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Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions
In the thirteen years since the first report of pfhrp2-deleted parasites in 2010, the World Health Organization (WHO) has found that 40 of 47 countries surveyed worldwide have reported pfhrp2/3 gene deletions. Due to a high prevalence of pfhrp2/3 deletions causing false-negative HRP2 RDTs, in the la...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615018/ https://www.ncbi.nlm.nih.gov/pubmed/37905102 http://dx.doi.org/10.1101/2023.10.21.23297352 |
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author | Watson, Oliver J. Tran, Thu Nguyen-Anh Zupko, Robert J Symons, Tasmin Thomson, Rebecca Visser, Theodoor Rumisha, Susan Dzianach, Paulina A Hathaway, Nicholas Kim, Isaac Juliano, Jonathan J. Bailey, Jeffrey A. Slater, Hannah Okell, Lucy Gething, Peter Ghani, Azra Boni, Maciej F Parr, Jonathan B. Cunningham, Jane |
author_facet | Watson, Oliver J. Tran, Thu Nguyen-Anh Zupko, Robert J Symons, Tasmin Thomson, Rebecca Visser, Theodoor Rumisha, Susan Dzianach, Paulina A Hathaway, Nicholas Kim, Isaac Juliano, Jonathan J. Bailey, Jeffrey A. Slater, Hannah Okell, Lucy Gething, Peter Ghani, Azra Boni, Maciej F Parr, Jonathan B. Cunningham, Jane |
author_sort | Watson, Oliver J. |
collection | PubMed |
description | In the thirteen years since the first report of pfhrp2-deleted parasites in 2010, the World Health Organization (WHO) has found that 40 of 47 countries surveyed worldwide have reported pfhrp2/3 gene deletions. Due to a high prevalence of pfhrp2/3 deletions causing false-negative HRP2 RDTs, in the last five years, Eritrea, Djibouti and Ethiopia have switched or started switching to using alternative RDTs, that target pan-specific-pLDH or P. falciparum specific-pLDH alone of in combination with HRP2. However, manufacturing of alternative RDTs has not been brought to scale and there are no WHO prequalified combination tests that use Pf-pLDH instead of HRP2 for P. falciparum detection. For these reasons, the continued spread of pfhrp2/3 deletions represents a growing public health crisis that threatens efforts to control and eliminate P. falciparum malaria. National malaria control programmes, their implementing partners and test developers desperately seek pfhrp2/3 deletion data that can inform their immediate and future resource allocation. In response, we use a mathematical modelling approach to evaluate the global risk posed by pfhrp2/3 deletions and explore scenarios for how deletions will continue to spread in Africa. We incorporate current best estimates of the prevalence of pfhrp2/3 deletions and conduct a literature review to estimate model parameters known to impact the selection of pfhrp2/3 deletions for each malaria endemic country. We identify 20 countries worldwide to prioritise for surveillance and future deployment of alternative RDT, based on quickly selecting for pfhrp2/3 deletions once established. In scenarios designed to explore the continued spread of deletions in Africa, we identify 10 high threat countries that are most at risk of deletions both spreading to and subsequently being rapidly selected for. If HRP2-based RDTs continue to be relied on for malaria case management, we predict that the major route for pfhrp2 deletions to spread is south out from the current hotspot in the Horn of Africa, moving through East Africa over the next 20 years. We explore the variation in modelled timelines through an extensive parameter sensitivity analysis and despite wide uncertainties, we identify three countries that have not yet switched RDTs (Senegal, Zambia and Kenya) that are robustly identified as high risk for pfhrp2/3 deletions. These results provide a refined and updated prediction model for the emergence of pfhrp2/3 deletions in an effort to help guide pfhrp2/3 policy and prioritise future surveillance efforts and innovation. |
format | Online Article Text |
id | pubmed-10615018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106150182023-10-31 Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions Watson, Oliver J. Tran, Thu Nguyen-Anh Zupko, Robert J Symons, Tasmin Thomson, Rebecca Visser, Theodoor Rumisha, Susan Dzianach, Paulina A Hathaway, Nicholas Kim, Isaac Juliano, Jonathan J. Bailey, Jeffrey A. Slater, Hannah Okell, Lucy Gething, Peter Ghani, Azra Boni, Maciej F Parr, Jonathan B. Cunningham, Jane medRxiv Article In the thirteen years since the first report of pfhrp2-deleted parasites in 2010, the World Health Organization (WHO) has found that 40 of 47 countries surveyed worldwide have reported pfhrp2/3 gene deletions. Due to a high prevalence of pfhrp2/3 deletions causing false-negative HRP2 RDTs, in the last five years, Eritrea, Djibouti and Ethiopia have switched or started switching to using alternative RDTs, that target pan-specific-pLDH or P. falciparum specific-pLDH alone of in combination with HRP2. However, manufacturing of alternative RDTs has not been brought to scale and there are no WHO prequalified combination tests that use Pf-pLDH instead of HRP2 for P. falciparum detection. For these reasons, the continued spread of pfhrp2/3 deletions represents a growing public health crisis that threatens efforts to control and eliminate P. falciparum malaria. National malaria control programmes, their implementing partners and test developers desperately seek pfhrp2/3 deletion data that can inform their immediate and future resource allocation. In response, we use a mathematical modelling approach to evaluate the global risk posed by pfhrp2/3 deletions and explore scenarios for how deletions will continue to spread in Africa. We incorporate current best estimates of the prevalence of pfhrp2/3 deletions and conduct a literature review to estimate model parameters known to impact the selection of pfhrp2/3 deletions for each malaria endemic country. We identify 20 countries worldwide to prioritise for surveillance and future deployment of alternative RDT, based on quickly selecting for pfhrp2/3 deletions once established. In scenarios designed to explore the continued spread of deletions in Africa, we identify 10 high threat countries that are most at risk of deletions both spreading to and subsequently being rapidly selected for. If HRP2-based RDTs continue to be relied on for malaria case management, we predict that the major route for pfhrp2 deletions to spread is south out from the current hotspot in the Horn of Africa, moving through East Africa over the next 20 years. We explore the variation in modelled timelines through an extensive parameter sensitivity analysis and despite wide uncertainties, we identify three countries that have not yet switched RDTs (Senegal, Zambia and Kenya) that are robustly identified as high risk for pfhrp2/3 deletions. These results provide a refined and updated prediction model for the emergence of pfhrp2/3 deletions in an effort to help guide pfhrp2/3 policy and prioritise future surveillance efforts and innovation. Cold Spring Harbor Laboratory 2023-10-31 /pmc/articles/PMC10615018/ /pubmed/37905102 http://dx.doi.org/10.1101/2023.10.21.23297352 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Watson, Oliver J. Tran, Thu Nguyen-Anh Zupko, Robert J Symons, Tasmin Thomson, Rebecca Visser, Theodoor Rumisha, Susan Dzianach, Paulina A Hathaway, Nicholas Kim, Isaac Juliano, Jonathan J. Bailey, Jeffrey A. Slater, Hannah Okell, Lucy Gething, Peter Ghani, Azra Boni, Maciej F Parr, Jonathan B. Cunningham, Jane Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions |
title | Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions |
title_full | Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions |
title_fullStr | Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions |
title_full_unstemmed | Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions |
title_short | Global risk of selection and spread of Plasmodium falciparum histidine-rich protein 2 and 3 gene deletions |
title_sort | global risk of selection and spread of plasmodium falciparum histidine-rich protein 2 and 3 gene deletions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615018/ https://www.ncbi.nlm.nih.gov/pubmed/37905102 http://dx.doi.org/10.1101/2023.10.21.23297352 |
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