Adaptive evolution of malaria parasites in French Guiana: Reversal of chloroquine resistance by acquisition of a mutation in pfcrt

Autor: Sarah K. Volkman, Lise Musset, Eric Legrand, Stanislaw J. Gabryszewski, Dyann F. Wirth, Béatrice Volney, Eli L. Moss, Stéphane Pelleau, Satish K. Dhingra, Daniel E. Neafsey, David A. Fidock, Jessica Casteras
Přispěvatelé: Laboratoire de Parasitologie, Centre National de Référence du Paludisme - Région Antilles-Guyane, Institut Pasteur de la Guyane - Réseau International des Instituts Pasteur - WHO Collaborating Center for Surveillance of Antimalarial Drug Resistance, Broad Institute of MIT and Harvard (BROAD INSTITUTE), Broad Institute of MIT and Harvard, Department of Microbiology and Immunology, Columbia University College of Physicians and Surgeons, Harvard School of Public Health, This work was supported by European Commission Grant REGPOT-CT-2011-285837-430 STRonGer (to S.P.), AgenceNationale de la Recherche Investissements d’Avenir Grant ANR-10-LABX-25-01(to S.P. and L.M.), NIH Grants R01AI50234 (to D.A.F.) and R01AI109023 (to D.A.F.),and the Institut de Veille Sanitaire. Sequencing was supported, in part, byNational Institute of Allergy and Infectious Diseases, NIH, Department ofHealth and Human Services Contract HHSN272200900018C., ANR-10-LABX-25-01/10-LABX-0025, CEBA, CEnter of the study of Biodiversity in Amazonia(2010), European Project : 285837, EC:FP7:REGPOT, FP7-REGPOT-2011-1, STRONGER(2011), Centre National de Référence du Paludisme [Cayenne, Guyane française] (CNR - laboratoire associé), Institut Pasteur de la Guyane, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Columbia University College of Physicians and Surgeons, ANR-10-LABX-0025,CEBA,CEnter of the study of Biodiversity in Amazonia(2010), European Project: 285837,EC:FP7:REGPOT,FP7-REGPOT-2011-1,STRONGER(2011), Centre National de Référence du Paludisme [Cayenne, Guyane française] (CNR), Centre National de Référence du Paludisme - Laboratoire de parasitologie [Cayenne, Guyane française] (CNR)
Jazyk: angličtina
Rok vydání: 2015
Předmět:
[SDV]Life Sciences [q-bio]
Protozoan Proteins
Drug resistance
MESH: Genetic Markers
MESH: Genotype
Chloroquine
Genotype
[SDV.SPEE] Life Sciences [q-bio]/Public Health and Epidemiology
MESH: Quinolines/chemistry
MESH: Inhibitory Concentration 50
Genetics
education.field_of_study
Multidisciplinary
biology
MESH: Chloroquine/therapeutic use
Biological Sciences
MESH: Malaria/drug therapy
3. Good health
[SDV] Life Sciences [q-bio]
[SDV.MP.PAR] Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology
medicine.drug
PfCRT
MESH: Plasmodium falciparum/drug effects
Population
Plasmodium falciparum
MESH: Plasmodium falciparum/genetics
malaria
MESH: Membrane Transport Proteins/genetics
MESH: Phenotype
Evolution
Molecular

Piperaquine
evolution
MESH: Evolution
Molecular

MESH: French Guiana
parasitic diseases
medicine
Humans
MESH: Genome
[SDV.MP.PAR]Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology
Allele
education
MESH: Prevalence
MESH: Principal Component Analysis
drug resistance
MESH: Humans
MESH: Alleles
Membrane Transport Proteins
MESH: Retrospective Studies
MESH: Haplotypes
biology.organism_classification
medicine.disease
MESH: Protozoan Proteins/genetics
Mutation
MESH: Mutation
MESH: Drug Resistance/genetics
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
Malaria
Zdroj: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2015, 112 (37), pp.11672-7
Proceedings of the National Academy of Sciences of the United States of America, 2015, 112 (37), pp.11672-11677. ⟨10.1073/pnas.1507142112⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2015, 112 (37), pp.11672-11677. ⟨10.1073/pnas.1507142112⟩
ISSN: 0027-8424
1091-6490
DOI: 10.1073/pnas.1507142112⟩
Popis: Comment in : Fusion of field studies and the laboratory solves a puzzle in antimalarial resistance. [Proc Natl Acad Sci U S A. 2015]; International audience; In regions with high malaria endemicity, the withdrawal of chloroquine (CQ) as first-line treatment of Plasmodium falciparum infections has typically led to the restoration of CQ susceptibility through the reexpansion of the wild-type (WT) allele K76 of the chloroquine resistance transporter gene (pfcrt) at the expense of less fit mutant alleles carrying the CQ resistance (CQR) marker K76T. In low-transmission settings, such as South America, drug resistance mutations can attain 100% prevalence, thereby precluding the return of WT parasites after the complete removal of drug pressure. In French Guiana, despite the fixation of the K76T allele, the prevalence of CQR isolates progressively dropped from >90% to
Databáze: OpenAIRE