Please use this identifier to cite or link to this item: https://accedacris.ulpgc.es/handle/10553/49971
DC FieldValueLanguage
dc.contributor.authorTavío, María M.en_US
dc.contributor.authorPerilli, Mariagraziaen_US
dc.contributor.authorVila, Jordien_US
dc.contributor.authorBecerro, Pinoen_US
dc.contributor.authorCasañas, Lucíaen_US
dc.contributor.authorAmicosante, Gianfrancoen_US
dc.contributor.authorTeresa Jiménez De Anta, Maríaen_US
dc.date.accessioned2018-11-24T12:13:19Z-
dc.date.available2018-11-24T12:13:19Z-
dc.date.issued2004en_US
dc.identifier.issn0378-1097en_US
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/49971-
dc.description.abstractThe effect of salicylate, a marRAB inducer, on the resistance to beta-lactams was characterized in an AmpC beta-lactamase hyperproducer Morganella morganii clinical isolate (the M1 strain). Results were compared with those of the effect of salicylate in a wild-type M. morganii strain. Salicylate induced a decreased susceptibility to nalidixic acid, norfloxacin and tetracycline and simultaneously increased the susceptibility to beta-lactams apparently due to the repression of AmpC P-lactamase synthesis in the M1 strain. Likewise, salicylate only repressed 46 kDa outer membrane protein expression in the wild-type strain, since the clinical isolate M1 did not express it.en_US
dc.languageengen_US
dc.relation.ispartofFEMS Microbiology Lettersen_US
dc.sourceFEMS Microbiology Letters[ISSN 0378-1097],v. 238(1), p. 139-144 (Septiembre 2004)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320103 Microbiología clínicaen_US
dc.subject.otherMultiple Antibiotic-Resistanceen_US
dc.subject.otherEnterobacter-Cloacaeen_US
dc.subject.otherEscherichia-Colien_US
dc.subject.otherOuter-Membraneen_US
dc.subject.otherExpressionen_US
dc.subject.otherProteusen_US
dc.subject.otherPorinsen_US
dc.titleSalicylate decreases production of AmpC type β-lactamases and increases susceptibility to β-lactams in a Morganella morganii clinical isolateen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.femsle.2004.07.030en_US
dc.identifier.scopus4444265064-
dc.identifier.isi000223805600020-
dc.contributor.authorscopusid6701659492-
dc.contributor.authorscopusid7004624865-
dc.contributor.authorscopusid7202012753-
dc.contributor.authorscopusid8983721300-
dc.contributor.authorscopusid6506636019-
dc.contributor.authorscopusid7006729208-
dc.contributor.authorscopusid6506989655-
dc.description.lastpage144en_US
dc.identifier.issue1-
dc.description.firstpage139en_US
dc.relation.volume238en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid2590173-
dc.contributor.daisngid358961-
dc.contributor.daisngid24031-
dc.contributor.daisngid12436681-
dc.contributor.daisngid3869833-
dc.contributor.daisngid144499-
dc.contributor.daisngid459288-
dc.description.numberofpages6en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Tavio, MM-
dc.contributor.wosstandardWOS:Perilli, M-
dc.contributor.wosstandardWOS:Vila, J-
dc.contributor.wosstandardWOS:Becerro, P-
dc.contributor.wosstandardWOS:Casanas, L-
dc.contributor.wosstandardWOS:Amicosante, G-
dc.contributor.wosstandardWOS:de Anta, MTJ-
dc.date.coverdateSeptiembre 2004en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr1,84-
dc.description.jcrqQ3-
dc.description.scieSCIE-
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR Investigación Básica y Aplicada en Ciencias de la Salud-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0002-1808-7461-
crisitem.author.parentorgDepartamento de Ciencias Clínicas-
crisitem.author.fullNameTavío Pérez, María Del Mar-
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