Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , |
Idioma: | eng |
Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Texto Completo: | http://hdl.handle.net/1822/26047 |
Resumo: | Medical device-associated infections caused by pathogens such as Staphylococcus epidermidis might involve biofilm formation and those are particularly challenging. The involvement of antibiotic resistant Staphylococci, exacerbates the problem. Rifampicin cannot be used as a single agent to treat infections because of the rapid selection of resistant mutants. However, combinations of rifampicin with other anti-staphylococcal agents could prevent the emergence of rifampicin resistance during therapy. N-acetylcisteine (NAC) decreases biofilm formation by a variety of bacteria and reduces the production of extracellular polysaccharide matrix. The goal of this study was to assess the antimicrobial activity of NAC in combination with rifampicin against biofilm of S. epidermidis. Two S. epidermidis strains biofilm-producing (9142 and 1457) were used in this study. 1xMIC (4mg/ml) and 10xMIC (40mg/ml) of NAC and 10mg/l of rifampicin, based on preliminary in vitro data, were added to 24h biofilm cells. Biofilm susceptibility to tested antimicrobial agents was assessed through scanning electron microscopy, crystal violet staining (total biofilm biomass) and cellular viability through XTT and colony forming units (CFU). The effect of NAC 1xMIC was similar to that of the control. Rifampicin, NAC 10xMIC alone and NAC-rifampicin combination (independently of NAC concentration used) showed significant bactericidal effect, promoting a 3-4 log10 decrease in biofilm cells. In conclusion, the results didn’t point to any synergistic effect between the two agents. Nevertheless, NAC seems to be a possible alternative to antibiotics in the treatment of infections associated to S. epidermidis biofilm. |
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Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilmsMedical device-associated infections caused by pathogens such as Staphylococcus epidermidis might involve biofilm formation and those are particularly challenging. The involvement of antibiotic resistant Staphylococci, exacerbates the problem. Rifampicin cannot be used as a single agent to treat infections because of the rapid selection of resistant mutants. However, combinations of rifampicin with other anti-staphylococcal agents could prevent the emergence of rifampicin resistance during therapy. N-acetylcisteine (NAC) decreases biofilm formation by a variety of bacteria and reduces the production of extracellular polysaccharide matrix. The goal of this study was to assess the antimicrobial activity of NAC in combination with rifampicin against biofilm of S. epidermidis. Two S. epidermidis strains biofilm-producing (9142 and 1457) were used in this study. 1xMIC (4mg/ml) and 10xMIC (40mg/ml) of NAC and 10mg/l of rifampicin, based on preliminary in vitro data, were added to 24h biofilm cells. Biofilm susceptibility to tested antimicrobial agents was assessed through scanning electron microscopy, crystal violet staining (total biofilm biomass) and cellular viability through XTT and colony forming units (CFU). The effect of NAC 1xMIC was similar to that of the control. Rifampicin, NAC 10xMIC alone and NAC-rifampicin combination (independently of NAC concentration used) showed significant bactericidal effect, promoting a 3-4 log10 decrease in biofilm cells. In conclusion, the results didn’t point to any synergistic effect between the two agents. Nevertheless, NAC seems to be a possible alternative to antibiotics in the treatment of infections associated to S. epidermidis biofilm.University of SouthamptonUniversidade do MinhoLeite, BrunaGomes, F. I.Teixeira, P.Souza, ClovisPizzolitto, ElisabethOliveira, Rosário20102010-01-01T00:00:00Zconference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/1822/26047enginfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-11T07:30:12Zoai:repositorium.sdum.uminho.pt:1822/26047Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T16:29:14.536454Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms |
title |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms |
spellingShingle |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms Leite, Bruna |
title_short |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms |
title_full |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms |
title_fullStr |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms |
title_full_unstemmed |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms |
title_sort |
Effect of N-Acetylcysteine alone and in combination with rifampicin on Staphylococcus epidermidis biofilms |
author |
Leite, Bruna |
author_facet |
Leite, Bruna Gomes, F. I. Teixeira, P. Souza, Clovis Pizzolitto, Elisabeth Oliveira, Rosário |
author_role |
author |
author2 |
Gomes, F. I. Teixeira, P. Souza, Clovis Pizzolitto, Elisabeth Oliveira, Rosário |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Leite, Bruna Gomes, F. I. Teixeira, P. Souza, Clovis Pizzolitto, Elisabeth Oliveira, Rosário |
description |
Medical device-associated infections caused by pathogens such as Staphylococcus epidermidis might involve biofilm formation and those are particularly challenging. The involvement of antibiotic resistant Staphylococci, exacerbates the problem. Rifampicin cannot be used as a single agent to treat infections because of the rapid selection of resistant mutants. However, combinations of rifampicin with other anti-staphylococcal agents could prevent the emergence of rifampicin resistance during therapy. N-acetylcisteine (NAC) decreases biofilm formation by a variety of bacteria and reduces the production of extracellular polysaccharide matrix. The goal of this study was to assess the antimicrobial activity of NAC in combination with rifampicin against biofilm of S. epidermidis. Two S. epidermidis strains biofilm-producing (9142 and 1457) were used in this study. 1xMIC (4mg/ml) and 10xMIC (40mg/ml) of NAC and 10mg/l of rifampicin, based on preliminary in vitro data, were added to 24h biofilm cells. Biofilm susceptibility to tested antimicrobial agents was assessed through scanning electron microscopy, crystal violet staining (total biofilm biomass) and cellular viability through XTT and colony forming units (CFU). The effect of NAC 1xMIC was similar to that of the control. Rifampicin, NAC 10xMIC alone and NAC-rifampicin combination (independently of NAC concentration used) showed significant bactericidal effect, promoting a 3-4 log10 decrease in biofilm cells. In conclusion, the results didn’t point to any synergistic effect between the two agents. Nevertheless, NAC seems to be a possible alternative to antibiotics in the treatment of infections associated to S. epidermidis biofilm. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010 2010-01-01T00:00:00Z |
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conference object |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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publishedVersion |
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http://hdl.handle.net/1822/26047 |
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http://hdl.handle.net/1822/26047 |
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eng |
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eng |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
University of Southampton |
publisher.none.fl_str_mv |
University of Southampton |
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