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Determining the Targets of Fluopsin C Action on Gram-Negative and Gram-Positive Bacteria

dc.contributor.authorPerez Navarro, Miguel Octavio
dc.contributor.authorDilarri, Guilherme [UNESP]
dc.contributor.authorSimionato, Ane Stefano
dc.contributor.authorGrzegorczyk, Kathlen
dc.contributor.authorDealis, Mickely Liuti
dc.contributor.authorCano, Barbara Gionco
dc.contributor.authorBarazetti, Andre Riedi
dc.contributor.authorAfonso, Leandro
dc.contributor.authorChryssafidis, Andreas Lazaros
dc.contributor.authorFerreira, Henrique [UNESP]
dc.contributor.authorAndrade, Galdino
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv Estado Santa Catarina
dc.date.accessioned2020-12-10T20:03:24Z
dc.date.available2020-12-10T20:03:24Z
dc.date.issued2020-06-04
dc.description.abstractThe antibiotic activity of metalloantibiotic compounds has been evaluated since the 90s, and many different modes of action were characterized. In the last decade, the effects of secondary metabolites produced byPseudomonas aeruginosaLV strain, including a cupric compound identified as Fluopsin C, were tested against many pathogenic bacteria strains, proving their high antibiotic activity. In the present study, the bactericidal mechanisms of action of Fluopsin C and the semi-purified fraction F4A were elucidated. The results found in electron microscopy [scanning electron microscopy (SEM) and transmission electronic microscopy (TEM)] demonstrated that both Fluopsin C and F4A are affecting the cytoplasmatic membrane of Gram-positive and Gram-negative bacteria. These results were confirmed by fluorescence microscopy, where these bacteria presented permeabilization of their cytoplasmatic membranes after contact with the semi-purified fraction and pure compound. Using electronic and fluorescence microscopy, along with bacterial mutant strains with marked divisional septum, the membrane was defined as the primary target of Fluopsin C in the tested bacteria.en
dc.description.affiliationUniv Estadual Londrina, Dept Microbiol, Microbial Ecol Lab, Londrina, Parana, Brazil
dc.description.affiliationUniv Estadual Paulista, Inst Biosci, Dept Biochem & Microbiol, Rio Claro, Brazil
dc.description.affiliationUniv Estado Santa Catarina, Ctr Agrovet Sci, Dept Vet Med, Lages, SC, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biosci, Dept Biochem & Microbiol, Rio Claro, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipAraucaria Foundation
dc.format.extent11
dc.identifierhttp://dx.doi.org/10.3389/fmicb.2020.01076
dc.identifier.citationFrontiers In Microbiology. Lausanne: Frontiers Media Sa, v. 11, 11 p., 2020.
dc.identifier.doi10.3389/fmicb.2020.01076
dc.identifier.issn1664-302X
dc.identifier.urihttp://hdl.handle.net/11449/197012
dc.identifier.wosWOS:000543335100001
dc.language.isoeng
dc.publisherFrontiers Media Sa
dc.relation.ispartofFrontiers In Microbiology
dc.sourceWeb of Science
dc.subjectbactericidal mechanism of action
dc.subjectXanthomonas
dc.subjectKPC
dc.subjectMRSA
dc.subjectelectronic microscopy
dc.subjectfluorescence microscopy
dc.titleDetermining the Targets of Fluopsin C Action on Gram-Negative and Gram-Positive Bacteriaen
dc.typeArtigo
dcterms.rightsHolderFrontiers Media Sa
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Rio Claropt
unesp.departmentBioquímica e Microbiologia - IBpt

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