Biofilm Localization in the Vertical Wall of Shaking 96-Well Plates

Microtiter plates with 96 wells are being increasingly used for biofilm studies due to their high throughput, low cost, easy handling, and easy application of several analytical methods to evaluate different biofilm parameters. These methods provide bulk information about the biofilm formed in each...

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Main Authors: Luciana C. Gomes, Joana M. R. Moreira, Manuel Simões, Luís F. Melo, Filipe J. Mergulhão
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:Scientifica
Online Access:http://dx.doi.org/10.1155/2014/231083
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spelling doaj-f0e3ceabd2a14a33a1a09ba8330906672020-11-25T01:11:43ZengHindawi LimitedScientifica2090-908X2014-01-01201410.1155/2014/231083231083Biofilm Localization in the Vertical Wall of Shaking 96-Well PlatesLuciana C. Gomes0Joana M. R. Moreira1Manuel Simões2Luís F. Melo3Filipe J. Mergulhão4LEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, PortugalLEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, PortugalLEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, PortugalLEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, PortugalLEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, PortugalMicrotiter plates with 96 wells are being increasingly used for biofilm studies due to their high throughput, low cost, easy handling, and easy application of several analytical methods to evaluate different biofilm parameters. These methods provide bulk information about the biofilm formed in each well but lack in detail, namely, regarding the spatial location of the biofilms. This location can be obtained by microscopy observation using optical and electron microscopes, but these techniques have lower throughput and higher cost and are subjected to equipment availability. This work describes a differential crystal violet (CV) staining method that enabled the determination of the spatial location of Escherichia coli biofilms formed in the vertical wall of shaking 96-well plates. It was shown that the biofilms were unevenly distributed on the wall with denser cell accumulation near the air-liquid interface. The results were corroborated by scanning electron microscopy and a correlation was found between biofilm accumulation and the wall shear strain rates determined by computational fluid dynamics. The developed method is quicker and less expensive and has a higher throughput than the existing methods available for spatial location of biofilms in microtiter plates.http://dx.doi.org/10.1155/2014/231083
collection DOAJ
language English
format Article
sources DOAJ
author Luciana C. Gomes
Joana M. R. Moreira
Manuel Simões
Luís F. Melo
Filipe J. Mergulhão
spellingShingle Luciana C. Gomes
Joana M. R. Moreira
Manuel Simões
Luís F. Melo
Filipe J. Mergulhão
Biofilm Localization in the Vertical Wall of Shaking 96-Well Plates
Scientifica
author_facet Luciana C. Gomes
Joana M. R. Moreira
Manuel Simões
Luís F. Melo
Filipe J. Mergulhão
author_sort Luciana C. Gomes
title Biofilm Localization in the Vertical Wall of Shaking 96-Well Plates
title_short Biofilm Localization in the Vertical Wall of Shaking 96-Well Plates
title_full Biofilm Localization in the Vertical Wall of Shaking 96-Well Plates
title_fullStr Biofilm Localization in the Vertical Wall of Shaking 96-Well Plates
title_full_unstemmed Biofilm Localization in the Vertical Wall of Shaking 96-Well Plates
title_sort biofilm localization in the vertical wall of shaking 96-well plates
publisher Hindawi Limited
series Scientifica
issn 2090-908X
publishDate 2014-01-01
description Microtiter plates with 96 wells are being increasingly used for biofilm studies due to their high throughput, low cost, easy handling, and easy application of several analytical methods to evaluate different biofilm parameters. These methods provide bulk information about the biofilm formed in each well but lack in detail, namely, regarding the spatial location of the biofilms. This location can be obtained by microscopy observation using optical and electron microscopes, but these techniques have lower throughput and higher cost and are subjected to equipment availability. This work describes a differential crystal violet (CV) staining method that enabled the determination of the spatial location of Escherichia coli biofilms formed in the vertical wall of shaking 96-well plates. It was shown that the biofilms were unevenly distributed on the wall with denser cell accumulation near the air-liquid interface. The results were corroborated by scanning electron microscopy and a correlation was found between biofilm accumulation and the wall shear strain rates determined by computational fluid dynamics. The developed method is quicker and less expensive and has a higher throughput than the existing methods available for spatial location of biofilms in microtiter plates.
url http://dx.doi.org/10.1155/2014/231083
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