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dc.contributor.authorOlsen, Jaran S.
dc.contributor.authorSkogan, Gunnar
dc.contributor.authorFykse, Else Marie
dc.contributor.authorRawlinson, Elizabeth L. A.
dc.contributor.authorTomaso, Herbert
dc.contributor.authorGranum, Per Einar
dc.contributor.authorBlatny, Janet
dc.date.accessioned2017-10-06T08:25:43Z
dc.date.accessioned2017-10-09T06:51:17Z
dc.date.available2017-10-06T08:25:43Z
dc.date.available2017-10-09T06:51:17Z
dc.date.issued2007
dc.identifier.citationOlsen, Skogan, Fykse, Rawlinson, Tomaso, Granum, Blatny. Genetic distribution of 295 Bacillus cereus group members based on adk-screening in combination with MLST (Multilocus Sequence Typing) used for validating a primer targeting a chromosomal locus in B. anthracis. Journal of Microbiological Methods. 2007;71(3):265-274en_GB
dc.identifier.urihttp://hdl.handle.net/20.500.12242/671
dc.identifier.urihttps://ffi-publikasjoner.archive.knowledgearc.net/handle/20.500.12242/671
dc.descriptionOlsen, Jaran S.; Skogan, Gunnar; Fykse, Else Marie; Rawlinson, Elizabeth L. A.; Tomaso, Herbert; Granum, Per Einar; Blatny, Janet. Genetic distribution of 295 Bacillus cereus group members based on adk-screening in combination with MLST (Multilocus Sequence Typing) used for validating a primer targeting a chromosomal locus in B. anthracis. Journal of Microbiological Methods 2007 ;Volum 71.(3) s. 265-274en_GB
dc.description.abstractThe genetic distribution of 295 Bacillus cereus group members has been investigated by using a modified Multilocus Sequence Typing method (MLST). By comparing the nucleic acid sequence of the adk gene fragment, isolates of B. cereus group members most related to B. anthracis may be easily identified. The genetic distribution, with focus on the B. anthracis close neighbours, was used to evaluate a new primer set for specific identification of B. anthracis. This primer set, BA5510-1/2, targeted the putative B. anthracis specific gene BA5510. Real-time PCR using BA5510-1/2 amplified the target fragment from all B. anthracis strains tested and only two (of 289) non-B. anthracis strains analysed. This is one of the most thoroughly validated chromosomal B. anthracis markers for real-time PCR identification, in which the screened collection contained several very closely related B. anthracis strains.en_GB
dc.language.isoenen_GB
dc.titleGenetic distribution of 295 Bacillus cereus group members based on adk-screening in combination with MLST (Multilocus Sequence Typing) used for validating a primer targeting a chromosomal locus in B. anthracisen_GB
dc.title.alternativeGenetic distribution of 295 Bacillus cereus group members based on adk-screening in combination with MLST (Multilocus Sequence Typing) used for validating a primer targeting a chromosomal locus in B. anthracisen_GB
dc.typeArticleen_GB
dc.date.updated2017-10-06T08:25:43Z
dc.identifier.cristinID617452
dc.identifier.cristinID617452
dc.identifier.doi10.1016/j.mimet.2007.10.001
dc.source.issn0167-7012
dc.source.issn1872-8359
dc.type.documentJournal article
dc.relation.journalJournal of Microbiological Methods


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