dc.creatorMaestre Buitrago, Amanda Elena
dc.creatorHawkins, Vivian N
dc.creatorAuliff, Alyson
dc.creatorPrajapati, Surendra Kumar
dc.creatorRungsihirunrat, Kanchana
dc.creatorHapuarachchi, Hapuarachchige C
dc.creatorO'Neil, Michael T
dc.creatorCheng, Qin
dc.creatorJoshi, Hema
dc.creatorNa Bangchang, Kesara
dc.creatorHopkins Sibley, Carol
dc.date2023-06-01T16:35:11Z
dc.date2023-06-01T16:35:11Z
dc.date2008
dc.date.accessioned2024-04-23T14:19:38Z
dc.date.available2024-04-23T14:19:38Z
dc.identifier1475-2875
dc.identifierhttps://hdl.handle.net/10495/35241
dc.identifier10.1186/1475-2875-7-72
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/9229528
dc.descriptionABSTRACT: Background: In order to maximize the useful therapeutic life of antimalarial drugs, it is crucial to understand the mechanisms by which parasites resistant to antimalarial drugs are selected and spread in natural populations. Recent work has demonstrated that pyrimethamine-resistance conferring mutations in Plasmodium falciparum dihydrofolate reductase (dhfr) have arisen rarely de novo, but spread widely in Asia and Africa. The origin and spread of mutations in Plasmodium vivax dhfr were assessed by constructing haplotypes based on sequencing dhfr and its flanking regions. Methods: The P. vivax dhfr coding region, 792 bp upstream and 683 bp downstream were amplified and sequenced from 137 contemporary patient isolates from Colombia, India, Indonesia, Papua New Guinea, Sri Lanka, Thailand, and Vanuatu. A repeat motif located 2.6 kb upstream of dhfr was also sequenced from 75 of 137 patient isolates, and mutational relationships among the haplotypes were visualized using the programme Network. Results: Synonymous and non-synonymous single nucleotide polymorphisms (SNPs) within the dhfr coding region were identified, as was the well-documented in-frame insertion/deletion (indel). SNPs were also identified upstream and downstream of dhfr, with an indel and a highly polymorphic repeat region identified upstream of dhfr. The regions flanking dhfr were highly variable. The double mutant (58R/117N) dhfr allele has evolved from several origins, because the 58R is encoded by at least 3 different codons. The triple (58R/61M/117T) and quadruple (57L/61M/117T/173F, 57I/58R/61M/117T and 57L/58R/61M/117T) mutant alleles had at least three independent origins in Thailand, Indonesia, and Papua New Guinea/Vanuatu. Conclusion: It was found that the P. vivax dhfr coding region and its flanking intergenic regions are highly polymorphic and that mutations in P. vivax dhfr that confer antifolate resistance have arisen several times in the Asian region. This contrasts sharply with the selective sweep of rare antifolate resistant alleles observed in the P. falciparum populations in Asia and Africa. The finding of multiple origins of resistance-conferring mutations has important implications for drug policy.
dc.descriptionCOL0014064
dc.format12
dc.formatapplication/pdf
dc.formatapplication/pdf
dc.languageeng
dc.publisherBMC (BioMed Central)
dc.publisherGEBIOMIC (Genética y Bioquímica de Microorganismos)
dc.publisherLondres, Inglaterra
dc.relationMalar. J.
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightshttp://creativecommons.org/licenses/by/2.5/co/
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.rightshttps://creativecommons.org/licenses/by/4.0/
dc.subjectAntimalaricos
dc.subjectAntimalarials
dc.subjectCodón
dc.subjectCodon
dc.subjectADN, protozoario
dc.subjectDNA, Protozoan
dc.subjectResistencia a Medicamentos
dc.subjectDrug Resistance
dc.subjectMalaria, Vivax
dc.subjectPlasmodium vivax
dc.subjectPolymorphism, Single Nucleotide
dc.subjectPolimorfismo, Nucleótido Único
dc.subjectPirimetamina
dc.subjectPyrimethamine
dc.subjectTetrahidrofolato deshidrogenasa
dc.subjectTetrahydrofolate Dehydrogenase
dc.titleMultiple origins of resistance-conferring mutations in Plasmodium vivax dihydrofolate reductase
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typehttp://purl.org/coar/resource_type/c_2df8fbb1
dc.typehttps://purl.org/redcol/resource_type/ART
dc.typeArtículo de investigación


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