Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCR

Multispecies biofilms are an important healthcare problem and may lead to persistent infections. These infections are difficult to treat, as cells in a biofilm are highly resistant to antimicrobial agents. While increasingly being recognized as important, the properties of multispecies biofilms rema...

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Main Authors: Sarah Tavernier, Tom Coenye
Format: Article
Language:English
Published: PeerJ Inc. 2015-02-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/787.pdf
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author Sarah Tavernier
Tom Coenye
author_facet Sarah Tavernier
Tom Coenye
author_sort Sarah Tavernier
collection DOAJ
description Multispecies biofilms are an important healthcare problem and may lead to persistent infections. These infections are difficult to treat, as cells in a biofilm are highly resistant to antimicrobial agents. While increasingly being recognized as important, the properties of multispecies biofilms remain poorly studied. In order to do so, the quantification of the individual species is needed. The current cultivation-based approaches can lead to an underestimation of the actual cell number and are time-consuming. In the present study we set up a culture-independent approach based on propidium monoazide qPCR (PMA-qPCR) to quantify Pseudomonas aeruginosa in a multispecies biofilm. As a proof of concept, we explored the influence of the combined presence of Staphylococcus aureus, Streptococcus anginosus and Burkholderia cenocepacia on the antimicrobial susceptibility of P. aeruginosa using this PMA-qPCR approach.
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spelling doaj.art-53d4e83cbd2e4276994a1b1d2b0c846a2023-12-03T10:14:41ZengPeerJ Inc.PeerJ2167-83592015-02-013e78710.7717/peerj.787787Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCRSarah Tavernier0Tom Coenye1Laboratory of Pharmaceutical Microbiology, Ghent University, Ghent, BelgiumLaboratory of Pharmaceutical Microbiology, Ghent University, Ghent, BelgiumMultispecies biofilms are an important healthcare problem and may lead to persistent infections. These infections are difficult to treat, as cells in a biofilm are highly resistant to antimicrobial agents. While increasingly being recognized as important, the properties of multispecies biofilms remain poorly studied. In order to do so, the quantification of the individual species is needed. The current cultivation-based approaches can lead to an underestimation of the actual cell number and are time-consuming. In the present study we set up a culture-independent approach based on propidium monoazide qPCR (PMA-qPCR) to quantify Pseudomonas aeruginosa in a multispecies biofilm. As a proof of concept, we explored the influence of the combined presence of Staphylococcus aureus, Streptococcus anginosus and Burkholderia cenocepacia on the antimicrobial susceptibility of P. aeruginosa using this PMA-qPCR approach.https://peerj.com/articles/787.pdfBiofilm Pseudomonas aeruginosa ResistancePMA-qPCR
spellingShingle Sarah Tavernier
Tom Coenye
Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCR
PeerJ
Biofilm
Pseudomonas aeruginosa
Resistance
PMA-qPCR
title Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCR
title_full Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCR
title_fullStr Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCR
title_full_unstemmed Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCR
title_short Quantification of Pseudomonas aeruginosa in multispecies biofilms using PMA-qPCR
title_sort quantification of pseudomonas aeruginosa in multispecies biofilms using pma qpcr
topic Biofilm
Pseudomonas aeruginosa
Resistance
PMA-qPCR
url https://peerj.com/articles/787.pdf
work_keys_str_mv AT sarahtavernier quantificationofpseudomonasaeruginosainmultispeciesbiofilmsusingpmaqpcr
AT tomcoenye quantificationofpseudomonasaeruginosainmultispeciesbiofilmsusingpmaqpcr