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Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan
Plasmodium vivax Duffy Binding Protein (PvDBP) is essential for interacting with Duffy antigen receptor for chemokines (DARC) on the surface of red blood cells to allow invasion. Earlier whole genome sequence analyses provided evidence for the duplications of PvDBP. It is unclear whether PvDBP dupli...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358875/ https://www.ncbi.nlm.nih.gov/pubmed/37471337 http://dx.doi.org/10.1371/journal.pone.0287668 |
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author | Ahmed, Safaa Pestana, Kareen Ford, Anthony Elfaki, Mohammed Gamil, Eiman Elamin, Arwa F. Hamad, Samuel Omer Elfaki, Tarig Mohamed Abukashawa, Sumaia Mohamed Ahmed Lo, Eugenia Abdel Hamid, Muzamil M. |
author_facet | Ahmed, Safaa Pestana, Kareen Ford, Anthony Elfaki, Mohammed Gamil, Eiman Elamin, Arwa F. Hamad, Samuel Omer Elfaki, Tarig Mohamed Abukashawa, Sumaia Mohamed Ahmed Lo, Eugenia Abdel Hamid, Muzamil M. |
author_sort | Ahmed, Safaa |
collection | PubMed |
description | Plasmodium vivax Duffy Binding Protein (PvDBP) is essential for interacting with Duffy antigen receptor for chemokines (DARC) on the surface of red blood cells to allow invasion. Earlier whole genome sequence analyses provided evidence for the duplications of PvDBP. It is unclear whether PvDBP duplications play a role in recent increase of P. vivax in Sudan and in Duffy-negative individuals. In this study, the prevalence and type of PvDBP duplications, and its relationship to demographic and clinical features were investigated. A total of 200 malaria-suspected blood samples were collected from health facilities in Khartoum, River Nile, and Al-Obied. Among them, 145 were confirmed to be P. vivax, and 43 (29.7%) had more than one PvDBP copies with up to four copies being detected. Both the Malagasy and Cambodian types of PvDBP duplication were detected. No significant difference was observed between the two types of duplications between Duffy groups. Parasitemia was significantly higher in samples with the Malagasy-type than those without duplications. No significant difference was observed in PvDBP duplication prevalence and copy number among study sites. The functional significance of PvDBP duplications, especially those Malagasy-type that associated with higher parasitemia, merit further investigations. |
format | Online Article Text |
id | pubmed-10358875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103588752023-07-21 Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan Ahmed, Safaa Pestana, Kareen Ford, Anthony Elfaki, Mohammed Gamil, Eiman Elamin, Arwa F. Hamad, Samuel Omer Elfaki, Tarig Mohamed Abukashawa, Sumaia Mohamed Ahmed Lo, Eugenia Abdel Hamid, Muzamil M. PLoS One Research Article Plasmodium vivax Duffy Binding Protein (PvDBP) is essential for interacting with Duffy antigen receptor for chemokines (DARC) on the surface of red blood cells to allow invasion. Earlier whole genome sequence analyses provided evidence for the duplications of PvDBP. It is unclear whether PvDBP duplications play a role in recent increase of P. vivax in Sudan and in Duffy-negative individuals. In this study, the prevalence and type of PvDBP duplications, and its relationship to demographic and clinical features were investigated. A total of 200 malaria-suspected blood samples were collected from health facilities in Khartoum, River Nile, and Al-Obied. Among them, 145 were confirmed to be P. vivax, and 43 (29.7%) had more than one PvDBP copies with up to four copies being detected. Both the Malagasy and Cambodian types of PvDBP duplication were detected. No significant difference was observed between the two types of duplications between Duffy groups. Parasitemia was significantly higher in samples with the Malagasy-type than those without duplications. No significant difference was observed in PvDBP duplication prevalence and copy number among study sites. The functional significance of PvDBP duplications, especially those Malagasy-type that associated with higher parasitemia, merit further investigations. Public Library of Science 2023-07-20 /pmc/articles/PMC10358875/ /pubmed/37471337 http://dx.doi.org/10.1371/journal.pone.0287668 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Ahmed, Safaa Pestana, Kareen Ford, Anthony Elfaki, Mohammed Gamil, Eiman Elamin, Arwa F. Hamad, Samuel Omer Elfaki, Tarig Mohamed Abukashawa, Sumaia Mohamed Ahmed Lo, Eugenia Abdel Hamid, Muzamil M. Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan |
title | Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan |
title_full | Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan |
title_fullStr | Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan |
title_full_unstemmed | Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan |
title_short | Prevalence and distribution of Plasmodium vivax Duffy Binding Protein gene duplications in Sudan |
title_sort | prevalence and distribution of plasmodium vivax duffy binding protein gene duplications in sudan |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358875/ https://www.ncbi.nlm.nih.gov/pubmed/37471337 http://dx.doi.org/10.1371/journal.pone.0287668 |
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