Method Article

Detecting Bacterial Contamination Using Magneto-fluorescent Nanosensors

July 8th, 2025

In This Article

Abstract

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Source: Shelby, T., Sulthana, S., McAfee, J., Banerjee, T., Santra, S. Foodborne Pathogen Screening Using Magneto-fluorescent Nanosensor: Rapid Detection of E. Coli O157:H7. J. Vis. Exp. (2017).

This video demonstrates a technique to detect bacterial contaminants in food and water samples using nanosensors. The target pathogenic bacteria are detected through a combination of magnetic relaxation and fluorescence emission modalities.

Protocol

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1. Rapid Detection of E. coli O157:H7 using MFnS

  1. Spike various PBS solutions (1X, pH 7.4, 300 µL) with increasing amounts of the 10-6 bacterial stock, resulting in CFU ranges from 1-100. Add a consistent amount of MFnS (100 µL) to these solutions.
  2. Create one baseline solution that contains only PBS (1X, pH 7.4, 300 µL) and MFnS (100 µL).
  3. Incubate solutions for 30 min at 37 °C and then allow them to cool to room temperature.
  4. Transfer individual solutions to the magnetic relaxometer (0.47 Tesla) and record changes in relaxation times (T2) relative to the CFUs in each solution.
    1. To record changes in T2 values, begin by measuring the T2 value of the baseline solution that contains only PBS and MFnS.
      1. Place the solution in the magnetic relaxometer. Open the respective software, select the "T2 relaxation" setting, and press "measure."
      2. Following the collection of the baseline T2, measure the T2 values of the additional solutions that were spiked with various concentrations of bacteria.
        Note: The change in T2 is equivalent to baseline T2 subtracted from the spiked T2.
  5. Remove samples from the magnetic relaxometer and centrifuge the tubes at 2880 x g for 10 min.
  6. Decant the supernatant and resuspend bacterial pellets in 100 µL of PBS (1X, pH 7.4).
  7. Add 80 µL of each resuspension to a 96-well plate and record fluorescence intensities at 595 nm.
    Note: Testing can be repeated using different solvents, including lake water, milk, and others, as described in the results section.

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Disclosures

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No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Ferrous Chloride TetrahydrateFisher ScientificI90-500
Ferric Chloride HexahydrateFisher ScientificI88-500
Ammonium HydroxideFisher ScientificA669S-500
Hydrochloric AcidFisher ScientificA144S-500
Polyacryllic AcidSigma-Aldrich323667-100G
EDCThermofisher Scientific22980
NHSFisher ScientificAC157270250
Anti-E. coli O111 antibodySera care5310-0352
Anti-E. coli O157:H7 antibody [P3C6Abcamab75244
DiI StainFisher ScientificD282
Nutrient BrothDifco233000
Freeze-dried E. coli O157:H7 pelletATCC700728
Magnetic RelaxomteterBrukermq20
ZetasizerMalvernNANO-ZS90
Plate ReaderTecanInfinite M200 PRO
Magnetic ColumnQuadroMACS130-090-976
CentrifugeEppendorf5804 Series
Centrifuge (accuSpin Micro 17)Fisher Scientific13-100-676
Floor Model Shaking IncubatorSHEL LABSSI5
Analytical BalanceMetler ToledoME104E
Digital Vortex MixerFisher Scientific02-215-370
Open-Air Rocking ShakerFisher Scientific02-217-765

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Tags

Magneto fluorescent NanosensorsBacterial Contamination DetectionMagnetic RelaxationFluorescence EmissionT2 Relaxation TimeBacterial CFU DetectionCentrifugation IsolationMagnetic RelaxometerNanosensor ClusteringFoodborne Pathogen Screening

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