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Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies

More than 35,000 new cases of human brucellosis were reported in 2010 by the Chinese Center for Disease Control and Prevention. An attenuated B. melitensis vaccine M5-90 is currently used for vaccination of sheep and goats in China. In the study, a periplasmic protein BP26 from M5-90 was characteriz...

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Autores principales: Qiu, Jinlang, Wang, Wenjing, Wu, Jingbo, Zhang, Hui, Wang, Yuanzhi, Qiao, Jun, Chen, Chuangfu, Gao, Goege F., Allain, Jean-Pierre, Li, Chengyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311636/
https://www.ncbi.nlm.nih.gov/pubmed/22457830
http://dx.doi.org/10.1371/journal.pone.0034246
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author Qiu, Jinlang
Wang, Wenjing
Wu, Jingbo
Zhang, Hui
Wang, Yuanzhi
Qiao, Jun
Chen, Chuangfu
Gao, Goege F.
Allain, Jean-Pierre
Li, Chengyao
author_facet Qiu, Jinlang
Wang, Wenjing
Wu, Jingbo
Zhang, Hui
Wang, Yuanzhi
Qiao, Jun
Chen, Chuangfu
Gao, Goege F.
Allain, Jean-Pierre
Li, Chengyao
author_sort Qiu, Jinlang
collection PubMed
description More than 35,000 new cases of human brucellosis were reported in 2010 by the Chinese Center for Disease Control and Prevention. An attenuated B. melitensis vaccine M5-90 is currently used for vaccination of sheep and goats in China. In the study, a periplasmic protein BP26 from M5-90 was characterized for its epitope reactivity with mouse monoclonal and sheep antibodies. A total of 29 monoclonal antibodies (mAbs) against recombinant BP26 (rBP26) were produced, which were tested for reactivity with a panel of BP26 peptides, three truncated rBP26 and native BP26 containing membrane protein extracts (NMP) of B. melitensis M5-90 in ELISA and Western-Blot. The linear, semi-conformational and conformational epitopes from native BP26 were identified. Two linear epitopes recognized by mAbs were revealed by 28 of 16mer overlapping peptides, which were accurately mapped as the core motif of amino acid residues (93)DRDLQTGGI(101) (position 93 to 101) or residues (104)QPIYVYPD(111), respectively. The reactivity of linear epitope peptides, rBP26 and NMP was tested with 137 sheep sera by ELISAs, of which the two linear epitopes had 65–70% reactivity and NMP 90% consistent with the results of a combination of two standard serological tests. The results were helpful for evaluating the reactivity of BP26 antigen in M5-90.
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spelling pubmed-33116362012-03-28 Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies Qiu, Jinlang Wang, Wenjing Wu, Jingbo Zhang, Hui Wang, Yuanzhi Qiao, Jun Chen, Chuangfu Gao, Goege F. Allain, Jean-Pierre Li, Chengyao PLoS One Research Article More than 35,000 new cases of human brucellosis were reported in 2010 by the Chinese Center for Disease Control and Prevention. An attenuated B. melitensis vaccine M5-90 is currently used for vaccination of sheep and goats in China. In the study, a periplasmic protein BP26 from M5-90 was characterized for its epitope reactivity with mouse monoclonal and sheep antibodies. A total of 29 monoclonal antibodies (mAbs) against recombinant BP26 (rBP26) were produced, which were tested for reactivity with a panel of BP26 peptides, three truncated rBP26 and native BP26 containing membrane protein extracts (NMP) of B. melitensis M5-90 in ELISA and Western-Blot. The linear, semi-conformational and conformational epitopes from native BP26 were identified. Two linear epitopes recognized by mAbs were revealed by 28 of 16mer overlapping peptides, which were accurately mapped as the core motif of amino acid residues (93)DRDLQTGGI(101) (position 93 to 101) or residues (104)QPIYVYPD(111), respectively. The reactivity of linear epitope peptides, rBP26 and NMP was tested with 137 sheep sera by ELISAs, of which the two linear epitopes had 65–70% reactivity and NMP 90% consistent with the results of a combination of two standard serological tests. The results were helpful for evaluating the reactivity of BP26 antigen in M5-90. Public Library of Science 2012-03-23 /pmc/articles/PMC3311636/ /pubmed/22457830 http://dx.doi.org/10.1371/journal.pone.0034246 Text en Qiu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Qiu, Jinlang
Wang, Wenjing
Wu, Jingbo
Zhang, Hui
Wang, Yuanzhi
Qiao, Jun
Chen, Chuangfu
Gao, Goege F.
Allain, Jean-Pierre
Li, Chengyao
Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies
title Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies
title_full Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies
title_fullStr Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies
title_full_unstemmed Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies
title_short Characterization of Periplasmic Protein BP26 Epitopes of Brucella melitensis Reacting with Murine Monoclonal and Sheep Antibodies
title_sort characterization of periplasmic protein bp26 epitopes of brucella melitensis reacting with murine monoclonal and sheep antibodies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311636/
https://www.ncbi.nlm.nih.gov/pubmed/22457830
http://dx.doi.org/10.1371/journal.pone.0034246
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