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Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia

Superantigens are proteins comprising a group of molecules produced by various microorganisms. They are involved in pathogenesis of several human diseases. The aim of the study was the comparison of susceptibility to antibiotics and antimicrobial peptides (AMPs) of Staphylococcus aureus (SA) strains...

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Autores principales: Baranska-Rybak, Wioletta, Cirioni, Oscar, Dawgul, Malgorzata, Sokolowska-Wojdylo, Malgorzata, Naumiuk, Lukasz, Szczerkowska-Dobosz, Aneta, Nowicki, Roman, Roszkiewicz, Jadwiga, Kamysz, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265250/
https://www.ncbi.nlm.nih.gov/pubmed/22312551
http://dx.doi.org/10.1155/2011/270932
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author Baranska-Rybak, Wioletta
Cirioni, Oscar
Dawgul, Malgorzata
Sokolowska-Wojdylo, Malgorzata
Naumiuk, Lukasz
Szczerkowska-Dobosz, Aneta
Nowicki, Roman
Roszkiewicz, Jadwiga
Kamysz, Wojciech
author_facet Baranska-Rybak, Wioletta
Cirioni, Oscar
Dawgul, Malgorzata
Sokolowska-Wojdylo, Malgorzata
Naumiuk, Lukasz
Szczerkowska-Dobosz, Aneta
Nowicki, Roman
Roszkiewicz, Jadwiga
Kamysz, Wojciech
author_sort Baranska-Rybak, Wioletta
collection PubMed
description Superantigens are proteins comprising a group of molecules produced by various microorganisms. They are involved in pathogenesis of several human diseases. The aim of the study was the comparison of susceptibility to antibiotics and antimicrobial peptides (AMPs) of Staphylococcus aureus (SA) strains producing staphylococcal enterotoxins SEA, SEB, SEC, SED, and TSST-1 and nonproducing ones. In the group of the total 28 of the patients with erythrodermia the presence of SA was confirmed in 24 cases. The total of 14 strains of SA excreted enterotoxins SEA, SEC, SED, and TSST-1. We did not observe that strains producing mentioned superantigens were less susceptible to AMPs (aurein 1.2, citropin 1.1, lipopeptide, protegrin 1, tachyplesin 3, temporin A, and uperin 3.6). The opposite situation was observed in conventional antibiotics. SA strains excreting tested superantigens had higher MICs and MBCs than nonproducing ones. The interesting finding considering the high efficacy of AMPs, against all examined strains of SA, makes them attractive candidates for therapeutic implication.
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spelling pubmed-32652502012-02-06 Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia Baranska-Rybak, Wioletta Cirioni, Oscar Dawgul, Malgorzata Sokolowska-Wojdylo, Malgorzata Naumiuk, Lukasz Szczerkowska-Dobosz, Aneta Nowicki, Roman Roszkiewicz, Jadwiga Kamysz, Wojciech Chemother Res Pract Research Article Superantigens are proteins comprising a group of molecules produced by various microorganisms. They are involved in pathogenesis of several human diseases. The aim of the study was the comparison of susceptibility to antibiotics and antimicrobial peptides (AMPs) of Staphylococcus aureus (SA) strains producing staphylococcal enterotoxins SEA, SEB, SEC, SED, and TSST-1 and nonproducing ones. In the group of the total 28 of the patients with erythrodermia the presence of SA was confirmed in 24 cases. The total of 14 strains of SA excreted enterotoxins SEA, SEC, SED, and TSST-1. We did not observe that strains producing mentioned superantigens were less susceptible to AMPs (aurein 1.2, citropin 1.1, lipopeptide, protegrin 1, tachyplesin 3, temporin A, and uperin 3.6). The opposite situation was observed in conventional antibiotics. SA strains excreting tested superantigens had higher MICs and MBCs than nonproducing ones. The interesting finding considering the high efficacy of AMPs, against all examined strains of SA, makes them attractive candidates for therapeutic implication. Hindawi Publishing Corporation 2011 2011-05-12 /pmc/articles/PMC3265250/ /pubmed/22312551 http://dx.doi.org/10.1155/2011/270932 Text en Copyright © 2011 Wioletta Baranska-Rybak et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Baranska-Rybak, Wioletta
Cirioni, Oscar
Dawgul, Malgorzata
Sokolowska-Wojdylo, Malgorzata
Naumiuk, Lukasz
Szczerkowska-Dobosz, Aneta
Nowicki, Roman
Roszkiewicz, Jadwiga
Kamysz, Wojciech
Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia
title Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia
title_full Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia
title_fullStr Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia
title_full_unstemmed Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia
title_short Activity of Antimicrobial Peptides and Conventional Antibiotics against Superantigen Positive Staphylococcus aureus Isolated from the Patients with Neoplastic and Inflammatory Erythrodermia
title_sort activity of antimicrobial peptides and conventional antibiotics against superantigen positive staphylococcus aureus isolated from the patients with neoplastic and inflammatory erythrodermia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265250/
https://www.ncbi.nlm.nih.gov/pubmed/22312551
http://dx.doi.org/10.1155/2011/270932
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