Bacteriophage cocktail-mediated inhibition of Pseudomonas aeruginosa biofilm on endotracheal tube surface

dc.commentsCEB54122por
dc.contributor.authorOliveira, Viviane C.por
dc.contributor.authorMacedo, Ana P.por
dc.contributor.authorMelo, Luís Daniel Rodriguespor
dc.contributor.authorSantos, Sílvio Roberto Brancopor
dc.contributor.authorHermann, Paula R. S.por
dc.contributor.authorSilva-Lovato, Cláudia H.por
dc.contributor.authorParanhos, Helena F. O.por
dc.contributor.authorAndrade, Denisepor
dc.contributor.authorWatanabe, Evandropor
dc.date.accessioned2021-03-19T10:29:49Z
dc.date.available2021-03-19T10:29:49Z
dc.date.issued2021
dc.date.updated2021-02-15T17:00:06Z
dc.description.abstractAlthough different strategies to control biofilm formation on endotracheal tubes have been proposed, there are scarce scientific data on applying phages for both removing and preventing Pseudomonas aeruginosa biofilms on the device surface. Here, the anti-biofilm capacity of five bacteriophages was evaluated by a high content screening assay. We observed that biofilms were significantly reduced after phage treatment, especially in multidrug-resistant strains. Considering the anti-biofilm screens, two phages were selected as cocktail components, and the cocktail’s ability to prevent colonization of the endotracheal tube surface was tested in a dynamic biofilm model. Phage-coated tubes were challenged with different P. aeruginosa strains. The biofilm growth was monitored from 24 to 168 h by colony forming unit counting, metabolic activity assessment, and biofilm morphology observation. The phage cocktail promoted differences of bacterial colonization; nonetheless, the action was strain dependent. Phage cocktail coating did not promote substantial changes in metabolic activity. Scanning electron microscopy revealed a higher concentration of biofilm cells in control, while tower-like structures could be observed on phage cocktail-coated tubes. These results demonstrate that with the development of new coating strategies, phage therapy has potential in controlling the endotracheal tube-associated biofilm.por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion
dc.description.sponsorshipThis work was supported by the São Paulo Research Foundation (FAPESP) under the grants 2018/09757-0, 2019/13271-9 and 2020/03405-5, as well as the National Council for Scientific and Technological Development (CNPq) under the grant 405622/2018-0.por
dc.distributioninternationalpor
dc.identifier.citationOliveira, Viviane C.; Macedo, Ana P.; Melo, Luís Daniel Rodrigues; Santos, Sílvio Roberto Branco; Hermann, Paula R. S.; Silva-Lovato, Cláudia H.; Paranhos, Helena F. O.; Andrade, Denise; Watanabe, Evandro, Bacteriophage cocktail-mediated inhibition of Pseudomonas aeruginosa biofilm on endotracheal tube surface. Antibiotics, 10(1), 78-78, 2021por
dc.identifier.doi10.3390/antibiotics10010078por
dc.identifier.eissn2079-6382por
dc.identifier.issn2079-6382por
dc.identifier.urihttps://hdl.handle.net/1822/70860
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherMDPIpor
dc.relation.publisherversionhttps://www.mdpi.com/2079-6382/10/1/78por
dc.rightsopenAccesspor
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/por
dc.subjectbacteriophagepor
dc.subjectbiofilmpor
dc.subjectPseudomonas aeruginosapor
dc.subjectendotracheal tubepor
dc.subject.wosScience & Technologypor
dc.titleBacteriophage cocktail-mediated inhibition of Pseudomonas aeruginosa biofilm on endotracheal tube surfacepor
dc.typearticle
dspace.entity.typePublicationen
oaire.citationConferencePlaceBasel, Switzerland
oaire.citationEndPage78por
oaire.citationIssue1por
oaire.citationStartPage78por
oaire.citationVolume10por
oaire.versionVoRpor
sdum.journalAntibioticspor

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