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Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide

Staphylococcus aureus and coagulase-negative staphylococci (CoNS) have become the main causative agents of medical device-related infections due to their biofilm-forming capability, which protects them from the host’s immune system and from the action of antimicrobials. This study evaluated the abil...

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Autores principales: de Oliveira, Adilson, Pinheiro-Hubinger, Luiza, Pereira, Valéria Cataneli, Riboli, Danilo Flávio Moraes, Martins, Katheryne Benini, Romero, Letícia Calixto, da Cunha, Maria de Lourdes Ribeiro de Souza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300745/
https://www.ncbi.nlm.nih.gov/pubmed/34356800
http://dx.doi.org/10.3390/antibiotics10070879
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author de Oliveira, Adilson
Pinheiro-Hubinger, Luiza
Pereira, Valéria Cataneli
Riboli, Danilo Flávio Moraes
Martins, Katheryne Benini
Romero, Letícia Calixto
da Cunha, Maria de Lourdes Ribeiro de Souza
author_facet de Oliveira, Adilson
Pinheiro-Hubinger, Luiza
Pereira, Valéria Cataneli
Riboli, Danilo Flávio Moraes
Martins, Katheryne Benini
Romero, Letícia Calixto
da Cunha, Maria de Lourdes Ribeiro de Souza
author_sort de Oliveira, Adilson
collection PubMed
description Staphylococcus aureus and coagulase-negative staphylococci (CoNS) have become the main causative agents of medical device-related infections due to their biofilm-forming capability, which protects them from the host’s immune system and from the action of antimicrobials. This study evaluated the ability of RNA III inhibiting peptide (RIP) to inhibit biofilm formation in 10 strains isolated from clinical materials, including one S. aureus strain, two S. epidermidis, two S. haemolyticus, two S. lugdunensis, and one isolate each of the following species: S. warneri, S. hominis, and S. saprophyticus. The isolates were selected from a total of 200 strains evaluated regarding phenotypic biofilm production and the presence and expression of the ica operon. The isolates were cultured in trypticase soy broth with 2% glucose in 96-well polystyrene plates containing catheter segments in the presence and absence of RIP. The catheter segments were observed by scanning electron microscopy. The results showed inhibition of biofilm formation in the presence of RIP in all CoNS isolates; however, RIP did not interfere with biofilm formation by S. aureus. RIP is a promising tool that might be used in the future for the prevention of biofilm-related infections caused by CoNS.
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spelling pubmed-83007452021-07-24 Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide de Oliveira, Adilson Pinheiro-Hubinger, Luiza Pereira, Valéria Cataneli Riboli, Danilo Flávio Moraes Martins, Katheryne Benini Romero, Letícia Calixto da Cunha, Maria de Lourdes Ribeiro de Souza Antibiotics (Basel) Article Staphylococcus aureus and coagulase-negative staphylococci (CoNS) have become the main causative agents of medical device-related infections due to their biofilm-forming capability, which protects them from the host’s immune system and from the action of antimicrobials. This study evaluated the ability of RNA III inhibiting peptide (RIP) to inhibit biofilm formation in 10 strains isolated from clinical materials, including one S. aureus strain, two S. epidermidis, two S. haemolyticus, two S. lugdunensis, and one isolate each of the following species: S. warneri, S. hominis, and S. saprophyticus. The isolates were selected from a total of 200 strains evaluated regarding phenotypic biofilm production and the presence and expression of the ica operon. The isolates were cultured in trypticase soy broth with 2% glucose in 96-well polystyrene plates containing catheter segments in the presence and absence of RIP. The catheter segments were observed by scanning electron microscopy. The results showed inhibition of biofilm formation in the presence of RIP in all CoNS isolates; however, RIP did not interfere with biofilm formation by S. aureus. RIP is a promising tool that might be used in the future for the prevention of biofilm-related infections caused by CoNS. MDPI 2021-07-20 /pmc/articles/PMC8300745/ /pubmed/34356800 http://dx.doi.org/10.3390/antibiotics10070879 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Oliveira, Adilson
Pinheiro-Hubinger, Luiza
Pereira, Valéria Cataneli
Riboli, Danilo Flávio Moraes
Martins, Katheryne Benini
Romero, Letícia Calixto
da Cunha, Maria de Lourdes Ribeiro de Souza
Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide
title Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide
title_full Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide
title_fullStr Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide
title_full_unstemmed Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide
title_short Staphylococcal Biofilm on the Surface of Catheters: Electron Microscopy Evaluation of the Inhibition of Biofilm Growth by RNAIII Inhibiting Peptide
title_sort staphylococcal biofilm on the surface of catheters: electron microscopy evaluation of the inhibition of biofilm growth by rnaiii inhibiting peptide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300745/
https://www.ncbi.nlm.nih.gov/pubmed/34356800
http://dx.doi.org/10.3390/antibiotics10070879
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