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<jats:title>Abstract</jats:title><jats:p>The rapid and aggressive spread of artemisinin-resistant <jats:italic>Plasmodium falciparum</jats:italic> carrying the <jats:italic>kelch13</jats:italic> C580Y mutation is a growing threat to malaria elimination in Southeast Asia, but there is no evidence of their spread to other regions. We conducted cross-sectional surveys in 2016 and 2017 at two clinics in Wewak, Papua New Guinea (PNG) where we identified three infections caused by C580Y mutants among 239 genotyped clinical samples. One of these mutants exhibited the highest survival rate (6.8%) among all parasites surveyed in ring-stage survival assays (RSA) for artemisinin. Analyses of <jats:italic>kelch13</jats:italic> flanking regions, and comparisons of deep sequencing data from 389 clinical samples from PNG, Indonesian Papua and Western Cambodia, suggested an independent origin of the Wewak C580Y mutation, showing that the mutants possess several distinctive genetic features. Identity by descent (IBD) showed that multiple portions of the mutants’ genomes share a common origin with parasites found in Indonesian Papua, comprising several mutations within genes previously associated with drug resistance, such as <jats:italic>mdr1, ferredoxin, atg18</jats:italic> and <jats:italic>pnp</jats:italic>. These findings suggest that a <jats:italic>P. falciparum</jats:italic> lineage spreading on the island of New Guinea has gradually acquired a complex ensemble of variants, including <jats:italic>kelch13</jats:italic> C580Y, which may affect the parasites’ drug sensitivity. This worrying development reinforces the need for increased surveillance of the evolving parasite populations on the island, to contain the spread of resistance.</jats:p>

Original publication

DOI

10.1101/621813

Type

Journal article

Publisher

Cold Spring Harbor Laboratory

Publication Date

18/07/2019