Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/89168
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dc.contributor.authorRocamora, Francesen
dc.contributor.authorZhu, Leien
dc.contributor.authorLiong, Kek Yeeen
dc.contributor.authorDondorp, Arjenen
dc.contributor.authorMiotto, Olivoen
dc.contributor.authorMok, Sachelen
dc.contributor.authorBozdech, Zbyneken
dc.contributor.editorCooper, Rolanden
dc.date.accessioned2018-05-18T06:11:42Zen
dc.date.accessioned2019-12-06T17:19:22Z-
dc.date.available2018-05-18T06:11:42Zen
dc.date.available2019-12-06T17:19:22Z-
dc.date.issued2018en
dc.identifier.citationRocamora, F., Zhu, L., Liong, K. Y., Dondorp, A., Miotto, O., Mok, S., et al. (2018). Oxidative stress and protein damage responses mediate artemisinin resistance in malaria parasites. PLOS Pathogens, 14(3), e1006930-.en
dc.identifier.issn1553-7366en
dc.identifier.urihttps://hdl.handle.net/10356/89168-
dc.identifier.urihttp://hdl.handle.net/10220/44831en
dc.description.abstractDue to their remarkable parasitocidal activity, artemisinins represent the key components of first-line therapies against Plasmodium falciparum malaria. However, the decline in efficacy of artemisinin-based drugs jeopardizes global efforts to control and ultimately eradicate the disease. To better understand the resistance phenotype, artemisinin-resistant parasite lines were derived from two clones of the 3D7 strain of P. falciparum using a selection regimen that mimics how parasites interact with the drug within patients. This long term in vitro selection induced profound stage-specific resistance to artemisinin and its relative compounds. Chemosensitivity and transcriptional profiling of artemisinin-resistant parasites indicate that enhanced adaptive responses against oxidative stress and protein damage are associated with decreased artemisinin susceptibility. This corroborates our previous findings implicating these cellular functions in artemisinin resistance in natural infections. Genomic characterization of the two derived parasite lines revealed a spectrum of sequence and copy number polymorphisms that could play a role in regulating artemisinin response, but did not include mutations in pfk13, the main marker of artemisinin resistance in Southeast Asia. Taken together, here we present a functional in vitro model of artemisinin resistance that is underlined by a new set of genetic polymorphisms as potential genetic markers.en
dc.description.sponsorshipMOE (Min. of Education, S’pore)en
dc.description.sponsorshipNMRC (Natl Medical Research Council, S’pore)en
dc.format.extent29 p.en
dc.language.isoenen
dc.relation.ispartofseriesPLOS Pathogensen
dc.rights© 2018 Rocamora et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectArtemisinin Resistanceen
dc.subjectParasitesen
dc.titleOxidative stress and protein damage responses mediate artemisinin resistance in malaria parasitesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen
dc.identifier.doi10.1371/journal.ppat.1006930en
dc.description.versionPublished versionen
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