Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/136232
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dc.creatorMonteiro, C
dc.creatorCosta, F
dc.creatorPirttilä, A
dc.creatorTejesvi, M
dc.creatorMartins, MCL
dc.date.accessioned2021-09-20T10:52:11Z-
dc.date.available2021-09-20T10:52:11Z-
dc.date.issued2019
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/10216/136232-
dc.description.abstractUrinary catheters are extensively used in hospitals, being responsible for about 75% of hospital-acquired infections. In this work, a de novo designed antimicrobial peptide (AMP) Chain201D was studied in the context of urinary catheter-associated infections. Chain201D showed excellent antimicrobial activity against relevant ATCC strains and clinical isolates of bacteria and yeast and demonstrated high stability in a wide range of temperatures, pH and salt concentrations. Moreover, the bactericidal activity of Chain201D immobilized on a model surface was studied against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), some of the most prevalent strains found in urinary catheter-associated infections. Chain201D was successfully tethered to ((1-mercapto-11-undecyl)-(tetra(ethylene glycol) (EG4)) terminated self-assembled monolayers (SAMs), (EG4-SAMs), activated by 1,1'-Carbonyldiimidazole (CDI) at different concentrations. Chain201D surfaces can bind and kill by contact a high percentage of adherent bacteria. These achievements are obtained without any peptide modification (for chemoselective conjugation) and without the use of a spacer. Moreover, increased amounts of immobilized AMP lead to higher numbers of adhered/dead bacteria, revealing a concentration-dependent behaviour and demonstrating that Chain201D has excellent potential for developing antimicrobial urinary catheters.
dc.description.sponsorshipAntINFECT: Bioengineered Advanced Therapies for Problematic Infected Wounds POCI-01-0145-FEDER-031781) and Institute for Research and Innovation in Health Sciences (UID/BIM/04293/2019). C. Monteiro would like to acknowledge national funding through FCT – Fundação para a Ciência e a Tecnologia, I.P., provided by the contract-program and according to numbers 4, 5 and 6 of art. 23 of Law no. 57/2016 of 29th August, as amended by Law no. 57/2017 of 19th July. Professor Paula Gomes from Faculdade de Ciências da Universidade do Porto (FC-UP), Porto Peptide Synthesis Facility (POP-UP) for CEM 7 peptide. The funding received from Tekes, Finland (3331/31/2014) is thankfully acknowledged.
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofScientific Reports, vol.9(1):10753
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.meshAnti-Infective Agents / therapeutic use
dc.subject.meshAntimicrobial Cationic Peptides / therapeutic use
dc.subject.meshCatheter-Related Infections / prevention & control
dc.subject.meshEndophytes / chemistry
dc.subject.meshEricaceae / chemistry
dc.subject.meshEscherichia coli / drug effects
dc.subject.meshHumans
dc.subject.meshKlebsiella pneumoniae / drug effects
dc.subject.meshMicrobial Sensitivity Tests
dc.subject.meshPseudomonas aeruginosa / drug effects
dc.subject.meshStaphylococcus aureus / drug effects
dc.subject.meshUrinary Catheterization / adverse effects
dc.subject.meshUrinary Catheterization / methods
dc.subject.meshUrinary Catheters / adverse effects
dc.subject.meshUrinary Catheters / microbiology
dc.titlePrevention of urinary catheter-associated infections by coating antimicrobial peptides from crowberry endophytes
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.1038/s41598-019-47108-5
dc.relation.publisherversionhttps://www.nature.com/articles/s41598-019-47108-5
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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