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Plasmodium berghei

(Redirected from Plasmodium berghei ANKA)

Plasmodium berghei is a single-celled parasite causing rodent malaria. It is in the Plasmodium subgenus Vinckeia.

Plasmodium berghei
Blood-borne forms
Blood-borne forms
Scientific classification Edit this classification
Domain: Eukaryota
Clade: Diaphoretickes
Clade: SAR
Clade: Alveolata
Phylum: Apicomplexa
Class: Aconoidasida
Order: Haemospororida
Family: Plasmodiidae
Genus: Plasmodium
Species:
P. berghei
Binomial name
Plasmodium berghei
Vincke & Lips, 1948
Strains

Originally, isolated from thicket rats in Central Africa, P. berghei is one of four Plasmodium species that have been described in African murine rodents, the others being P. chabaudi, P. vinckei, and P. yoelii. Due to its ability to infect rodents and relative ease of genetic engineering, P. berghei is a popular model organism for the study of human malaria.

Biology

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Like all malaria parasites of mammals, including the four human malaria parasites, P. berghei is transmitted by Anopheles mosquitoes and it infects the liver after being injected into the bloodstream by a bite of an infected female mosquito. After a short period (a few days) of development and multiplication, these parasites leave the liver and invade erythrocytes (red blood cells). The multiplication of the parasite in the blood causes the pathology such as anaemia and damage of essential organs of the host such as lungs, liver, spleen. P. berghei infections may also affect the brain and can be the cause of cerebral complications in laboratory mice (cerebral murine malaria, CMM). These symptoms are to a certain degree comparable to symptoms of cerebral malaria in patients infected with the human malaria parasite Plasmodium falciparum.[3]

Although sexuality is necessary in vivo in P. berghei as normal for most sexual organisms, it is a stark competitive disadvantage in vitro. Sinha et al., 2014 implement both mechanical passaging and competitive assay to demonstrate the advantage of loss of gametocyte production: During mechanical passage successive generations are found to naturally trend toward lower gametocytaemia; and nonsexuals outcompete sexuals rapidly when placed together in vitro.[4]: 575 

Immunochemistry

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Endothelin 1 has an uncertain role in producing cerebral murine malaria.[2] Martins et al., 2016 find blockade of endothelin-1 prevents CMM and its symptoms and supplementation helps to produce it.[2] Subramaniam et al., 2015 find mice increase production of BTNL2 during infection and so it is probably protective.[2] Chertow et al., 2015 find the asymmetric dimethylarginine-to-arginine ratio is indicative of disease severity in mice with P. berghei ANKA.[5][6] This ratio is a metric of arginine bioavailability and in this disease they find it predicts degree of endothelial dysfunction.[5][6]

Strains

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Some strains produce cerebral murine malaria and some do not.[2]

  • ANKA produces CMM.[2] Martins et al., 2016 find endothelin-1 production is vital to CMM disease progression.[1] Subramaniam et al., 2015 find mice respond to ANKA by increasing BTNL2.[2] Chertow et al., 2015 find arginine metabolism indicative of disease severity.[5][6]
  • NK65 notably does not produce CMM.[2] Martins et al., 2016 find NK65 can produce CMM under supplementation of endothelin-1.[2]

See section above for specific molecules' interactions.

Distribution

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Plasmodium berghei is found in the forests of Central Africa, where its natural cyclic hosts are the thicket rat (Grammomys surdaster) and the mosquito (Anopheles dureni).

Hosts

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Plasmodium berghei was first identified in the thicket rat (Grammomys surdaster). It has also been described in Leggada bella, Praomys jacksoni and Thamnomys surdaster.[citation needed] In research laboratories, various rodents can be infected, such as mice (Mus musculus), rats and gerbils (Meriones unguiculatus).[7] In M. musculus ⇔ P. b. ANKA, downregulation of responses is necessary to prevent self-inflicted damage leading to CMM.[8][9]: 97  Specifically, Sarfo et al., 2011 finds mice produce the cytokine interleukin-10 (cIL-10) to suppress otherwise-potentially-deadly CMM damage from others of their own immune factors.[8][9]

The natural insect host of P. berghei is likely Anopheles dureni, however in laboratory conditions it has also been shown to infect An. stephensi.[citation needed]

Gene interactions

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In Mus musculus ⇔ the P. b. ANKA strain various genes affect the incidence of cerebral murine malaria. Kassa et al., 2016 finds several genes to be of no effect:

They find one improves survival probability:

An. gambiae's hemocytes transcribe a wide array of molecular responses to Plasmodium infections.[10][11]: 138 [12][13][14][15]: 221  In response to this species, Baton et al., 2009 find this includes increased expression of the prophenoloxidase gene, cascading to increase phenoloxidase and thereby melanization.[10][11]: 138 [12][13][14][15]: 221 

Treatment

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Some phytochemicals show efficacy against P. berghei. Bankole et al., 2016 find Markhamia tomentosa to be highly effective, comparable to chloroquine, while Monoon longifolium is also significantly effective. They find Trichilia heudelotii to be ineffective.[16]

History

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This species was first described by Vincke and Lips in 1948 in the Belgian Congo.[17]

 
Live P. berghei expressing GFP (green) in erythrocytes; visualised using a fluorescence microscope
 
Infected mouse, with P. berghei in the lungs, spleen and adipose tissue. Transgenic parasites are visualized by their expression of the bioluminescent reporter protein Luciferase
 
A liver cell with P. berghei (a schizont with daughter parasites) expressing mCherry (red). Here the parasite membrane is stained green with an antibody, while the nuclei of liver cells and parasites are stained with DAPI (blue)

Research

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Plasmodium berghei infection of laboratory mouse strains is frequently used in research as a model for human malaria.[18] In the laboratory the natural hosts have been replaced by a number of commercially available laboratory mouse strains, and the mosquito Anopheles stephensi, which is comparatively easily reared and maintained under defined laboratory conditions.

P. berghei is used as a model organism for the investigation of human malaria because of its similarity to the Plasmodium species which cause human malaria. P. berghei has a very similar life-cycle to the species that infect humans, and it causes disease in mice which has signs similar to those seen in human malaria. Importantly, P. berghei can be genetically manipulated more easily than the species which infect humans, making it a useful model for research into Plasmodium genetics.

In several aspects the pathology caused by P. berghei in mice differs from malaria caused by P. falciparum in humans. In particular, while death from P. falciparum malaria in humans is most frequently caused by the accumulation of red blood cells in the blood vessels of the brain, it is unclear to what extent this occurs in mice infected with P. berghei.[18] Instead, in P. berghei infection, mice are found to have an accumulation of immune cells in brain blood vessels.[18] This has led some to question the use of P. berghei infections in mice as an appropriate model of cerebral malaria in humans.[18]

P. berghei can be genetically manipulated in the laboratory using standard genetic engineering technologies. Consequently, this parasite is often used for the analysis of the function of malaria genes using the technology of genetic modification.[19][20][21] Additionally, the genome of P. berghei has been sequenced and it shows a high similarity, both in structure and gene content, with the genome of the primate malaria parasite Plasmodium falciparum.[22][23][24]

A number of genetically modified P. berghei lines have been generated which express fluorescent reporter proteins such as Green Fluorescent Protein (GFP) and mCherry (red) or bioluminescent reporters such as Luciferase. These transgenic parasites are important tools to study and visualize the parasites in the living host.[25][26]

P. berghei is used in research programs for development and screening of anti-malarial drugs and for the development of an effective vaccine against malaria.[27]

References

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  1. ^ a b c d e f g Torre, Sabrina; Langlais, David; Gros, Philippe (2018-06-19). "Genetic analysis of cerebral malaria in the mouse model infected with Plasmodium berghei". Mammalian Genome. 29 (7–8). Springer Science+Business Media: 488–506. doi:10.1007/s00335-018-9752-9. ISSN 0938-8990. PMID 29922917. S2CID 49309005. International Mammalian Genome Society.
  2. ^ a b c d e f g h i 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.
  3. ^ Franke-Fayard B, et al. (2010). "Sequestration and tissue accumulation of human malaria parasites: can we learn anything from rodent models of malaria?". PLOS Pathogens. 6 (9): e1001032. doi:10.1371/journal.ppat.1001032. PMC 2947991. PMID 20941396.
  4. ^ Josling, Gabrielle A.; Llinás, Manuel (2015-08-14). "Sexual development in Plasmodium parasites: knowing when it's time to commit". Nature Reviews Microbiology. 13 (9). Nature Portfolio: 573–587. doi:10.1038/nrmicro3519. ISSN 1740-1526. PMID 26272409. S2CID 2182486.
  5. ^ a b c Ngai, Michelle; Weckman, Andrea M.; Erice, Clara; McDonald, Chloe R.; Cahill, Lindsay S.; Sled, John G.; Kain, Kevin C. (2020). "Malaria in Pregnancy and Adverse Birth Outcomes: New Mechanisms and Therapeutic Opportunities". Trends in Parasitology. 36 (2). Cell Press: 127–137. doi:10.1016/j.pt.2019.12.005. ISSN 1471-4922. PMID 31864896. S2CID 209446589.
  6. ^ a b c Kayano, Ana Carolina A. V.; Dos-Santos, João Conrado K.; Bastos, Marcele F.; Carvalho, Leonardo J.; Aliberti, Júlio; Costa, Fabio T. M. (2016). Andrews-Polymenis, H. L. (ed.). "Pathophysiological Mechanisms in Gaseous Therapies for Severe Malaria". Infection and Immunity. 84 (4). American Society for Microbiology: 874–882. doi:10.1128/iai.01404-15. ISSN 0019-9567. PMC 4807480. PMID 26831465. S2CID 29927044.
  7. ^ Junaid, Quazim Olawale; Khaw, Loke Tim; Mahmud, Rohela; Ong, Kien Chai; Lau, Yee Ling; Borade, Prajakta Uttam; Liew, Jonathan Wee Kent; Sivanandam, Sinnadurai; Wong, Kum Thong; Vythilingam, Indra (2017). "Pathogenesis of Plasmodium berghei ANKA infection in the gerbil (Meriones unguiculatus) as an experimental model for severe malaria". Parasite. 24: 38. doi:10.1051/parasite/2017040. PMC 5642054. PMID 29034874.  
  8. ^ a b Xu, Zhilu; Zhang, Xiang; Lau, Jennie; Yu, Jun (2016). "C-X-C". Expert Reviews in Molecular Medicine. 18. Cambridge University Press (CUP): 1–11. doi:10.1017/erm.2016.16. ISSN 1462-3994. PMID 27669973. S2CID 28322523.
  9. ^ a b Fillatreau, S.; O’Garra, A. (2014). Interleukin-10 in Health and Disease. Current Topics in Microbiology and Immunology. Vol. 20. Berlin, Heidelberg: Springer Berlin Heidelberg. p. 649. doi:10.1007/978-3-662-43492-5. ISBN 978-3-662-43491-8. ISSN 0070-217X. PMC 6387150. PMID 30717382. {{cite book}}: |journal= ignored (help)
  10. ^ a b Smith, Ryan C; Vega-Rodríguez, Joel; Jacobs-Lorena, Marcelo (2014). "The Plasmodium bottleneck: malaria parasite losses in the mosquito vector". Memórias do Instituto Oswaldo Cruz. 109 (5). FapUNIFESP (SciELO): 644–661. doi:10.1590/0074-0276130597. ISSN 0074-0276. PMC 4156458. PMID 25185005.
  11. ^ a b Willis, Judith H.; Papandreou, Nikos C.; Iconomidou, Vassiliki A.; Hamodrakas, Stavros J. (2012). "5 Cuticular Proteins". In Gilbert, Lawrence I. (ed.). Insect Molecular Biology and Biochemistry. Elsevier. pp. x+563. ISBN 978-0-12-384747-8. OCLC 742299021.
  12. ^ a b Clayton, April M.; Dong, Yuemei; Dimopoulos, George (2014). "The Anopheles Innate Immune System in the Defense against Malaria Infection". Journal of Innate Immunity. 6 (2). Karger Publishers: 169–181. doi:10.1159/000353602. ISSN 1662-8128. PMC 3939431. PMID 23988482.
  13. ^ a b Hillyer, Julián F.; Strand, Michael R. (2014). "Mosquito hemocyte-mediated immune responses". Current Opinion in Insect Science. 3. Elsevier: 14–21. doi:10.1016/j.cois.2014.07.002. ISSN 2214-5745. PMC 4190037. PMID 25309850. NIHMSID 615755.
  14. ^ a b Cheng, Gong; Liu, Yang; Wang, Penghua; Xiao, Xiaoping (2016). "Mosquito Defense Strategies against Viral Infection". Trends in Parasitology. 32 (3). Cell Press: 177–186. doi:10.1016/j.pt.2015.09.009. ISSN 1471-4922. PMC 4767563. PMID 26626596.
  15. ^ a b Hillyer, Julián F. (2010). "Mosquito Immunity". In Söderhäll, Kenneth (ed.). Invertebrate Immunity. Advances in Experimental Medicine and Biology. Vol. 708. Boston, MA: Springer Nature. pp. 218–238. doi:10.1007/978-1-4419-8059-5_12. ISBN 978-1-4419-8058-8. ISSN 0065-2598. PMID 21528701.
  16. ^ Dkhil, Mohamed A.; Al-Quraishy, Saleh; Al-Shaebi, Esam M.; Abdel-Gaber, Rewaida; Thagfan, Felwa Abdullah; Qasem, Mahmood A.A. (2021). "Medicinal plants as a fight against murine blood-stage malaria". Saudi Journal of Biological Sciences. 28 (3). Elsevier: 1723–1738. doi:10.1016/j.sjbs.2020.12.014. ISSN 1319-562X. PMC 7938113. PMID 33732056. S2CID 232241302. Saudi Biological Society.
  17. ^ Vincke, I.H. and Lips, M. (1948) Un nouveau plasmodium d'un rongeur sauvage du Congo: Plasmodium berghei n.sp. Annales de la Société Belge de Médecine Tropicale 28, 97-104
  18. ^ a b c d Craig AG; Grau GE; Janse C; Kazura JW; Milner D; Barnwell JW; Turner G; Langhorne J (February 2012). "The Role of Animal Models for Research on Severe Malaria". PLOS Pathogens. 8 (2): e1002401. doi:10.1371/journal.ppat.1002401. PMC 3271056. PMID 22319438.
  19. ^ Janse CJ; Ramesar J; Waters AP (2006). "High-efficiency transfection and drug selection of genetically transformed blood stages of the rodent malaria parasite Plasmodium berghei". Nature Protocols. 1 (1): 346–56. doi:10.1038/nprot.2006.53. PMID 17406255. S2CID 20096737.
  20. ^ Janse C.J.; et al. (2011). "A genotype and phenotype database of genetically modified malaria-parasites". Trends in Parasitology. 27 (1): 31–39. doi:10.1016/j.pt.2010.06.016. PMID 20663715.
  21. ^ Khan SM; Kroeze H; Franke-Fayard B; Janse CJ (2013). "Standardization in Generating and Reporting Genetically Modified Rodent Malaria Parasites: The RMGMDB Database". Malaria. Methods in Molecular Biology. Vol. 923. pp. 139–50. doi:10.1007/978-1-62703-026-7_9. ISBN 978-1-62703-025-0. PMID 22990775.
  22. ^ Hall; et al. (2005). "A comprehensive survey of the Plasmodium life cycle by genomic, transcriptomic, and proteomic analyses". Science. 307 (5706): 82–6. Bibcode:2005Sci...307...82H. doi:10.1126/science.1103717. PMID 15637271. S2CID 7230793.
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  24. ^ Otto TD; et al. (2014). "A comprehensive evaluation of rodent malaria parasite genomes and gene expression". BMC Biology. 12: 86. doi:10.1186/s12915-014-0086-0. PMC 4242472. PMID 25359557.
  25. ^ Amino R, Ménard R, Frischknecht F (2005). "In vivo imaging of malaria parasites--recent advances and future directions". Current Opinion in Microbiology. 8 (4): 407–14. doi:10.1016/j.mib.2005.06.019. PMID 16019254.
  26. ^ Franke-Fayard B, Waters AP, Janse CJ (2006). "Real-time in vivo imaging of transgenic bioluminescent blood stages of rodent malaria parasites in mice". Nature Protocols. 1 (1): 476–85. doi:10.1038/nprot.2006.69. PMID 17406270. S2CID 20812965.
  27. ^ Khan SM, Janse CJ, Kappe SH, Mikolajczak SA (2012). "Genetic engineering of attenuated malaria parasites for vaccination". Current Opinion in Biotechnology. 23 (6): 908–916. doi:10.1016/j.copbio.2012.04.003. PMID 22560204.
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