Publication:
Rapid qualitative urinary tract infection pathogen identification by SeptiFast real-time PCR

cris.virtual.author-orcid0000-0003-3525-8477
cris.virtualsource.author-orcid69d2b3da-aa71-4d06-a336-6a1f32d3c935
cris.virtualsource.author-orcid9a3662ad-4a37-4511-a187-1d6fc3aa6063
cris.virtualsource.author-orcidb6cd5251-35a7-4f2a-bcca-35d2b4146404
dc.contributor.authorLehmann, Lutz Eric
dc.contributor.authorHauser, Stefan
dc.contributor.authorMalinka, Thomas
dc.contributor.authorKlaschik, Sven
dc.contributor.authorWeber, Stefan U
dc.contributor.authorSchewe, Jens-Christian
dc.contributor.authorStüber, Frank
dc.contributor.authorBook, Malte
dc.date.accessioned2024-10-11T09:09:22Z
dc.date.available2024-10-11T09:09:22Z
dc.date.issued2011
dc.description.abstractBackground Urinary tract infections (UTI) are frequent in outpatients. Fast pathogen identification is mandatory for shortening the time of discomfort and preventing serious complications. Urine culture needs up to 48 hours until pathogen identification. Consequently, the initial antibiotic regimen is empirical. Aim To evaluate the feasibility of qualitative urine pathogen identification by a commercially available real-time PCR blood pathogen test (SeptiFast®) and to compare the results with dipslide and microbiological culture. Design of study Pilot study with prospectively collected urine samples. Setting University hospital. Methods 82 prospectively collected urine samples from 81 patients with suspected UTI were included. Dipslide urine culture was followed by microbiological pathogen identification in dipslide positive samples. In parallel, qualitative DNA based pathogen identification (SeptiFast®) was performed in all samples. Results 61 samples were SeptiFast® positive, whereas 67 samples were dipslide culture positive. The inter-methodological concordance of positive and negative findings in the gram+, gram- and fungi sector was 371/410 (90%), 477/492 (97%) and 238/246 (97%), respectively. Sensitivity and specificity of the SeptiFast® test for the detection of an infection was 0.82 and 0.60, respectively. SeptiFast® pathogen identifications were available at least 43 hours prior to culture results. Conclusion The SeptiFast® platform identified bacterial DNA in urine specimens considerably faster compared to conventional culture. For UTI diagnosis sensitivity and specificity is limited by its present qualitative setup which does not allow pathogen quantification. Future quantitative assays may hold promise for PCR based UTI pathogen identification as a supplementation of conventional culture methods.
dc.description.numberOfPages1
dc.description.sponsorshipUniversitätsklinik für Anästhesiologie und Schmerztherapie
dc.identifier.doi10.7892/boris.6055
dc.identifier.isi000287392700055
dc.identifier.pmid21359187
dc.identifier.publisherDOI10.1371/journal.pone.0017146
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/76617
dc.language.isoen
dc.publisherPublic Library of Science
dc.publisher.placeLawrence, Kans.
dc.relation.ispartofPLoS ONE
dc.relation.issn1932-6203
dc.relation.organizationDCD5A442BADCE17DE0405C82790C4DE2
dc.titleRapid qualitative urinary tract infection pathogen identification by SeptiFast real-time PCR
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue2
oaire.citation.startPagee17146
oaire.citation.volume6
oairecerif.author.affiliationUniversitätsklinik für Anästhesiologie und Schmerztherapie
oairecerif.author.affiliationUniversitätsklinik für Anästhesiologie und Schmerztherapie
oairecerif.author.affiliationUniversitätsklinik für Anästhesiologie und Schmerztherapie
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unibe.description.ispublishedpub
unibe.eprints.legacyId6055
unibe.journal.abbrevTitlePLOS ONE
unibe.refereedTRUE
unibe.subtype.articlejournal

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