Abstract

A nucleic acid aptamer that specifically recognizes methicillin-resistant Staphylococcus aureus (MRSA) has been immobilized on magnetic nanoparticles to capture the target bacteria prior to mass spectrometry analysis. After the MRSA species were captured, they were further eluted from the nanoparticles and identified using matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS). The combination of aptamer-based capture/enrichment and MS analysis of microorganisms took advantage of the selectivity of both techniques and should enhance the accuracy of MRSA identification. The capture and elution efficiencies for MRSA were optimized by examining factors such as incubation time, temperature, and elution solvents. The aptamer-modified magnetic nanoparticles showed a capture rate of more than 90% under the optimized condition, whereas the capture rates were less than 11% for non-target bacteria. The as-prepared nanoparticles exhibited only a 5% decrease in the capture rate and a 9% decrease in the elution rate after 10 successive cycles of utilization. Most importantly, the aptamer-modified nanoparticles revealed an excellent selectivity towards MRSA in bacterial mixtures. The capture of MRSA at a concentration of 102 CFU/mL remained at a good percentage of 82% even when the other two species were at 104 times higher concentration (106 CFU/mL). Further, the eluted MRSA bacteria were successfully identified using MALDI mass spectrometry.

Highlights

  • The particle surface was modified with carboxylic groups through a reaction with polyacrylic acid (PA) to form PA-modified magnetic silica nanoparticles (PAMNPs)

  • We evaluated the amount of aptamer bound with 1 mg of PAMNPs after the mixture was incubated for 3 h

  • We describe a highly specific and robust method for capturing and analyzing methicillin-resistant Staphylococcus aureus. This method employed synthetic magnetic nanoparticles modified with nucleic acid aptamers to capture MRSA

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Summary

Results and Discussion

The selectivity of aptamer-modified magnetic nanoparticles towards MRSA bacteria was investigated. The particle surface was modified with carboxylic groups through a reaction with polyacrylic acid (PA) to form PA-modified magnetic silica. The selectivity of aptamer-modified magnetic nanoparticles to of 12 wards MRSA bacteria was investigated. The magnetic iron oxide core was coated with silica via the sol-gel method. The particle surface was modified with carboxylic groups through a reaction with polyacrylic acid (PA) to form PA-modified magnetic silica nanoparticles (PAMNPs). PAMNPs through reaction between the amino group in the aptamer and the carboxyl group in the particles

IR Spectra of PAMNPs
Conjugation of Aptamers with PAMNPs
Bacterial Capture Efficiency of PAMNP-Aptamer
Optimization
Materials and Reagents
Instruments
Bacterial Samples
Capture and Elution of Bacteria
Conclusions
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