熱帯熱マラリア原虫

関: Plasmodium falciparum

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the 16th letter of the Roman alphabet (同)p
a river in western Thailand; a major tributary of the Chao Phraya (同)Ping River

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/04/03 20:27:27」(JST)

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Plasmodium falciparum is a protozoan parasite, one of the species of Plasmodium that cause malaria in humans. It is transmitted by the female Anopheles mosquito. Malaria caused by this species (also called malignant^[1] or falciparum^[2] malaria) is the most dangerous form of malaria,^[3] with the highest rates of complications and mortality. As of 2006, there were an estimated 247 million human malarial infections (98% in Africa, 70% being 5 years or younger).^[4] It is much more prevalent in sub-Saharan Africa than in many other regions of the world; in most African countries, over 75% of cases were due to P. falciparum, whereas in most other countries with malaria transmission, other, less virulent plasmodial species predominate. Almost every malarial death is caused by P. falciparum.^[4]

1 Background
2 Plasmodium life cycle
3 Pathogenesis
4 Microscopic appearance
5 The Plasmodium falciparum genome
6 Influence of P. falciparum on the human genome
- 6.1 P. falciparum and sickle cell anemia
7 Known vectors
8 Origins and Evolution
9 Treatment
- 9.1 Uncomplicated falciparum malaria
- 9.2 Severe falciparum malaria
- 9.3 History of falciparum treatment
10 Vaccination
11 See also
12 References
13 Sources and further reading
- 13.1 Overview
- 13.2 Spatial distribution
- 13.3 Blood slides
- 13.4 Case histories
- 13.5 Pathology due to Plasmodium falciparum
- 13.6 Plasmodium falciparum genome data
- 13.7 Other

Background[edit]

Malaria is caused by an infection with protozoa of the genus Plasmodium. The name malaria, from the Italian mala aria, meaning "bad air", comes from the linkage suggested by Giovanni Maria Lancisi (1717) of malaria with the poisonous vapours of swamps. This species name comes from the Latin falx, meaning "sickle", and parere meaning "to give birth". The organism itself was first seen by Laveran on November 6, 1880 at a military hospital in Constantine, Algeria, when he discovered a microgametocyte exflagellating. Patrick Manson (1894) hypothesised that mosquitoes could transmit malaria. This hypothesis was experimentally confirmed independently by Giovanni Battista Grassi and Ronald Ross in 1898. Grassi (1900) proposed an exerythrocytic stage in the life cycle, later confirmed by Short, Garnham, Covell and Shute (1948), who found Plasmodium vivax in the human liver.

Around the world, malaria is the most significant parasitic disease of humans, and claims the lives of more children worldwide than any other infectious disease. Since 1900, the area of the world exposed to malaria has been halved, yet two billion more people are presently exposed. Morbidity, as well as mortality, is substantial. Infection rates in children in endemic areas are of the order of 50%: Chronic infection has been shown to reduce school scores by up to 15%. Reduction in the incidence of malaria coincides with increased economic output.^[5]

While there are no effective vaccines for any of the six or more species that cause human malaria, drugs have been employed for centuries. In 1640, Huan del Vego first employed the tincture of the cinchona bark for treating malaria; the native Indians of Peru and Ecuador had been using it even earlier for treating fevers. Thompson (1650) introduced this "Jesuits' bark" to England. Its first recorded use there was by Dr John Metford of Northampton in 1656. Morton (1696) presented the first detailed description of the clinical picture of malaria and of its treatment with cinchona. Gize (1816) studied the extraction of crystalline quinine from the cinchona bark, and Pelletier and Caventou (1820) in France extracted pure quinine alkaloids, which they named quinine and cinchonine.

Plasmodium life cycle[edit]

Pathogenesis[edit]

Plasmodium falciparum causes severe malaria via a distinctive property not shared by any other human malaria, that of sequestration. Within the 48-hour asexual blood stage cycle, the mature forms change the surface properties of infected red blood cells, causing them to stick to blood vessels (a process called cytoadherence). This leads to obstruction of the microcirculation and results in dysfunction of multiple organs, typically the brain in cerebral malaria.^[7]

Microscopic appearance[edit]

Blood smear from a P. falciparum culture (K1 strain - asexual forms) - several red blood cells have ring stages inside them. Close to the center, there is a schizont and on the left a trophozoite.

Among medical professionals, the preferred method to diagnose malaria and determine which species of Plasmodium is causing the infection is by examination of a blood film under microscope in a laboratory. Each species has distinctive physical characteristics that are apparent under a microscope. In P. falciparum, only early (ring-form) trophozoites and gametocytes are seen in the peripheral blood. It is unusual to see mature trophozoites or schizonts in peripheral blood smears, as these are usually sequestered in the tissues. The parasitised erythrocytes are not enlarged, and it is common to see cells with more than one parasite within them (multiply parasitised erythrocytes). On occasion, faint, comma-shaped, red dots called "Maurer's dots" are seen on the red cell surface. The comma-shaped dots can also appear as pear-shaped blotches.

The Plasmodium falciparum genome[edit]

In 1995, a consortium, the malaria genome project (MGP), was set up to sequence the genome of P. falciparum. The genome of its mitochondrion was reported in 1995, that of the nonphotosynthetic plastid known as the apicoplast in 1996,^[8] and the sequence of the first nuclear chromosome (chromosome 2) in 1998. The sequence of chromosome 3 was reported in 1999, and the entire genome on 3 October 2002.^[9] Annotated genome data can now be fully analyzed at several database resources including the UCSC Malaria Genome Browser, PlasmoDB and GeneDB. The ~24 megabase genome is extremely AT-rich (~80%) and is organised into 14 chromosomes: Just over 5,300 genes were described.

Influence of P. falciparum on the human genome[edit]

The presence of the parasite in human populations caused selection in the human genome in a multitude of ways, as humans have been forced to develop resistance to the disease. Beet, a doctor working in Southern Rhodesia (now Zimbabwe) in 1948, first suggested that sickle-cell disease could offer some protection to malaria. This suggestion was reiterated by J. B. S. Haldane in 1949, who suggested that thalassaemia could provide similar protection. This hypothesis has since been confirmed and has been extended to hemoglobin C and hemoglobin E, abnormalities in ankyrin and spectrin (ovalocytosis, elliptocytosis), in glucose-6-phosphate dehydrogenase deficiency and pyruvate kinase deficiency, loss of the Gerbich antigen (glycophorin C) and the Duffy antigen on the erythrocytes, thalassemias and variations in the major histocompatibility complex classes 1 and 2 and CD32 and CD36.

P. falciparum and sickle cell anemia[edit]

Further information: Genetic resistance to malaria

Individuals with sickle-cell anemia or sickle-cell trait do have reduced parasitemia when compared to wild-type individuals for the hemoglobin protein in red blood cells. Studies have shown these genetic deviations of hemoglobin from normal states provide protection against the deadly parasite that causes malaria (Allison, 1954).

Of the six malarial parasites, P. falciparum causes the most fatal and medically severe form. Malaria is prevalent in tropical countries with an incidence of 300 million per year and a mortality rate of 1 to 2 million per year. Roughly 50% of all malarial infections are caused by P. falciparum (Roberts and Janovy Jr., 2005). Upon infection via a bite from an infected Anopheles mosquito, sporozoites devastate the human body by first infecting the liver. While in the liver, sporozoites undergo asexual development and merozoites are released into the bloodstream. The trophozoites further develop and reproduce by invading red blood cells. During the reproduction cycle, Plasmodium falciparum produces up to 40,000 merozoites in one day. Other blood sporozoans, such as Plasmodium vivax, Plasmodium ovale, and Plasmodium malariae, that infect humans and cause malaria do not have such a productive cycle for invasion. The process of bursting red blood cells does not have any symptoms, however destruction of the cells does cause anemia, since the bone marrow cannot compensate for the damage. When red blood cells rupture, hemozoin wastes cause cytokine release, chills, and then fever (Roberts and Janovy Jr., 2005).

Plasmodium falciparum trophozoites develop sticky knobs in red blood cells, which then adhere to endothelial cells in blood vessels, thus evading clearance in the spleen. The acquired adhesive nature of the red blood cells may cause cerebral malaria when sequestered cells prevent oxygenation of the brain. Symptoms of cerebral malaria include impaired consciousness, convulsions, neurological disorder, and coma (Brown University). Additional complications from Plasmodium falciparum induced malaria include advanced immunosuppression (Roberts and Janovy Jr., 2005).

Individuals with sickle-cell trait and sickle-cell anemia are privileged because they have altered sticky knobs. Research by Cholera, R., Brittain, N., Gillrie, M. et al. (2007) has shown that parasitemia (the ability of a parasite to infect) because merozoites of each parasite species that cause malaria invade the red blood cell in three stages: contact, attachment, and endocytosis. Individuals suffering from sickle-cell anemia have deformed red blood cells that interfere with the attachment phase, and Plasmodium falciparum and the other forms of malaria have trouble with endocytosis.

These individuals have reduced attachment when compared to red blood cells with the normally functioning hemoglobin because of differing protein interactions. In normal circumstances, merozoites enter red blood cells through two PfEMP-1 protein-dependent interactions. These interactions promote the malaria inflammatory response associated with symptoms of chills and fever. When these proteins are impaired, as in sickle-cell cases, parasites cannot undergo cytoadherance interactions and cannot infect the cells; therefore, sickle-cell-anemic individuals and individuals carrying the sickle-cell trait have lower parasite loads and shorter time for symptoms than individuals expressing normal red blood cells (Mockenhaupt, 2004).

Individuals with sickle-cell anemia may also experience greatly reduced symptoms of malaria because Plasmodium falciparum trophozoites cannot bind to hemoglobin in order to form sticky knobs. Without knob-binding complexes, which is an exclusive feature of Plasmodium falciparum, red blood cells do not stick to endothelial walls of blood vessels, and infected individuals do not experience symptoms such as cerebral malaria (Cholera, R., Brittain, N., Gillrie, M. et al. 2007).

Many may wonder why natural selection has not phased out sickle-cell anemia. The answer lies within answers generated by Cholera, R., Brittain, N., Gillrie, M. et al. (2007). Individuals with sickle-cell trait are greatly desired in areas where malarial infections are endemic. Malaria kills between 1 and 2 million people per year. It is the leading cause of death among children in tropical regions. Individuals with sickle-cell deformities are able to fight Plasmodium parasite infections and do not become victims of malarial demise. Therefore, individuals expressing the genes and individuals carrying genes are selected to remain within the population (Allison 1964). It is no surprise that the incidence of sickle-cell anemia matches that of endemic regions for malarial infections.

Known vectors[edit]

Anopheles gambiae (Principal vector)^[10]
Anopheles albimanus
Anopheles freeborni
Anopheles maculatus
Anopheles stephensi

Origins and Evolution[edit]

The closest relative of Plasmodium falciparum is Plasmodium reichenowi, a parasite of chimpanzees. P. falciparum and P. reichenowi are not closely related to the other Plasmodium species that parasitize humans, or indeed mammals in general. It has been argued that these two species originated from a parasite of birds.^[11] More recent analyses do not support this, however, instead suggesting that the ability to parasitize mammals evolved only once within the genus Plasmodium.^[12]

New evidence based on analysis of more than 1,100 mitochondrial, apicoplastic, and nuclear DNA sequences has suggested that Plasmodium falciparum may in fact have speciated from a lineage present in gorillas.^[13]^[14]^[15]

According to this theory, P. falciparum and P. reichenowi may both represent host switches from an ancestral line that infected primarily gorillas; P. falciparum went on to infect primarily humans, while P. reichenowi specialized in chimpanzees. The ongoing debate over the evolutionary origin of Plasmodium falciparum will likely be the focus of continuing genetic study.^[16]

A third species that appears to related to these two has been discovered: Plasmodium gaboni. This putative species is currently (2009) known only from two DNA sequences and awaits a full species description before it can be regarded as valid.

Molecular clock analyses suggest that P. falciparum is as old as the human line; the two species diverged at the same time as humans and chimpanzees.^[17] However, low levels of polymorphism within the P. falciparum genome suggest a much more recent origin.^[18] It may be that this discrepancy exists because P. falciparum is old, but its population recently underwent a great expansion.^[19] Some evidence still indicates that P. reichenowi was the ancestor of P. falciparum.^[20] The timing of this event is unclear at present but it has been proposed that it may have occurred about 10,000 years ago.

More recently, P. falciparum has evolved in response to human interventions. Most strains of malaria can be treated with chloroquine, but P. falciparum has developed resistance to this treatment. A combination of quinine and tetracycline has also been used, but there are strains of P. falciparum that have grown resistant to this treatment as well. Different strains of P. falciparum have grown resistant to different treatments. Often, the resistance of the strain depends on where it was contracted. Many cases of malaria that come from parts of the Caribbean and west of the Panama Canal as well as the Middle East and Egypt can often be treated with chloroquine, since they have not yet developed resistance. Nearly all cases contracted in Africa, India, and southeast Asia have grown resistant to this medication, and there have been cases in Thailand and Cambodia in which the strain has been resistant to nearly all treatments. Often the strain grows resistant to the treatment in areas where the use is not as tightly regulated.

Like most apicomplexans, malaria parasites harbor a plastid, an apicoplast, similar to plant chloroplasts, which they probably acquired by engulfing (or being invaded by) a eukaryotic alga, and retaining the algal plastid as a distinctive organelle encased within four membranes - (see endosymbiotic theory). The apicoplast, is an essential organelle, thought to be involved in the synthesis of lipids and several other compounds, and it provides an attractive target for antimalarial drug development, in particular in light of the emergence of parasites resistant to chloroquine and other existing antimalarial agents.

Treatment[edit]

Uncomplicated falciparum malaria[edit]

According to WHO guidelines 2010,^[21] artemisinin-based combination therapies (ACTs) are the recommended first line antimalarial treatments for uncomplicated malaria caused by P. falciparum.^[21] The following ACTs are recommended by the WHO:^[21]

artemether plus lumefantrine
artesunate plus amodiaquine
artesunate plus mefloquine
artesunate plus sulfadoxine-pyrimethamine
dihydroartemisinin plus piperaquine

The choice of ACT in a country or region will be based on the level of resistance to the constituents in the combination.^[21] Artemisinin and its derivatives should not be used as monotherapy in uncomplicated falciparum malaria.^[21] As second-line antimalarial treatment, when initial treatment doesn’t work or stops working, it is recommended to use an alternative ACT known to be effective in the region, such as:

Artesunate plus tetracycline or doxycycline or clindamycin.^[21]
Quinine plus tetracycline or doxycycline or clindamycin^[21]

Any of these combinations are to be given for 7 days.^[21]

A Cochrane systematic review published in 2014, provided evidence that in Africa the overall treatment failure was lesser for dihydroartemisinin-piperaquine when compared to artemether-lumefantrine and both drugs had PCR adjusted failure rates of less than 5%.However in Asian countries, dihydroartemisinin-piperaquine was found to be better tolerated but as effective as artesunate plus mefloquine. ^[22]

For pregnant women, the recommended first-line treatment during the first trimester is quinine plus clindamycin for 7 days.^[21] Artesunate plus clindamycin for 7 days is indicated if this treatment fails.^[21] Still, an ACT is indicated only if this is the only treatment immediately available, or if treatment with 7-day quinine plus clindamycin fails or if there is uncertainty of compliance with a 7-day treatment.^[21] In second and third trimesters, the recommended treatment is an ACT known to be effective in the country/region or artesunate plus clindamycin for 7 days, or quinine plus clindamycin for 7 days.^[21] Lactating women should receive standard antimalarial treatment (including ACTs) except for dapsone, primaquine and tetracyclines.

In infants and young children, the recommended first-line treatment is ACTs, with attention to accurate dosing and ensuring the administered dose is retained.^[21]

For travellers returning to non-endemic countries, any of the following is recommended:^[21]

atovaquone-proguanil
artemether-lumefantrine;
quinine plus doxycycline or clindamycin.

Severe falciparum malaria[edit]

In severe falciparum malaria, it is recommended that rapid clinical assessment and confirmation of the diagnosis be made, followed by administration of full doses of parenteral antimalarial treatment without delay with whichever effective antimalarial is first available.^[21]

For adults, intravenous (IV) or intramuscular (IM) artesunate is recommended.^[21] Quinine is an acceptable alternative if parenteral artesunate is not available.^[21]

For children, especially in the malaria-endemic areas of Africa, any the following antimalarial medicines is recommended:^[21]

artesunate IV or IM
quinine (IV infusion or divided IM injection)
artemether IM. It should be used only if none of the alternatives are available, as its absorption may be erratic.^[21]

Parenteral antimalarials should be administered for a minimum of 24 hours in the treatment of severe malaria, irrespective of the patient's ability to tolerate oral medication earlier.^[21] Thereafter, it is recommended to complete treatment by giving a complete course of any of the following:^[21]

an ACT
artesunate plus clindamycin or doxycycline
quinine plus clindamycin or doxycycline

If complete treatment of severe malaria is not possible, it is recommended that patients be given pre-referral treatment and referred immediately to an appropriate facility for further treatment. The following are options for pre-referral treatment:^[21]

rectal artesunate
quinine IM
artesunate IM
artemether IM

History of falciparum treatment[edit]

Attempts to make synthetic antimalarials began in 1891. Atabrine, developed in 1933, was used widely throughout the Pacific in World War II but was deeply unpopular because of the yellowing of the skin it caused. In the late 1930s, the Germans developed chloroquine, which went into use in the North African campaigns. Mao Zedong encouraged Chinese scientists to find new antimalarials after seeing the casualties in the Vietnam War. Artemisinin was discovered in the 1970s based on a medicine described in China in the year 340. This new drug became known to Western scientists in the late 1980s and early 1990s and is now a standard treatment. In 1976, P. falciparum was successfully cultured in vitro for the first time, which facilitated the development of new drugs substantially.^[23] A 2008 study published in the New England Journal of Medicine highlighted the emergence of artemisinin-resistant strains of P.falciparum in Cambodia.^[24]

Vaccination[edit]

Although an antimalarial vaccine is urgently needed, infected individuals never develop a sterilizing (complete) immunity, making the prospects for such a vaccine dim. The parasites live inside cells, where they are largely hidden from the immune response. Infection has a profound effect on the immune system including immune suppression. Dendritic cells suffer a maturation defect following interaction with infected erythrocytes and become unable to induce protective liver-stage immunity. Infected erythrocytes directly adhere to and activate peripheral blood B cells from nonimmune donors. The var gene products, a group of highly expressed surface antigens, bind the Fab and Fc fragments of human immunoglobulins in a fashion similar to protein A to Staphylococcus aureus, which may offer some protection to the parasite from the human immune system. Despite the poor prospects for a fully protective vaccine, it may be possible to develop a vaccine that would reduce the severity of malaria for children living in endemic areas.

References[edit]

^ Rich, S. M.; Leendertz, F. H.; Xu, G.; Lebreton, M.; Djoko, C. F.; Aminake, M. N.; Takang, E. E.; Diffo, J. L. D.; Pike, B. L.; Rosenthal, B. M.; Formenty, P.; Boesch, C.; Ayala, F. J.; Wolfe, N. D. (2009). "The origin of malignant malaria". Proceedings of the National Academy of Sciences 106 (35): 14902–14907. doi:10.1073/pnas.0907740106. PMC 2720412. PMID 19666593. edit
^ Perkins, D. J.; Were, T.; Davenport, G. C.; Kempaiah, P.; Hittner, J. B.; Ong'Echa, J. M. (2011). "Severe malarial anemia: Innate immunity and pathogenesis". International journal of biological sciences 7 (9): 1427–1442. doi:10.7150/ijbs.7.1427. PMC 3221949. PMID 22110393. edit
^ Perlmann, P; Troye-Blomberg, M (2000). "Malaria blood-stage infection and its control by the immune system". Folia biologica 46 (6): 210–8. PMID 11140853.
^ ^a ^b "World Malaria Report 2008". World Health Organisation. 2008. p. 10. Retrieved 2009-08-17.
^ http://www.ijern.com/images/February-2013/13.pdf
^ Biodiversity of the Malaria in the World, Sylvie Manguin et al. Editorial John Libbey, 2008. p. 23
^ Dondorp AM, Pongponratn E, White NJ (February 2004). "Reduced microcirculatory flow in severe falciparum malaria: pathophysiology and electron-microscopic pathology". Acta Trop. 89 (3): 309–17. doi:10.1016/j.actatropica.2003.10.004. PMID 14744557.
^ Wilson RJ; Denny PW; Preiser PR et al. (August 1996). "Complete gene map of the plastid-like DNA of the malaria parasite Plasmodium falciparum". Journal of Molecular Biology 261 (2): 155–72. doi:10.1006/jmbi.1996.0449. PMID 8757284.
^ Gardner MJ; Hall N; Fung E; and others; Berriman, Matthew; Hyman, Richard W.; Carlton, Jane M.; Pain, Arnab; Nelson, Karen E.; Bowman, Sharen; Paulsen, Ian T.; James, Keith; Eisen, Jonathan A.; Rutherford, Kim; Salzberg, Steven L.; Craig, Alister; Kyes, Sue; Chan, Man-Suen; Nene, Vishvanath; Shallom, Shamira J.; Suh, Bernard; Peterson, Jeremy; Angiuoli, Sam; Pertea, Mihaela; Allen, Jonathan; Selengut, Jeremy; Haft, Daniel; Mather, Michael W.; Vaidya, Akhil B. et al. (October 2002). "Genome sequence of the human malaria parasite Plasmodium falciparum". Nature 419 (6906): 498–511. Bibcode:2002Natur.419..498G. doi:10.1038/nature01097. PMID 12368864.
^ Mbogo CM; Mwangangi JM; Nzovu J et al. (June 2003). "Spatial and temporal heterogeneity of Anopheles mosquitoes and Plasmodium falciparum transmission along the Kenyan coast". Am. J. Trop. Med. Hyg. 68 (6): 734–42. PMID 12887036.
^ Rathore, D; Wahl AM, Sullivan M, McCutchan TF (2001-04-25). "A phylogenetic comparison of gene trees constructed from plastid, mitochondrial and genomic DNA of Plasmodium species". Molecular and Biochemical Parasitology 114 (1): 89–94. doi:10.1016/S0166-6851(01)00241-9. PMID 11356517.
^ Yotoko, KSC; C Elisei (November 2006). "Malaria parasites (Apicomplexa, Haematozoea) and their relationships with their hosts: is there an evolutionary cost for the specialization?". Journal of Zoological Systematics and Evolutionary Research 44 (4): 265–73. doi:10.1111/j.1439-0469.2006.00377.x.
^ Liu, W; Y Li, GH Learn, RS Rudicell, JD Robertson, BF Keele, JN Ndjango, CM Sanz, DB Morgan, S Locatelli, MK Gonder, PJ Kranzusch, PD Walsh, E Delaporte, E Mpoudi-Ngole, AV Georgiev, MN Muller, GM Shaw, M Peeters, PM Sharp, JC Rayner, BH Hahn (2010). "Origin of the human malaria parasite Plasmodium falciparum in gorillas". Nature 467 (7314): 420–5. Bibcode:2010Natur.467..420L. doi:10.1038/nature09442. PMC 2997044. PMID 20864995.
^ Duval, L; M Fourment, E Nerrienet, D Rousset, SA Sadeuh, SM Goodman, NV Andriaholinirina, M Randrianarivelojosia, RE Paul, V Robert, FJ Ayala, F Ariey (2010). "African apes as reservoirs of Plasmodium falciparum and the origin and diversification of the Laverania subgenus". Proceedings of the National Academy of Sciences of the United States of America 107 (23): 10561–6. Bibcode:2010PNAS..10710561D. doi:10.1073/pnas.1005435107. PMC 2890828. PMID 20498054.
^ Rayner, J; WM Liu, M Peeters, PM Sharp, BH Hahn (2011). "A plethora of Plasmodium species in wild apes: a source of human infection?". Trends in Parasitology 467 (5): 222. doi:10.1016/J.Pt.2011.01.006.
^ Prugnolle, F; P Durand, B Ollomo, L Duval, F Ariey, C Arnathau, JP Gonzalez, E Leroy, F Renaud (2011). "A Fresh Look at the Origin of Plasmodium falciparum, the Most Malignant Malaria Agent". In Manchester, Marianne. PLOS Pathogens 7 (2): e1001283. doi:10.1371/journal.ppat.1001283. PMC 3044689. PMID 21383971.
^ Escalante, AA; E Barrio, FJ Ayala (1995). "Evolutionary origin of human and primate malarias: evidence from the circumsporozoite protein gene". Molecular Biology and Evolution 12 (4): 616–26. ISSN 0737-4038. PMID 7659017.
^ Hartl, DH (January 2004). "The origin of malaria: mixed messages from genetic diversity". Nature Reviews Microbiology 2 (1): 15–22. doi:10.1038/nrmicro795. PMID 15035005.
^ Joy, DA; Feng X, Mu J, Furuya T, Chotivanich K, Krettli AU, Ho M, Wang A, White NJ, Suh E, Beerli P, Su XZ. (2003-04-11). "Early origin and recent expansion of Plasmodium falciparum". Science 300 (5617): 318–21. Bibcode:2003Sci...300..318J. doi:10.1126/science.1081449. PMID 12690197.
^ Rich SM, Leendertz FH, Xu G, Lebreton M, Djoko CF, Aminake MN, Takang EE, Diffo JL, Pike BL, Rosenthal BM, Formenty P, Boesch C, Ayala FJ, Wolfe ND; Leendertz; Xu; Lebreton; Djoko; Aminake; Takang; Diffo; Pike; Rosenthal; Formenty; Boesch; Ayala; Wolfe (2009). "The origin of malignant malaria". Proc Natl Acad Sci USA 106 (35): 14902–7. Bibcode:2009PNAS..10614902R. doi:10.1073/pnas.0907740106. PMC 2720412. PMID 19666593.
^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j ^k ^l ^m ⁿ ^o ^p ^q ^r ^s ^t ^u ^v Guidelines for the treatment of malaria, second edition Authors: WHO. Number of pages: 194. Publication date: 2010. Languages: English. ISBN 978-92-4-154792-5
^ Babalwa Zani et al. (2014). "Dihydroartemisinin-piperaquine for treating uncomplicated Plasmodium falciparum malaria". Cochrane Database of Systematic Reviews 1. doi:10.1002/14651858.CD010927.
^ Trager, W; J B Jensen (1976-08-20). "Human malaria parasites in continuous culture". Science 193 (4254): 673–5. Bibcode:1976Sci...193..673T. doi:10.1126/science.781840. PMID 781840.
^ Noedl H, Se Y, Schaecher K, Smith BL, Socheat D, Fukuda MM (December 2008). "Evidence of artemisinin-resistant malaria in western Cambodia". N. Engl. J. Med. 359 (24): 2619–20. doi:10.1056/NEJMc0805011. PMID 19064625.

Sources and further reading[edit]

Overview[edit]

Introductory
Overview
Malaria biology
Life cycle cartoon

Spatial distribution[edit]

Malaria Atlas Project

Blood slides[edit]

Blood forms
Blood forms
Blood forms
Blood forms
Multiple blood forms
Female gametocyte
Female gametocyte

Case histories[edit]

Case 1
Case 2
Case 3
Case 4

Pathology due to Plasmodium falciparum[edit]

Brain

Gross pathology
Low power H & E stain
High power H & E stain showing parasite adherence to the vessel walls

Spleen

Gross pathology
Low power H & E
Smear preparation
Smear preparation

Liver

Low power H & E
High power H & E

Kidney

Low power H & E
High power H & E
High power H & E
Membrane stain
Membrane stain