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dc.contributor.authorFraser, TA
dc.contributor.authorBell, MG
dc.contributor.authorHarris, PNA
dc.contributor.authorBell, SC
dc.contributor.authorBergh, H
dc.contributor.authorNguyen, TK
dc.contributor.authorKidd, TJ
dc.contributor.authorNimmo, GR
dc.contributor.authorSarovich, DS
dc.contributor.authorPrice, EP
dc.date.accessioned2019-11-13T04:02:49Z
dc.date.available2019-11-13T04:02:49Z
dc.date.issued2019
dc.identifier.issn2057-5858
dc.identifier.doi10.1099/mgen.0.000307
dc.identifier.urihttp://hdl.handle.net/10072/389128
dc.description.abstractStenotrophomonas maltophilia is emerging as an important cause of disease in nosocomial and community-acquired settings, including bloodstream, wound and catheter-associated infections. Cystic fibrosis (CF) airways also provide optimal growth conditions for various opportunistic pathogens with high antibiotic tolerance, including S. maltophilia. Currently, there is no rapid, cost-effective and accurate molecular method for detecting this potentially life-threatening pathogen, particularly in polymicrobial specimens, suggesting that its true prevalence is underestimated. Here, we used large-scale comparative genomics to identify a specific genetic target for S. maltophilia, with subsequent development and validation of a real-time PCR assay for its detection. Analysis of 167 Stenotrophomonas spp. genomes identified a conserved 4 kb region in S. maltophilia, which was targeted for Black Hole Quencher assay design. Our assay yielded the positive detection of 89 of 89 (100%) clinical S. maltophilia strains, and no amplification of 23 non-S. maltophilia clinical isolates. S. maltophilia was detected in 10 of 16 CF sputa, demonstrating the assay's utility for direct detection in respiratory specimens. The assay demonstrated good sensitivity, with limits of detection and quantitation on pure culture of ~10 and ~100 genome equivalents, respectively. Our assay provides a highly specific, sensitive and cost-effective method for the accurate identification of S. maltophilia, and will improve the diagnosis and treatment of this under-recognized pathogen by enabling its accurate and rapid detection from polymicrobial clinical and environmental samples.
dc.description.peerreviewedYes
dc.languageEnglish
dc.publisherMicrobiology Society
dc.publisher.placeUnited Kingdom
dc.relation.ispartofpagefrom1
dc.relation.ispartofpageto11
dc.relation.ispartofissue10
dc.relation.ispartofjournalMicrobial genomics
dc.relation.ispartofvolume5
dc.subject.fieldofresearchMicrobiology
dc.subject.fieldofresearchGenetics
dc.subject.fieldofresearchcode0605
dc.subject.fieldofresearchcode0604
dc.subject.keywordsStenotrophomonas maltophilia
dc.subject.keywordscomparative genomics
dc.subject.keywordsdiagnostics
dc.titleQuantitative real-time PCR assay for the rapid identification of the intrinsically multidrug-resistant bacterial pathogen Stenotrophomonas maltophilia
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationFraser, TA; Bell, MG; Harris, PNA; Bell, SC; Bergh, H; Nguyen, TK; Kidd, TJ; Nimmo, GR; Sarovich, DS; Price, EP, Quantitative real-time PCR assay for the rapid identification of the intrinsically multidrug-resistant bacterial pathogen Stenotrophomonas maltophilia, Microbial genomics, 2019, 5 (10), pp. 1-11
dcterms.licensehttp://creativecommons.org/licenses/by/4.0/
dc.date.updated2019-11-12T01:22:55Z
dc.description.versionPublished
gro.rights.copyright© 2019 The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
gro.hasfulltextFull Text
gro.griffith.authorNimmo, Graeme R.


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