High-throughput genotyping of Plasmodium vivax in the Peruvian Amazon via molecular inversion probes

Plasmodium vivax transmission occurs throughout the tropics and is an emerging threat in areas of Plasmodium falciparum decline, causing relapse infections that complicate treatment and control. Targeted sequencing for P. falciparum has been widely deployed to detect population structure and the geographic spread of antimalarial and diagnostic resistance. However, there are fewer such tools for P. vivax. Leveraging global variation data, we designed four molecular inversion probe (MIP) genotyping panels targeting geographically differentiating SNPs, neutral SNPs, putative antimalarial resistance genes, and vaccine candidate genes. We deployed these MIP panels on 866 infections from the Peruvian Amazon and identified transmission networks with clonality (IBD[identity by descent]>0.99), copy number variation in Pvdbp and multiple Pvrbps, mutations in antimalarial resistance orthologs, and balancing selection in 13 vaccine candidate genes. Our MIP panels are the broadest genotyping panel currently available and are poised for successful deployment in other regions of P. vivax transmission.

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Publication Details

Journal
Nature Communications
Published
2024-11-25
DOI
https://doi.org/10.1038/s41467-024-54731-y
Citations
5
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
2.71

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article

High-throughput genotyping of Plasmodium vivax in the Peruvian Amazon via molecular inversion probes

David Giesbrecht, Karamoko Niaré, Alfred Simkin, Hugo O. Valdivia et al.
5 citations
Nature Communications
Malaria Research and Control
2.71
article

High-throughput genotyping of Plasmodium vivax in the Peruvian Amazon via molecular inversion probes

David Giesbrecht, Karamoko Niaré, Alfred Simkin, Hugo O. Valdivia, Danielle L. Pannebaker, Jeffrey A. Bailey, Özkan Aydemir, Rebecca Crudale, Zachary R. Popkin-Hall, Jonathan J. Juliano, Isaac E. Kim, Abebe A. Fola, Juan F. Sánchez
article en
5 citations

Abstract

Plasmodium vivax transmission occurs throughout the tropics and is an emerging threat in areas of Plasmodium falciparum decline, causing relapse infections that complicate treatment and control. Targeted sequencing for P. falciparum has been widely deployed to detect population structure and the geographic spread of antimalarial and diagnostic resistance. However, there are fewer such tools for P. vivax. Leveraging global variation data, we designed four molecular inversion probe (MIP) genotyping panels targeting geographically differentiating SNPs, neutral SNPs, putative antimalarial resistance genes, and vaccine candidate genes. We deployed these MIP panels on 866 infections from the Peruvian Amazon and identified transmission networks with clonality (IBD[identity by descent]>0.99), copy number variation in Pvdbp and multiple Pvrbps, mutations in antimalarial resistance orthologs, and balancing selection in 13 vaccine candidate genes. Our MIP panels are the broadest genotyping panel currently available and are poised for successful deployment in other regions of P. vivax transmission.

Nature CommunicationsVol. 15(1)
University of North Carolina at Chapel Hill (US), University of Massachusetts Chan Medical School (US), Brown University (US), United States Naval Medical Research Unit SOUTH (PE)
U.S. Department of Defense, U.S. Navy, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 9%
Malaria Research and Control
2.71
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