Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2012 |
| Outros Autores: | , |
| Idioma: | eng |
| Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
| Texto Completo: | http://hdl.handle.net/1822/25686 |
Resumo: | Due to widespread and indiscriminate use of conventional antibiotics, bacteria have acquired a resistant phenotype in response to those antimicrobials pressure. Therefore, microbial infections associated with biofilms have become hard to treat with conventional therapy. The development of microbial drug resistance and drugrelated toxicity has promoted the search for new alternatives, to control, mostly, healthcare-associated infections. Terpinen-4-ol is the major component of tea tree essential oil and has shown strong antimicrobial properties as a single agent against planktonic cultures. Colistin is an antimicrobial peptide with great antimicrobial activity, essentially against Gram-negative bacteria, such as P. aeruginosa. The aim of this study was to explore the synergism between terpinen-4-ol and colistin, using low doses of each natural antimicrobial, to control the establishment of P. aeruginosa biofilms. Biofilms were formed in the presence of both antmicrobials, alone or in combination, being after characterized by total biomass, through crystal violet, and number of cultivable bacterial cells (log CFU/cm2). Data related with the individual antimicrobial activity of terpinen-4-ol revealed that the biomass of P.aeruginosa biofilms was significantly reduced for 0.19 % (v/v), though it not affected the viability of cells even for the highest concentration tested (0.38 % (v/v)). On the other hand, colistin promoted a significantly reduction of the biofilm mass but only for concentrations higher than 1 μg ml-1. The number of viable cells entrapped within the biofilms was only affect for colistin doses higher for 4 μg ml-1. The association of terpinen-4-ol (0.19 % (v/v)) with colistin revealed to be a very efficient prophylactic strategy, as it impaired significantly biofilm formation. In fact, it was observed biofilm mass reductions closed to 100 % and significant decreases of the numbers of viable biofilm-cells (3-5 log of reduction) even for the lowest colistin concentration tested (0.5 μg ml-1). These data highlighted the promising antibiofilm activity of association of natural compounds, as antimicrobial peptides and secondary metabolites of essential oils, suggesting that this combination may have prophylactic potential for the prevention of P. aeruginosa biofilm-associated infections. |
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Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formationTerpinen-4-olAntimicrobial peptidesColistinBiofilmsProphylactic strategiesAntimicrobial synergismDue to widespread and indiscriminate use of conventional antibiotics, bacteria have acquired a resistant phenotype in response to those antimicrobials pressure. Therefore, microbial infections associated with biofilms have become hard to treat with conventional therapy. The development of microbial drug resistance and drugrelated toxicity has promoted the search for new alternatives, to control, mostly, healthcare-associated infections. Terpinen-4-ol is the major component of tea tree essential oil and has shown strong antimicrobial properties as a single agent against planktonic cultures. Colistin is an antimicrobial peptide with great antimicrobial activity, essentially against Gram-negative bacteria, such as P. aeruginosa. The aim of this study was to explore the synergism between terpinen-4-ol and colistin, using low doses of each natural antimicrobial, to control the establishment of P. aeruginosa biofilms. Biofilms were formed in the presence of both antmicrobials, alone or in combination, being after characterized by total biomass, through crystal violet, and number of cultivable bacterial cells (log CFU/cm2). Data related with the individual antimicrobial activity of terpinen-4-ol revealed that the biomass of P.aeruginosa biofilms was significantly reduced for 0.19 % (v/v), though it not affected the viability of cells even for the highest concentration tested (0.38 % (v/v)). On the other hand, colistin promoted a significantly reduction of the biofilm mass but only for concentrations higher than 1 μg ml-1. The number of viable cells entrapped within the biofilms was only affect for colistin doses higher for 4 μg ml-1. The association of terpinen-4-ol (0.19 % (v/v)) with colistin revealed to be a very efficient prophylactic strategy, as it impaired significantly biofilm formation. In fact, it was observed biofilm mass reductions closed to 100 % and significant decreases of the numbers of viable biofilm-cells (3-5 log of reduction) even for the lowest colistin concentration tested (0.5 μg ml-1). These data highlighted the promising antibiofilm activity of association of natural compounds, as antimicrobial peptides and secondary metabolites of essential oils, suggesting that this combination may have prophylactic potential for the prevention of P. aeruginosa biofilm-associated infections.International Conference on Antimicrobial Research (ICAR 2012)Universidade do MinhoCoelho, Filipa Alexandra Baltar LoboAlves, Diana Filipa BarrosPereira, Maria Olívia20122012-01-01T00:00:00Zconference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/1822/25686enginfo: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:RCAAP2024-05-11T06:32:43Zoai:repositorium.sdum.uminho.pt:1822/25686Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T15:56:37.398060Repositórios 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 |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation |
| title |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation |
| spellingShingle |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation Coelho, Filipa Alexandra Baltar Lobo Terpinen-4-ol Antimicrobial peptides Colistin Biofilms Prophylactic strategies Antimicrobial synergism |
| title_short |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation |
| title_full |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation |
| title_fullStr |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation |
| title_full_unstemmed |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation |
| title_sort |
Terpinen-4-ol combined with colistin effectively impairs Pseudomonas aeruginosa biofilm formation |
| author |
Coelho, Filipa Alexandra Baltar Lobo |
| author_facet |
Coelho, Filipa Alexandra Baltar Lobo Alves, Diana Filipa Barros Pereira, Maria Olívia |
| author_role |
author |
| author2 |
Alves, Diana Filipa Barros Pereira, Maria Olívia |
| author2_role |
author author |
| dc.contributor.none.fl_str_mv |
Universidade do Minho |
| dc.contributor.author.fl_str_mv |
Coelho, Filipa Alexandra Baltar Lobo Alves, Diana Filipa Barros Pereira, Maria Olívia |
| dc.subject.por.fl_str_mv |
Terpinen-4-ol Antimicrobial peptides Colistin Biofilms Prophylactic strategies Antimicrobial synergism |
| topic |
Terpinen-4-ol Antimicrobial peptides Colistin Biofilms Prophylactic strategies Antimicrobial synergism |
| description |
Due to widespread and indiscriminate use of conventional antibiotics, bacteria have acquired a resistant phenotype in response to those antimicrobials pressure. Therefore, microbial infections associated with biofilms have become hard to treat with conventional therapy. The development of microbial drug resistance and drugrelated toxicity has promoted the search for new alternatives, to control, mostly, healthcare-associated infections. Terpinen-4-ol is the major component of tea tree essential oil and has shown strong antimicrobial properties as a single agent against planktonic cultures. Colistin is an antimicrobial peptide with great antimicrobial activity, essentially against Gram-negative bacteria, such as P. aeruginosa. The aim of this study was to explore the synergism between terpinen-4-ol and colistin, using low doses of each natural antimicrobial, to control the establishment of P. aeruginosa biofilms. Biofilms were formed in the presence of both antmicrobials, alone or in combination, being after characterized by total biomass, through crystal violet, and number of cultivable bacterial cells (log CFU/cm2). Data related with the individual antimicrobial activity of terpinen-4-ol revealed that the biomass of P.aeruginosa biofilms was significantly reduced for 0.19 % (v/v), though it not affected the viability of cells even for the highest concentration tested (0.38 % (v/v)). On the other hand, colistin promoted a significantly reduction of the biofilm mass but only for concentrations higher than 1 μg ml-1. The number of viable cells entrapped within the biofilms was only affect for colistin doses higher for 4 μg ml-1. The association of terpinen-4-ol (0.19 % (v/v)) with colistin revealed to be a very efficient prophylactic strategy, as it impaired significantly biofilm formation. In fact, it was observed biofilm mass reductions closed to 100 % and significant decreases of the numbers of viable biofilm-cells (3-5 log of reduction) even for the lowest colistin concentration tested (0.5 μg ml-1). These data highlighted the promising antibiofilm activity of association of natural compounds, as antimicrobial peptides and secondary metabolites of essential oils, suggesting that this combination may have prophylactic potential for the prevention of P. aeruginosa biofilm-associated infections. |
| publishDate |
2012 |
| dc.date.none.fl_str_mv |
2012 2012-01-01T00:00:00Z |
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conference object |
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info:eu-repo/semantics/publishedVersion |
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publishedVersion |
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http://hdl.handle.net/1822/25686 |
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http://hdl.handle.net/1822/25686 |
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eng |
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eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
International Conference on Antimicrobial Research (ICAR 2012) |
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International Conference on Antimicrobial Research (ICAR 2012) |
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reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
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