Enzyme-linked immunosorbent assay using monoclonal antibodies for identification of mycobacteria from early cultures

C P Verstijnen, H M Ly, K Polman, C Richter, S P Smits, S Y Maselle, P Peerbooms, D Rienthong, N Montreewasuwat, S Koanjanart

    Research output: Contribution to journalA1: Web of Science-articlepeer-review

    Abstract

    A simple enzyme-linked immunosorbent assay (ELISA) for the identification of cultured mycobacteria belonging to the Mycobacterium tuberculosis complex, the Mycobacterium avium complex, and Mycobacterium kansasii has been developed (R. Schöningh, C. P. H. J. Verstijnen, S. Kuijper, and A. H. J. Kolk. J. Clin. Microbiol. 28:708-713, 1990). The test for the routine identification of cultured mycobacteria was introduced in five clinical laboratories located in Tanzania, Thailand, Vietnam, and The Netherlands. The ELISA can be conducted without an ELISA reader since the test can be read visually. The results of identification of 255 strains of the M. tuberculosis complex by microbiological means and by ELISA were compared; the specificity and the sensitivity were 100%. For the M. avium complex, the specificity was 100% and the sensitivity was 64%. All 26 M. kansasii strains tested could be identified as M. kansasii. The ELISA described here proved to be useful in both well- and modestly equipped laboratories and may replace the microbiological method of identification of M. tuberculosis and M. kansasii.

    Original languageEnglish
    JournalJournal of Clinical Microbiology
    Volume29
    Issue number7
    Pages (from-to)1372-1375
    Number of pages4
    ISSN0095-1137
    Publication statusPublished - 1991

    Keywords

    • Antibodies, Monoclonal
    • Enzyme-Linked Immunosorbent Assay
    • Evaluation Studies as Topic
    • Humans
    • Mycobacterium
    • Mycobacterium Infections
    • Mycobacterium avium Complex
    • Mycobacterium tuberculosis
    • Nontuberculous Mycobacteria
    • Sensitivity and Specificity
    • Journal Article
    • Research Support, Non-U.S. Gov't
    • Research Support, U.S. Gov't, Non-P.H.S.

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