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Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation

Opportunistic foodborne pathogens such as Staphylococcus aureus (S. aureus) can cause a wide variety of threats to public health. There is an urgent clinical need for a fast, simple, low-cost, and sensitive method. Here, we designed a fluorescence-based aptamer biosensor (aptasensor) for S. aureus d...

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Autores principales: Li, Na, Zhang, Ying, Wei, Tiancheng, Yang, Tao, Bao, Qing, Cheng, Qichao, Mao, Chuanbin, Shuai, Yajun, Yang, Mingying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321366/
https://www.ncbi.nlm.nih.gov/pubmed/37416905
http://dx.doi.org/10.1039/d3ra01555f
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author Li, Na
Zhang, Ying
Wei, Tiancheng
Yang, Tao
Bao, Qing
Cheng, Qichao
Mao, Chuanbin
Shuai, Yajun
Yang, Mingying
author_facet Li, Na
Zhang, Ying
Wei, Tiancheng
Yang, Tao
Bao, Qing
Cheng, Qichao
Mao, Chuanbin
Shuai, Yajun
Yang, Mingying
author_sort Li, Na
collection PubMed
description Opportunistic foodborne pathogens such as Staphylococcus aureus (S. aureus) can cause a wide variety of threats to public health. There is an urgent clinical need for a fast, simple, low-cost, and sensitive method. Here, we designed a fluorescence-based aptamer biosensor (aptasensor) for S. aureus detection using core–shell structured upconversion nanoparticles (CS-UCNPs) as a beacon. A S. aureus-specific aptamer was modified on the surface of CS-UCNPs for binding pathogens. The S. aureus bound to CS-UCNPs can then be isolated from the detection system by simple low-speed centrifugation. Thus, an aptasensor was successfully established for the detection of S. aureus. The fluorescence intensity of CS-UCNPs correlated with the concentration of S. aureus within the range of 6.36 × 10(2) to 6.36 × 10(8) CFU mL(−1), resulting in the detected limit of S. aureus being 60 CFU mL(−1). The aptasensor performed well in real food samples (milk) with a detection limit of 146 CFU mL(−1) for S. aureus. Furthermore, we applied our aptasensor in chicken muscles for S. aureus detection, and compared it with the plate count gold standard method. There was no significant difference between our aptasensor and the plate count method within the detected limit, while the time for the aptasensor (0.58 h) was shorter than that of the plate count method (3–4 d). Therefore, we succeeded in the design of a simple, sensitive and fast CS-UCNPs aptasensor for S. aureus detection. This aptasensor system would have the potential for the detection of a wide range of bacterial species by switching the corresponding aptamer.
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spelling pubmed-103213662023-07-06 Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation Li, Na Zhang, Ying Wei, Tiancheng Yang, Tao Bao, Qing Cheng, Qichao Mao, Chuanbin Shuai, Yajun Yang, Mingying RSC Adv Chemistry Opportunistic foodborne pathogens such as Staphylococcus aureus (S. aureus) can cause a wide variety of threats to public health. There is an urgent clinical need for a fast, simple, low-cost, and sensitive method. Here, we designed a fluorescence-based aptamer biosensor (aptasensor) for S. aureus detection using core–shell structured upconversion nanoparticles (CS-UCNPs) as a beacon. A S. aureus-specific aptamer was modified on the surface of CS-UCNPs for binding pathogens. The S. aureus bound to CS-UCNPs can then be isolated from the detection system by simple low-speed centrifugation. Thus, an aptasensor was successfully established for the detection of S. aureus. The fluorescence intensity of CS-UCNPs correlated with the concentration of S. aureus within the range of 6.36 × 10(2) to 6.36 × 10(8) CFU mL(−1), resulting in the detected limit of S. aureus being 60 CFU mL(−1). The aptasensor performed well in real food samples (milk) with a detection limit of 146 CFU mL(−1) for S. aureus. Furthermore, we applied our aptasensor in chicken muscles for S. aureus detection, and compared it with the plate count gold standard method. There was no significant difference between our aptasensor and the plate count method within the detected limit, while the time for the aptasensor (0.58 h) was shorter than that of the plate count method (3–4 d). Therefore, we succeeded in the design of a simple, sensitive and fast CS-UCNPs aptasensor for S. aureus detection. This aptasensor system would have the potential for the detection of a wide range of bacterial species by switching the corresponding aptamer. The Royal Society of Chemistry 2023-07-05 /pmc/articles/PMC10321366/ /pubmed/37416905 http://dx.doi.org/10.1039/d3ra01555f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Li, Na
Zhang, Ying
Wei, Tiancheng
Yang, Tao
Bao, Qing
Cheng, Qichao
Mao, Chuanbin
Shuai, Yajun
Yang, Mingying
Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation
title Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation
title_full Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation
title_fullStr Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation
title_full_unstemmed Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation
title_short Upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of Staphylococcus aureus by low-speed centrifugation
title_sort upconversion nanoparticle-based aptasensor for rapid and ultrasensitive detection of staphylococcus aureus by low-speed centrifugation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321366/
https://www.ncbi.nlm.nih.gov/pubmed/37416905
http://dx.doi.org/10.1039/d3ra01555f
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