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http://hdl.handle.net/11452/29556
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DC Field | Value | Language |
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dc.date.accessioned | 2022-11-24T11:22:28Z | - |
dc.date.available | 2022-11-24T11:22:28Z | - |
dc.date.issued | 2015-12-07 | - |
dc.identifier.citation | Aybey, A. ve Demirkan, E. (2016). "Inhibition of quorum sensing-controlled virulence factors in Pseudomonas aeruginosa by human serum paraoxonase". Journal of Medical Microbiology, 65(2), 105-113. | en_US |
dc.identifier.issn | 0022-2615 | - |
dc.identifier.issn | 1473-5644 | - |
dc.identifier.uri | https://doi.org/10.1099/jmm.0.000206 | - |
dc.identifier.uri | https://www.microbiologyresearch.org/content/journal/jmm/10.1099/jmm.0.000206 | - |
dc.identifier.uri | http://hdl.handle.net/11452/29556 | - |
dc.description.abstract | The role of quorum sensing (QS) in the regulation of virulence factor production in Pseudomonas aeruginosa is well established. Increased antibiotic resistance in this bacterium has led to the search for new treatment options, and inhibition of the QS system has been explored for potential therapeutic benefits. If the use of QS inhibitory agents were to lead to a reduction in bacterial virulence, new approaches in the treatment of P. aeruginosa infections could be further developed. Accordingly, we examined whether human serum paraoxonase 1 (hPON1), which uses lactonase activity to hydrolyse N-acyl homoserine lactones, could cleave P. aeruginosa-derived signalling molecules. hPON1 was purified using ammonium sulfate precipitation and hydrophobic interaction chromatography (Sepharose 4B-L-tyrosine-1-naphthylamine). Different concentrations of hPON1 were found to reduce various virulence factors including pyocyanin, rhamnolipid, elastase, staphylolytic LasA protease and alkaline protease. Although treatment with 0.1-10 mg hPON1 ml(-1) did not show a highly inhibitory effect on elastase and staphylolytic LasA protease production, it resulted in good inhibitory effects on alkaline protease production at concentrations as low as 0.1 mg ml(-1). hPON1 also reduced the production of pyocyanin and rhamnolipid at a concentration of 1.25 mg ml(-1) (within a range of 0.312-5 mg ml(-1)). In addition, rhamnolipid, an effective biosurfactant reported to stimulate the biodegradation of hydrocarbons, was able to degrade oil only in the absence of hPON1. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Microbiology | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Microbiology | en_US |
dc.subject | Lasa protease | en_US |
dc.subject | Alkaline protease | en_US |
dc.subject | Transcriptional activator | en_US |
dc.subject | Epithelial-cells | en_US |
dc.subject | Enzyme-activity | en_US |
dc.subject | Exotoxin-a | en_US |
dc.subject | Elastase | en_US |
dc.subject | Signal | en_US |
dc.subject | Lactone | en_US |
dc.subject | Purification | en_US |
dc.subject.mesh | Aryldialkylphosphatase | en_US |
dc.subject.mesh | Bacterial proteins | en_US |
dc.subject.mesh | Endopeptidases | en_US |
dc.subject.mesh | Gene expression regulation, bacterial | en_US |
dc.subject.mesh | Glycolipids | en_US |
dc.subject.mesh | Host-pathogen interactions | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Metalloendopeptidases | en_US |
dc.subject.mesh | Pseudomonas aeruginosa | en_US |
dc.subject.mesh | Pseudomonas infections | en_US |
dc.subject.mesh | Pyocyanine | en_US |
dc.subject.mesh | Quorum sensing | en_US |
dc.subject.mesh | Virulence factors | en_US |
dc.title | Inhibition of quorum sensing-controlled virulence factors in Pseudomonas aeruginosa by human serum paraoxonase | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000373752300001 | tr_TR |
dc.identifier.scopus | 2-s2.0-84959288351 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü. | tr_TR |
dc.relation.bap | HDP (F)-2013/29 | tr_TR |
dc.identifier.startpage | 105 | tr_TR |
dc.identifier.endpage | 113 | tr_TR |
dc.identifier.volume | 65 | tr_TR |
dc.identifier.issue | 2 | tr_TR |
dc.relation.journal | Journal of Medical Microbiology | en_US |
dc.contributor.buuauthor | Aybey, Aynur | - |
dc.contributor.buuauthor | Demirkan, Elif | - |
dc.contributor.researcherid | ABI-4472-2020 | tr_TR |
dc.identifier.pubmed | 26654051 | tr_TR |
dc.subject.wos | Microbiology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q3 | en_US |
dc.contributor.scopusid | 55353798200 | tr_TR |
dc.contributor.scopusid | 23469245200 | tr_TR |
dc.subject.scopus | Quorum Sensing; Pseudomonas Aeruginosa; N-Octanoylhomoserine Lactone | en_US |
dc.subject.emtree | 1 naphthylamine | en_US |
dc.subject.emtree | Alkaline proteinase | en_US |
dc.subject.emtree | Ammonium sulfate | en_US |
dc.subject.emtree | Aryldialkylphosphatase | en_US |
dc.subject.emtree | Biosurfactant | en_US |
dc.subject.emtree | Elastase | en_US |
dc.subject.emtree | Gluconolactonase | en_US |
dc.subject.emtree | Hydrocarbon | en_US |
dc.subject.emtree | LasA protease | en_US |
dc.subject.emtree | Levo tyrosine 1 naphthylamine | en_US |
dc.subject.emtree | N acylhomoserine lactone | en_US |
dc.subject.emtree | Oil | en_US |
dc.subject.emtree | Proteinase | en_US |
dc.subject.emtree | Pyocyanine | en_US |
dc.subject.emtree | Rhamnolipid | en_US |
dc.subject.emtree | Sepharose | en_US |
dc.subject.emtree | Unclassified drug | en_US |
dc.subject.emtree | Virulence factor | en_US |
dc.subject.emtree | Aryldialkylphosphatase | en_US |
dc.subject.emtree | Bacterial protein | en_US |
dc.subject.emtree | Glycolipid | en_US |
dc.subject.emtree | Metalloproteinase | en_US |
dc.subject.emtree | PON1 protein | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Staphylolytic protease | en_US |
dc.subject.emtree | Virulence factor | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Bacterial strain | en_US |
dc.subject.emtree | Bacterial virulence | en_US |
dc.subject.emtree | Biodegradation | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Enzyme activity | en_US |
dc.subject.emtree | Enzyme inhibition | en_US |
dc.subject.emtree | Enzyme purification | en_US |
dc.subject.emtree | Hydrophobic interaction chromatography | en_US |
dc.subject.emtree | Nonhuman | en_US |
dc.subject.emtree | Precipitation | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Pseudomonas aeruginosa | en_US |
dc.subject.emtree | Quorum sensing | en_US |
dc.subject.emtree | Signal transduction | en_US |
dc.subject.emtree | Enzymology | en_US |
dc.subject.emtree | Gene expression regulation | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Host pathogen interaction | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Isolation and purification | en_US |
dc.subject.emtree | Metabolism | en_US |
dc.subject.emtree | Microbiology | en_US |
dc.subject.emtree | Physiology | en_US |
dc.subject.emtree | Pseudomonas aeruginosa | en_US |
dc.subject.emtree | Pseudomonas infection | en_US |
Appears in Collections: | Scopus Web of Science |
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