Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.

This article describes Bacteria ID Chips ('BacChips'): an inexpensive, portable, and autonomous microfluidic platform for identifying pathogenic strains of bacteria. BacChips consist of a set of microchambers and channels molded in the elastomeric polymer, poly(dimethylsiloxane) (PDMS). Ea...

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Main Authors: Jack Y Ho, Nate J Cira, John A Crooks, Josue Baeza, Douglas B Weibel
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3407151?pdf=render
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author Jack Y Ho
Nate J Cira
John A Crooks
Josue Baeza
Douglas B Weibel
author_facet Jack Y Ho
Nate J Cira
John A Crooks
Josue Baeza
Douglas B Weibel
author_sort Jack Y Ho
collection DOAJ
description This article describes Bacteria ID Chips ('BacChips'): an inexpensive, portable, and autonomous microfluidic platform for identifying pathogenic strains of bacteria. BacChips consist of a set of microchambers and channels molded in the elastomeric polymer, poly(dimethylsiloxane) (PDMS). Each microchamber is preloaded with mono-, di-, or trisaccharides and dried. Pressing the layer of PDMS into contact with a glass coverslip forms the device; the footprint of the device in this article is ∼6 cm(2). After assembly, BacChips are degased under large negative pressure and are stored in vacuum-sealed plastic bags. To use the device, the bag is opened, a sample containing bacteria is introduced at the inlet of the device, and the degased PDMS draws the sample into the central channel and chambers. After the liquid at the inlet is consumed, air is drawn into the BacChip via the inlet and provides a physical barrier that separates the liquid samples in adjacent microchambers. A pH indicator is admixed with the samples prior to their loading, enabling the metabolism of the dissolved saccharides in the microchambers to be visualized. Importantly, BacChips operate without external equipment or instruments. By visually detecting the growth of bacteria using ambient light after ∼4 h, we demonstrate that BacChips with ten microchambers containing different saccharides can reproducibly detect the ESKAPE panel of pathogens, including strains of: Enterococcus faecalis, Enteroccocus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter aerogenes, and Enterobacter cloacae. This article describes a BacChip for point-of-care detection of ESKAPE pathogens and a starting point for designing multiplexed assays that identify bacterial strains from clinical samples and simultaneously determine their susceptibility to antibiotics.
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spelling doaj.art-565df6ac6fd94efa965987c428c389e12022-12-21T18:23:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0177e4124510.1371/journal.pone.0041245Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.Jack Y HoNate J CiraJohn A CrooksJosue BaezaDouglas B WeibelThis article describes Bacteria ID Chips ('BacChips'): an inexpensive, portable, and autonomous microfluidic platform for identifying pathogenic strains of bacteria. BacChips consist of a set of microchambers and channels molded in the elastomeric polymer, poly(dimethylsiloxane) (PDMS). Each microchamber is preloaded with mono-, di-, or trisaccharides and dried. Pressing the layer of PDMS into contact with a glass coverslip forms the device; the footprint of the device in this article is ∼6 cm(2). After assembly, BacChips are degased under large negative pressure and are stored in vacuum-sealed plastic bags. To use the device, the bag is opened, a sample containing bacteria is introduced at the inlet of the device, and the degased PDMS draws the sample into the central channel and chambers. After the liquid at the inlet is consumed, air is drawn into the BacChip via the inlet and provides a physical barrier that separates the liquid samples in adjacent microchambers. A pH indicator is admixed with the samples prior to their loading, enabling the metabolism of the dissolved saccharides in the microchambers to be visualized. Importantly, BacChips operate without external equipment or instruments. By visually detecting the growth of bacteria using ambient light after ∼4 h, we demonstrate that BacChips with ten microchambers containing different saccharides can reproducibly detect the ESKAPE panel of pathogens, including strains of: Enterococcus faecalis, Enteroccocus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter aerogenes, and Enterobacter cloacae. This article describes a BacChip for point-of-care detection of ESKAPE pathogens and a starting point for designing multiplexed assays that identify bacterial strains from clinical samples and simultaneously determine their susceptibility to antibiotics.http://europepmc.org/articles/PMC3407151?pdf=render
spellingShingle Jack Y Ho
Nate J Cira
John A Crooks
Josue Baeza
Douglas B Weibel
Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.
PLoS ONE
title Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.
title_full Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.
title_fullStr Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.
title_full_unstemmed Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.
title_short Rapid identification of ESKAPE bacterial strains using an autonomous microfluidic device.
title_sort rapid identification of eskape bacterial strains using an autonomous microfluidic device
url http://europepmc.org/articles/PMC3407151?pdf=render
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