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Estimation of parasite age and synchrony status in Plasmodium falciparum infections
Human malaria parasites have complex but poorly understood population dynamics inside their human host. In some but not all infections, parasites progress synchronously through the 48 h lifecycle following erythrocyte invasion, such that at any one time there is a limited spread of parasites at a pa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331735/ https://www.ncbi.nlm.nih.gov/pubmed/32616767 http://dx.doi.org/10.1038/s41598-020-67817-6 |
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author | Ciuffreda, Laura Zoiku, Felix Kwame Quashie, Neils B. Ranford-Cartwright, Lisa C. |
author_facet | Ciuffreda, Laura Zoiku, Felix Kwame Quashie, Neils B. Ranford-Cartwright, Lisa C. |
author_sort | Ciuffreda, Laura |
collection | PubMed |
description | Human malaria parasites have complex but poorly understood population dynamics inside their human host. In some but not all infections, parasites progress synchronously through the 48 h lifecycle following erythrocyte invasion, such that at any one time there is a limited spread of parasites at a particular time (hours) post-invasion. Patients presenting with older parasites, and with asynchronous infections, have been reported to have higher risks of fatal outcomes, associated with higher parasite biomass and multiplication rates respectively. However, practical tools to assess synchrony and estimate parasite age post-invasion in patient samples are lacking. We have developed a novel method based on three genes differentially expressed over the parasite intra-erythrocytic lifecycle, and applied it to samples from patients with uncomplicated malaria attending two health clinics in Ghana. We found that most patients presented with synchronous infections, and with parasites within 12 h of erythrocyte invasion. Finally we investigated if clinical features such as fever and parasite density could act as predictors of parasite age and synchrony. The new method is a simple and practicable approach to study parasite dynamics in naturally-infected patients, and is a significant improvement on the subjective microscopical methods for parasite staging in vivo, aiding patient management. |
format | Online Article Text |
id | pubmed-7331735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73317352020-07-06 Estimation of parasite age and synchrony status in Plasmodium falciparum infections Ciuffreda, Laura Zoiku, Felix Kwame Quashie, Neils B. Ranford-Cartwright, Lisa C. Sci Rep Article Human malaria parasites have complex but poorly understood population dynamics inside their human host. In some but not all infections, parasites progress synchronously through the 48 h lifecycle following erythrocyte invasion, such that at any one time there is a limited spread of parasites at a particular time (hours) post-invasion. Patients presenting with older parasites, and with asynchronous infections, have been reported to have higher risks of fatal outcomes, associated with higher parasite biomass and multiplication rates respectively. However, practical tools to assess synchrony and estimate parasite age post-invasion in patient samples are lacking. We have developed a novel method based on three genes differentially expressed over the parasite intra-erythrocytic lifecycle, and applied it to samples from patients with uncomplicated malaria attending two health clinics in Ghana. We found that most patients presented with synchronous infections, and with parasites within 12 h of erythrocyte invasion. Finally we investigated if clinical features such as fever and parasite density could act as predictors of parasite age and synchrony. The new method is a simple and practicable approach to study parasite dynamics in naturally-infected patients, and is a significant improvement on the subjective microscopical methods for parasite staging in vivo, aiding patient management. Nature Publishing Group UK 2020-07-02 /pmc/articles/PMC7331735/ /pubmed/32616767 http://dx.doi.org/10.1038/s41598-020-67817-6 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ciuffreda, Laura Zoiku, Felix Kwame Quashie, Neils B. Ranford-Cartwright, Lisa C. Estimation of parasite age and synchrony status in Plasmodium falciparum infections |
title | Estimation of parasite age and synchrony status in Plasmodium falciparum infections |
title_full | Estimation of parasite age and synchrony status in Plasmodium falciparum infections |
title_fullStr | Estimation of parasite age and synchrony status in Plasmodium falciparum infections |
title_full_unstemmed | Estimation of parasite age and synchrony status in Plasmodium falciparum infections |
title_short | Estimation of parasite age and synchrony status in Plasmodium falciparum infections |
title_sort | estimation of parasite age and synchrony status in plasmodium falciparum infections |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331735/ https://www.ncbi.nlm.nih.gov/pubmed/32616767 http://dx.doi.org/10.1038/s41598-020-67817-6 |
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