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Global scenario of Plasmodium vivax occurrence and resistance pattern

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JOURNAL OF BASIC MICROBIOLOGY
卷 62, 期 12, 页码 1417-1428

出版社

WILEY
DOI: 10.1002/jobm.202200316

关键词

drug resistance; malaria; molecular marker; Plasmodium; resistance

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This article discusses the endemicity of P. vivax malaria, a historical overview of antimalarial drugs, the emergence of drug resistance, the global distribution of molecular markers, and various measures taken to reduce the malaria burden caused by P. vivax infection and its resistance.
Malaria caused by Plasmodium vivax is comparatively less virulent than Plasmodium falciparum, which can also lead to severe disease and death. It shows a wide geographical distribution. Chloroquine serves as a drug of choice, with primaquine as a radical cure. However, with the appearance of resistance to chloroquine and treatment has been shifted to artemisinin combination therapy followed by primaquine as a radical cure. Sulphadoxine-pyrimethamine, mefloquine, and atovaquone-proguanil are other drugs of choice in chloroquine-resistant areas, and later resistance was soon reported for these drugs also. The emergence of drug resistance serves as a major hurdle to controlling and eliminating malaria. The discovery of robust molecular markers and regular surveillance for the presence of mutations in malaria-endemic areas would serve as a helpful tool to combat drug resistance. Here, in this review, we will discuss the endemicity of P. vivax, a historical overview of antimalarial drugs, the appearance of drug resistance and molecular markers with their global distribution along with different measures taken to reduce malaria burden due to P. vivax infection and their resistance.

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