Electrophoretic and dielectrophoretic approaches to separations can provide unique capabilities. In the past, capillary and microchip-based approaches to electrophoresis have demonstrated extremely high-resolution separations. More recently, dielectrophoretic systems have shown excellent results for the separation of bioparticles. Here we demonstrate resolution of a difficult pair of targets: gentamicin resistant and susceptible strains of Staphylococcus epidermidis. This separation has significant potential implications for healthcare. This establishes a foundation for biophysical separations as a direct diagnostic tool, potentially improving nearly every figure of merit for diagnostics and antibiotic stewardship. The separations are performed on a modified gradient insulator-based dielectrophoresis (g-iDEP) system and demonstrate that the presence of antibiotic resistance enzymes (or secondary effects) produces a sufficient degree of electrophysical difference to allow separation. The differentiating factor is the ratio of electrophoretic to dielectrophoretic mobilities. This factor is 4.6 ± 0.6 × 109 V m−2 for the resistant strain, versus 9.2 ± 0.4 × 109 V m−2 for the susceptible strain. Using g-iDEP separation, this difference produces clear and easily discerned differentiation of the two strains.
Details
- Biophysical Separation of Staphylococcus Epidermidis Strains Based on Antibiotic Resistance
- Jones, Paul (Author)
- Hilton, Shannon (Author)
- Davis, Paige (Author)
- McLemore, Ryan (Author)
- McLaren, Alex (Author)
- Hayes, Mark (Author)
- Department of Chemistry and Biochemistry (Contributor)
- Digital object identifier: 10.1039/C5AN00906E
- Identifier TypeInternational standard serial numberIdentifier Value0003-2654
- View the article in the Analyst at http://pubs.rsc.org/en/Content/ArticleLanding/2015/AN/C5AN00906E
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Jones, Paul V.; Huey, Shannon; Davis, Paige; McLemore, Ryan; McLaren, Alex; Hayes, Mark A. (2015) Biophysical separation of Staphylococcus epidermidis strains based on antibiotic resistance, The Analyst 140(15):5152-5161 DOI: 10.1039/C5AN00906E