Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/100527
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dc.contributor.authorBorlee, Bradley R.en
dc.contributor.authorNielsen, Thomas E.en
dc.contributor.authorParsek, Matthew R.en
dc.contributor.authorRybtke, Morten Theilen
dc.contributor.authorMurakami, Keijien
dc.contributor.authorIrie, Yasuhikoen
dc.contributor.authorHentzer, Mortenen
dc.contributor.authorGivskov, Michaelen
dc.contributor.authorTolker-Nielsen, Timen
dc.date.accessioned2013-07-05T02:39:35Zen
dc.date.accessioned2019-12-06T20:24:03Z-
dc.date.available2013-07-05T02:39:35Zen
dc.date.available2019-12-06T20:24:03Z-
dc.date.copyright2012en
dc.date.issued2012en
dc.identifier.citationRybtke, M. T., Borlee, B. R., Murakami, K., Irie, Y., Hentzer, M., Nielsen, T. E., et al. (2012). Fluorescence-based reporter for gauging cyclic Di-GMP levels in Pseudomonas aeruginosa. Applied and Environmental Microbiology, 78(15), 5060-5069.en
dc.identifier.issn0099-2240en
dc.identifier.urihttps://hdl.handle.net/10356/100527-
dc.description.abstractThe increased tolerance toward the host immune system and antibiotics displayed by biofilm-forming Pseudomonas aeruginosa and other bacteria in chronic infections such as cystic fibrosis bronchopneumonia is of major concern. Targeting of biofilm formation is believed to be a key aspect in the development of novel antipathogenic drugs that can augment the effect of classic antibiotics by decreasing antimicrobial tolerance. The second messenger cyclic di-GMP is a positive regulator of biofilm formation, and cyclic di-GMP signaling is now regarded as a potential target for the development of antipathogenic compounds. Here we describe the development of fluorescent monitors that can gauge the cellular level of cyclic di-GMP in P. aeruginosa. We have created cyclic di-GMP level reporters by transcriptionally fusing the cyclic di-GMP-responsive cdrA promoter to genes encoding green fluorescent protein. We show that the reporter constructs give a fluorescent readout of the intracellular level of cyclic di-GMP in P. aeruginosa strains with different levels of cyclic di-GMP. Furthermore, we show that the reporters are able to detect increased turnover of cyclic di-GMP mediated by treatment of P. aeruginosa with the phosphodiesterase inducer nitric oxide. Considering that biofilm formation is a necessity for the subsequent development of a chronic infection and therefore a pathogenicity trait, the reporters display a significant potential for use in the identification of novel antipathogenic compounds targeting cyclic di-GMP signaling, as well as for use in research aiming at understanding the biofilm biology of P. aeruginosa.en
dc.language.isoenen
dc.relation.ispartofseriesApplied and environmental microbiologyen
dc.rights© 2012 American Society for Microbiology.en
dc.titleFluorescence-based reporter for gauging cyclic Di-GMP levels in Pseudomonas aeruginosaen
dc.typeJournal Articleen
dc.identifier.doi10.1128/AEM.00414-12en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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