Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms

Detalhes bibliográficos
Autor(a) principal: Akturk, Ergun
Data de Publicação: 2019
Outros Autores: Melo, Luís Daniel Rodrigues, Oliveira, Hugo Alexandre Mendes, Santos, Sílvio Roberto Branco, Azeredo, Joana
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/1822/63982
Resumo: Bacteria-associated polymicrobial biofilms are sessile microbial aggregates of different species adhered to surfaces and encased in a self-produced extracellular polymeric matrix, which shows a high degree of tolerance/resistance to disinfection by chemicals, antibiotics, and to the human immune system. Pseudomonas aeruginosa and Staphylococcus aureus are versatile bacterial pathogens and common etiological agents of several chronic infections, namely otitis media, oral infections, surgical-side infections, diabetic foot ulcers, and cystic fibrosis. In this study we aimed at assessing the efficacy of phages (vB_PaM_EPA1) to control P. aeruginosa and S. aureus polymicrobial biofilms, alone and combined with Gentamicin (GEN). The phage and the antibiotic were simultaneously or sequentially combined and added to 48 hours-old biofilms. After 24 hours treatment the number of viable cells were enumerated by CFU counting and observed under confocal laser microscopy with fluorescence probes. Probes were designed to specifically target the bacterial species and consists of a recombinant tail fibre protein P. aeruginosa-specific fused to mCherry (mCherry+TFP) and a cell wall binding domain of a phage endolysin, S. aureus specific, fused to GFP (GFP+CBD). Results showed that phage-drug combinations greatly reduced the number of P. aeruginosa viable cells, ranging from 4.06 to 6.32 orders-of-magnitude. The best treatment outcome was observed with sequential treatment by combing first EPA1 and then GEN. Overall, our results support the phenomenon that combination of phages and antibiotics are very effective against P. aeruginosa in dual-species biofilms when applied sequentially, and this constitutes a good strategy to control biofilm-associated infections.
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spelling Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilmsBacteria-associated polymicrobial biofilms are sessile microbial aggregates of different species adhered to surfaces and encased in a self-produced extracellular polymeric matrix, which shows a high degree of tolerance/resistance to disinfection by chemicals, antibiotics, and to the human immune system. Pseudomonas aeruginosa and Staphylococcus aureus are versatile bacterial pathogens and common etiological agents of several chronic infections, namely otitis media, oral infections, surgical-side infections, diabetic foot ulcers, and cystic fibrosis. In this study we aimed at assessing the efficacy of phages (vB_PaM_EPA1) to control P. aeruginosa and S. aureus polymicrobial biofilms, alone and combined with Gentamicin (GEN). The phage and the antibiotic were simultaneously or sequentially combined and added to 48 hours-old biofilms. After 24 hours treatment the number of viable cells were enumerated by CFU counting and observed under confocal laser microscopy with fluorescence probes. Probes were designed to specifically target the bacterial species and consists of a recombinant tail fibre protein P. aeruginosa-specific fused to mCherry (mCherry+TFP) and a cell wall binding domain of a phage endolysin, S. aureus specific, fused to GFP (GFP+CBD). Results showed that phage-drug combinations greatly reduced the number of P. aeruginosa viable cells, ranging from 4.06 to 6.32 orders-of-magnitude. The best treatment outcome was observed with sequential treatment by combing first EPA1 and then GEN. Overall, our results support the phenomenon that combination of phages and antibiotics are very effective against P. aeruginosa in dual-species biofilms when applied sequentially, and this constitutes a good strategy to control biofilm-associated infections.This study was supported by FCT under the scope of the strategic funding of UID/BIO/04469/2013 unit and COMPETE 2020 (POCI-01-0145-FEDER-006684) and the Project PTDC/BBB-BSS/6471/2014 (FEDER: POCI-01-0145-FEDER-016643) and also supported by BioTecNorte operation (NORTE-01-0145-FEDER-000004) funded by the European Regional Development Fund under the scope of Norte2020 - Programa Operacional Regional do Norte. EA acknowledge FCT for the funding through grant PD/BD/135254/2017.info:eu-repo/semantics/publishedVersionUniversidade do MinhoAkturk, ErgunMelo, Luís Daniel RodriguesOliveira, Hugo Alexandre MendesSantos, Sílvio Roberto BrancoAzeredo, Joana2019-08-042019-08-04T00:00:00Zconference posterinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/1822/63982engAkturk, Ergun; Melo, Luís D. R.; Oliveira, Hugo; Santos, Sílvio B.; Azeredo, Joana, Interaction of Phage and Gentamicin Combinations in Pseudomonas aeruginosa and Staphylococcus aureus Polymicrobial Biofilms. 23rd Biennial Evergreen International Phage Meeting. Olympia, USA, Aug 4-9, 190, 2019.10.13140/RG.2.2.32064.48649blogs.evergreen.edu/phage/about/meetings/2019-2/info: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:RCAAP2024-05-11T04:31:09Zoai:repositorium.sdum.uminho.pt:1822/63982Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:50:48.039271Repositórios 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 Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
title Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
spellingShingle Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
Akturk, Ergun
title_short Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
title_full Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
title_fullStr Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
title_full_unstemmed Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
title_sort Interaction of phage and gentamicin combinations in Pseudomonas aeruginosa and Staphylococcus aureus polymicrobial biofilms
author Akturk, Ergun
author_facet Akturk, Ergun
Melo, Luís Daniel Rodrigues
Oliveira, Hugo Alexandre Mendes
Santos, Sílvio Roberto Branco
Azeredo, Joana
author_role author
author2 Melo, Luís Daniel Rodrigues
Oliveira, Hugo Alexandre Mendes
Santos, Sílvio Roberto Branco
Azeredo, Joana
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Akturk, Ergun
Melo, Luís Daniel Rodrigues
Oliveira, Hugo Alexandre Mendes
Santos, Sílvio Roberto Branco
Azeredo, Joana
description Bacteria-associated polymicrobial biofilms are sessile microbial aggregates of different species adhered to surfaces and encased in a self-produced extracellular polymeric matrix, which shows a high degree of tolerance/resistance to disinfection by chemicals, antibiotics, and to the human immune system. Pseudomonas aeruginosa and Staphylococcus aureus are versatile bacterial pathogens and common etiological agents of several chronic infections, namely otitis media, oral infections, surgical-side infections, diabetic foot ulcers, and cystic fibrosis. In this study we aimed at assessing the efficacy of phages (vB_PaM_EPA1) to control P. aeruginosa and S. aureus polymicrobial biofilms, alone and combined with Gentamicin (GEN). The phage and the antibiotic were simultaneously or sequentially combined and added to 48 hours-old biofilms. After 24 hours treatment the number of viable cells were enumerated by CFU counting and observed under confocal laser microscopy with fluorescence probes. Probes were designed to specifically target the bacterial species and consists of a recombinant tail fibre protein P. aeruginosa-specific fused to mCherry (mCherry+TFP) and a cell wall binding domain of a phage endolysin, S. aureus specific, fused to GFP (GFP+CBD). Results showed that phage-drug combinations greatly reduced the number of P. aeruginosa viable cells, ranging from 4.06 to 6.32 orders-of-magnitude. The best treatment outcome was observed with sequential treatment by combing first EPA1 and then GEN. Overall, our results support the phenomenon that combination of phages and antibiotics are very effective against P. aeruginosa in dual-species biofilms when applied sequentially, and this constitutes a good strategy to control biofilm-associated infections.
publishDate 2019
dc.date.none.fl_str_mv 2019-08-04
2019-08-04T00:00:00Z
dc.type.driver.fl_str_mv conference poster
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/63982
url http://hdl.handle.net/1822/63982
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Akturk, Ergun; Melo, Luís D. R.; Oliveira, Hugo; Santos, Sílvio B.; Azeredo, Joana, Interaction of Phage and Gentamicin Combinations in Pseudomonas aeruginosa and Staphylococcus aureus Polymicrobial Biofilms. 23rd Biennial Evergreen International Phage Meeting. Olympia, USA, Aug 4-9, 190, 2019.
10.13140/RG.2.2.32064.48649
blogs.evergreen.edu/phage/about/meetings/2019-2/
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
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