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Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis

BACKGROUND: Bovine purified protein derivative (bPPD) and avian purified protein derivative (aPPD) are widely used for bovine tuberculosis diagnosis. However, little is known about their qualitative and quantitative characteristics, which makes their standardisation difficult. In addition, bPPD can...

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Autores principales: Infantes-Lorenzo, José Antonio, Moreno, Inmaculada, Risalde, María de los Ángeles, Roy, Álvaro, Villar, Margarita, Romero, Beatriz, Ibarrola, Nieves, de la Fuente, José, Puentes, Eugenia, de Juan, Lucía, Gortázar, Christian, Bezos, Javier, Domínguez, Lucas, Domínguez, Mercedes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669029/
https://www.ncbi.nlm.nih.gov/pubmed/29142508
http://dx.doi.org/10.1186/s12014-017-9171-z
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author Infantes-Lorenzo, José Antonio
Moreno, Inmaculada
Risalde, María de los Ángeles
Roy, Álvaro
Villar, Margarita
Romero, Beatriz
Ibarrola, Nieves
de la Fuente, José
Puentes, Eugenia
de Juan, Lucía
Gortázar, Christian
Bezos, Javier
Domínguez, Lucas
Domínguez, Mercedes
author_facet Infantes-Lorenzo, José Antonio
Moreno, Inmaculada
Risalde, María de los Ángeles
Roy, Álvaro
Villar, Margarita
Romero, Beatriz
Ibarrola, Nieves
de la Fuente, José
Puentes, Eugenia
de Juan, Lucía
Gortázar, Christian
Bezos, Javier
Domínguez, Lucas
Domínguez, Mercedes
author_sort Infantes-Lorenzo, José Antonio
collection PubMed
description BACKGROUND: Bovine purified protein derivative (bPPD) and avian purified protein derivative (aPPD) are widely used for bovine tuberculosis diagnosis. However, little is known about their qualitative and quantitative characteristics, which makes their standardisation difficult. In addition, bPPD can give false-positive tuberculosis results because of sequence homology between Mycobacterium bovis (M. bovis) and M. avium proteins. Thus, the objective of this study was to carry out a proteomic characterisation of bPPD, aPPD and an immunopurified subcomplex from bPPD called P22 in order to identify proteins contributing to cross-reactivity among these three products in tuberculosis diagnosis. METHODS: Trypsin digests of bPPD, aPPD and P22 were analysed by nanoscale liquid chromatography-electrospray ionization tandem mass spectrometry. Mice were immunised with bPPD or aPPD, and their serum was tested by indirect ELISA for reactivity against these preparations as well as against P22. RESULTS: A total of 456 proteins were identified in bPPD, 1019 in aPPD and 118 in P22; 146 of these proteins were shared by bPPD and aPPD, and 43 were present in all three preparations. Candidate proteins that may cause cross-reactivity between bPPD and aPPD were identified based on protein abundance and antigenic propensity. Serum reactivity experiments indicated that P22 may provide greater specificity than bPPD with similar sensitivity for ELISA-type detection of antibodies against M. tuberculosis complex. CONCLUSION: The subpreparation from bPPD called P22 may be an alternative to bPPD for serodiagnosis of bovine tuberculosis, since it shares fewer proteins with aPPD than bPPD does, reducing risk of cross-reactivity with anti-M. avium antibodies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12014-017-9171-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-56690292017-11-15 Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis Infantes-Lorenzo, José Antonio Moreno, Inmaculada Risalde, María de los Ángeles Roy, Álvaro Villar, Margarita Romero, Beatriz Ibarrola, Nieves de la Fuente, José Puentes, Eugenia de Juan, Lucía Gortázar, Christian Bezos, Javier Domínguez, Lucas Domínguez, Mercedes Clin Proteomics Research BACKGROUND: Bovine purified protein derivative (bPPD) and avian purified protein derivative (aPPD) are widely used for bovine tuberculosis diagnosis. However, little is known about their qualitative and quantitative characteristics, which makes their standardisation difficult. In addition, bPPD can give false-positive tuberculosis results because of sequence homology between Mycobacterium bovis (M. bovis) and M. avium proteins. Thus, the objective of this study was to carry out a proteomic characterisation of bPPD, aPPD and an immunopurified subcomplex from bPPD called P22 in order to identify proteins contributing to cross-reactivity among these three products in tuberculosis diagnosis. METHODS: Trypsin digests of bPPD, aPPD and P22 were analysed by nanoscale liquid chromatography-electrospray ionization tandem mass spectrometry. Mice were immunised with bPPD or aPPD, and their serum was tested by indirect ELISA for reactivity against these preparations as well as against P22. RESULTS: A total of 456 proteins were identified in bPPD, 1019 in aPPD and 118 in P22; 146 of these proteins were shared by bPPD and aPPD, and 43 were present in all three preparations. Candidate proteins that may cause cross-reactivity between bPPD and aPPD were identified based on protein abundance and antigenic propensity. Serum reactivity experiments indicated that P22 may provide greater specificity than bPPD with similar sensitivity for ELISA-type detection of antibodies against M. tuberculosis complex. CONCLUSION: The subpreparation from bPPD called P22 may be an alternative to bPPD for serodiagnosis of bovine tuberculosis, since it shares fewer proteins with aPPD than bPPD does, reducing risk of cross-reactivity with anti-M. avium antibodies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12014-017-9171-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-02 /pmc/articles/PMC5669029/ /pubmed/29142508 http://dx.doi.org/10.1186/s12014-017-9171-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Infantes-Lorenzo, José Antonio
Moreno, Inmaculada
Risalde, María de los Ángeles
Roy, Álvaro
Villar, Margarita
Romero, Beatriz
Ibarrola, Nieves
de la Fuente, José
Puentes, Eugenia
de Juan, Lucía
Gortázar, Christian
Bezos, Javier
Domínguez, Lucas
Domínguez, Mercedes
Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis
title Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis
title_full Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis
title_fullStr Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis
title_full_unstemmed Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis
title_short Proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis
title_sort proteomic characterisation of bovine and avian purified protein derivatives and identification of specific antigens for serodiagnosis of bovine tuberculosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669029/
https://www.ncbi.nlm.nih.gov/pubmed/29142508
http://dx.doi.org/10.1186/s12014-017-9171-z
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