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A lab-on-chip for malaria diagnosis and surveillance

BACKGROUND: Access to timely and accurate diagnostic tests has a significant impact in the management of diseases of global concern such as malaria. While molecular diagnostics satisfy this need effectively in developed countries, barriers in technology, reagent storage, cost and expertise have hamp...

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Autores principales: Taylor, Brian J, Howell, Anita, Martin, Kimberly A, Manage, Dammika P, Gordy, Walter, Campbell, Stephanie D, Lam, Samantha, Jin, Albert, Polley, Spencer D, Samuel, Roshini A, Atrazhev, Alexey, Stickel, Alex J, Birungi, Josephine, Mbonye, Anthony K, Pilarski, Linda M, Acker, Jason P, Yanow, Stephanie K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029813/
https://www.ncbi.nlm.nih.gov/pubmed/24885206
http://dx.doi.org/10.1186/1475-2875-13-179
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author Taylor, Brian J
Howell, Anita
Martin, Kimberly A
Manage, Dammika P
Gordy, Walter
Campbell, Stephanie D
Lam, Samantha
Jin, Albert
Polley, Spencer D
Samuel, Roshini A
Atrazhev, Alexey
Stickel, Alex J
Birungi, Josephine
Mbonye, Anthony K
Pilarski, Linda M
Acker, Jason P
Yanow, Stephanie K
author_facet Taylor, Brian J
Howell, Anita
Martin, Kimberly A
Manage, Dammika P
Gordy, Walter
Campbell, Stephanie D
Lam, Samantha
Jin, Albert
Polley, Spencer D
Samuel, Roshini A
Atrazhev, Alexey
Stickel, Alex J
Birungi, Josephine
Mbonye, Anthony K
Pilarski, Linda M
Acker, Jason P
Yanow, Stephanie K
author_sort Taylor, Brian J
collection PubMed
description BACKGROUND: Access to timely and accurate diagnostic tests has a significant impact in the management of diseases of global concern such as malaria. While molecular diagnostics satisfy this need effectively in developed countries, barriers in technology, reagent storage, cost and expertise have hampered the introduction of these methods in developing countries. In this study a simple, lab-on-chip PCR diagnostic was created for malaria that overcomes these challenges. METHODS: The platform consists of a disposable plastic chip and a low-cost, portable, real-time PCR machine. The chip contains a desiccated hydrogel with reagents needed for Plasmodium specific PCR. Chips can be stored at room temperature and used on demand by rehydrating the gel with unprocessed blood, avoiding the need for sample preparation. These chips were run on a custom-built instrument containing a Peltier element for thermal cycling and a laser/camera setup for amplicon detection. RESULTS: This diagnostic was capable of detecting all Plasmodium species with a limit of detection for Plasmodium falciparum of 2 parasites/μL of blood. This exceeds the sensitivity of microscopy, the current standard for diagnosis in the field, by ten to fifty-fold. In a blind panel of 188 patient samples from a hyper-endemic region of malaria transmission in Uganda, the diagnostic had high sensitivity (97.4%) and specificity (93.8%) versus conventional real-time PCR. The test also distinguished the two most prevalent malaria species in mixed infections, P. falciparum and Plasmodium vivax. A second blind panel of 38 patient samples was tested on a streamlined instrument with LED-based excitation, achieving a sensitivity of 96.7% and a specificity of 100%. CONCLUSIONS: These results describe the development of a lab-on-chip PCR diagnostic from initial concept to ready-for-manufacture design. This platform will be useful in front-line malaria diagnosis, elimination programmes, and clinical trials. Furthermore, test chips can be adapted to detect other pathogens for a differential diagnosis in the field. The flexibility, reliability, and robustness of this technology hold much promise for its use as a novel molecular diagnostic platform in developing countries.
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spelling pubmed-40298132014-05-22 A lab-on-chip for malaria diagnosis and surveillance Taylor, Brian J Howell, Anita Martin, Kimberly A Manage, Dammika P Gordy, Walter Campbell, Stephanie D Lam, Samantha Jin, Albert Polley, Spencer D Samuel, Roshini A Atrazhev, Alexey Stickel, Alex J Birungi, Josephine Mbonye, Anthony K Pilarski, Linda M Acker, Jason P Yanow, Stephanie K Malar J Methodology BACKGROUND: Access to timely and accurate diagnostic tests has a significant impact in the management of diseases of global concern such as malaria. While molecular diagnostics satisfy this need effectively in developed countries, barriers in technology, reagent storage, cost and expertise have hampered the introduction of these methods in developing countries. In this study a simple, lab-on-chip PCR diagnostic was created for malaria that overcomes these challenges. METHODS: The platform consists of a disposable plastic chip and a low-cost, portable, real-time PCR machine. The chip contains a desiccated hydrogel with reagents needed for Plasmodium specific PCR. Chips can be stored at room temperature and used on demand by rehydrating the gel with unprocessed blood, avoiding the need for sample preparation. These chips were run on a custom-built instrument containing a Peltier element for thermal cycling and a laser/camera setup for amplicon detection. RESULTS: This diagnostic was capable of detecting all Plasmodium species with a limit of detection for Plasmodium falciparum of 2 parasites/μL of blood. This exceeds the sensitivity of microscopy, the current standard for diagnosis in the field, by ten to fifty-fold. In a blind panel of 188 patient samples from a hyper-endemic region of malaria transmission in Uganda, the diagnostic had high sensitivity (97.4%) and specificity (93.8%) versus conventional real-time PCR. The test also distinguished the two most prevalent malaria species in mixed infections, P. falciparum and Plasmodium vivax. A second blind panel of 38 patient samples was tested on a streamlined instrument with LED-based excitation, achieving a sensitivity of 96.7% and a specificity of 100%. CONCLUSIONS: These results describe the development of a lab-on-chip PCR diagnostic from initial concept to ready-for-manufacture design. This platform will be useful in front-line malaria diagnosis, elimination programmes, and clinical trials. Furthermore, test chips can be adapted to detect other pathogens for a differential diagnosis in the field. The flexibility, reliability, and robustness of this technology hold much promise for its use as a novel molecular diagnostic platform in developing countries. BioMed Central 2014-05-09 /pmc/articles/PMC4029813/ /pubmed/24885206 http://dx.doi.org/10.1186/1475-2875-13-179 Text en Copyright © 2014 Taylor et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Taylor, Brian J
Howell, Anita
Martin, Kimberly A
Manage, Dammika P
Gordy, Walter
Campbell, Stephanie D
Lam, Samantha
Jin, Albert
Polley, Spencer D
Samuel, Roshini A
Atrazhev, Alexey
Stickel, Alex J
Birungi, Josephine
Mbonye, Anthony K
Pilarski, Linda M
Acker, Jason P
Yanow, Stephanie K
A lab-on-chip for malaria diagnosis and surveillance
title A lab-on-chip for malaria diagnosis and surveillance
title_full A lab-on-chip for malaria diagnosis and surveillance
title_fullStr A lab-on-chip for malaria diagnosis and surveillance
title_full_unstemmed A lab-on-chip for malaria diagnosis and surveillance
title_short A lab-on-chip for malaria diagnosis and surveillance
title_sort lab-on-chip for malaria diagnosis and surveillance
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029813/
https://www.ncbi.nlm.nih.gov/pubmed/24885206
http://dx.doi.org/10.1186/1475-2875-13-179
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