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

Authors :
Lucas Domínguez
Mercedes Domínguez
Javier Bezos
Margarita Villar
Christian Gortázar
Inmaculada Moreno
Álvaro Roy
Nieves Ibarrola
Eugenia Puentes
Lucía de Juan
José de la Fuente
José Antonio Infantes-Lorenzo
Beatriz Romero
María Ángeles Risalde
Comunidad de Madrid
European Commission
CSIC - Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA)
Ministerio de Economía, Industria y Competitividad (España)
Ministerio de Educación, Cultura y Deporte (España)
Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (España)
Comunidad de Madrid (España)
Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname, Repisalud, Instituto de Salud Carlos III (ISCIII), Clinical Proteomics, Vol 14, Iss 1, Pp 1-10 (2017), Clinical Proteomics, Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid, Consejería de Sanidad de la Comunidad de Madrid
Publication Year :
2017
Publisher :
BioMed Central, 2017.

Abstract

[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.<br />This work was supported by the Ministerio de Economía, Industria y Competitividad of Spain (RTC-2016-4746-2), the Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria of Spain (RTA2015-00043-C02-02) and the TAVS-CM Programme of the Comunidad de Madrid (S2013/ABI-2747), cofinanced by the FEDER fund “A way to build Europe”. Jose Antonio Infantes-Lorenzo was supported by an FPU contract-fellowship (Formación de Profesorado Universitario) from the Ministerio de Educación, Cultura y Deporte of the Spanish Government (FPU2013/6000). Alvaro Roy is the recipient of an Industrial Doctorate contract (DI-15-08110) funded by the Spanish Ministerio de Economía, Industria y Competitividad and the European Social Fund.

Details

Database :
OpenAIRE
Journal :
Digital.CSIC. Repositorio Institucional del CSIC, instname, Repisalud, Instituto de Salud Carlos III (ISCIII), Clinical Proteomics, Vol 14, Iss 1, Pp 1-10 (2017), Clinical Proteomics, Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid, Consejería de Sanidad de la Comunidad de Madrid
Accession number :
edsair.doi.dedup.....4248ef3d6371fd36a5f650144f7d9509