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A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay

[Image: see text] Rapid and low-cost pathogen diagnostic approaches are critical for clinical decision-making procedures. Cultivating bacteria often takes days to identify pathogens and provide antimicrobial susceptibilities. The delay in diagnosis may result in compromised treatment and inappropria...

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Autores principales: Wu, Tsung-Feng, Chen, Yu-Chen, Wang, Wei-Chung, Fang, Yen-Chi, Fukuoka, Scott, Pride, David T., Pak, On Shun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276042/
https://www.ncbi.nlm.nih.gov/pubmed/30555900
http://dx.doi.org/10.1021/acscentsci.8b00447
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author Wu, Tsung-Feng
Chen, Yu-Chen
Wang, Wei-Chung
Fang, Yen-Chi
Fukuoka, Scott
Pride, David T.
Pak, On Shun
author_facet Wu, Tsung-Feng
Chen, Yu-Chen
Wang, Wei-Chung
Fang, Yen-Chi
Fukuoka, Scott
Pride, David T.
Pak, On Shun
author_sort Wu, Tsung-Feng
collection PubMed
description [Image: see text] Rapid and low-cost pathogen diagnostic approaches are critical for clinical decision-making procedures. Cultivating bacteria often takes days to identify pathogens and provide antimicrobial susceptibilities. The delay in diagnosis may result in compromised treatment and inappropriate antibiotic use. Over the past decades, molecular-based techniques have significantly shortened pathogen identification turnaround time with high accuracy. However, these assays often use complex fluorescent labeling and nucleic acid amplification processes, which limit their use in resource-limited settings. In this work, we demonstrate a wash-free molecular agglutination assay with a straightforward mixing and incubation step that significantly simplifies procedures of molecular testing. By targeting the 16S rRNA gene of pathogens, we perform a rapid pathogen identification within 30 min on a dark-field imaging microfluidic cytometry platform. The dark-field images with low background noise can be obtained using a narrow beam scanning technique with off-the-shelf complementary metal oxide semiconductor (CMOS) imagers such as smartphone cameras. We utilize a machine learning algorithm to deconvolute topological features of agglutinated clusters and thus quantify the abundance of bacteria. Consequently, we unambiguously distinguish Escherichia coli positive from other E. coli negative among 50 clinical urinary tract infection samples with 96% sensitivity and 100% specificity. Furthermore, we also apply this quantitative detection approach to achieve rapid antimicrobial susceptibility testing within 3 h. This work exhibits easy-to-use protocols, high sensitivity, and short turnaround time for point-of-care testing uses.
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spelling pubmed-62760422018-12-15 A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay Wu, Tsung-Feng Chen, Yu-Chen Wang, Wei-Chung Fang, Yen-Chi Fukuoka, Scott Pride, David T. Pak, On Shun ACS Cent Sci [Image: see text] Rapid and low-cost pathogen diagnostic approaches are critical for clinical decision-making procedures. Cultivating bacteria often takes days to identify pathogens and provide antimicrobial susceptibilities. The delay in diagnosis may result in compromised treatment and inappropriate antibiotic use. Over the past decades, molecular-based techniques have significantly shortened pathogen identification turnaround time with high accuracy. However, these assays often use complex fluorescent labeling and nucleic acid amplification processes, which limit their use in resource-limited settings. In this work, we demonstrate a wash-free molecular agglutination assay with a straightforward mixing and incubation step that significantly simplifies procedures of molecular testing. By targeting the 16S rRNA gene of pathogens, we perform a rapid pathogen identification within 30 min on a dark-field imaging microfluidic cytometry platform. The dark-field images with low background noise can be obtained using a narrow beam scanning technique with off-the-shelf complementary metal oxide semiconductor (CMOS) imagers such as smartphone cameras. We utilize a machine learning algorithm to deconvolute topological features of agglutinated clusters and thus quantify the abundance of bacteria. Consequently, we unambiguously distinguish Escherichia coli positive from other E. coli negative among 50 clinical urinary tract infection samples with 96% sensitivity and 100% specificity. Furthermore, we also apply this quantitative detection approach to achieve rapid antimicrobial susceptibility testing within 3 h. This work exhibits easy-to-use protocols, high sensitivity, and short turnaround time for point-of-care testing uses. American Chemical Society 2018-11-05 2018-11-28 /pmc/articles/PMC6276042/ /pubmed/30555900 http://dx.doi.org/10.1021/acscentsci.8b00447 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Wu, Tsung-Feng
Chen, Yu-Chen
Wang, Wei-Chung
Fang, Yen-Chi
Fukuoka, Scott
Pride, David T.
Pak, On Shun
A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay
title A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay
title_full A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay
title_fullStr A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay
title_full_unstemmed A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay
title_short A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay
title_sort rapid and low-cost pathogen detection platform by using a molecular agglutination assay
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276042/
https://www.ncbi.nlm.nih.gov/pubmed/30555900
http://dx.doi.org/10.1021/acscentsci.8b00447
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