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Plasmodium ovale

Molecular classification
Other
01

Overview

Plasmodium ovale is a species of protozoan parasite that infects humans and causes tertian malaria, characterized by fever episodes recurring every ~49 hours[3][5][9]. It is transmitted by the bite of infected Anopheles mosquitoes and can form dormant liver stages (hypnozoites) that cause relapses years after the initial infection[1][3][5]. Two genetic types exist, Plasmodium ovale curtisi and Plasmodium ovale wallikeri[1][7][8]. In the human host, the parasite infects red blood cells, leading to symptoms such as fever, anemia, splenomegaly, and potential hypoglycemia[1][7]. Treatment typically involves chloroquine and primaquine to clear both blood and liver stages; alternative therapies may include artemether-lumefantrine and atovaquone-proguanil[5][6]. Although studied for molecular targets (e.g., MSP1, spect-1, GPI-anchored proteins) in vaccine and drug discovery efforts[8], "Plasmodium ovale" itself is not a defined molecular target such as a receptor, enzyme, or transporter, but rather the causative pathogen of a human infectious disease.

Other names
Plasmodium ovale curtisiPlasmodium ovale wallikeriP. ovale
02

Mechanism of action

Inhibition of hemoglobin digestion, Eradication of liver hypnozoites, Disruption of parasite DNA replication and mitochondrial function

03

Biological functions

InfectionErythrocyte invasionLiver stage dormancyGametocyte formation
04

Disease associations

Infection (Malaria)
05

Safety considerations

Drug resistanceRelapses due to liver dormancyMisidentification with Plasmodium vivaxDrug toxicity (e.g., chloroquine overdose)
06

Interacting drugs

Chloroquine

3 more in the full profile.

07

Biomarkers

Merozoite surface protein 1 (MSP1)Genetic markers for P. ovale curtisi and wallikeri

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