Plasmodium yoelii

Plasmodium yoelii
Scientific classification
Domain:	Eukaryota
Clade:	Diaphoretickes
Clade:	SAR
Clade:	Alveolata
Phylum:	Apicomplexa
Class:	Aconoidasida
Order:	Haemospororida
Family:	Plasmodiidae
Genus:	Plasmodium
Species:	P. yoelii
Binomial name
	Plasmodium yoelii; Landau, Michel and Adam, 1968
Subspecies
	Plasmodium yoelii killicki ; Plasmodium yoelii nigeriensis ; Plasmodium yoelii yoelli ;

Plasmodium yoelii is a parasite of the genus Plasmodium subgenus Vinckeia. As in all Plasmodium species, P. yoelii has both vertebrate and insect hosts. The vertebrate hosts for this parasite are mammals.

Taxonomy

This species was described in 1968 by Landau, Michel and Adam. Three subspecies are recognised:

Strains

P. yoelii 17XNL^[1]

Distribution

This species occurs in Africa.

Vectors

The natural vectors of this species are not currently known. One possible is the female Anopheles mosquito which serves as a vector for Plasmodium vivax.

Hosts

This species infects Thamnomys rutilans.

Pathogenesis

P. yoelii impairs immune responses including impairing responses to other pathogens. Fewer granulocytes move out from the bone marrow and in a separate action induces the rodent's own heme oxygenase 1 (HO-1). Although HO-1 induction is a tolerance response by the host to malaria – preventing damage caused by the host's own immune response – the reduced reactive oxygen species production takes away a weapon vital to fighting some unrelated microbes. Cunnington et al. 2012 find mice tolerating P. yoelii 17XNL do not clear coinfections with other pathogens as easily as they normally would.^[1]

Notes

It is used in the laboratory to infect mice, as a model of human malaria, particularly with respect to the immune response. It is advantageous to have a whole-animal model of malaria because often it is difficult to know which factors to study in vitro, particularly in a complex system like the immune system. Moreover, for many experiments it is not ethical or practical to use humans.

One of the special things about this particular model is that it has two strains with vastly different pathogenicity. These are generally referred to as the "lethal" and "non-lethal" strains of the species. Comparison of these two strains can be used to deduce which factors may contribute to more serious malaria infections in humans.

References

^ ^a ^b Moxon, Christopher A.; Gibbins, Matthew P.; McGuinness, Dagmara; Milner, Danny A.; Marti, Matthias (2020-01-24). "New Insights into Malaria Pathogenesis". Annual Review of Pathology: Mechanisms of Disease. 15 (1). Annual Reviews: 315–343. doi:10.1146/annurev-pathmechdis-012419-032640. ISSN 1553-4006. PMID 31648610. S2CID 204882296.

External links

Information about the genome and genes of P. yoelii

www.genedb.org/Homepage/PyoeliiYM

[Moxon-et-al-2020-1] Moxon, Christopher A.; Gibbins, Matthew P.; McGuinness, Dagmara; Milner, Danny A.; Marti, Matthias (2020-01-24). "New Insights into Malaria Pathogenesis". Annual Review of Pathology: Mechanisms of Disease. 15 (1). Annual Reviews: 315–343. doi:10.1146/annurev-pathmechdis-012419-032640. ISSN 1553-4006. PMID 31648610. S2CID 204882296.

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