Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/77240
DC FieldValueLanguage
dc.contributor.authorPompilio, Ariannaen_US
dc.contributor.authorRanalli, Marcoen_US
dc.contributor.authorPiccirilli, Alessandraen_US
dc.contributor.authorPerilli, Mariagraziaen_US
dc.contributor.authorVukovic, Draganaen_US
dc.contributor.authorSavic, Branislavaen_US
dc.contributor.authorKrutova, Marcelaen_US
dc.contributor.authorDrevinek, Pavelen_US
dc.contributor.authorJonas, Danielen_US
dc.contributor.authorFiscarelli, Ersilia V.en_US
dc.contributor.authorAssanti, Vanessa Tuccio Guarnaen_US
dc.contributor.authorTavío Pérez, María Del Maren_US
dc.contributor.authorArtiles, Fernandoen_US
dc.contributor.authorDi Bonaventura, Giovannien_US
dc.date.accessioned2021-01-18T15:53:40Z-
dc.date.available2021-01-18T15:53:40Z-
dc.date.issued2021en_US
dc.identifier.otherScopus-
dc.identifier.urihttp://hdl.handle.net/10553/77240-
dc.description.abstractThe ability to form biofilms is a recognized trait of Stenotrophomonas maltophilia, but the extent of its clinical relevance is still unclear. The present multicenter prospective study (ANSELM) aims at investigating the association between biofilm formation and clinical outcomes of S. maltophilia infections. One hundred and nine isolates were collected from various geographical origins and stratified according to their clinical relevance. Biofilm formation was evaluated by the microtiter plate assay and correlated with microbiological and clinical data from the associated strains. Antibiotic susceptibility of the planktonic cells was tested by the disk diffusion technique, while antibiotic activity against mature biofilms was spectrophotometrically assessed. Most strains (91.7%) were able to form biofilm, although bloodborne strains produced biofilm amounts significantly higher than strains causing hospital-rather than community-acquired infections, and those recognized as “definite” pathogens. Biofilm formation efficiency was positively correlated with mechanical ventilation (p = 0.032), whereas a negative relationship was found with antibiotic resistance (r2 = 0.107; p < 0.001), specifically in the case of the pathogenic strains. Mature S. maltophilia biofilms were markedly more resistant (up to 128 times) to cotrimoxazole and levofloxacin compared with their planktonic counterparts, especially in the case of bloodborne strains. Our findings indicate that biofilm formation by S. maltophilia is obviously a contributing factor in the pathogenesis of infections, especially in deep ones, thus warranting additional studies with larger cohort of patients and isolates.en_US
dc.languageengen_US
dc.relation.ispartofMicroorganismsen_US
dc.sourceMicroorganisms [EISSN 2076-2607], v. 9 (1), p. 1-25, (Enero 2021)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3201 Ciencias clínicasen_US
dc.subject3207 Patologíaen_US
dc.subject.otherAntibiotic Resistanceen_US
dc.subject.otherBiofilm Formationen_US
dc.subject.otherClinical Relevanceen_US
dc.subject.otherMulticenter Studyen_US
dc.subject.otherStenotrophomonas Maltophiliaen_US
dc.titleBiofilm formation among stenotrophomonas maltophilia isolates has clinical relevance: The ANSELM prospective multicenter studyen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/microorganisms9010049en_US
dc.identifier.scopus85098854444-
dc.contributor.authorscopusid24765379300-
dc.contributor.authorscopusid57221337920-
dc.contributor.authorscopusid57189041486-
dc.contributor.authorscopusid7004624865-
dc.contributor.authorscopusid7005414538-
dc.contributor.authorscopusid7004671656-
dc.contributor.authorscopusid54585433400-
dc.contributor.authorscopusid6603477890-
dc.contributor.authorscopusid7005318464-
dc.contributor.authorscopusid6602405539-
dc.contributor.authorscopusid57221326460-
dc.contributor.authorscopusid6701659492-
dc.contributor.authorscopusid6507261074-
dc.contributor.authorscopusid7003845013-
dc.identifier.eissn2076-2607-
dc.identifier.issue1-
dc.relation.volume9en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages26en_US
dc.utils.revisionen_US
dc.date.coverdateEnero 2021en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,862
dc.description.jcr4,926
dc.description.sjrqQ2
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds10,4
item.grantfulltextopen-
item.fulltextCon texto completo-
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-
Appears in Collections:Artículos
Adobe PDF (5,46 MB)
Show simple item record

Google ScholarTM

Check

Altmetric


Share



Export metadata



Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.