Development of high resolution melting analysis for the diagnosis of human malaria

Molecular detection has overcome limitations of microscopic examination by providing greater sensitivity and specificity in Plasmodium species detection. The objective of the present study was to develop a quantitative real-time polymerase chain reaction coupled with high-resolution melting (qRT-PCR...

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Main Authors: Chua, Kek Heng, Lim, Siew Chee, Ng, Ching Ching, Lee, Ping Chin, Lim, Yvonne Ai Lian, Lau, Tze Pheng, Chai, Hwa Chia
Format: Article
Language:English
English
Published: Nature Publishing Group 2015
Subjects:
Online Access:https://eprints.ums.edu.my/id/eprint/19365/1/Development%20of%20high%20resolution%20melting%20analysis%20for%20the%20diagnosis%20of%20human%20malaria.pdf
https://eprints.ums.edu.my/id/eprint/19365/7/Development%20of%20high%20resolution%20melting%20analysis%20for%20the%20diagnosis%20of%20human%20malaria.pdf
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author Chua, Kek Heng
Lim, Siew Chee
Ng, Ching Ching
Lee, Ping Chin
Lim, Yvonne Ai Lian
Lau, Tze Pheng
Chai, Hwa Chia
author_facet Chua, Kek Heng
Lim, Siew Chee
Ng, Ching Ching
Lee, Ping Chin
Lim, Yvonne Ai Lian
Lau, Tze Pheng
Chai, Hwa Chia
author_sort Chua, Kek Heng
collection UMS
description Molecular detection has overcome limitations of microscopic examination by providing greater sensitivity and specificity in Plasmodium species detection. The objective of the present study was to develop a quantitative real-time polymerase chain reaction coupled with high-resolution melting (qRT-PCR-HRM) assay for rapid, accurate and simultaneous detection of all five human Plasmodium spp. A pair of primers targeted the 18S SSU rRNA gene of the Plasmodium spp. was designed for qRT-PCR-HRM assay development. Analytical sensitivity and specificity of the assay were evaluated. Samples collected from 229 malaria suspected patients recruited from Sabah, Malaysia were screened using the assay and results were compared with data obtained using PlasmoNexTM, a hexaplex PCR system. The qRT-PCR-HRM assay was able to detect and discriminate the five Plasmodium spp. with lowest detection limits of 1–100 copy numbers without nonspecific amplifications. The detection of Plasmodium spp. in clinical samples using this assay also achieved 100% concordance with that obtained using PlasmoNexTM. This indicated that the diagnostic sensitivity and specificity of this assay in Plasmodium spp. detection is comparable with those of PlasmoNexTM. The qRT-PCR-HRM assay is simple, produces results in two hours and enables high-throughput screening. Thus, it is an alternative method for rapid and accurate malaria diagnosis.
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spelling ums.eprints-193652021-04-30T06:55:10Z https://eprints.ums.edu.my/id/eprint/19365/ Development of high resolution melting analysis for the diagnosis of human malaria Chua, Kek Heng Lim, Siew Chee Ng, Ching Ching Lee, Ping Chin Lim, Yvonne Ai Lian Lau, Tze Pheng Chai, Hwa Chia RC Internal medicine Molecular detection has overcome limitations of microscopic examination by providing greater sensitivity and specificity in Plasmodium species detection. The objective of the present study was to develop a quantitative real-time polymerase chain reaction coupled with high-resolution melting (qRT-PCR-HRM) assay for rapid, accurate and simultaneous detection of all five human Plasmodium spp. A pair of primers targeted the 18S SSU rRNA gene of the Plasmodium spp. was designed for qRT-PCR-HRM assay development. Analytical sensitivity and specificity of the assay were evaluated. Samples collected from 229 malaria suspected patients recruited from Sabah, Malaysia were screened using the assay and results were compared with data obtained using PlasmoNexTM, a hexaplex PCR system. The qRT-PCR-HRM assay was able to detect and discriminate the five Plasmodium spp. with lowest detection limits of 1–100 copy numbers without nonspecific amplifications. The detection of Plasmodium spp. in clinical samples using this assay also achieved 100% concordance with that obtained using PlasmoNexTM. This indicated that the diagnostic sensitivity and specificity of this assay in Plasmodium spp. detection is comparable with those of PlasmoNexTM. The qRT-PCR-HRM assay is simple, produces results in two hours and enables high-throughput screening. Thus, it is an alternative method for rapid and accurate malaria diagnosis. Nature Publishing Group 2015 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/19365/1/Development%20of%20high%20resolution%20melting%20analysis%20for%20the%20diagnosis%20of%20human%20malaria.pdf text en https://eprints.ums.edu.my/id/eprint/19365/7/Development%20of%20high%20resolution%20melting%20analysis%20for%20the%20diagnosis%20of%20human%20malaria.pdf Chua, Kek Heng and Lim, Siew Chee and Ng, Ching Ching and Lee, Ping Chin and Lim, Yvonne Ai Lian and Lau, Tze Pheng and Chai, Hwa Chia (2015) Development of high resolution melting analysis for the diagnosis of human malaria. Scientific Reports, 5 (15671). pp. 1-13. ISSN 2045-2322 http://doi.org/10.1038/srep15671
spellingShingle RC Internal medicine
Chua, Kek Heng
Lim, Siew Chee
Ng, Ching Ching
Lee, Ping Chin
Lim, Yvonne Ai Lian
Lau, Tze Pheng
Chai, Hwa Chia
Development of high resolution melting analysis for the diagnosis of human malaria
title Development of high resolution melting analysis for the diagnosis of human malaria
title_full Development of high resolution melting analysis for the diagnosis of human malaria
title_fullStr Development of high resolution melting analysis for the diagnosis of human malaria
title_full_unstemmed Development of high resolution melting analysis for the diagnosis of human malaria
title_short Development of high resolution melting analysis for the diagnosis of human malaria
title_sort development of high resolution melting analysis for the diagnosis of human malaria
topic RC Internal medicine
url https://eprints.ums.edu.my/id/eprint/19365/1/Development%20of%20high%20resolution%20melting%20analysis%20for%20the%20diagnosis%20of%20human%20malaria.pdf
https://eprints.ums.edu.my/id/eprint/19365/7/Development%20of%20high%20resolution%20melting%20analysis%20for%20the%20diagnosis%20of%20human%20malaria.pdf
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