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Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection
BACKGROUND: Malaria, due to Plasmodium ovale, can be challenging to diagnose due to clinically mild disease and low parasite burden. Two genetically distinct sub-species of P. ovale exist: Plasmodium ovale curtisi (classic) and Plasmodium ovale wallikeri (variant). It is presently unknown if the sub...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103354/ https://www.ncbi.nlm.nih.gov/pubmed/27832785 http://dx.doi.org/10.1186/s12936-016-1601-2 |
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author | Phuong, Melissa S. Lau, Rachel Ralevski, Filip Boggild, Andrea K. |
author_facet | Phuong, Melissa S. Lau, Rachel Ralevski, Filip Boggild, Andrea K. |
author_sort | Phuong, Melissa S. |
collection | PubMed |
description | BACKGROUND: Malaria, due to Plasmodium ovale, can be challenging to diagnose due to clinically mild disease and low parasite burden. Two genetically distinct sub-species of P. ovale exist: Plasmodium ovale curtisi (classic) and Plasmodium ovale wallikeri (variant). It is presently unknown if the sub-species causing infection affects performance of malaria diagnostic tests. The aim of this work was to understand how the genetically distinct sub-species, P. o. curtisi and P. o. wallikeri, affect malaria diagnostic tests. METHODS: Plasmodium ovale-positive whole blood specimens were sub-speciated by PCR and sequencing of 18S rRNA and dhfr-ts. Parasitaemia, morphology, pan-aldolase positivity, 18S copy number, and dhfr-ts sequences were compared between sub-species. RESULTS: From 2006 to 2015, 49 P. ovale isolates were identified, of which 22 were P. o. curtisi and 27 P. o. wallikeri; 80% were identified in the last five years, and 88% were acquired in West Africa. Sub-species did not differ by parasitaemia, 18S copy number, or pan-aldolase positivity. Lack of Schüffner’s stippling was over-represented among P. o. wallikeri isolates (p = 0.02). Several nucleotide polymorphisms between the sub-species were observed, but they do not occur at sites believed to relate to antifolate binding. CONCLUSIONS: Plasmodium ovale is increasing among travellers to West Africa, although sub-species do not differ significantly by parasitologic features such as parasitaemia. Absence of Schüffner’s stippling may be a feature specific to P. o. wallikeri and is a novel finding. |
format | Online Article Text |
id | pubmed-5103354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51033542016-11-10 Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection Phuong, Melissa S. Lau, Rachel Ralevski, Filip Boggild, Andrea K. Malar J Research BACKGROUND: Malaria, due to Plasmodium ovale, can be challenging to diagnose due to clinically mild disease and low parasite burden. Two genetically distinct sub-species of P. ovale exist: Plasmodium ovale curtisi (classic) and Plasmodium ovale wallikeri (variant). It is presently unknown if the sub-species causing infection affects performance of malaria diagnostic tests. The aim of this work was to understand how the genetically distinct sub-species, P. o. curtisi and P. o. wallikeri, affect malaria diagnostic tests. METHODS: Plasmodium ovale-positive whole blood specimens were sub-speciated by PCR and sequencing of 18S rRNA and dhfr-ts. Parasitaemia, morphology, pan-aldolase positivity, 18S copy number, and dhfr-ts sequences were compared between sub-species. RESULTS: From 2006 to 2015, 49 P. ovale isolates were identified, of which 22 were P. o. curtisi and 27 P. o. wallikeri; 80% were identified in the last five years, and 88% were acquired in West Africa. Sub-species did not differ by parasitaemia, 18S copy number, or pan-aldolase positivity. Lack of Schüffner’s stippling was over-represented among P. o. wallikeri isolates (p = 0.02). Several nucleotide polymorphisms between the sub-species were observed, but they do not occur at sites believed to relate to antifolate binding. CONCLUSIONS: Plasmodium ovale is increasing among travellers to West Africa, although sub-species do not differ significantly by parasitologic features such as parasitaemia. Absence of Schüffner’s stippling may be a feature specific to P. o. wallikeri and is a novel finding. BioMed Central 2016-11-10 /pmc/articles/PMC5103354/ /pubmed/27832785 http://dx.doi.org/10.1186/s12936-016-1601-2 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Phuong, Melissa S. Lau, Rachel Ralevski, Filip Boggild, Andrea K. Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection |
title | Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection |
title_full | Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection |
title_fullStr | Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection |
title_full_unstemmed | Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection |
title_short | Parasitological correlates of Plasmodium ovale curtisi and Plasmodium ovale wallikeri infection |
title_sort | parasitological correlates of plasmodium ovale curtisi and plasmodium ovale wallikeri infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103354/ https://www.ncbi.nlm.nih.gov/pubmed/27832785 http://dx.doi.org/10.1186/s12936-016-1601-2 |
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