The DOI matches its Crossref record; 139 of the 139 references it cites were found in a registry or an index.
Plasmodium—a brief introduction to the parasites causing human malaria and their basic biology
Open accessAbstract
Malaria is one of the most devastating infectious diseases of humans. It is problematic clinically and economically as it prevails in poorer countries and regions, strongly hindering socioeconomic development. The causative agents of malaria are unicellular protozoan parasites belonging to the genus Plasmodium. These parasites infect not only humans but also other vertebrates, from reptiles and birds to mammals. To date, over 200 species of Plasmodium have been formally described, and each species infects a certain range of hosts. Plasmodium species that naturally infect humans and cause malaria in large areas of the world are limited to five—P. falciparum, P. vivax, P. malariae, P. ovale and P. knowlesi. The first four are specific for humans, while P. knowlesi is naturally maintained in macaque monkeys and causes zoonotic malaria widely in South East Asia. Transmission of Plasmodium species between vertebrate hosts depends on an insect vector, which is usually the mosquito. The vector is not just a carrier but the definitive host, where sexual reproduction of Plasmodium species occurs, and the parasite’s development in the insect is essential for transmission to the next vertebrate host. The range of insect species that can support the critical development of Plasmodium depends on the individual parasite species, but all five Plasmodium species causing malaria in humans are transmitted exclusively by anopheline mosquitoes. Plasmodium species have remarkable genetic flexibility which lets them adapt to alterations in the environment, giving them the potential to quickly develop resistance to therapeutics such as antimalarials and to change host specificity. In this article, selected topics involving the Plasmodium species that cause malaria in humans are reviewed.
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Cites
Genome sequence of the human malaria parasite Plasmodium falciparum
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“However, as the genomic information encoded in the nuclear genome of the parasites became available [110], it gradually became evident that the Plasmodium apicoplast is involved in plant-type metabolic pathways including isoprenoid biosynthesis [111], type II fatty acid biosynthesis [112] and haem biosynthesis [113].”
BackgroundSpread of Artemisinin Resistance in Plasmodium falciparum Malaria
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A large focus of naturally acquired Plasmodium knowlesi infections in human beings
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Quinine, an old anti-malarial drug in a modern world: role in the treatment of malaria
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Plasmodium knowlesi Malaria in Humans Is Widely Distributed and Potentially Life Threatening
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Mefloquine resistance in Plasmodium falciparum and increased pfmdr1 gene copy number
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Cited by
Functions of double‐negative B cells in autoimmune diseases, infections, and cancers
Chung, M. K. Y., Gong, L., Kwong, D. L., Lee, V. H., Lee, A. W., Guan, X., Kam, N., & Dai, W. (2023) · EMBO Molecular Medicine · doi:10.15252/emmm.202217341 · Cited by 73
Metadata
- Authors
- Sato, S.
- Venue
- Journal of Physiological Anthropology
- Published
- 2021-01-07
- Volume
- 40
- Issue
- 1
- Pages
- 1-1
- ISSN
- 1880-6791 (ISSN-L)
- 1880-6805
- OpenAlex
- W3120666957
- Cited by
- 404
- References
- 139
- FWCI
- 46.30
- Type
- journal article
- Language
- en
- Open access
- gold
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