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Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities()

It has been proposed that ovale malaria in humans is caused by two closely related but distinct species of malaria parasite, Plasmodium ovale curtisi and Plasmodium ovale wallikeri. It was recently shown that these two parasite types are sympatric at the country level. However, it remains possible t...

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Autores principales: Oguike, Mary Chiaka, Betson, Martha, Burke, Martina, Nolder, Debbie, Stothard, J. Russell, Kleinschmidt, Immo, Proietti, Carla, Bousema, Teun, Ndounga, Mathieu, Tanabe, Kazuyuki, Ntege, Edward, Culleton, Richard, Sutherland, Colin J.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084460/
https://www.ncbi.nlm.nih.gov/pubmed/21315074
http://dx.doi.org/10.1016/j.ijpara.2011.01.004
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author Oguike, Mary Chiaka
Betson, Martha
Burke, Martina
Nolder, Debbie
Stothard, J. Russell
Kleinschmidt, Immo
Proietti, Carla
Bousema, Teun
Ndounga, Mathieu
Tanabe, Kazuyuki
Ntege, Edward
Culleton, Richard
Sutherland, Colin J.
author_facet Oguike, Mary Chiaka
Betson, Martha
Burke, Martina
Nolder, Debbie
Stothard, J. Russell
Kleinschmidt, Immo
Proietti, Carla
Bousema, Teun
Ndounga, Mathieu
Tanabe, Kazuyuki
Ntege, Edward
Culleton, Richard
Sutherland, Colin J.
author_sort Oguike, Mary Chiaka
collection PubMed
description It has been proposed that ovale malaria in humans is caused by two closely related but distinct species of malaria parasite, Plasmodium ovale curtisi and Plasmodium ovale wallikeri. It was recently shown that these two parasite types are sympatric at the country level. However, it remains possible that localised geographic, temporal or ecological barriers exist within endemic countries which prevent recombination between the genomes of the two species. Here, using conventional and real-time quantitative PCR (qPCR) methods specifically designed to discriminate P. o. curtisi and P. o. wallikeri, it is shown that both species are present among clinic attendees in Congo-Brazzaville, and occur simultaneously both in lake-side and inland districts in Uganda and on Bioko Island, Equatorial Guinea. Thus P. o. curtisi and P. o. wallikeri in these localities are exactly sympatric in both time and space. These findings are consistent with the existence of a biological barrier, rather than geographical or ecological factors, preventing recombination between P. o. curtisi and P. o. wallikeri. In cross-sectional surveys carried out in Uganda and Bioko, our results show that infections with P. ovale spp. are more common than previously thought, occurring at a frequency of 1–6% in population samples, with both proposed species contributing to ovale malaria in six sites. Malaria elimination programmes in Africa need to include strategies for control of P. o. curtisi and P. o. wallikeri.
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spelling pubmed-30844602011-06-28 Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities() Oguike, Mary Chiaka Betson, Martha Burke, Martina Nolder, Debbie Stothard, J. Russell Kleinschmidt, Immo Proietti, Carla Bousema, Teun Ndounga, Mathieu Tanabe, Kazuyuki Ntege, Edward Culleton, Richard Sutherland, Colin J. Int J Parasitol Article It has been proposed that ovale malaria in humans is caused by two closely related but distinct species of malaria parasite, Plasmodium ovale curtisi and Plasmodium ovale wallikeri. It was recently shown that these two parasite types are sympatric at the country level. However, it remains possible that localised geographic, temporal or ecological barriers exist within endemic countries which prevent recombination between the genomes of the two species. Here, using conventional and real-time quantitative PCR (qPCR) methods specifically designed to discriminate P. o. curtisi and P. o. wallikeri, it is shown that both species are present among clinic attendees in Congo-Brazzaville, and occur simultaneously both in lake-side and inland districts in Uganda and on Bioko Island, Equatorial Guinea. Thus P. o. curtisi and P. o. wallikeri in these localities are exactly sympatric in both time and space. These findings are consistent with the existence of a biological barrier, rather than geographical or ecological factors, preventing recombination between P. o. curtisi and P. o. wallikeri. In cross-sectional surveys carried out in Uganda and Bioko, our results show that infections with P. ovale spp. are more common than previously thought, occurring at a frequency of 1–6% in population samples, with both proposed species contributing to ovale malaria in six sites. Malaria elimination programmes in Africa need to include strategies for control of P. o. curtisi and P. o. wallikeri. Elsevier Science 2011-05 /pmc/articles/PMC3084460/ /pubmed/21315074 http://dx.doi.org/10.1016/j.ijpara.2011.01.004 Text en © 2011 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Oguike, Mary Chiaka
Betson, Martha
Burke, Martina
Nolder, Debbie
Stothard, J. Russell
Kleinschmidt, Immo
Proietti, Carla
Bousema, Teun
Ndounga, Mathieu
Tanabe, Kazuyuki
Ntege, Edward
Culleton, Richard
Sutherland, Colin J.
Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities()
title Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities()
title_full Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities()
title_fullStr Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities()
title_full_unstemmed Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities()
title_short Plasmodium ovale curtisi and Plasmodium ovale wallikeri circulate simultaneously in African communities()
title_sort plasmodium ovale curtisi and plasmodium ovale wallikeri circulate simultaneously in african communities()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084460/
https://www.ncbi.nlm.nih.gov/pubmed/21315074
http://dx.doi.org/10.1016/j.ijpara.2011.01.004
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