A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation
Abstract Background The use of highly sensitive molecular tools in malaria diagnosis is currently largely restricted to research and epidemiological settings, but will ultimately be essential during elimination and potentially eradication. Accurate diagnosis and differentiation down to species level...
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ftdoajarticles:oai:doaj.org/article:73ae9e71510945b4b56a279b8ae48c58 2023-05-15T15:09:29+02:00 A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation Aline Lamien-Meda Hans-Peter Fuehrer David Leitsch Harald Noedl 2021-02-01T00:00:00Z https://doi.org/10.1186/s12936-021-03662-w https://doaj.org/article/73ae9e71510945b4b56a279b8ae48c58 EN eng BMC https://doi.org/10.1186/s12936-021-03662-w https://doaj.org/toc/1475-2875 doi:10.1186/s12936-021-03662-w 1475-2875 https://doaj.org/article/73ae9e71510945b4b56a279b8ae48c58 Malaria Journal, Vol 20, Iss 1, Pp 1-8 (2021) Malaria qPCR HRM Plasmodium Plasmodium falciparum Plasmodium ovale wallikeri Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 article 2021 ftdoajarticles https://doi.org/10.1186/s12936-021-03662-w 2022-12-31T04:38:29Z Abstract Background The use of highly sensitive molecular tools in malaria diagnosis is currently largely restricted to research and epidemiological settings, but will ultimately be essential during elimination and potentially eradication. Accurate diagnosis and differentiation down to species levels, including the two Plasmodium ovale species and zoonotic variants of the disease, will be important for the understanding of changing epidemiological patterns of the disease. Methods A qPCR-high resolution melting (HRM) method was to detect and differentiate all human Plasmodium species with one forward and one reverse primer set. The HRM detection method was further refined using a hydrolysis probe to specifically discriminate Plasmodium falciparum. Results Out of the 113 samples tested with the developed HRM-qPCR- P. falciparum probe assay, 96 (85.0 %) single infections, 12 (10.6 %) mixed infections, and 5 (4.4 %) were Plasmodium negative. The results were concordant with those of the nested PCR at 98.2 %. The assay limit of detection was varied from 21.47 to 46.43 copies /µl, equivalent to 1–2.11 parasites/µl. All P. falciparum infections were confirmed with the associated Taqman probe. Conclusions Although the dependence on qPCR currently limits its deployment in resource-limited environments, this assay is highly sensitive and specific, easy to perform and convenient for Plasmodium mono-infection and may provide a novel tool for rapid and accurate malaria diagnosis also in epidemiological studies. Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Malaria Journal 20 1 |
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Open Polar |
collection |
Directory of Open Access Journals: DOAJ Articles |
op_collection_id |
ftdoajarticles |
language |
English |
topic |
Malaria qPCR HRM Plasmodium Plasmodium falciparum Plasmodium ovale wallikeri Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 |
spellingShingle |
Malaria qPCR HRM Plasmodium Plasmodium falciparum Plasmodium ovale wallikeri Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 Aline Lamien-Meda Hans-Peter Fuehrer David Leitsch Harald Noedl A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation |
topic_facet |
Malaria qPCR HRM Plasmodium Plasmodium falciparum Plasmodium ovale wallikeri Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 |
description |
Abstract Background The use of highly sensitive molecular tools in malaria diagnosis is currently largely restricted to research and epidemiological settings, but will ultimately be essential during elimination and potentially eradication. Accurate diagnosis and differentiation down to species levels, including the two Plasmodium ovale species and zoonotic variants of the disease, will be important for the understanding of changing epidemiological patterns of the disease. Methods A qPCR-high resolution melting (HRM) method was to detect and differentiate all human Plasmodium species with one forward and one reverse primer set. The HRM detection method was further refined using a hydrolysis probe to specifically discriminate Plasmodium falciparum. Results Out of the 113 samples tested with the developed HRM-qPCR- P. falciparum probe assay, 96 (85.0 %) single infections, 12 (10.6 %) mixed infections, and 5 (4.4 %) were Plasmodium negative. The results were concordant with those of the nested PCR at 98.2 %. The assay limit of detection was varied from 21.47 to 46.43 copies /µl, equivalent to 1–2.11 parasites/µl. All P. falciparum infections were confirmed with the associated Taqman probe. Conclusions Although the dependence on qPCR currently limits its deployment in resource-limited environments, this assay is highly sensitive and specific, easy to perform and convenient for Plasmodium mono-infection and may provide a novel tool for rapid and accurate malaria diagnosis also in epidemiological studies. |
format |
Article in Journal/Newspaper |
author |
Aline Lamien-Meda Hans-Peter Fuehrer David Leitsch Harald Noedl |
author_facet |
Aline Lamien-Meda Hans-Peter Fuehrer David Leitsch Harald Noedl |
author_sort |
Aline Lamien-Meda |
title |
A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation |
title_short |
A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation |
title_full |
A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation |
title_fullStr |
A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation |
title_full_unstemmed |
A powerful qPCR-high resolution melting assay with taqman probe in Plasmodium species differentiation |
title_sort |
powerful qpcr-high resolution melting assay with taqman probe in plasmodium species differentiation |
publisher |
BMC |
publishDate |
2021 |
url |
https://doi.org/10.1186/s12936-021-03662-w https://doaj.org/article/73ae9e71510945b4b56a279b8ae48c58 |
geographic |
Arctic |
geographic_facet |
Arctic |
genre |
Arctic |
genre_facet |
Arctic |
op_source |
Malaria Journal, Vol 20, Iss 1, Pp 1-8 (2021) |
op_relation |
https://doi.org/10.1186/s12936-021-03662-w https://doaj.org/toc/1475-2875 doi:10.1186/s12936-021-03662-w 1475-2875 https://doaj.org/article/73ae9e71510945b4b56a279b8ae48c58 |
op_doi |
https://doi.org/10.1186/s12936-021-03662-w |
container_title |
Malaria Journal |
container_volume |
20 |
container_issue |
1 |
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1766340671251152896 |