Please use this identifier to cite or link to this item: http://hdl.handle.net/10311/306
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dc.contributor.authorMatsheka, M.I.
dc.contributor.authorLastovica, A.J.
dc.contributor.authorElisha, B.G.
dc.date.accessioned2009-04-21T10:36:39Z
dc.date.available2009-04-21T10:36:39Z
dc.date.issued2001
dc.identifier.citationMatsheka, M.I et al (2001) Molecular Identification of Campylobacter concisus, Journal of Clinical Microbiology, vol. 39 (10), pp. 3684–3689en
dc.identifier.issn0095-1137
dc.identifier.urihttp://hdl.handle.net/10311/306
dc.description.abstractA 1.6-kb DNA fragment isolated from a Campylobacter concisus genomic library gave C. concisus-specific restriction fragment length patterns when it was used as a probe in hybridization studies. All of the strains tested, including type strains and clinical isolates, contained a 0.5-kb HindIII fragment that hybridized to the probe. DNA sequencing of the 1.6-kb fragment identified three open reading frames (ORFs). One of the ORFs encodes the carboxy terminus of GyrB, and the translational products of ORF2 and ORF3 showed similarity to hypothetical proteins, previously identified in Campylobacter jejuni. DNA-DNA hybridization studies with a fragment internal to ORF3 showed that this sequence was responsible for the signal observed with the 0.5-kb HindIII fragment. A rapid PCR assay was developed and evaluated. Primers that annealed to the extremities of the 1.6-kb fragment were used to obtain an amplicon of the correct size from both reference and clinical strains of C. concisus.en
dc.language.isoenen
dc.publisherAmerican Society for Microbiology. http://jcm.asm.org/en
dc.subjectCampylobacter concisusen
dc.subjectDNA sequencingen
dc.subjectPCR assayen
dc.titleMolecular Identification of Campylobacter concisusen
dc.typePublished Articleen
Appears in Collections:Research articles (Dept of Biological Sciences)

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