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Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR

There is a critical need for developing new malaria diagnostic tools that are sensitive, cost effective and capable of performing large scale diagnosis. The real-time PCR methods are particularly robust for large scale screening and they can be used in malaria control and elimination programs. We ha...

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Autores principales: Lucchi, Naomi W., Narayanan, Jothikumar, Karell, Mara A., Xayavong, Maniphet, Kariuki, Simon, DaSilva, Alexandre J., Hill, Vincent, Udhayakumar, Venkatachalam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577666/
https://www.ncbi.nlm.nih.gov/pubmed/23437209
http://dx.doi.org/10.1371/journal.pone.0056677
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author Lucchi, Naomi W.
Narayanan, Jothikumar
Karell, Mara A.
Xayavong, Maniphet
Kariuki, Simon
DaSilva, Alexandre J.
Hill, Vincent
Udhayakumar, Venkatachalam
author_facet Lucchi, Naomi W.
Narayanan, Jothikumar
Karell, Mara A.
Xayavong, Maniphet
Kariuki, Simon
DaSilva, Alexandre J.
Hill, Vincent
Udhayakumar, Venkatachalam
author_sort Lucchi, Naomi W.
collection PubMed
description There is a critical need for developing new malaria diagnostic tools that are sensitive, cost effective and capable of performing large scale diagnosis. The real-time PCR methods are particularly robust for large scale screening and they can be used in malaria control and elimination programs. We have designed novel self-quenching photo-induced electron transfer (PET) fluorogenic primers for the detection of P. falciparum and the Plasmodium genus by real-time PCR. A total of 119 samples consisting of different malaria species and mixed infections were used to test the utility of the novel PET-PCR primers in the diagnosis of clinical samples. The sensitivity and specificity were calculated using a nested PCR as the gold standard and the novel primer sets demonstrated 100% sensitivity and specificity. The limits of detection for P. falciparum was shown to be 3.2 parasites/µl using both Plasmodium genus and P. falciparum-specific primers and 5.8 parasites/µl for P. ovale, 3.5 parasites/µl for P. malariae and 5 parasites/µl for P. vivax using the genus specific primer set. Moreover, the reaction can be duplexed to detect both Plasmodium spp. and P. falciparum in a single reaction. The PET-PCR assay does not require internal probes or intercalating dyes which makes it convenient to use and less expensive than other real-time PCR diagnostic formats. Further validation of this technique in the field will help to assess its utility for large scale screening in malaria control and elimination programs.
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spelling pubmed-35776662013-02-22 Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR Lucchi, Naomi W. Narayanan, Jothikumar Karell, Mara A. Xayavong, Maniphet Kariuki, Simon DaSilva, Alexandre J. Hill, Vincent Udhayakumar, Venkatachalam PLoS One Research Article There is a critical need for developing new malaria diagnostic tools that are sensitive, cost effective and capable of performing large scale diagnosis. The real-time PCR methods are particularly robust for large scale screening and they can be used in malaria control and elimination programs. We have designed novel self-quenching photo-induced electron transfer (PET) fluorogenic primers for the detection of P. falciparum and the Plasmodium genus by real-time PCR. A total of 119 samples consisting of different malaria species and mixed infections were used to test the utility of the novel PET-PCR primers in the diagnosis of clinical samples. The sensitivity and specificity were calculated using a nested PCR as the gold standard and the novel primer sets demonstrated 100% sensitivity and specificity. The limits of detection for P. falciparum was shown to be 3.2 parasites/µl using both Plasmodium genus and P. falciparum-specific primers and 5.8 parasites/µl for P. ovale, 3.5 parasites/µl for P. malariae and 5 parasites/µl for P. vivax using the genus specific primer set. Moreover, the reaction can be duplexed to detect both Plasmodium spp. and P. falciparum in a single reaction. The PET-PCR assay does not require internal probes or intercalating dyes which makes it convenient to use and less expensive than other real-time PCR diagnostic formats. Further validation of this technique in the field will help to assess its utility for large scale screening in malaria control and elimination programs. Public Library of Science 2013-02-20 /pmc/articles/PMC3577666/ /pubmed/23437209 http://dx.doi.org/10.1371/journal.pone.0056677 Text en 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.
Narayanan, Jothikumar
Karell, Mara A.
Xayavong, Maniphet
Kariuki, Simon
DaSilva, Alexandre J.
Hill, Vincent
Udhayakumar, Venkatachalam
Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR
title Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR
title_full Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR
title_fullStr Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR
title_full_unstemmed Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR
title_short Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR
title_sort molecular diagnosis of malaria by photo-induced electron transfer fluorogenic primers: pet-pcr
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577666/
https://www.ncbi.nlm.nih.gov/pubmed/23437209
http://dx.doi.org/10.1371/journal.pone.0056677
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