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Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis

Francisella tularensis is a potential biowarfare/bioterrorism agent and zoonotic pathogen that causes tularemia; thus, surveillance of F. tularensis and first-level emergency response using point-of-care testing (POCT) are essential. The UPT-LF POCT assay was established to quantitatively detect F....

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Autores principales: Hua, Fei, Zhang, Pingping, Zhang, Fuli, Zhao, Yong, Li, Chunfeng, Sun, Chongyun, Wang, Xiaochen, Yang, Ruifu, Wang, Chengbin, Yu, Ailian, Zhou, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660431/
https://www.ncbi.nlm.nih.gov/pubmed/26608358
http://dx.doi.org/10.1038/srep17178
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author Hua, Fei
Zhang, Pingping
Zhang, Fuli
Zhao, Yong
Li, Chunfeng
Sun, Chongyun
Wang, Xiaochen
Yang, Ruifu
Wang, Chengbin
Yu, Ailian
Zhou, Lei
author_facet Hua, Fei
Zhang, Pingping
Zhang, Fuli
Zhao, Yong
Li, Chunfeng
Sun, Chongyun
Wang, Xiaochen
Yang, Ruifu
Wang, Chengbin
Yu, Ailian
Zhou, Lei
author_sort Hua, Fei
collection PubMed
description Francisella tularensis is a potential biowarfare/bioterrorism agent and zoonotic pathogen that causes tularemia; thus, surveillance of F. tularensis and first-level emergency response using point-of-care testing (POCT) are essential. The UPT-LF POCT assay was established to quantitatively detect F. tularensis within 15 min, and the sensitivity of the assay was 10(4) CFU · mL(−1) (100 CFU/test). The linear quantitative range covered five orders of magnitude, and the coefficients of variation were less than 10%. Except Shigella dysenteriae, UPT-LF showed excellent specificity to four strains that are also potential biowarfare/bioterrorism agents and 13 food-borne pathogenic strains. Samples with pH 2–13, high ion strengths (≥2 mol · L(−1) solution of KCl and NaCl), high viscosities (≤50 mg · mL(−1) PEG20000 or ≥20% glycerol), and high concentrations of biomacromolecules (≥400 mg · mL(−1) bovine serum albumin or ≥80 mg · mL(−1) casein) showed little influence on the assay. For practical utilization, the tolerance limits for seven powders and eight viscera were determined, and operation errors of liquid measurement demonstrated a minor influence on the strip. Ftu-UPT-LF is a candidate POCT method because of its excellent sensitivity, specificity, and stability in complex samples, as well as low operation error.
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spelling pubmed-46604312015-12-02 Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis Hua, Fei Zhang, Pingping Zhang, Fuli Zhao, Yong Li, Chunfeng Sun, Chongyun Wang, Xiaochen Yang, Ruifu Wang, Chengbin Yu, Ailian Zhou, Lei Sci Rep Article Francisella tularensis is a potential biowarfare/bioterrorism agent and zoonotic pathogen that causes tularemia; thus, surveillance of F. tularensis and first-level emergency response using point-of-care testing (POCT) are essential. The UPT-LF POCT assay was established to quantitatively detect F. tularensis within 15 min, and the sensitivity of the assay was 10(4) CFU · mL(−1) (100 CFU/test). The linear quantitative range covered five orders of magnitude, and the coefficients of variation were less than 10%. Except Shigella dysenteriae, UPT-LF showed excellent specificity to four strains that are also potential biowarfare/bioterrorism agents and 13 food-borne pathogenic strains. Samples with pH 2–13, high ion strengths (≥2 mol · L(−1) solution of KCl and NaCl), high viscosities (≤50 mg · mL(−1) PEG20000 or ≥20% glycerol), and high concentrations of biomacromolecules (≥400 mg · mL(−1) bovine serum albumin or ≥80 mg · mL(−1) casein) showed little influence on the assay. For practical utilization, the tolerance limits for seven powders and eight viscera were determined, and operation errors of liquid measurement demonstrated a minor influence on the strip. Ftu-UPT-LF is a candidate POCT method because of its excellent sensitivity, specificity, and stability in complex samples, as well as low operation error. Nature Publishing Group 2015-11-26 /pmc/articles/PMC4660431/ /pubmed/26608358 http://dx.doi.org/10.1038/srep17178 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hua, Fei
Zhang, Pingping
Zhang, Fuli
Zhao, Yong
Li, Chunfeng
Sun, Chongyun
Wang, Xiaochen
Yang, Ruifu
Wang, Chengbin
Yu, Ailian
Zhou, Lei
Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis
title Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis
title_full Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis
title_fullStr Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis
title_full_unstemmed Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis
title_short Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of Francisella tularensis
title_sort development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid detection of francisella tularensis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660431/
https://www.ncbi.nlm.nih.gov/pubmed/26608358
http://dx.doi.org/10.1038/srep17178
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