Abstract |
The pertussis toxin (PT) promoter region is a frequently used target for DNA-based diagnosis of pertussis and parapertussis infections. The reported polymorphism in this region has also allowed discrimination of species in mixtures with several Bordetella species by their specific PCR amplicon restriction patterns. In the present study, we investigated the degree of polymorphism in order to confirm the reliability of the assay. Five different sequence types of the amplified 239- or 249-bp region were found among the 33 Bordetella pertussis, B. parapertussis, and B. bronchiseptica American Type Culture Collection reference strains and patient isolates analyzed. According to the sequences that were obtained and according to the PT promoter sequences already available in the databases, restriction enzyme analysis with TaqI, BglI, and HaeII, which gave four different patterns, can be performed to reliably identify B. pertussis, B. parapertussis, and B. bronchiseptica.
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Authors | M Nygren, E Reizenstein, M Ronaghi, J Lundeberg |
Journal | Journal of clinical microbiology
(J Clin Microbiol)
Vol. 38
Issue 1
Pg. 55-60
(Jan 2000)
ISSN: 0095-1137 [Print] United States |
PMID | 10618063
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DNA, Bacterial
- Virulence Factors, Bordetella
- Pertussis Toxin
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Topics |
- Base Sequence
- Bordetella
(classification, genetics)
- Bordetella Infections
(diagnosis)
- Bordetella bronchiseptica
(classification, genetics)
- Bordetella pertussis
(classification, genetics)
- DNA, Bacterial
(isolation & purification)
- Electrophoresis, Agar Gel
- Molecular Sequence Data
- Pertussis Toxin
- Polymerase Chain Reaction
- Polymorphism, Genetic
- Promoter Regions, Genetic
- Sequence Analysis, DNA
- Sequence Homology, Amino Acid
- Virulence Factors, Bordetella
(genetics)
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