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Colorimetric Solid-Phase Capture Hybridization Assay for Detection of Amplified Borrelia burgdorferi DNA
Author(s) -
Frédéric Mansy,
Bernard Hoyois,
Michel J. Vos,
A. Van Elsen,
Alex Bollen,
Edmond Godfroid
Publication year - 1996
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/96211rr03
Subject(s) - borrelia burgdorferi , microbiology and biotechnology , lyme disease , agarose gel electrophoresis , biology , polymerase chain reaction , dna–dna hybridization , agarose , dna , oligonucleotide , hybridization probe , virology , gene , genetics , antibody
To simplify detection procedures of DNA fragments resulting from PCR, we developed a colorimetric microplate hybridization assay. This format was used for the identification of Borrelia burgdorferi sensu lato, the causal agent of Lyme disease. The system relied on the use of a specific capture probe covalently linked to polystyrene plates and a specific polybiotinylated detection probe. DNA fragments, resulting from PCR and sandwiched between these two probes, were detected by enzymatic color development. The new detection format outperformed agarose gel electrophoresis of PCR products in sensitivity and specificity Moreover, in view of its rapidity and simplicity, the system proved appropriate for the routine diagnostic analysis of clinical specimens from Lyme disease patients. The proposed detection format can be adapted easily to other DNA targets and is suitable for automation.

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