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Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry

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 nanopartic...

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Autores principales: Liu, Yu-Chen, Kumar, Katragunta, Wu, Cheng-Hsiu, Chang, Kai-Chih, Chiang, Cheng-Kang, Ho, Yen-Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234742/
https://www.ncbi.nlm.nih.gov/pubmed/34207373
http://dx.doi.org/10.3390/ijms22126571
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author Liu, Yu-Chen
Kumar, Katragunta
Wu, Cheng-Hsiu
Chang, Kai-Chih
Chiang, Cheng-Kang
Ho, Yen-Peng
author_facet Liu, Yu-Chen
Kumar, Katragunta
Wu, Cheng-Hsiu
Chang, Kai-Chih
Chiang, Cheng-Kang
Ho, Yen-Peng
author_sort Liu, Yu-Chen
collection PubMed
description 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 10(2) CFU/mL remained at a good percentage of 82% even when the other two species were at 10(4) times higher concentration (10(6) CFU/mL). Further, the eluted MRSA bacteria were successfully identified using MALDI mass spectrometry.
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spelling pubmed-82347422021-06-27 Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry Liu, Yu-Chen Kumar, Katragunta Wu, Cheng-Hsiu Chang, Kai-Chih Chiang, Cheng-Kang Ho, Yen-Peng Int J Mol Sci Article 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 10(2) CFU/mL remained at a good percentage of 82% even when the other two species were at 10(4) times higher concentration (10(6) CFU/mL). Further, the eluted MRSA bacteria were successfully identified using MALDI mass spectrometry. MDPI 2021-06-18 /pmc/articles/PMC8234742/ /pubmed/34207373 http://dx.doi.org/10.3390/ijms22126571 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Yu-Chen
Kumar, Katragunta
Wu, Cheng-Hsiu
Chang, Kai-Chih
Chiang, Cheng-Kang
Ho, Yen-Peng
Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry
title Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry
title_full Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry
title_fullStr Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry
title_full_unstemmed Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry
title_short Selective Capture and Identification of Methicillin-Resistant Staphylococcus aureus by Combining Aptamer-Modified Magnetic Nanoparticles and Mass Spectrometry
title_sort selective capture and identification of methicillin-resistant staphylococcus aureus by combining aptamer-modified magnetic nanoparticles and mass spectrometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234742/
https://www.ncbi.nlm.nih.gov/pubmed/34207373
http://dx.doi.org/10.3390/ijms22126571
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