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Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria

BACKGROUND: Molecular diagnostic methods can complement existing tools to improve the diagnosis of malaria. However, they require good laboratory infrastructure thereby restricting their use to reference laboratories and research studies. Therefore, adopting molecular tools for routine use in malari...

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Autores principales: Lucchi, Naomi W., Demas, Allison, Narayanan, Jothikumar, Sumari, Deborah, Kabanywanyi, Abdunoor, Kachur, S. Patrick, Barnwell, John W., Udhayakumar, Venkatachalam
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966401/
https://www.ncbi.nlm.nih.gov/pubmed/21060829
http://dx.doi.org/10.1371/journal.pone.0013733
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author Lucchi, Naomi W.
Demas, Allison
Narayanan, Jothikumar
Sumari, Deborah
Kabanywanyi, Abdunoor
Kachur, S. Patrick
Barnwell, John W.
Udhayakumar, Venkatachalam
author_facet Lucchi, Naomi W.
Demas, Allison
Narayanan, Jothikumar
Sumari, Deborah
Kabanywanyi, Abdunoor
Kachur, S. Patrick
Barnwell, John W.
Udhayakumar, Venkatachalam
author_sort Lucchi, Naomi W.
collection PubMed
description BACKGROUND: Molecular diagnostic methods can complement existing tools to improve the diagnosis of malaria. However, they require good laboratory infrastructure thereby restricting their use to reference laboratories and research studies. Therefore, adopting molecular tools for routine use in malaria endemic countries will require simpler molecular platforms. The recently developed loop-mediated isothermal amplification (LAMP) method is relatively simple and can be improved for better use in endemic countries. In this study, we attempted to improve this method for malaria diagnosis by using a simple and portable device capable of performing both the amplification and detection (by fluorescence) of LAMP in one platform. We refer to this as the RealAmp method. METHODOLOGY AND SIGNIFICANT FINDINGS: Published genus-specific primers were used to test the utility of this method. DNA derived from different species of malaria parasites was used for the initial characterization. Clinical samples of P. falciparum were used to determine the sensitivity and specificity of this system compared to microscopy and a nested PCR method. Additionally, directly boiled parasite preparations were compared with a conventional DNA isolation method. The RealAmp method was found to be simple and allowed real-time detection of DNA amplification. The time to amplification varied but was generally less than 60 minutes. All human-infecting Plasmodium species were detected. The sensitivity and specificity of RealAmp in detecting P. falciparum was 96.7% and 91.7% respectively, compared to microscopy and 98.9% and 100% respectively, compared to a standard nested PCR method. In addition, this method consistently detected P. falciparum from directly boiled blood samples. CONCLUSION: This RealAmp method has great potential as a field usable molecular tool for diagnosis of malaria. This tool can provide an alternative to conventional PCR based diagnostic methods for field use in clinical and operational programs.
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spelling pubmed-29664012010-11-08 Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria Lucchi, Naomi W. Demas, Allison Narayanan, Jothikumar Sumari, Deborah Kabanywanyi, Abdunoor Kachur, S. Patrick Barnwell, John W. Udhayakumar, Venkatachalam PLoS One Research Article BACKGROUND: Molecular diagnostic methods can complement existing tools to improve the diagnosis of malaria. However, they require good laboratory infrastructure thereby restricting their use to reference laboratories and research studies. Therefore, adopting molecular tools for routine use in malaria endemic countries will require simpler molecular platforms. The recently developed loop-mediated isothermal amplification (LAMP) method is relatively simple and can be improved for better use in endemic countries. In this study, we attempted to improve this method for malaria diagnosis by using a simple and portable device capable of performing both the amplification and detection (by fluorescence) of LAMP in one platform. We refer to this as the RealAmp method. METHODOLOGY AND SIGNIFICANT FINDINGS: Published genus-specific primers were used to test the utility of this method. DNA derived from different species of malaria parasites was used for the initial characterization. Clinical samples of P. falciparum were used to determine the sensitivity and specificity of this system compared to microscopy and a nested PCR method. Additionally, directly boiled parasite preparations were compared with a conventional DNA isolation method. The RealAmp method was found to be simple and allowed real-time detection of DNA amplification. The time to amplification varied but was generally less than 60 minutes. All human-infecting Plasmodium species were detected. The sensitivity and specificity of RealAmp in detecting P. falciparum was 96.7% and 91.7% respectively, compared to microscopy and 98.9% and 100% respectively, compared to a standard nested PCR method. In addition, this method consistently detected P. falciparum from directly boiled blood samples. CONCLUSION: This RealAmp method has great potential as a field usable molecular tool for diagnosis of malaria. This tool can provide an alternative to conventional PCR based diagnostic methods for field use in clinical and operational programs. Public Library of Science 2010-10-29 /pmc/articles/PMC2966401/ /pubmed/21060829 http://dx.doi.org/10.1371/journal.pone.0013733 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Lucchi, Naomi W.
Demas, Allison
Narayanan, Jothikumar
Sumari, Deborah
Kabanywanyi, Abdunoor
Kachur, S. Patrick
Barnwell, John W.
Udhayakumar, Venkatachalam
Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria
title Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria
title_full Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria
title_fullStr Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria
title_full_unstemmed Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria
title_short Real-Time Fluorescence Loop Mediated Isothermal Amplification for the Diagnosis of Malaria
title_sort real-time fluorescence loop mediated isothermal amplification for the diagnosis of malaria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966401/
https://www.ncbi.nlm.nih.gov/pubmed/21060829
http://dx.doi.org/10.1371/journal.pone.0013733
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