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PMID: 8039659 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Rapid typing of group A streptococci by the use of DNA amplification and non-radioactive allele-specific oligonucleotide probes.

FEMS microbiology letters ·Vol. 119 ·No. 1-2 ·1994-06-01 ·Pages 19-25

Kaufhold A, Podbielski A, Baumgarten G, Blokpoel M, Top J, Schouls L

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.

MeSH Terms
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,genetics
Chemicals
Antigens, Bacterial Bacterial Outer Membrane Proteins Bacterial Proteins Carrier Proteins Oligonucleotide Probes streptococcal M protein
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kaufhold A
Institute of Medical Microbiology, Technical University (RWTH) Aachen, FRG.
Podbielski A
Baumgarten G
Blokpoel M
Top J
Schouls L
Article Info
Journal
FEMS microbiology letters
Abbr.
FEMS Microbiol Lett
ISSN
0378-1097
Published
1994-06-01
Pages
19-25
Language
English
Region
England
NLM ID
7705721
Subset
IM
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