Abstract
A system for rapid colorimetric detection of specific genome DNA fragments amplified by the polymerase chain reaction (PCR) is described that has been designed to allow direct solid-phase sequencing of positive samples. The amplified material is immobilized on magnetic beads by using the biotin streptavidin system. An Escherichia coli lac operator DNA sequence is incorporated in the amplified material during the second step of a nested primer procedure. This 21-base-pair sequence is used for a general colorimetric detection with a fusion protein consisting of the E. coli Lac repressor and beta-galactosidase. Positive samples can be treated subsequently with alkali to obtain a single-stranded DNA template suitable for direct genomic sequencing. This method to detect immobilized amplified nucleic acids (DIANA) is well adapted for automated or semiautomated clinical assays. Here, we show that it can be used to detect and sequence Chlamydia trachomatis genomic DNA in clinical samples.
MeSH Terms
Amino Acid Sequence
Base Sequence
Chlamydia Infections/diagnosis
Chlamydia trachomatis/genetics
Colorimetry/methods
DNA, Bacterial/analysis,genetics
Escherichia coli/genetics
Genes, Bacterial
Humans
Lac Operon
Molecular Sequence Data
Oligonucleotide Probes/chemical synthesis
Polymerase Chain Reaction/methods
Recombinant Fusion Proteins/isolation & purification
Spectrometry, Fluorescence/methods
beta-Galactosidase/genetics,isolation & purification
Chemicals
DNA, Bacterial
Oligonucleotide Probes
Recombinant Fusion Proteins
beta-Galactosidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wahlberg J
Department of Biochemistry and Biotechnology, Royal Institute of Technology, Stockholm, Sweden.
Lundeberg J
Hultman T
Uhlén M
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