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Plasmodium vivax and Drug Resistance

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Resistance to antimalarial drugs is a threat to global efforts to eliminate malaria by 2030. Currently, treatment for vivax malaria uses chloroquine or ACT for uncomplicated P. vivax whereas primaquine is given to eliminate latent liver stage infections (a method known as radical cure). Studies on P. vivax resistance to antimalarials and the molecular basis of resistance lags far behind the P. falciparum as in vitro cultivation of the P. vivax has not yet been established. Therefore, data on the P. vivax resistance to any antimalarial drugs are generated through in vivo studies or through monitoring of antimalarial treatments in mixed species infection. Indirect evidence through drug selective pressure on the parasites genome, as evidenced by the presence of the molecular marker(s) for drug resistance in areas where P. falciparum and P. vivax are distributed in sympatry may reflect, although require validation, the status of P. vivax resistance. This review focuses on the currently available data that may represent the state-of-the art of the P. vivax resistance status to antimalarial to anticipate the challenge for malaria elimination by 2030.
Title: Plasmodium vivax and Drug Resistance
Description:
Resistance to antimalarial drugs is a threat to global efforts to eliminate malaria by 2030.
Currently, treatment for vivax malaria uses chloroquine or ACT for uncomplicated P.
vivax whereas primaquine is given to eliminate latent liver stage infections (a method known as radical cure).
Studies on P.
vivax resistance to antimalarials and the molecular basis of resistance lags far behind the P.
falciparum as in vitro cultivation of the P.
vivax has not yet been established.
Therefore, data on the P.
vivax resistance to any antimalarial drugs are generated through in vivo studies or through monitoring of antimalarial treatments in mixed species infection.
Indirect evidence through drug selective pressure on the parasites genome, as evidenced by the presence of the molecular marker(s) for drug resistance in areas where P.
falciparum and P.
vivax are distributed in sympatry may reflect, although require validation, the status of P.
vivax resistance.
This review focuses on the currently available data that may represent the state-of-the art of the P.
vivax resistance status to antimalarial to anticipate the challenge for malaria elimination by 2030.

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