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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c447t-c701d26516779df9ecbc190091bd61ffc478a591676a244a11625b6fe2a081f23
cites cdi_FETCH-LOGICAL-c447t-c701d26516779df9ecbc190091bd61ffc478a591676a244a11625b6fe2a081f23
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container_issue 3
container_start_page 354
container_title Veterinary microbiology
container_volume 151
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
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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><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 &amp; 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&amp;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. 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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 &amp; control</subject><subject>Cell Line</subject><subject>developing countries</subject><subject>diagnostic techniques</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. 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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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identifier ISSN: 0378-1135
ispartof Veterinary microbiology, 2011-08, Vol.151 (3), p.354-362
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source ScienceDirect Freedom Collection
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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