{ "labelLang" : "hun", "responseDate" : "2024-03-28 15:34", "paging" : { "last" : true, "first" : true, "totalPages" : 1, "totalElements" : 1, "totalUncutElements" : 1, "totalEstimatedElements" : 1, "size" : 10, "number" : 1, "numberOfElements" : 1, "sort" : [ { "direction" : "DESC", "property" : "publishedYear", "ascending" : false }, { "direction" : "ASC", "property" : "firstAuthor", "ascending" : true } ] }, "content" : [ { "otype" : "JournalArticle", "mtid" : 30409867, "status" : "VALIDATED", "published" : true, "comment" : "Department of Microbiology and Biotechnology, Szent István University, Budapest, Hungary \n Department of Medical Microbiology and Immunobiology, University of Szeged, Szeged, Hungary \n Cited By :5 \n Export Date: 31 July 2020 \n CODEN: PHYRE \n Correspondence Address: Kiskó, G.; Department of Microbiology and Biotechnology, Szent István UniversityHungary; email: kisko.gabriella@etk.szie.hu \n Chemicals/CAS: carvacrol, 499-75-2; ciprofloxacin, 85721-33-1; crystal violet, 467-63-0, 548-62-9; ethidium bromide, 1239-45-8; para cymene, 99-87-6; tetracycline, 23843-90-5, 60-54-8, 64-75-5, 8021-86-1; thymoquinone, 490-91-5; 4-cymene; Anti-Bacterial Agents; Anti-Infective Agents; Benzoquinones; carvacrol; Monoterpenes; Oils, Volatile; Plant Extracts; thymoquinone \n Manufacturers: Sigma Aldrich, Germany; MP Biomedicals, France \n Funding details: GINOP‐2.3.2‐15‐2016‐ 00012 \n Funding details: European Social Fund, ESF, EFOP‐3.6.3‐VEKOP‐16‐2017‐00005 EFOP‐ 3.6.3‐VEKOP‐16‐2017‐00009 \n Funding details: Magyar Tudományos Akadémia, MTA \n Funding details: European Commission, EC \n Funding details: European Social Fund, ESF, EFOP‐3.6.3‐VEKOP‐16‐2017‐ 00005, EFOP‐3.6.3‐VEKOP‐16‐2017‐00009 \n Funding details: European Commission, EC \n Funding details: Magyar Tudományos Akadémia, MTA \n Funding text 1: European Union and co‐financed by the European Social Fund, Grant/Award Number: EFOP‐3.6.3‐VEKOP‐16‐2017‐00005 EFOP‐ 3.6.3‐VEKOP‐16‐2017‐00009; János Bolyai Research Scholarship of the Hungarian Academy of Sciences; University of Szeged, Grant/ Award Number: GINOP‐2.3.2‐15‐2016‐ 00012; European Union and the State of Hungary and co‐financed by the European Social Fund, Grant/Award Number: TÁMOP 4.2.4. A/2‐11‐1‐2012‐0001; ÚNKP‐18‐3 New National Excellence Program of the Ministry of Human Capacities of Hungary \n Funding text 2: The study was supported by the European Union and co‐financed by the European Social Fund (grants EFOP‐3.6.3‐VEKOP‐16‐2017‐ 00005 and EFOP‐3.6.3‐VEKOP‐16‐2017‐00009). This research was supported by the European Union and the State of Hungary and co‐ financed by the European Social Fund in the framework of TÁMOP 4.2.4. A/2‐11‐1‐2012‐0001 “National Excellence Program.” This study was supported by the GINOP‐2.3.2‐15‐2016‐00012 project (University of Szeged, Hungary). Gabriella Spengler was supported by the János Bolyai Research Scholarship of the Hungarian Academy of Sciences. Annamária Kincses was supported by the ÚNKP‐18‐3 New National Excellence Program of the Ministry of Human Capacities of Hungary. Authors express special thanks to Professor Éva Szőke, Department of Pharmacognosy, Semmelweis University, Budapest, for preparation of the essential oil used in the experiments.\nDepartment of Microbiology and Biotechnology, Szent István University, Budapest, Hungary \n Department of Medical Microbiology and Immunobiology, University of Szeged, Szeged, Hungary \n Cited By :9 \n Export Date: 18 January 2021 \n CODEN: PHYRE \n Correspondence Address: Kiskó, G.; Department of Microbiology and Biotechnology, Szent István UniversityHungary; email: kisko.gabriella@etk.szie.hu \n Chemicals/CAS: carvacrol, 499-75-2; ciprofloxacin, 85721-33-1; crystal violet, 467-63-0, 548-62-9; ethidium bromide, 1239-45-8; para cymene, 99-87-6; tetracycline, 23843-90-5, 60-54-8, 64-75-5, 8021-86-1; thymoquinone, 490-91-5; 4-cymene; Anti-Bacterial Agents; Anti-Infective Agents; Benzoquinones; carvacrol; Monoterpenes; Oils, Volatile; Plant Extracts; thymoquinone \n Manufacturers: Sigma Aldrich, Germany; MP Biomedicals, France \n Funding details: Szegedi Tudományegyetem, SZTE, GINOP‐2.3.2‐15‐2016‐ 00012 \n Funding details: European Social Fund, ESF, EFOP‐3.6.3‐VEKOP‐16‐2017‐00005 EFOP‐ 3.6.3‐VEKOP‐16‐2017‐00009 \n Funding details: Magyar Tudományos Akadémia, MTA \n Funding details: European Commission, EC \n Funding details: Szegedi Tudományegyetem, SZTE \n Funding details: European Social Fund, ESF, A/2‐11‐1‐2012‐0001, EFOP‐3.6.3‐VEKOP‐16‐2017‐ 00005, EFOP‐3.6.3‐VEKOP‐16‐2017‐00009 \n Funding details: Magyar Tudományos Akadémia, MTA \n Funding details: European Commission, EC \n Funding text 1: European Union and co‐financed by the European Social Fund, Grant/Award Number: EFOP‐3.6.3‐VEKOP‐16‐2017‐00005 EFOP‐ 3.6.3‐VEKOP‐16‐2017‐00009; János Bolyai Research Scholarship of the Hungarian Academy of Sciences; University of Szeged, Grant/ Award Number: GINOP‐2.3.2‐15‐2016‐ 00012; European Union and the State of Hungary and co‐financed by the European Social Fund, Grant/Award Number: TÁMOP 4.2.4. A/2‐11‐1‐2012‐0001; ÚNKP‐18‐3 New National Excellence Program of the Ministry of Human Capacities of Hungary \n Funding text 2: The study was supported by the European Union and co‐financed by the European Social Fund (grants EFOP‐3.6.3‐VEKOP‐16‐2017‐ 00005 and EFOP‐3.6.3‐VEKOP‐16‐2017‐00009). This research was supported by the European Union and the State of Hungary and co‐ financed by the European Social Fund in the framework of TÁMOP 4.2.4. A/2‐11‐1‐2012‐0001 “National Excellence Program.” This study was supported by the GINOP‐2.3.2‐15‐2016‐00012 project (University of Szeged, Hungary). Gabriella Spengler was supported by the János Bolyai Research Scholarship of the Hungarian Academy of Sciences. Annamária Kincses was supported by the ÚNKP‐18‐3 New National Excellence Program of the Ministry of Human Capacities of Hungary. 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"publishedYear" : 2019, "abstractText" : "Nigella sativa essential oil (EO) and its compounds (thymoquinone, carvacrol, and p-cymene) have a broad antimicrobial spectrum. The aim of this study was to investigate the antimicrobial and resistance modifying activity of N. sativa EO, thymoquinone, carvacrol, and p-cymene against one methicillin susceptible and one methicillin resistant Staphylococcus aureus strain. N. sativa EO, thymoquinone, carvacrol, and p-cymene were assessed for antimicrobial activity and modulation of antimicrobial resistance (by broth microdilution), inhibition of antimicrobial efflux (by ethidium bromide [EtBr] accumulation assay), relative expression of mepA gene (by real-time reverse transcriptase quantitative polymerase chain reaction), membrane disrupting effect (by LIVE/DEAD BacLight™ Kit), and finally antibiofilm activity (by the crystal violet assay). Both strains of S. aureus were susceptible to N. sativa EO, thymoquinone, and carvacrol. N. sativa EO and carvacrol induced the increase of EtBr accumulated by both S. aureus strains. Membrane integrity of ATCC strain was disrupted by carvacrol and p-cymene, whereas for the methicillin resistant S. aureus (MRSA) strain the membrane integrity was disrupted by each compound. 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