Please use this identifier to cite or link to this item: https://doi.org/10.3390/pathogens5010003
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dc.titleBrighter Fluorescent Derivatives of UTI89 Utilizing a Monomeric vGFP
dc.contributor.authorEshaghi, Majid
dc.contributor.authorMehershahi, Kurosh S
dc.contributor.authorChen, Swaine L
dc.date.accessioned2019-06-03T04:09:47Z
dc.date.available2019-06-03T04:09:47Z
dc.date.issued2016-03-01
dc.identifier.citationEshaghi, Majid, Mehershahi, Kurosh S, Chen, Swaine L (2016-03-01). Brighter Fluorescent Derivatives of UTI89 Utilizing a Monomeric vGFP. PATHOGENS 5 (1). ScholarBank@NUS Repository. https://doi.org/10.3390/pathogens5010003
dc.identifier.issn2076-0817
dc.identifier.issn2076-0817
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/155007
dc.description.abstract© 2016 by the authors; licensee MDPI, Basel, Switzerland. Fluorescent proteins, especially green fluorescent protein (GFP), have been instrumental in understanding urinary tract infection pathogenesis by uropathogenic Escherichia coli (UPEC). We have used a recently developed GFP variant, vsfGFP-9, to create new plasmid- and chromosome-based GFP derivatives of the UPEC strain UTI89. The vsfGFP-9 strains are nearly 10 x brighter with no in vitro growth or in vivo virulence defects compared to previously reported GFP-expressing UTI89 strains. The chromosomal vsfGFP-9 strain is equivalent to the wild type UTI89 during in vivo UTI, while both plasmid GFP constructs have an equivalent virulence defect compared to non-plasmid carrying UTI89. These new vsfGFP-9 expressing strains should be useful for further studies of the pathogenesis of UTI89, and similar strategies can be used to create improved fluorescent derivatives of other UPEC strains.
dc.language.isoen
dc.publisherMDPI
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectMicrobiology
dc.subjecturinary tract infection
dc.subjectGFP
dc.subjecturopathogenic Escherichia coli
dc.subjectUROPATHOGENIC ESCHERICHIA-COLI
dc.subjectURINARY-TRACT-INFECTIONS
dc.subjectPROTEIN
dc.subjectEXPRESSION
dc.subjectGENE
dc.subjectSELECTION
dc.subjectCELLS
dc.typeArticle
dc.date.updated2019-06-03T02:43:06Z
dc.contributor.departmentMEDICINE
dc.description.doi10.3390/pathogens5010003
dc.description.sourcetitlePATHOGENS
dc.description.volume5
dc.description.issue1
dc.description.placeSWITZERLAND
dc.published.statePublished
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