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Table 3_Application of a new highly multiplexed amplicon sequencing tool to evaluate Plasmodium falciparum antimalarial resistance and relatedness in individual and pooled samples from Dschang, Cameroon.xlsx

Title: Table 3_Application of a new highly multiplexed amplicon sequencing tool to evaluate Plasmodium falciparum antimalarial resistance and relatedness in individual and pooled samples from Dschang, Cameroon.xlsx
Authors: Jacob M. Sadler; Alfred Simkin; Valery P. K. Tchuenkam; Isabela Gerdes Gyuricza; Abebe A. Fola; Kevin Wamae; Ashenafi Assefa; Karamoko Niaré; Kyaw Thwai; Samuel J. White; William J. Moss; Rhoel R. Dinglasan; Sandrine Eveline Nsango; Christopher B. Tume; Jonathan B. Parr; Innocent Mbulli Ali; Jeffrey A. Bailey; Jonathan J. Juliano
Publication Year: 2025
Collection: Frontiers: Figshare
Subject Terms: Parasitology; malaria; Plasmodium falciparum; antimalarial resistance; genetic relatedness; amplicon sequencing
Description: Background Resistance to antimalarial drugs remains a major obstacle to malaria elimination. Multiplexed, targeted amplicon sequencing is being adopted for surveilling resistance and dissecting the genetics of complex malaria infections. Moreover, genotyping of parasites and detection of molecular markers drug resistance in resource-limited regions requires open-source protocols for processing samples, using accessible reagents, and rapid methods for processing numerous samples including pooled sequencing. Methods Plasmodium falciparum Streamlined Multiplex Antimalarial Resistance and Relatedness Testing (Pf-SMARRT) is a PCR-based amplicon panel consisting of 15 amplicons targeting antimalarial resistance mutations and 9 amplicons targeting hypervariable regions. This assay uses oligonucleotide primers in two pools and a non-proprietary library and barcoding approach. Results We evaluated Pf-SMARRT using control mocked dried blood spots (DBS) at varying levels of parasitemia and a mixture of 3D7 and Dd2 strains at known frequencies, showing the ability to genotype at low parasite density and recall within-sample allele frequencies. We then piloted Pf-SMARRT to genotype 100 parasite isolates collected from uncomplicated malaria cases at three health facilities in Dschang, Western Cameroon. Antimalarial resistance genotyping showed high levels of sulfadoxine-pyrimethamine resistance mutations, including 31% prevalence of the DHPS A613S mutation. No K13 candidate or validated artemisinin partial resistance mutations were detected, but one low-level non-synonymous change was observed. Pf-SMARRT’s hypervariable targets, used to assess complexity of infections and parasite diversity and relatedness, showed similar levels and patterns compared to molecular inversion probe (MIP) sequencing. While there was strong concordance of antimalarial resistance mutations between individual samples and pools, low-frequency variants in the pooled samples were often missed. Conclusion Overall, Pf-SMARRT is a robust tool for ...
Document Type: dataset
Language: unknown
Relation: https://figshare.com/articles/dataset/Table_3_Application_of_a_new_highly_multiplexed_amplicon_sequencing_tool_to_evaluate_Plasmodium_falciparum_antimalarial_resistance_and_relatedness_in_individual_and_pooled_samples_from_Dschang_Cameroon_xlsx/28349921
DOI: 10.3389/fpara.2024.1509261.s002
Availability: https://doi.org/10.3389/fpara.2024.1509261.s002; https://figshare.com/articles/dataset/Table_3_Application_of_a_new_highly_multiplexed_amplicon_sequencing_tool_to_evaluate_Plasmodium_falciparum_antimalarial_resistance_and_relatedness_in_individual_and_pooled_samples_from_Dschang_Cameroon_xlsx/28349921
Rights: CC BY 4.0
Accession Number: edsbas.F26A66F
Database: BASE