Abstract
Purpose: Tuberculosis (TB) is a major infectious disease and is responsible for two million deaths annually. For the identification and quantitation of Mycobacterium tuberculosis (M. tuberculosis), a causative agent of TB, a sandwich enzyme-linked immunosorbent assay (ELISA) against the MPT64 protein of M. tuberculosis, an antigen marker of the M. tuberculosis complex, was developed. Materials and Methods: The MPT64 protein was expressed, and anti-MPT64 monoclonal antibodies were prepared. A sandwich ELISA was established using recombinant MPT64 protein and anti-MPT64 monoclonal antibodies. The sandwich MPT64 ELISA was evaluated using reference and clinical mycobacterial strains. Results: The sandwich MPT64 ELISA detected MPT64 protein from 2.1 ng/mL to 250 ng/mL (equivalent to 1.7×10 4 CFU/mL and 2.0×10 6 CFU/mL). All 389 clinical M. tuberculosis isolates tested positive in the sandwich MPT64 ELISA (sensitivity, 100%), and the assay showed no cross reactivity to any tested nontuberculous mycobacterial strain (specificity, 100%). Conclusion: The sandwich MPT64 ELISA is a highly sensitive and quantitative test for MPT64 protein, which can identify M. tuberculosis. © Yonsei University College of Medicine 2014.
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Ji, M., Cho, B., Cho, Y. S., Park, S. Y., Cho, S. N., Jeon, B. Y., & Yoon, B. S. (2014). Development of a quantitative sandwich enzyme-linked immunosorbent assay for detecting the MPT64 antigen of mycobacterium tuberculosis. Yonsei Medical Journal, 55(3), 746–752. https://doi.org/10.3349/ymj.2014.55.3.746
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