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Plasmodium vivax is a protozoal parasite and a human pathogen.This parasite is the most frequent and widely distributed cause of recurring malaria. [2] Although it is less virulent than Plasmodium falciparum, the deadliest of the five human malaria parasites, P. vivax malaria infections can lead to severe disease and death, often due to splenomegaly (a pathologically enlarged spleen).
Schüffner's dots refers to a hematological finding that is associated with malaria, [1] exclusively found in infections caused by Plasmodium ovale or Plasmodium vivax. [ 2 ] Plasmodium vivax induces morphologic alterations in infected host erythrocytes that are visible by light microscopy in Romanowsky-stained blood smears as multiple brick ...
Subgenus Plasmodium Bray 1963 emend. Garnham 1964; Subgenus Sauramoeba Garnham 1966; Subgenus Vinckeia Garnham 1964; Genus Polychromophilus Landau et al 1984; Genus Rayella Dasgupta 1967; Genus Saurocytozoon Lainson & Shaw 1969; Genus †Vetufebrus Poinar 2011; The genus Mesnilium is the only taxon that infects fish. The genus has a single ...
Plasmodium malariae is a parasitic protozoan that causes malaria in humans. It is one of several species of Plasmodium parasites that infect other organisms as pathogens, also including Plasmodium falciparum and Plasmodium vivax, responsible for most malarial infection.
Within the subgenus Plasmodium, P. vivax groups with an Asian clade which appears to be rooted in Africa. P. malaria and P. ovale both belong to an African clade and are more closely related to each other than to P. vivax. Within the subgenus Laverinia P. falciparum and P. reichenowi form a clade while the other four known species form a second ...
Plasmodium is a genus of unicellular eukaryotes that are obligate parasites of vertebrates and insects.The life cycles of Plasmodium species involve development in a blood-feeding insect host which then injects parasites into a vertebrate host during a blood meal.
The PHIST proteins are exported to the cytoplasm of the infected erythrocyte. The human malaria parasites P. falciparum and P. vivax have shown a lineage-specific expansion of proteins with this domain. [1] Of the two PHIST genes in the mouse parasite P. berghei, only one is required for infection. [3]
The most common form of MSPs are anchored to the merozoite surface with glycophosphatidylinositol, a short glycolipid often used for protein anchoring. Additional forms include integral membrane proteins and peripherally associated proteins, which are found to a lesser extent than glycophosphatidylinositol anchored proteins, or (GPI)-anchored proteins, on the merozoite surface. [4]