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Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans
BACKGROUND: The entry of PCR-based techniques into malaria diagnostics has improved the sensitivity and specificity of the detection of Plasmodium infections. It has been shown that humans are regularly infected by at least six different Plasmodium species. The MC004 real-time PCR assay for malaria...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274047/ https://www.ncbi.nlm.nih.gov/pubmed/34247622 http://dx.doi.org/10.1186/s12936-021-03842-8 |
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author | van Bergen, Kim Stuitje, Toon Akkers, Robert Vermeer, Eric Castel, Rob Mank, Theo |
author_facet | van Bergen, Kim Stuitje, Toon Akkers, Robert Vermeer, Eric Castel, Rob Mank, Theo |
author_sort | van Bergen, Kim |
collection | PubMed |
description | BACKGROUND: The entry of PCR-based techniques into malaria diagnostics has improved the sensitivity and specificity of the detection of Plasmodium infections. It has been shown that humans are regularly infected by at least six different Plasmodium species. The MC004 real-time PCR assay for malaria diagnosis is a novel single-tube assay that has been developed for the purpose of simultaneously detecting all Plasmodium species known to infect humans, and discrimination between Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae, Plasmodium ovale wallikeri, Plasmodium ovale curtisi, Plasmodium knowlesi (including differentiation of three strains) and Plasmodium cynomolgi (including differentiation of three strains). Detection and identification of Plasmodium species relies on molecular beacon probe-based melting curve analysis. In addition, this assay might be used to quantify the parasitaemia of at least P. falciparum by calculating the level of parasitaemia directly from the Cq-value. METHODS: The samples used in this study comprised reference samples, patient samples, and synthetic controls. The following analytical performance characteristics of the MC004 assay were determined: analytical specificity, limit of detection, the ability to detect mixed infections, and the potential to determine the level of parasitaemia of P. falciparum, including assessment of within-run and between-run precisions. RESULTS: No false positive or false negative results were observed. The limit of detection of P. falciparum was 1 × 10(–3) IU/mL (WHO standard). Mixed infections with P. falciparum and non-falciparum species were correctly identified. A calibration curve could be established to quantify the parasitaemia of at least P. falciparum. The within-run and between-run precisions were less than 20% CV at the tested parasitaemia levels of 0.09%, 0.16%, 2.15% and 27.27%. CONCLUSION: Based upon the analytical performance characteristics that were determined, the MC004 assay showed performance suitable for use in clinical settings, as well as epidemiological studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-021-03842-8. |
format | Online Article Text |
id | pubmed-8274047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82740472021-07-13 Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans van Bergen, Kim Stuitje, Toon Akkers, Robert Vermeer, Eric Castel, Rob Mank, Theo Malar J Methodology BACKGROUND: The entry of PCR-based techniques into malaria diagnostics has improved the sensitivity and specificity of the detection of Plasmodium infections. It has been shown that humans are regularly infected by at least six different Plasmodium species. The MC004 real-time PCR assay for malaria diagnosis is a novel single-tube assay that has been developed for the purpose of simultaneously detecting all Plasmodium species known to infect humans, and discrimination between Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae, Plasmodium ovale wallikeri, Plasmodium ovale curtisi, Plasmodium knowlesi (including differentiation of three strains) and Plasmodium cynomolgi (including differentiation of three strains). Detection and identification of Plasmodium species relies on molecular beacon probe-based melting curve analysis. In addition, this assay might be used to quantify the parasitaemia of at least P. falciparum by calculating the level of parasitaemia directly from the Cq-value. METHODS: The samples used in this study comprised reference samples, patient samples, and synthetic controls. The following analytical performance characteristics of the MC004 assay were determined: analytical specificity, limit of detection, the ability to detect mixed infections, and the potential to determine the level of parasitaemia of P. falciparum, including assessment of within-run and between-run precisions. RESULTS: No false positive or false negative results were observed. The limit of detection of P. falciparum was 1 × 10(–3) IU/mL (WHO standard). Mixed infections with P. falciparum and non-falciparum species were correctly identified. A calibration curve could be established to quantify the parasitaemia of at least P. falciparum. The within-run and between-run precisions were less than 20% CV at the tested parasitaemia levels of 0.09%, 0.16%, 2.15% and 27.27%. CONCLUSION: Based upon the analytical performance characteristics that were determined, the MC004 assay showed performance suitable for use in clinical settings, as well as epidemiological studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-021-03842-8. BioMed Central 2021-07-12 /pmc/articles/PMC8274047/ /pubmed/34247622 http://dx.doi.org/10.1186/s12936-021-03842-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology van Bergen, Kim Stuitje, Toon Akkers, Robert Vermeer, Eric Castel, Rob Mank, Theo Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans |
title | Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans |
title_full | Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans |
title_fullStr | Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans |
title_full_unstemmed | Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans |
title_short | Evaluation of a novel real-time PCR assay for the detection, identification and quantification of Plasmodium species causing malaria in humans |
title_sort | evaluation of a novel real-time pcr assay for the detection, identification and quantification of plasmodium species causing malaria in humans |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274047/ https://www.ncbi.nlm.nih.gov/pubmed/34247622 http://dx.doi.org/10.1186/s12936-021-03842-8 |
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