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Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification
Staphylococcus epidermidis is a critical pathogen of nosocomial blood infections, resulting in significant morbidity and mortality. A piezoelectric quartz crystal microbalance (QCM) nucleic acid biosensor array using Au nanoparticle signal amplification was developed to rapidly detect S. epidermidis...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707461/ https://www.ncbi.nlm.nih.gov/pubmed/27873880 http://dx.doi.org/10.3390/s8106453 |
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author | Xia, Han Wang, Feng Huang, Qing Huang, Junfu Chen, Ming Wang, Jue Yao, Chunyan Chen, Qinghai Cai, Guoru Fu, Weiling |
author_facet | Xia, Han Wang, Feng Huang, Qing Huang, Junfu Chen, Ming Wang, Jue Yao, Chunyan Chen, Qinghai Cai, Guoru Fu, Weiling |
author_sort | Xia, Han |
collection | PubMed |
description | Staphylococcus epidermidis is a critical pathogen of nosocomial blood infections, resulting in significant morbidity and mortality. A piezoelectric quartz crystal microbalance (QCM) nucleic acid biosensor array using Au nanoparticle signal amplification was developed to rapidly detect S. epidermidis in clinical samples. The synthesized thiolated probes specific targeting S. epidermidis 16S rRNA gene were immobilized on the surface of QCM nucleic acid biosensor arrays. Hybridization was induced by exposing the immobilized probes to the PCR amplified fragments of S. epidermidis, resulting in a mass change and a consequent frequency shift of the QCM biosensor. To further enhance frequency shift results from above described hybridizations, streptavidin coated Au nanoparticles were conjugated to the PCR amplified fragments. The results showed that the lowest detection limit of current QCM system was 1.3×10(3) CFU/mL. A linear correlation was found when the concentration of S. epidermidis varied from 1.3×10(3) to 1.3×10(7) CFU/mL. In addition, 55 clinical samples were detected with both current QCM biosensor system and conventional clinical microbiological method, and the sensitivity and specificity of current QCM biosensor system were 97.14% and 100%, respectively. In conclusion, the current QCM system is a rapid, low-cost and sensitive method that can be used to identify infection of S. epidermidis in clinical samples. |
format | Online Article Text |
id | pubmed-3707461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-37074612013-07-10 Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification Xia, Han Wang, Feng Huang, Qing Huang, Junfu Chen, Ming Wang, Jue Yao, Chunyan Chen, Qinghai Cai, Guoru Fu, Weiling Sensors (Basel) Article Staphylococcus epidermidis is a critical pathogen of nosocomial blood infections, resulting in significant morbidity and mortality. A piezoelectric quartz crystal microbalance (QCM) nucleic acid biosensor array using Au nanoparticle signal amplification was developed to rapidly detect S. epidermidis in clinical samples. The synthesized thiolated probes specific targeting S. epidermidis 16S rRNA gene were immobilized on the surface of QCM nucleic acid biosensor arrays. Hybridization was induced by exposing the immobilized probes to the PCR amplified fragments of S. epidermidis, resulting in a mass change and a consequent frequency shift of the QCM biosensor. To further enhance frequency shift results from above described hybridizations, streptavidin coated Au nanoparticles were conjugated to the PCR amplified fragments. The results showed that the lowest detection limit of current QCM system was 1.3×10(3) CFU/mL. A linear correlation was found when the concentration of S. epidermidis varied from 1.3×10(3) to 1.3×10(7) CFU/mL. In addition, 55 clinical samples were detected with both current QCM biosensor system and conventional clinical microbiological method, and the sensitivity and specificity of current QCM biosensor system were 97.14% and 100%, respectively. In conclusion, the current QCM system is a rapid, low-cost and sensitive method that can be used to identify infection of S. epidermidis in clinical samples. Molecular Diversity Preservation International (MDPI) 2008-10-21 /pmc/articles/PMC3707461/ /pubmed/27873880 http://dx.doi.org/10.3390/s8106453 Text en © 2008 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Xia, Han Wang, Feng Huang, Qing Huang, Junfu Chen, Ming Wang, Jue Yao, Chunyan Chen, Qinghai Cai, Guoru Fu, Weiling Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification |
title | Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification |
title_full | Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification |
title_fullStr | Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification |
title_full_unstemmed | Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification |
title_short | Detection of Staphylococcus epidermidis by a Quartz Crystal Microbalance Nucleic Acid Biosensor Array Using Au Nanoparticle Signal Amplification |
title_sort | detection of staphylococcus epidermidis by a quartz crystal microbalance nucleic acid biosensor array using au nanoparticle signal amplification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707461/ https://www.ncbi.nlm.nih.gov/pubmed/27873880 http://dx.doi.org/10.3390/s8106453 |
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