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Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda
Histidine-rich protein 2 (HRP2)–based rapid diagnostic tests detect Plasmodium falciparum malaria and are used throughout sub-Saharan Africa. However, deletions in the pfhrp2 and related pfhrp3 (pfhrp2/3) genes threaten use of these tests. Therapeutic efficacy studies (TESs) enroll persons with symp...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888236/ https://www.ncbi.nlm.nih.gov/pubmed/35201739 http://dx.doi.org/10.3201/eid2803.211499 |
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author | Rogier, Eric McCaffery, Jessica N. Nace, Doug Svigel, Samaly Souza Assefa, Ashenafi Hwang, Jimee Kariuki, Simon Samuels, Aaron M. Westercamp, Nelli Ratsimbasoa, Arsène Randrianarivelojosia, Milijaona Uwimana, Aline Udhayakumar, Venkatachalam Halsey, Eric S. |
author_facet | Rogier, Eric McCaffery, Jessica N. Nace, Doug Svigel, Samaly Souza Assefa, Ashenafi Hwang, Jimee Kariuki, Simon Samuels, Aaron M. Westercamp, Nelli Ratsimbasoa, Arsène Randrianarivelojosia, Milijaona Uwimana, Aline Udhayakumar, Venkatachalam Halsey, Eric S. |
author_sort | Rogier, Eric |
collection | PubMed |
description | Histidine-rich protein 2 (HRP2)–based rapid diagnostic tests detect Plasmodium falciparum malaria and are used throughout sub-Saharan Africa. However, deletions in the pfhrp2 and related pfhrp3 (pfhrp2/3) genes threaten use of these tests. Therapeutic efficacy studies (TESs) enroll persons with symptomatic P. falciparum infection. We screened TES samples collected during 2016–2018 in Ethiopia, Kenya, Rwanda, and Madagascar for HRP2/3, pan-Plasmodium lactate dehydrogenase, and pan-Plasmodium aldolase antigen levels and selected samples with low levels of HRP2/3 for pfhrp2/3 genotyping. We observed deletion of pfhrp3 in samples from all countries except Kenya. Single-gene deletions in pfhrp2 were observed in 1.4% (95% CI 0.2%–4.8%) of Ethiopia samples and in 0.6% (95% CI 0.2%–1.6%) of Madagascar samples, and dual pfhrp2/3 deletions were noted in 2.0% (95% CI 0.4%–5.9%) of Ethiopia samples. Although this study was not powered for precise prevalence estimates, evaluating TES samples revealed a low prevalence of pfhrp2/3 deletions in most sites. |
format | Online Article Text |
id | pubmed-8888236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-88882362022-03-02 Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda Rogier, Eric McCaffery, Jessica N. Nace, Doug Svigel, Samaly Souza Assefa, Ashenafi Hwang, Jimee Kariuki, Simon Samuels, Aaron M. Westercamp, Nelli Ratsimbasoa, Arsène Randrianarivelojosia, Milijaona Uwimana, Aline Udhayakumar, Venkatachalam Halsey, Eric S. Emerg Infect Dis Research Histidine-rich protein 2 (HRP2)–based rapid diagnostic tests detect Plasmodium falciparum malaria and are used throughout sub-Saharan Africa. However, deletions in the pfhrp2 and related pfhrp3 (pfhrp2/3) genes threaten use of these tests. Therapeutic efficacy studies (TESs) enroll persons with symptomatic P. falciparum infection. We screened TES samples collected during 2016–2018 in Ethiopia, Kenya, Rwanda, and Madagascar for HRP2/3, pan-Plasmodium lactate dehydrogenase, and pan-Plasmodium aldolase antigen levels and selected samples with low levels of HRP2/3 for pfhrp2/3 genotyping. We observed deletion of pfhrp3 in samples from all countries except Kenya. Single-gene deletions in pfhrp2 were observed in 1.4% (95% CI 0.2%–4.8%) of Ethiopia samples and in 0.6% (95% CI 0.2%–1.6%) of Madagascar samples, and dual pfhrp2/3 deletions were noted in 2.0% (95% CI 0.4%–5.9%) of Ethiopia samples. Although this study was not powered for precise prevalence estimates, evaluating TES samples revealed a low prevalence of pfhrp2/3 deletions in most sites. Centers for Disease Control and Prevention 2022-03 /pmc/articles/PMC8888236/ /pubmed/35201739 http://dx.doi.org/10.3201/eid2803.211499 Text en https://creativecommons.org/licenses/by/4.0/Emerging Infectious Diseases is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Rogier, Eric McCaffery, Jessica N. Nace, Doug Svigel, Samaly Souza Assefa, Ashenafi Hwang, Jimee Kariuki, Simon Samuels, Aaron M. Westercamp, Nelli Ratsimbasoa, Arsène Randrianarivelojosia, Milijaona Uwimana, Aline Udhayakumar, Venkatachalam Halsey, Eric S. Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda |
title | Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda |
title_full | Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda |
title_fullStr | Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda |
title_full_unstemmed | Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda |
title_short | Plasmodium falciparum pfhrp2 and pfhrp3 Gene Deletions from Persons with Symptomatic Malaria Infection in Ethiopia, Kenya, Madagascar, and Rwanda |
title_sort | plasmodium falciparum pfhrp2 and pfhrp3 gene deletions from persons with symptomatic malaria infection in ethiopia, kenya, madagascar, and rwanda |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888236/ https://www.ncbi.nlm.nih.gov/pubmed/35201739 http://dx.doi.org/10.3201/eid2803.211499 |
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