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Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing
BACKGROUND: Plasmodium vivax is estimated to affect 75 million people annually. It is reportedly absent, however, from west and central Africa due to the high prevalence of the Duffy negative phenotype in the indigenous populations. Despite this, non-African travellers consistently return to their o...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546428/ https://www.ncbi.nlm.nih.gov/pubmed/18783630 http://dx.doi.org/10.1186/1475-2875-7-174 |
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author | Culleton, Richard L Mita, Toshihiro Ndounga, Mathieu Unger, Holger Cravo, Pedro VL Paganotti, Giacomo M Takahashi, Nobuyuki Kaneko, Akira Eto, Hideaki Tinto, Halidou Karema, Corine D'Alessandro, Umberto do Rosário, Virgilio Kobayakawa, Takatoshi Ntoumi, Francine Carter, Richard Tanabe, Kazuyuki |
author_facet | Culleton, Richard L Mita, Toshihiro Ndounga, Mathieu Unger, Holger Cravo, Pedro VL Paganotti, Giacomo M Takahashi, Nobuyuki Kaneko, Akira Eto, Hideaki Tinto, Halidou Karema, Corine D'Alessandro, Umberto do Rosário, Virgilio Kobayakawa, Takatoshi Ntoumi, Francine Carter, Richard Tanabe, Kazuyuki |
author_sort | Culleton, Richard L |
collection | PubMed |
description | BACKGROUND: Plasmodium vivax is estimated to affect 75 million people annually. It is reportedly absent, however, from west and central Africa due to the high prevalence of the Duffy negative phenotype in the indigenous populations. Despite this, non-African travellers consistently return to their own countries with P. vivax malaria after visiting this region. An attempt was made, therefore, to detect the presence of P. vivax parasites in blood samples collected from the indigenous populations of west and central Africa. METHODS: Parasite species typing (for all four human malaria parasites) was carried out by PCR on 2,588 blood samples collected from individuals from nine African malaria-endemic countries. RESULTS: Most infections (98.5%) were Plasmodium falciparum, Plasmodium malariae was identified in 8.5% of all infections, and Plasmodium ovale in 3.9%. The prevalence of both parasites varied greatly by country. Only one case of P. vivax was detected from Sao Tome, an island off the west coast of Africa, confirming the scarcity of this parasite in Africa. CONCLUSION: The prevalence of P. vivax in local populations in sub-Saharan Africa is very low, despite the frequent identification of this parasite in non-African travellers. |
format | Text |
id | pubmed-2546428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25464282008-09-20 Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing Culleton, Richard L Mita, Toshihiro Ndounga, Mathieu Unger, Holger Cravo, Pedro VL Paganotti, Giacomo M Takahashi, Nobuyuki Kaneko, Akira Eto, Hideaki Tinto, Halidou Karema, Corine D'Alessandro, Umberto do Rosário, Virgilio Kobayakawa, Takatoshi Ntoumi, Francine Carter, Richard Tanabe, Kazuyuki Malar J Research BACKGROUND: Plasmodium vivax is estimated to affect 75 million people annually. It is reportedly absent, however, from west and central Africa due to the high prevalence of the Duffy negative phenotype in the indigenous populations. Despite this, non-African travellers consistently return to their own countries with P. vivax malaria after visiting this region. An attempt was made, therefore, to detect the presence of P. vivax parasites in blood samples collected from the indigenous populations of west and central Africa. METHODS: Parasite species typing (for all four human malaria parasites) was carried out by PCR on 2,588 blood samples collected from individuals from nine African malaria-endemic countries. RESULTS: Most infections (98.5%) were Plasmodium falciparum, Plasmodium malariae was identified in 8.5% of all infections, and Plasmodium ovale in 3.9%. The prevalence of both parasites varied greatly by country. Only one case of P. vivax was detected from Sao Tome, an island off the west coast of Africa, confirming the scarcity of this parasite in Africa. CONCLUSION: The prevalence of P. vivax in local populations in sub-Saharan Africa is very low, despite the frequent identification of this parasite in non-African travellers. BioMed Central 2008-09-11 /pmc/articles/PMC2546428/ /pubmed/18783630 http://dx.doi.org/10.1186/1475-2875-7-174 Text en Copyright © 2008 Culleton et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Culleton, Richard L Mita, Toshihiro Ndounga, Mathieu Unger, Holger Cravo, Pedro VL Paganotti, Giacomo M Takahashi, Nobuyuki Kaneko, Akira Eto, Hideaki Tinto, Halidou Karema, Corine D'Alessandro, Umberto do Rosário, Virgilio Kobayakawa, Takatoshi Ntoumi, Francine Carter, Richard Tanabe, Kazuyuki Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing |
title | Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing |
title_full | Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing |
title_fullStr | Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing |
title_full_unstemmed | Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing |
title_short | Failure to detect Plasmodium vivax in West and Central Africa by PCR species typing |
title_sort | failure to detect plasmodium vivax in west and central africa by pcr species typing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546428/ https://www.ncbi.nlm.nih.gov/pubmed/18783630 http://dx.doi.org/10.1186/1475-2875-7-174 |
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