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A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria

BACKGROUND: P. ovale spp. infections are endemic across multiple African countries and are caused by two distinct non-recombining species, P. ovale curtisi (Poc) and P. ovale wallikeri (Pow). These species are thought to differ in clinical symptomatology and latency, but existing diagnostic assays h...

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Autores principales: He, Wenqiao, Sendor, Rachel, Potlapalli, Varun R., Kashamuka, Melchior M., Tshefu, Antoinette K., Phanzu, Fernandine, Kalonji, Albert, Ngasala, Billy, Thwai, Kyaw Lay, Juliano, Jonathan J., Lin, Jessica T., Parr, Jonathan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635243/
https://www.ncbi.nlm.nih.gov/pubmed/37961397
http://dx.doi.org/10.1101/2023.10.31.23297819
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author He, Wenqiao
Sendor, Rachel
Potlapalli, Varun R.
Kashamuka, Melchior M.
Tshefu, Antoinette K.
Phanzu, Fernandine
Kalonji, Albert
Ngasala, Billy
Thwai, Kyaw Lay
Juliano, Jonathan J.
Lin, Jessica T.
Parr, Jonathan B.
author_facet He, Wenqiao
Sendor, Rachel
Potlapalli, Varun R.
Kashamuka, Melchior M.
Tshefu, Antoinette K.
Phanzu, Fernandine
Kalonji, Albert
Ngasala, Billy
Thwai, Kyaw Lay
Juliano, Jonathan J.
Lin, Jessica T.
Parr, Jonathan B.
author_sort He, Wenqiao
collection PubMed
description BACKGROUND: P. ovale spp. infections are endemic across multiple African countries and are caused by two distinct non-recombining species, P. ovale curtisi (Poc) and P. ovale wallikeri (Pow). These species are thought to differ in clinical symptomatology and latency, but existing diagnostic assays have limited ability to detect and distinguish them. In this study, we developed a new duplex assay for the detection and differentiation of Poc and Pow that can be used to improve our understanding of these parasites. METHODS: Repetitive sequence motifs were identified in available Poc and Pow genomes and used for assay development and validation. We evaluated the analytical sensitivity and specificity of the best-performing assay using a panel of samples from Tanzania and the Democratic Republic of the Congo (DRC), then validated its performance using 55 P. ovale spp. samples and 40 non-ovale Plasmodium samples from the DRC. Poc and Pow prevalence among symptomatic individuals sampled across three provinces of the DRC were estimated. RESULTS: The best-performing Poc and Pow targets had 9 and 8 copies within the reference genomes, respectively. Our duplex assay had 100% specificity and 95% confidence lower limits of detection of 4.2 and 41.2 parasite genome equivalents/μl for Poc and Pow, respectively. Species was determined in 80% of all P. ovale spp.-positive field samples and 100% of those with >10 parasites/μl. Most P. ovale spp. field samples from the DRC were found to be Poc infections. CONCLUSIONS: We identified promising multi-copy targets for molecular detection and differentiation of Poc and Pow and used them to develop a new duplex real-time PCR assay that performed well when applied to diverse field samples. Though low-density Pow infections are not reliably detected, the assay is highly specific and can be used for high-throughput studies of P. ovale spp. epidemiology among symptomatic cases in malaria-endemic countries like the DRC.
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spelling pubmed-106352432023-11-13 A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria He, Wenqiao Sendor, Rachel Potlapalli, Varun R. Kashamuka, Melchior M. Tshefu, Antoinette K. Phanzu, Fernandine Kalonji, Albert Ngasala, Billy Thwai, Kyaw Lay Juliano, Jonathan J. Lin, Jessica T. Parr, Jonathan B. medRxiv Article BACKGROUND: P. ovale spp. infections are endemic across multiple African countries and are caused by two distinct non-recombining species, P. ovale curtisi (Poc) and P. ovale wallikeri (Pow). These species are thought to differ in clinical symptomatology and latency, but existing diagnostic assays have limited ability to detect and distinguish them. In this study, we developed a new duplex assay for the detection and differentiation of Poc and Pow that can be used to improve our understanding of these parasites. METHODS: Repetitive sequence motifs were identified in available Poc and Pow genomes and used for assay development and validation. We evaluated the analytical sensitivity and specificity of the best-performing assay using a panel of samples from Tanzania and the Democratic Republic of the Congo (DRC), then validated its performance using 55 P. ovale spp. samples and 40 non-ovale Plasmodium samples from the DRC. Poc and Pow prevalence among symptomatic individuals sampled across three provinces of the DRC were estimated. RESULTS: The best-performing Poc and Pow targets had 9 and 8 copies within the reference genomes, respectively. Our duplex assay had 100% specificity and 95% confidence lower limits of detection of 4.2 and 41.2 parasite genome equivalents/μl for Poc and Pow, respectively. Species was determined in 80% of all P. ovale spp.-positive field samples and 100% of those with >10 parasites/μl. Most P. ovale spp. field samples from the DRC were found to be Poc infections. CONCLUSIONS: We identified promising multi-copy targets for molecular detection and differentiation of Poc and Pow and used them to develop a new duplex real-time PCR assay that performed well when applied to diverse field samples. Though low-density Pow infections are not reliably detected, the assay is highly specific and can be used for high-throughput studies of P. ovale spp. epidemiology among symptomatic cases in malaria-endemic countries like the DRC. Cold Spring Harbor Laboratory 2023-10-31 /pmc/articles/PMC10635243/ /pubmed/37961397 http://dx.doi.org/10.1101/2023.10.31.23297819 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
He, Wenqiao
Sendor, Rachel
Potlapalli, Varun R.
Kashamuka, Melchior M.
Tshefu, Antoinette K.
Phanzu, Fernandine
Kalonji, Albert
Ngasala, Billy
Thwai, Kyaw Lay
Juliano, Jonathan J.
Lin, Jessica T.
Parr, Jonathan B.
A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria
title A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria
title_full A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria
title_fullStr A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria
title_full_unstemmed A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria
title_short A novel duplex qualitative real-time PCR assay for the detection and differentiation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri malaria
title_sort novel duplex qualitative real-time pcr assay for the detection and differentiation of plasmodium ovale curtisi and plasmodium ovale wallikeri malaria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635243/
https://www.ncbi.nlm.nih.gov/pubmed/37961397
http://dx.doi.org/10.1101/2023.10.31.23297819
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