Abstract
Because of the allelic variations within the M protein gene (emm gene) of group A streptococci, reliable typing of this important human pathogen can be accomplished by the use of emm gene-specific oligonucleotide probes. Two technical modifications (a reverse dot blot and a reverse line blot hybridization assay) of a novel approach for the type-specific identification of emm genes have been developed. Both procedures involved amplification of an emm gene by polymerase chain reaction. The non-radioactively labeled amplicon was subsequently hybridized to a membrane carrying an array of immobilized emm gene-specific oligonucleotide probes, thus allowing the simultaneous analysis of the gene polymorphism in a single hybridization reaction. The feasibility of these rapid and easy to perform methods was shown for the unequivocal identification of reference strains and clinical isolates belonging to 16 different M serotypes.
| Original language | English |
|---|---|
| Pages (from-to) | 19-25 |
| Number of pages | 7 |
| Journal | FEMS microbiology letters |
| Volume | 119 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 1 Jun 1994 |
| Externally published | Yes |
Keywords
- Alleles
- Antigens, Bacterial
- Bacterial Outer Membrane Proteins
- Bacterial Proteins/genetics
- Bacterial Typing Techniques
- Base Sequence
- Carrier Proteins
- Molecular Sequence Data
- Oligonucleotide Probes
- Polymerase Chain Reaction
- Streptococcus pyogenes/classification
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