Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samples

<p>Abstract</p> <p>Background</p> <p>The emergence of <it>Plasmodium knowlesi </it>in humans, which is in many cases misdiagnosed by microscopy as <it>Plasmodium malariae </it>due to the morphological similarity has contributed to the needs of de...

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Main Authors: Anthony Claudia N, Chin Lit-Chein, Cheong Fei-Wen, Palaeya Vanitha, Chang Phooi-Yee, Mahmud Rohela, Fong Mun-Yik, Lau Yee-Ling, Al-Mekhlafi Abdulsalam M, Chen Yeng
Format: Article
Language:English
Published: BMC 2011-07-01
Series:Malaria Journal
Online Access:http://www.malariajournal.com/content/10/1/197
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spelling doaj-51044ec51edf4927b928527594ffeb232020-11-24T21:13:57ZengBMCMalaria Journal1475-28752011-07-0110119710.1186/1475-2875-10-197Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samplesAnthony Claudia NChin Lit-CheinCheong Fei-WenPalaeya VanithaChang Phooi-YeeMahmud RohelaFong Mun-YikLau Yee-LingAl-Mekhlafi Abdulsalam MChen Yeng<p>Abstract</p> <p>Background</p> <p>The emergence of <it>Plasmodium knowlesi </it>in humans, which is in many cases misdiagnosed by microscopy as <it>Plasmodium malariae </it>due to the morphological similarity has contributed to the needs of detection and differentiation of malaria parasites. At present, nested PCR targeted on <it>Plasmodium </it>ssrRNA genes has been described as the most sensitive and specific method for Plasmodium detection. However, this method is costly and requires trained personnel for its implementation. Loop-mediated isothermal amplification (LAMP), a novel nucleic acid amplification method was developed for the clinical detection of <it>P. knowlesi</it>. The sensitivity and specificity of LAMP was evaluated in comparison to the results obtained via microscopic examination and nested PCR.</p> <p>Methods</p> <p>LAMP assay was developed based on <it>P. knowlesi </it>genetic material targeting the apical membrane antigen-1 (AMA-1) gene. The method uses six primers that recognize eight regions of the target DNA and it amplifies DNA within an hour under isothermal conditions (65°C) in a water-bath.</p> <p>Results</p> <p>LAMP is highly sensitive with the detection limit as low as ten copies for AMA-1. LAMP detected malaria parasites in all confirm cases (n = 13) of <it>P. knowlesi </it>infection (sensitivity, 100%) and none of the negative samples (specificity, 100%) within an hour. LAMP demonstrated higher sensitivity compared to nested PCR by successfully detecting a sample with very low parasitaemia (< 0.01%).</p> <p>Conclusion</p> <p>With continuous efforts in the optimization of this assay, LAMP may provide a simple and reliable test for detecting <it>P. knowlesi </it>malaria parasites in areas where malaria is prevalent.</p> http://www.malariajournal.com/content/10/1/197
collection DOAJ
language English
format Article
sources DOAJ
author Anthony Claudia N
Chin Lit-Chein
Cheong Fei-Wen
Palaeya Vanitha
Chang Phooi-Yee
Mahmud Rohela
Fong Mun-Yik
Lau Yee-Ling
Al-Mekhlafi Abdulsalam M
Chen Yeng
spellingShingle Anthony Claudia N
Chin Lit-Chein
Cheong Fei-Wen
Palaeya Vanitha
Chang Phooi-Yee
Mahmud Rohela
Fong Mun-Yik
Lau Yee-Ling
Al-Mekhlafi Abdulsalam M
Chen Yeng
Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samples
Malaria Journal
author_facet Anthony Claudia N
Chin Lit-Chein
Cheong Fei-Wen
Palaeya Vanitha
Chang Phooi-Yee
Mahmud Rohela
Fong Mun-Yik
Lau Yee-Ling
Al-Mekhlafi Abdulsalam M
Chen Yeng
author_sort Anthony Claudia N
title Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samples
title_short Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samples
title_full Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samples
title_fullStr Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samples
title_full_unstemmed Specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (LAMP) in blood samples
title_sort specific, sensitive and rapid detection of human <it>plasmodium knowlesi </it>infection by loop-mediated isothermal amplification (lamp) in blood samples
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2011-07-01
description <p>Abstract</p> <p>Background</p> <p>The emergence of <it>Plasmodium knowlesi </it>in humans, which is in many cases misdiagnosed by microscopy as <it>Plasmodium malariae </it>due to the morphological similarity has contributed to the needs of detection and differentiation of malaria parasites. At present, nested PCR targeted on <it>Plasmodium </it>ssrRNA genes has been described as the most sensitive and specific method for Plasmodium detection. However, this method is costly and requires trained personnel for its implementation. Loop-mediated isothermal amplification (LAMP), a novel nucleic acid amplification method was developed for the clinical detection of <it>P. knowlesi</it>. The sensitivity and specificity of LAMP was evaluated in comparison to the results obtained via microscopic examination and nested PCR.</p> <p>Methods</p> <p>LAMP assay was developed based on <it>P. knowlesi </it>genetic material targeting the apical membrane antigen-1 (AMA-1) gene. The method uses six primers that recognize eight regions of the target DNA and it amplifies DNA within an hour under isothermal conditions (65°C) in a water-bath.</p> <p>Results</p> <p>LAMP is highly sensitive with the detection limit as low as ten copies for AMA-1. LAMP detected malaria parasites in all confirm cases (n = 13) of <it>P. knowlesi </it>infection (sensitivity, 100%) and none of the negative samples (specificity, 100%) within an hour. LAMP demonstrated higher sensitivity compared to nested PCR by successfully detecting a sample with very low parasitaemia (< 0.01%).</p> <p>Conclusion</p> <p>With continuous efforts in the optimization of this assay, LAMP may provide a simple and reliable test for detecting <it>P. knowlesi </it>malaria parasites in areas where malaria is prevalent.</p>
url http://www.malariajournal.com/content/10/1/197
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