Expression, immunochemical characterization and localization of the Mycobacterium tuberculosis protein p27

• Published in: Tuberculosis (Edinburgh, Scotland) Vol. 85; no. 4; pp. 213 - 219
• Main Authors: Le Moigne, V., Robreau, G., Borot, C., Guesdon, J.-L., Mahana, W.
• Format: Journal Article
• Language: English
• Published: Scotland Elsevier Ltd 01.07.2005; Elsevier
• Subjects: Antibodies, Bacterial - immunology; Electrophoresis, Polyacrylamide Gel; Genes, Bacterial - immunology; Humans; Immunodiagnostic; Immunologic Techniques; Life Sciences; Lipoproteins - genetics; Lipoproteins - immunology; Lipoproteins - metabolism; Localization; Mycobacterium tuberculosis; Mycobacterium tuberculosis - immunology; p27; PPE; Recombinant Proteins - analysis; Tuberculosis - immunology; Mycobacterium tuberculosis; PPE; p27; Immunodiagnostic; Localization
• ISSN: 1472-9792; 1873-281X
• DOI: 10.1016/j.tube.2005.02.002

Rv2108 is a gene of the PPE family of Mycobacterium tuberculosis specific for this bacterial complex and that may encode a putative protein p27. This gene was amplified, inserted into bacterial vectors, sequenced, and expressed as a recombinant protein. Specific antibodies to this protein were generated and used for immunochemical characterization and cellular localization. Mass spectrometric analysis of the expressed protein revealed a molecule that corresponded to the p27 putative protein. The expressed protein was immunologically active, and reacted with antibodies from tuberculosis patient sera. Specific immunoblot analysis confirmed the presence of the p27 antigen in Mycobacterium bovis BCG strain and in human clinical isolates of M. tuberculosis, but not in other mycobacteria tested. Western blot and immunoelectron microscopic analysis of BCG strain indicated that the p27 protein is localized in the membrane of the cell. The specific expression of the p27 protein in the M. tuberculosis complex could provide a novel specific complimentary diagnostic test for the presence of and infection with M. tuberculosis.