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><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20110805</creationdate><title>The 16MΔvjbR as an ideal live attenuated vaccine candidate for differentiation between Brucella vaccination and infection</title><author>Wang, Yufei ; Bai, Yaoxia ; Qu, Qing ; Xu, Jie ; Chen, Yanfen ; Zhong, Zhijun ; Qiu, Yefeng ; Wang, Tongkun ; Du, Xinying ; Wang, Zhoujia ; Yu, Shuang ; Fu, Simei ; Yuan, Jing ; Zhen, Qing ; Yu, Yaqing ; Chen, Zeliang ; Huang, Liuyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-c701d26516779df9ecbc190091bd61ffc478a591676a244a11625b6fe2a081f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>antibodies</topic><topic>Antibody Formation</topic><topic>antigens</topic><topic>Applied microbiology</topic><topic>Bacterial Proteins - blood</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - immunology</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Brucella</topic><topic>Brucella melitensis</topic><topic>Brucella melitensis - genetics</topic><topic>Brucella melitensis - immunology</topic><topic>Brucella Vaccine - genetics</topic><topic>Brucella Vaccine - immunology</topic><topic>brucellosis</topic><topic>Brucellosis - immunology</topic><topic>Brucellosis - prevention & control</topic><topic>Cell Line</topic><topic>developing countries</topic><topic>diagnostic techniques</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Deletion</topic><topic>genes</topic><topic>Humans</topic><topic>immunity</topic><topic>immunoglobulin G</topic><topic>Immunoglobulin G - immunology</topic><topic>Interferon-gamma - immunology</topic><topic>interferons</topic><topic>interleukin-10</topic><topic>Interleukin-10 - immunology</topic><topic>kanamycin</topic><topic>Live attenuated vaccines</topic><topic>live vaccines</topic><topic>Macrophages - immunology</topic><topic>Macrophages - microbiology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>mutants</topic><topic>patients</topic><topic>quorum sensing</topic><topic>recombinant proteins</topic><topic>secretion</topic><topic>Sequence Deletion</topic><topic>vaccination</topic><topic>vaccine development</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</topic><topic>Vaccines, Attenuated - genetics</topic><topic>Vaccines, Attenuated - immunology</topic><topic>VjbR</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yufei</creatorcontrib><creatorcontrib>Bai, Yaoxia</creatorcontrib><creatorcontrib>Qu, Qing</creatorcontrib><creatorcontrib>Xu, Jie</creatorcontrib><creatorcontrib>Chen, Yanfen</creatorcontrib><creatorcontrib>Zhong, Zhijun</creatorcontrib><creatorcontrib>Qiu, Yefeng</creatorcontrib><creatorcontrib>Wang, Tongkun</creatorcontrib><creatorcontrib>Du, Xinying</creatorcontrib><creatorcontrib>Wang, Zhoujia</creatorcontrib><creatorcontrib>Yu, Shuang</creatorcontrib><creatorcontrib>Fu, Simei</creatorcontrib><creatorcontrib>Yuan, Jing</creatorcontrib><creatorcontrib>Zhen, Qing</creatorcontrib><creatorcontrib>Yu, Yaqing</creatorcontrib><creatorcontrib>Chen, Zeliang</creatorcontrib><creatorcontrib>Huang, Liuyu</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Veterinary microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Yufei</au><au>Bai, Yaoxia</au><au>Qu, Qing</au><au>Xu, Jie</au><au>Chen, Yanfen</au><au>Zhong, Zhijun</au><au>Qiu, Yefeng</au><au>Wang, Tongkun</au><au>Du, Xinying</au><au>Wang, Zhoujia</au><au>Yu, Shuang</au><au>Fu, Simei</au><au>Yuan, Jing</au><au>Zhen, Qing</au><au>Yu, Yaqing</au><au>Chen, Zeliang</au><au>Huang, Liuyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The 16MΔvjbR as an ideal live attenuated vaccine candidate for differentiation between Brucella vaccination and infection</atitle><jtitle>Veterinary microbiology</jtitle><addtitle>Vet Microbiol</addtitle><date>2011-08-05</date><risdate>2011</risdate><volume>151</volume><issue>3</issue><spage>354</spage><epage>362</epage><pages>354-362</pages><issn>0378-1135</issn><eissn>1873-2542</eissn><coden>VMICDQ</coden><abstract>Brucellosis brings great economic burdens for developing countries. Live attenuated vaccines are the most efficient means for prevention and control of animal
Brucellosis. However, the difficulties of differentiating of infection from vaccine immunization, which is essential for eradication programs, limit their applications. Therefore, the development of a vaccine that could differentiate infection from immunization will overcome the limitations and get extensive application. VjbR is a quorum sensing regulator involving in
Brucella's intracellular survival. The vjbR∷Tn5 mutants have been proven effective against wild type strain challenge, implying its possibility of use in vaccine candidate development. To further evaluate this candidate gene, in the present study, the antigenicity of purified recombinant VjbR protein was analyzed. Antibodies to
Brucella melitensis VjbR could be detected in sera from patients and animals with brucellosis but not in control ones, implying the potential use of this protein as a diagnostic antigen. Then a
vjbR mutant of
B. melitensis 16M was constructed by replacing the
vjbR with kanamycin gene. The mutant showed reduced survival in macrophage and mice. Vaccination of BALB/c mice with 16MΔvjbR conferred significant protective immunity against
B. melitensis strain 16M challenges, being equivalent to which induced by the license vaccine Rev.1. The
vjbR deletion mutant elicited an anti-
Brucella-specific immunoglobulin G response and induced the secretion of gamma interferon and interleukin-10. The most importance is that, the use of
vjbR mutants as vaccines in association with diagnostic tests based on the VjbR antigen would allow the serological differentiation between infected and vaccinated animals. These results suggest that 16MΔvjbR is an ideal live attenuated vaccine candidate against
B. melitensis and deserves further evaluation for vaccine development.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>21530111</pmid><doi>10.1016/j.vetmic.2011.03.031</doi><tpages>9</tpages></addata></record> |
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subjects | Animals antibodies Antibody Formation antigens Applied microbiology Bacterial Proteins - blood Bacterial Proteins - genetics Bacterial Proteins - immunology Bacteriology Biological and medical sciences Brucella Brucella melitensis Brucella melitensis - genetics Brucella melitensis - immunology Brucella Vaccine - genetics Brucella Vaccine - immunology brucellosis Brucellosis - immunology Brucellosis - prevention & control Cell Line developing countries diagnostic techniques Female Fundamental and applied biological sciences. Psychology Gene Deletion genes Humans immunity immunoglobulin G Immunoglobulin G - immunology Interferon-gamma - immunology interferons interleukin-10 Interleukin-10 - immunology kanamycin Live attenuated vaccines live vaccines Macrophages - immunology Macrophages - microbiology Mice Mice, Inbred BALB C Microbiology Miscellaneous mutants patients quorum sensing recombinant proteins secretion Sequence Deletion vaccination vaccine development Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) Vaccines, Attenuated - genetics Vaccines, Attenuated - immunology VjbR |
title | The 16MΔvjbR as an ideal live attenuated vaccine candidate for differentiation between Brucella vaccination and infection |
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