A microscope automated fluidic system to study bacterial processes in real time.
Most time lapse microscopy experiments studying bacterial processes ie growth, progression through the cell cycle and motility have been performed on thin nutrient agar pads. An important limitation of this approach is that dynamic perturbations of the experimental conditions cannot be easily perfor...
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2009-09-01
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doaj-3adeeccc04e74eef874e428940ab83462020-11-25T00:24:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-09-0149e728210.1371/journal.pone.0007282A microscope automated fluidic system to study bacterial processes in real time.Adrien DucretEtienne MaisonneuvePhilippe NotareschiAlain GrossiTâm MignotSam DukanMost time lapse microscopy experiments studying bacterial processes ie growth, progression through the cell cycle and motility have been performed on thin nutrient agar pads. An important limitation of this approach is that dynamic perturbations of the experimental conditions cannot be easily performed. In eukaryotic cell biology, fluidic approaches have been largely used to study the impact of rapid environmental perturbations on live cells and in real time. However, all these approaches are not easily applicable to bacterial cells because the substrata are in all cases specific and also because microfluidics nanotechnology requires a complex lithography for the study of micrometer sized bacterial cells. In fact, in many cases agar is the experimental solid substratum on which bacteria can move or even grow. For these reasons, we designed a novel hybrid micro fluidic device that combines a thin agar pad and a custom flow chamber. By studying several examples, we show that this system allows real time analysis of a broad array of biological processes such as growth, development and motility. Thus, the flow chamber system will be an essential tool to study any process that take place on an agar surface at the single cell level.http://europepmc.org/articles/PMC2748647?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Adrien Ducret Etienne Maisonneuve Philippe Notareschi Alain Grossi Tâm Mignot Sam Dukan |
spellingShingle |
Adrien Ducret Etienne Maisonneuve Philippe Notareschi Alain Grossi Tâm Mignot Sam Dukan A microscope automated fluidic system to study bacterial processes in real time. PLoS ONE |
author_facet |
Adrien Ducret Etienne Maisonneuve Philippe Notareschi Alain Grossi Tâm Mignot Sam Dukan |
author_sort |
Adrien Ducret |
title |
A microscope automated fluidic system to study bacterial processes in real time. |
title_short |
A microscope automated fluidic system to study bacterial processes in real time. |
title_full |
A microscope automated fluidic system to study bacterial processes in real time. |
title_fullStr |
A microscope automated fluidic system to study bacterial processes in real time. |
title_full_unstemmed |
A microscope automated fluidic system to study bacterial processes in real time. |
title_sort |
microscope automated fluidic system to study bacterial processes in real time. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2009-09-01 |
description |
Most time lapse microscopy experiments studying bacterial processes ie growth, progression through the cell cycle and motility have been performed on thin nutrient agar pads. An important limitation of this approach is that dynamic perturbations of the experimental conditions cannot be easily performed. In eukaryotic cell biology, fluidic approaches have been largely used to study the impact of rapid environmental perturbations on live cells and in real time. However, all these approaches are not easily applicable to bacterial cells because the substrata are in all cases specific and also because microfluidics nanotechnology requires a complex lithography for the study of micrometer sized bacterial cells. In fact, in many cases agar is the experimental solid substratum on which bacteria can move or even grow. For these reasons, we designed a novel hybrid micro fluidic device that combines a thin agar pad and a custom flow chamber. By studying several examples, we show that this system allows real time analysis of a broad array of biological processes such as growth, development and motility. Thus, the flow chamber system will be an essential tool to study any process that take place on an agar surface at the single cell level. |
url |
http://europepmc.org/articles/PMC2748647?pdf=render |
work_keys_str_mv |
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