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dc.contributor.authorGravningen, Kirsten Midttun
dc.contributor.authorChristerson, Linus
dc.contributor.authorFurberg, Anne-Sofie
dc.contributor.authorSimonsen, Gunnar Skov
dc.contributor.authorÖdman, Kristina
dc.contributor.authorStåhlsten, Anna
dc.contributor.authorHerrmann, Björn
dc.date.accessioned2013-03-13T15:16:33Z
dc.date.available2013-03-13T15:16:33Z
dc.date.issued2012
dc.description.abstractThe Chlamydia trachomatis incidence rate in Finnmark, the most northern and sparsely populated county in Norway, has been twice the national average. This population based cross-sectional study among Finnmark high school students had the following aims: i) to examine distribution of multilocus sequence types (STs) of C. trachomatis in a previously unmapped area, ii) to compare chlamydia genetic diversity in Finnmark with that of two urban regions, and iii) to compare discriminatory capacity of multilocus sequence typing (MLST) with conventional ompA sequencing in a large number of chlamydia specimens. ompA sequencing and a high-resolution MLST system based on PCR amplification and DNA sequencing of five highly variable genetic regions were used. Eighty chlamydia specimens from adolescents aged 15–20 years in Finnmark were collected in five high schools (n = 60) and from routine clinical samples in the laboratory (n = 20). These were compared to routine clinical samples from adolescents in Tromsø (n = 80) and Trondheim (n = 88), capitals of North and Central Norway, respectively. ompA sequencing detected 11 genotypes in 248 specimens from all three areas. MLST displayed 50 STs providing a five-fold higher resolution. Two-thirds of all STs were novel. The common ompA E/Bour genotype comprised 46% and resolved into 24 different STs. MLST identified the Swedish new variant of C. trachomatis not discriminated by ompA sequencing. Simpson's discriminatory index (D) was 0.93 for MLST, while a corrected Dc was 0.97. There were no statistically significant differences in ST genetic diversity between geographic areas. Finnmark had an atypical genovar distribution with G being predominant. This was mainly due to expansion of specific STs of which the novel ST161 was unique for Finnmark. MLST revealed multiple new STs and a larger genetic diversity in comparison to ompA sequencing and proved to be a useful tool in molecular epidemiology of chlamydia infectionsen
dc.descriptionGravningen's doctoral thesis, available in Munin at <a href=http://hdl.handle.net/10037/5649>http://hdl.handle.net/10037/5649</a>
dc.identifier.citationPLoS ONE (2012), vol. 7(3): e34452en
dc.identifier.cristinIDFRIDAID 960362
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pone.0034452
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/10037/5019
dc.identifier.urnURN:NBN:no-uit_munin_4693
dc.language.isoengen
dc.publisherPublic Library of Science (PLoS)en
dc.rights.accessRightsopenAccess
dc.subjectVDP::Medical disciplines: 700::Clinical medical disciplines: 750::Communicable diseases: 776en
dc.subjectVDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Infeksjonsmedisin: 776en
dc.titleMultilocus Sequence Typing of Genital Chlamydia trachomatis in Norway Reveals Multiple New Sequence Types and a Large Genetic Diversityen
dc.typeJournal articleen
dc.typeTidsskriftartikkelen
dc.typePeer revieweden


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