Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/49968
Campo DC | Valor | idioma |
---|---|---|
dc.contributor.author | Tavío, María M. | en_US |
dc.contributor.author | Perilli, Mariagrazia | en_US |
dc.contributor.author | Vila, Jordi | en_US |
dc.contributor.author | Becerro, Pino | en_US |
dc.contributor.author | Ruiz, Joaquím | en_US |
dc.contributor.author | Amicosante, Gianfranco | en_US |
dc.contributor.author | Jiménez De Anta, María T. | en_US |
dc.date.accessioned | 2018-11-24T12:11:55Z | - |
dc.date.available | 2018-11-24T12:11:55Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.issn | 1076-6294 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/49968 | - |
dc.description.abstract | The effect of ciprofloxacin and two marPAB inducers on the susceptibility to beta-lactam antibiotics in two AmpC beta-lactamase semiconstitutive producer Citrobacter freundii clinical isolates (the DM1 and DM2 strains) was studied. Possible changes in outer membrane protein expression, permeability to cephaloridine, active efflux, and hydrolytic activity of beta-lactamase-crude extracts were evaluated under the influence of ciprofloxacin, sodium salicylate, and 2,4-dinitrophenol. Results were compared with those of the effect of the same three chemicals on a normally beta-lactamase-inducible wild-type C. freundii strain. The three assayed compounds decreased beta-lactamase hydrolysis on cephaloridine in both the two clinical isolates as well as in the wild-type strain. However, only the DM1 and DM2 strains showed increased susceptibility to beta-lactams. Sodium salicylate and 2,4-dinitrophenol, but not ciprofloxacin, reduced the expression of a 45-kDa outer membrane protein in the three studied strains, which was accompanied by a 4- to 20-fold diminution in permeability to cephaloridine. In conclusion, two marRAB inducers and ciprofloxacin induced the Mar phenotype and repressed AmpC beta-lactamase synthesis in the DM1 and DM2 clinical isolates. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Microbial Drug Resistance | en_US |
dc.source | Microbial Drug Resistance[ISSN 1076-6294],v. 11(3), p. 225-231 (Septiembre 2005) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 320103 Microbiología clínica | en_US |
dc.subject.other | Multidrug Efflux Pump | en_US |
dc.subject.other | Escherichia-Coli | en_US |
dc.subject.other | Pseudomonas-Aeruginosa | en_US |
dc.subject.other | Antibiotic-Resistance | en_US |
dc.subject.other | Enterobacter-Cloacae | en_US |
dc.subject.other | Outer-Membrane | en_US |
dc.subject.other | Cephalosporins | en_US |
dc.subject.other | Quinolones | en_US |
dc.subject.other | Imipenem | en_US |
dc.subject.other | Strains | en_US |
dc.title | Ciprofloxacin, salicylate, and 2,4-dinitrophenol decrease production of AmpC-type β-lactamase in two Citrobacter freundii clinical isolates | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1089/mdr.2005.11.225 | en_US |
dc.identifier.scopus | 26444432340 | - |
dc.identifier.isi | 000232437200004 | - |
dc.contributor.authorscopusid | 6701659492 | - |
dc.contributor.authorscopusid | 7004624865 | - |
dc.contributor.authorscopusid | 7202012753 | - |
dc.contributor.authorscopusid | 8983721300 | - |
dc.contributor.authorscopusid | 35392400000 | - |
dc.contributor.authorscopusid | 7006729208 | - |
dc.contributor.authorscopusid | 35412061700 | - |
dc.description.lastpage | 231 | en_US |
dc.description.firstpage | 225 | en_US |
dc.relation.volume | 11 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.contributor.daisngid | 2590173 | - |
dc.contributor.daisngid | 358961 | - |
dc.contributor.daisngid | 24031 | - |
dc.contributor.daisngid | 12436681 | - |
dc.contributor.daisngid | 173728 | - |
dc.contributor.daisngid | 144499 | - |
dc.contributor.daisngid | 459288 | - |
dc.description.numberofpages | 7 | en_US |
dc.utils.revision | Sí | en_US |
dc.contributor.wosstandard | WOS:Tavio, MM | - |
dc.contributor.wosstandard | WOS:Perilli, M | - |
dc.contributor.wosstandard | WOS:Vila, J | - |
dc.contributor.wosstandard | WOS:Becerro, P | - |
dc.contributor.wosstandard | WOS:Ruiz, J | - |
dc.contributor.wosstandard | WOS:Amicosante, G | - |
dc.contributor.wosstandard | WOS:De Anta, MTJ | - |
dc.date.coverdate | Septiembre 2005 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.jcr | 2,072 | - |
dc.description.jcrq | Q2 | - |
dc.description.scie | SCIE | - |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | GIR Investigación Básica y Aplicada en Ciencias de la Salud | - |
crisitem.author.dept | Departamento de Ciencias Clínicas | - |
crisitem.author.orcid | 0000-0002-1808-7461 | - |
crisitem.author.parentorg | Departamento de Ciencias Clínicas | - |
crisitem.author.fullName | Tavío Pérez, María Del Mar | - |
Colección: | Artículos |
Citas SCOPUSTM
1
actualizado el 24-nov-2024
Citas de WEB OF SCIENCETM
Citations
1
actualizado el 24-nov-2024
Visitas
79
actualizado el 03-ago-2024
Google ScholarTM
Verifica
Altmetric
Comparte
Exporta metadatos
Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.