Time-dependent loss of invasive ability of Plasmodium berghei merozoites in vitro
- PMID: 325188
Time-dependent loss of invasive ability of Plasmodium berghei merozoites in vitro
Abstract
The invasive ability of Plasmodium berghei merozoites in vivo was studied following their artificial removal from parasitized mouse red cells using complement-mediated immune lysis in vitro and in vivo. Time-course experiments revealed that lysed preparations contained two components contributing to the parasites' infectivity in mice. One component, presumed to be free merozoites released from mature schizont-infected cells, rapidly lost infectivity with time at 1 to 2 C. A second minor component appeared to have more stability at this temperature, and could be accounted for as intact parasitized cells containing mature schizonts not lysed by the complement in vitro, but lysed by the recipients' plasma complement in vivo. Further experiments revealed that suspension of parasitized cells in an isotonic diluent and centrifugation at moderate speeds substantially removes the number of invasive free merozoites insolable from a given sample of infected blood by immune hemolysis.
Conclusions: merzoites, either contained within the confines of mature schizont-infected cells, or artificially removed from host cells, rapidly lose the ability to invade susceptible erythrocytes in vivo when suspended in an isotonic medium and held at 1 to 2 C in vitro.
Similar articles
-
Studies on the invasive ability of malarial merozoites (Plasmodium berghei).J Parasitol. 1977 Jun;63(3):448-54. J Parasitol. 1977. PMID: 405468
-
[Further observations of the course of Plasmodium berghei infection in the mouse].Tropenmed Parasitol. 1979 Mar;30(1):24-34. Tropenmed Parasitol. 1979. PMID: 375509 German.
-
Harvest of Plasmodium falciparum merozoites from continuous culture.Bull World Health Organ. 1979;57 Suppl 1(Suppl):63-8. Bull World Health Organ. 1979. PMID: 397009 Free PMC article.
-
The influence of cell type and culture medium on the in vitro cultivation of exoerythrocytic stages of Plasmodium berghei.J Parasitol. 1983 Apr;69(2):346-52. J Parasitol. 1983. PMID: 6343574
-
Schizont-infected cell enrichment in rodent malaria.J Parasitol. 1976 Oct;62(5):664-9. J Parasitol. 1976. PMID: 789847
Cited by
-
Differential drivers of intraspecific and interspecific competition during malaria-helminth co-infection.Parasitology. 2021 Aug;148(9):1030-1039. doi: 10.1017/S003118202100072X. Epub 2021 May 11. Parasitology. 2021. PMID: 33971991 Free PMC article.
-
Reduced erythrocyte susceptibility and increased host clearance of young parasites slows Plasmodium growth in a murine model of severe malaria.Sci Rep. 2015 May 6;5:9412. doi: 10.1038/srep09412. Sci Rep. 2015. PMID: 25944649 Free PMC article.
-
In vitro culture of Plasmodium berghei-ANKA maintains infectivity of mouse erythrocytes inducing cerebral malaria.Malar J. 2011 Nov 25;10:346. doi: 10.1186/1475-2875-10-346. Malar J. 2011. PMID: 22118493 Free PMC article.
-
Uncovering drivers of dose-dependence and individual variation in malaria infection outcomes.PLoS Comput Biol. 2020 Oct 8;16(10):e1008211. doi: 10.1371/journal.pcbi.1008211. eCollection 2020 Oct. PLoS Comput Biol. 2020. PMID: 33031367 Free PMC article.
-
Effect of mature blood-stage Plasmodium parasite sequestration on pathogen biomass in mathematical and in vivo models of malaria.Infect Immun. 2014 Jan;82(1):212-20. doi: 10.1128/IAI.00705-13. Epub 2013 Oct 21. Infect Immun. 2014. PMID: 24144725 Free PMC article.