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Biology of Plasmodium Parasite and Malaria Disease

This article provides an overview of the biology of Plasmodium parasite, the causative agent of malaria, including its life cycle, molecular characteristics, and clinical manifestations. It also discusses the different species of Plasmodium that infect humans and their impact on global health.

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Biology of Plasmodium Parasite and Malaria Disease

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  1. Biology of PlasmodiumZLY 201 By SHITTU, Olalere Dept. of Zoology University of Ilorin, Nigeria

  2. Introduction • Five species of Plasmodium parasite cause malaria, and there is growing awareness of the importance of each to global health. • The species infecting man include Plasmodium falciparum, P. malariae, P. ovale, P. vivaxand P. knowlesi. The majority of mortality and morbidity attributed to malaria are caused by P. falciparum because of its irregular but continuous episodes; however, P. malariae causes quartian fever, but not fatal, P. vivaxand P. ovale also causes a significant burden of disease referred to as tertian fever within 48hours. • The life cycle of all malaria parasites is complex and traverse vertebrates and mosquito. Infection by all Plasmodium spp. begins with the bite of an infected female Anopheles mosquito.

  3. Molecular Biology of Plasmodium All species examined to date have 14 chromosomes, one mitochondrion and one plastid (apicoplast, an organelle similar to a chloroplast). The chromosomes vary from 500 kilobases to 3.5 megabases in length. It is presumed that this is the pattern throughout the genus. The plastid, unlike those found in algae, is not photosynthetic. Its function is not fully known; however, it has been demonstrated that some essential metabolic pathways like isoprenoid, Fe-S clusters, fatty acid and phospholipid biosynthesis occurs in this organelle, and that it also still possess its own genome, partly shared with the nucleus. On a molecular level, the parasite damages red blood cells using plasmepsin enzymes (aspartic acid proteases) which degrade hemoglobin.

  4. Ultra structure of Plasmodium

  5. Malaria Life Cycle and Biology (i) Liver stage: 6 - 14 days (ii) Blood stage: 48 - 72 hrs (iii) Incubation period: 21 days (iv) Primary infections: Clinical disease of varying manifestations (v) Adults from endemic areas develop clinical immunity but carry low-grade parasitemia Apicomplexan life cycle: 1-zygote, 2-sporozoites, 3-merozoites, 4-gametes

  6. Malaria Parasite Biology, Clinical Disease and Immunity • Incubation period: Time between infections to first appearance of blood form parasites (varies between species). P. vivax and P. ovale have dormant liver form stage causing relapse infection (months to a year or more) • Chronicity of infection: P. malariae can be present in a host for up to 40 years • Asymptomatic carriers: Multiple exposures in individuals born in endemic countries or expatriates with prolonged residence develop partial immunity while carrying low-grade parasite burden • Parasite burden in asymptomatic carriers is not known • Infectious dose of blood form malaria parasites is very low

  7. Malaria Life Cycle and Biology (i) Liver stage: 6 - 14 days (ii) Blood stage: 48 - 72 hrs (iii) Incubation period: 21 days (iv) Primary infections: Clinical disease of varying manifestations (v) Adults from endemic areas develop clinical immunity but carry low-grade parasitemia

  8. Migration of Plasmodium Parasite

  9. The Life Cycle of Plasmodium Parasites

  10. The Life Cycle of Plasmodium Parasites • Malaria parasite exhibits a complex life cycle involving an insect vector (mosquito) and a vertebrate host (human). • In summary, malaria parasites undergo three distinct asexual replicative stages, viz; i. Exoerythrocytic schizogony, ii. blood stage schizogony, and iii. sporogony • All these stages result in the production of invasive forms (merozoites and sporozoites). A sexual reproduction occurs with the switch from vertebrate to invertebrate host and leads to the formation of the invasive ookinete. All invasive stages are characterized by the apical organelles typical of apicomplexan species.

  11. The Life Cycle of Plasmodium Parasites • All five species mentioned above exhibit a similar life cycle with only minor variations. • The infection is initiated when sporozoites are injected with the saliva of a feeding mosquito. Sporozoites are carried by the circulatory system to the liver and invade hepatocytes • The intracellular parasite undergoes an asexual replication known as exoerythrocytic schizogonywithin the hepatocyte (2-4). Exoerythrocytic schizogony culminates in the production of merozoites which are released into the bloodstream (5). A proportion of the liver-stage parasites from P. vivaxand P. ovale go through a dormant period instead of immediately undergoing asexual replication (i.e., stay temporarily at step 2).

  12. The Life Cycle of Plasmodium Parasites • These hypnozoites will reactivate several weeks to months (or years) after the primary infection and are responsible for relapses. Merozoites invade erythrocytes (6) and undergo a trophic period in which the parasite enlarges (7-8). The early trophozoite is often referred to as 'ring form' because of its morphology. 2.) Trophozoite enlargement is accompanied by an active metabolism including the ingestion of host cytoplasm and the proteolysis of hemoglobin into amino acids. The end of the trophic period is manifested by multiple rounds of nuclear division without cytokinesis resulting is a schizont (9). Merozoites bud from the mature schizont, also called a segmenter(10), and the merozoites are released following rupture of the infected erythrocyte (11).

  13. The Life Cycle of Plasmodium Parasites • Invasion of erythrocytes reinitiates another round of the blood-stage replicative cycle (6-11) (The blood stage is responsible for the pathology associated with malaria). 3.)The intermittent fever paroxyms are due to the synchronous lysis of the infected erythrocytes. P. malariae exhibits a 72 hour periodicity, whereas the other four species exhibit 48 hour cycles. 4.)However, P. falciparum often exhibits a continuous fever rather than the periodic paroxysm. P. falciparum also is responsible for more morbidity and mortality than the other species. This increase virulence is due in part to the higher levels of parasitaemia associated with P. falciparum infections.

  14. The Life Cycle of Plasmodium Parasites • In addition, more complications are associated with P. falciparum because of the sequestration of the trophozoite- and schizont-infected erythrocytes in the deep tissues. 5.) As an alternative to the asexual replicative cycle, the parasite can differentiate into sexual forms known as macro- or microgametocytes (12). The gametocytes are large parasites which fill up the erythrocyte, but only contain one nucleus. Ingestion of gametocytes by the mosquito vector induces gametogenesis (i.e., the production of gametes) and escape from the host erythrocyte.

  15. Factors which participate in the induction of gametogenesis include: • a drop in temperature, • an increase in carbon (iv) oxide, and • mosquito metabolites. 6.)Microgametes, formed by a process known as exflagellation (13), are flagellated forms which will fertilize the macrogamete (14) leading to a zygote (15). The zygote develops into a motile ookinete(16) which penetrates the gut epithelial cells and develops into an oocyst (17). The oocyst undergoes multiple rounds of asexual replication (18) resulting in the production of sporozoites (19). Rupture of the mature oocyst releases the sporozoites into the hemocoel (i.e., body cavity) of the mosquito (20). The sporozoites migrate to and invade the salivary glands, thus completing the life cycle.

  16. The stages of gametocyte development in Plasmodium falciparum

  17. Morphology of the different Plasmodium Parasites

  18. Morphology of the different Plasmodium Parasites

  19. Morphology of the different Plasmodium Parasites

  20. Morphology of the different Plasmodium Parasites

  21. End of Presentation

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