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Method Article

Colorimetric Paper-based Detection of Escherichia coli, Salmonella spp., and Listeria monocytogenes from Large Volumes of Agricultural Water

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DOI:

10.3791/51414

June 9th, 2014

In This Article

Summary

A protocol involving integrated concentration, enrichment, and end-point colorimetric detection of foodborne pathogens in large volumes of agricultural water is presented here. Water is filtered through Modified Moore Swabs (MMS), enriched with selective or non-selective media, and detection is performed using paper-based analytical devices (µPAD) imbedded with bacterial-indicative colorimetric substrates.

Abstract

This protocol describes rapid colorimetric detection of Escherichia coli, Salmonella spp., and Listeria monocytogenes from large volumes (10 L) of agricultural waters. Here, water is filtered through sterile Modified Moore Swabs (MMS), which consist of a simple gauze filter enclosed in a plastic cartridge, to concentrate bacteria. Following filtration, non-selective or selective enrichments for the target bacteria are performed in the MMS. For colorimetric detection of the target bacteria, the enrichments are then assayed using paper-based analytical devices (µPADs) embedded with bacteria-indicative substrates. Each substrate reacts with target-indicative bacterial enzymes, generating colored products that can be detected visually (qualitative detection) on the µPAD. Alternatively, digital images of the reacted µPADs can be generated with common scanning or photographic devices and analyzed using ImageJ software, allowing for more objective and standardized interpretation of results. Although the biochemical screening procedures are designed to identify the aforementioned bacterial pathogens, in some cases enzymes produced by background microbiota or the degradation of the colorimetric substrates may produce a false positive. Therefore, confirmation using a more discriminatory diagnostic is needed. Nonetheless, this bacterial concentration and detection platform is inexpensive, sensitive (0.1 CFU/ml detection limit), easy to perform, and rapid (concentration, enrichment, and detection are performed within approximately 24 hr), justifying its use as an initial screening method for the microbiological quality of agricultural water.

Introduction

It is important that foodborne disease agents are detected rapidly and preferably in field-based settings in order to reduce the burden of foodborne disease. Common strategies to detect foodborne bacterial pathogens include biochemical profiling, selective and differential culturing, immunological isolation and detection, and molecular detection. However, these methods are hampered by sporadic contamination, small sample sizes tested, the often low concentrations of the foodborne pathogenic bacteria, require long processing times, and/or are not applicable for field settings. Further, compounds in many food matrices are inhibitory to detection and diagnostic applicati....

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Protocol

1. Concentration of Bacteria from Large Volumes of Agricultural Water Using MMS

  1. MMS Preparation
    1. Cut a rectangular section of 4-ply cheesecloth measuring 40 x 12 cm.
    2. Fold the cheesecloth along both axes to obtain a rectangle of 20 x 6 cm.
    3. Roll the cheesecloth tightly along its long axis to form a cylindrical swab of approximately 6 cm tall and 3 cm in diameter.
    4. Autoclave the cheesecloth swab in aluminum foil, do not autoclave the cassette. Decontaminate the cassette by soaking it for 30 min in 10% household bleach, and deactivate the residual chlorine by soaking the cassette for 15 min in a sodium ....

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Results

As described in this protocol, concentration of bacteria using the MMS (Figure 1) can be performed within approximately 15-20 min. The MMS in constructed from acrylonitrile butadiene styrene (ABS) in two separate components; a lid and a cartridge both with an integrated spigot assembly into which a cylindrical cheesecloth swab is inserted (Figure 1A). Both components are then screwed together forming the MMS (Figure 1B). MMS-based processing is driven by a battery-powere.......

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Discussion

This protocol describes an integrated method for detecting E. coli, Salmonella spp., and L. monocytogenes in agricultural water. Here, MMS concentration of bacteria from large volumes (10 L) of agricultural water, is coupled with bacterial enrichment, and bacterial-indicative colorimetric detection using µPADs. The MMS procedure can cope with high particulate content in the water samples while concentrating the bacteria 10-fold, is robust and simple enough for field applications by minimal.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

We gratefully acknowledge funding for this project from the USDA National Institute of Food and Agriculture grants 2009-01208 and 2009-01984.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Agricultural waterIrrigation water, produce wash water, well water, etc.
Vinyl tubingWilmarBN-CVT1005 1/4" inner diameter,  3/8" outer diameter, available at:  http://www.wilmar.com
Modified Moore Swab cartridge Lumiere Diagnostics11 ½ cm in length and 4 ½ cm in width, available at:  http://www.lumierediagnostics.com.  Alternativelly, a non-disposable version of the cartridge can be used (refer to the text)
CheeseclothChesapeake Wiper & Supply, Inc.CC90Grade #90, 44 x 36 weave, available at:  www.raglady.com
Household BleachVariousSodium hypochlorite concentration approx. 6%
Sodium thiosulphate 5-hydrateMallinckrodt Baker Inc8100-04
ManifoldBuilt in-houseOptional, device can be constructed from PVC pipes and appropriate fittings
Peristaltic pumpMicron MetersRPP1300Available at:  http://www.micronmeters.com
Serological pipetteVariousDisposable, 10 ml
Universal preenrichment brothDifco223510
Buffered peptone waterDifco218105
Salmonella supplementBiomérieux Industry42650http://www.biomerieux-usa.com
VIDAS UP Listeria (LPT) BrothBiomérieux Industry410848http://www.biomerieux-usa.com
VancomycinSigma-Aldrich861987http://www.sigmaaldrich.com
Pipet-AidVariousDrummond DP-110 used here
Shaking incubatorVariousExcella E25, New Brunswick Scientific used here
Micropipette Various10 μl, 1 ml
Micropipette tipsVariousBarrier, 10 μl, 1 ml
1.5 microcentrifuge tubesVariousRNase- and DNase-free
Probe sonicatorQ Sonica LLCXL-2000 series
µPADsAvant Wax printed 7 mm diameter circles, with 4 pt line thickness. Contact Dr. Charles Henry for additional information
HEPES [N-(2-Hydroxyethyl)piperazine-N′-2-ethanesulfonic acid]Sigma-AldrichH3375
Bovine serum albuminSigma-AldrichA8022
Chlorophenol red-galactopyranoside (CPRG)Sigma-Aldrich59767
5-Bromo-4-chloro-3-indolyl-β-D-glucuronide (X-Gluc)Sigma-AldrichB8174
5-bromo-6-chloro-3 indolylcaprylate (magenta caprylate) Sigma-Aldrich53451
5-Bromo-4-chloro-myo-inositol phosphate (X-InP) Sigma-Aldrich38896
Petri dishes, polystyrene 100 mm by 15 mmVariousSterile
Flat bed scannerVariousXerox USB scanner
ImageJ softwareNational Institutes of Healthhttp://rsb.info.nih.gov/ij/

References

  1. Guidance for industry: Guide to minimize microbial food safety hazards for fresh fruits and vegetables. , U.S. Dept. of Health and Human Service, Food and Drug Administration, Center for Food Safety and Applied Nutrition (CFSAN). (1998).
  2. Bisha, B., Pérez-Méndez, A., Danyluk, M. D., Goodridge, L. D.

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Tags

Colorimetric DetectionPaper based Analytical DevicesModified Moore SwabPeristaltic PumpEnrichment BrothImageJ Analysis