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      Evaluation of Immunogenicity and Protective Efficacy Elicited by Mycobacterium bovis BCG Overexpressing Ag85A Protein against Mycobacterium tuberculosis Aerosol Infection

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          Abstract

          Mycobacterium bovis bacillus Calmette-Guérin (BCG) is currently the only vaccine available for preventing tuberculosis (TB), however, BCG has varying success in preventing pulmonary TB. In this study, a recombinant BCG (rBCG::Ag85A) strain overexpressing the immunodominant Ag85A antigen was constructed, and its immunogenicity and protective efficacy were evaluated. Our results indicated that the Ag85A protein was successfully overexpressed in rBCG::Ag85A, and the Ag85A peptide–MHC complexes on draining lymph node dendritic cells of C57BL/6 mice infected with rBCG::Ag85A were detectable 4 h post-infection. The C57BL/6 mice infected with this strain had stronger antigen-specific interferon-gamma (IFN-γ) responses and higher antibody titers than those immunized with BCG, and the protective experiments showed that rBCG::Ag85A can enhance protection against Mycobacterium tuberculosis ( M. tuberculosis) H37Rv infection compared to the BCG vaccine alone. Our results demonstrate the potential of rBCG::Ag85A as a candidate vaccine against TB.

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          Most cited references22

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          Variation in protection by BCG: implications of and for heterologous immunity.

          P E Fine (1995)
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            The success and failure of BCG - implications for a novel tuberculosis vaccine.

            Over the past 50 years, the Mycobacterium bovis bacille Calmette-Guérin (BCG) vaccine against tuberculosis (TB) has maintained its position as the world's most widely used vaccine, despite showing highly variable efficacy (0-80%) in different trials. The efficacy of BCG in adults is particularly poor in tropical and subtropical regions. Studies in animal models of TB, supported by data from clinical BCG trials in humans, indicate that this failure is related to pre-existing immune responses to antigens that are common to environmental mycobacteria and Mycobacterium tuberculosis. Here, we discuss the potential mechanisms behind the variation of BCG efficacy and their implications for an improved TB vaccination strategy.
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              Role of the major antigen of Mycobacterium tuberculosis in cell wall biogenesis.

              The dominant exported proteins and protective antigens of Mycobacterium tuberculosis are a triad of related gene products called the antigen 85 (Ag85) complex. Each has also been implicated in disease pathogenesis through its fibronectin-binding capacities. A carboxylesterase domain was found within the amino acid sequences of Ag85A, B, and C, and each protein acted as a mycolyltransferase involved in the final stages of mycobacterial cell wall assembly, as shown by direct enzyme assay and site-directed mutagenesis. Furthermore, the use of an antagonist (6-azido-6-deoxy-alpha, alpha'-trehalose) of this activity demonstrates that these proteins are essential and potential targets for new antimycobacterial drugs.
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                Author and article information

                Contributors
                Journal
                Front Cell Infect Microbiol
                Front Cell Infect Microbiol
                Front. Cell. Infect. Microbiol.
                Frontiers in Cellular and Infection Microbiology
                Frontiers Media S.A.
                2235-2988
                28 January 2016
                2016
                : 6
                : 3
                Affiliations
                [1] 1Jiangsu Key Laboratory of Zoonosis, Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University Yangzhou, China
                [2] 2ABSL-3 Lab, Wuhan University Wuhan, China
                [3] 3Unit of Innate Defense and Immune Modulation, Institute Pasteur of Shanghai, Chinese Academy of Sciences Shanghai, China
                Author notes

                Edited by: Nora Lía Padola, Universidad Nacional del Centro de la Provincia de Buenos Aires, Argentina

                Reviewed by: Yufeng Yao, Shanghai Jiao Tong University School of Medicine, China; Ram P. Kamal, Battelle, USA

                *Correspondence: Xin An Jiao jiao@ 123456yzu.edu.cn ;
                Article
                10.3389/fcimb.2016.00003
                4729882
                26858942
                8c6c22c3-624b-44ca-b558-b0dba73323ee
                Copyright © 2016 Xu, Chen, Hu, Meng, Wang, Rao, Zhang, Yin, Pan and Jiao.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or repr oduction is permitted which does not comply with these terms.

                History
                : 24 October 2015
                : 08 January 2016
                Page count
                Figures: 8, Tables: 0, Equations: 0, References: 27, Pages: 9, Words: 5740
                Categories
                Microbiology
                Original Research

                Infectious disease & Microbiology
                mycobacterium tuberculosis,recombinant bcg,ag85a,immunogenicity,protective efficacy

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