AI Article Synopsis

  • The study examines the differences between two related species of malaria-causing parasites: Plasmodium ovale curtisi and Plasmodium ovale wallikeri, focusing on their latency periods before symptoms appear.
  • Archived blood samples from UK malaria patients were analyzed using PCR to compare the duration of latency between the two species.
  • Results revealed that P ovale curtisi has a significantly longer latency period (85.7 days) compared to P ovale wallikeri (40.6 days), indicating that existing malaria control measures may need to be adapted to effectively manage ovale malaria.

Article Abstract

Objectives: Ovale malaria is caused by two closely related species of protozoan parasite: Plasmodium ovale curtisi and Plasmodium ovale wallikeri Although clearly distinct genetically, there have been no studies comparing the morphology, life cycle or epidemiology of these parasites. We tested the hypothesis that the two species differ in the duration of latency prior to presentation with symptoms of blood-stage infection.

Design: PCR was used to identify P ovale curtisi and P ovale wallikeri infections among archived blood from UK malaria patients. Latency periods, estimated as the time between entry into the UK and diagnosis of malaria, were compared between the two groups.

Setting: UK National Reference Laboratory.

Participants: None. Archived parasite material and surveillance data for 74 P ovale curtisi and 60 P ovale wallikeri infections were analysed. Additional epidemiological data were taken from a database of 1045 imported cases.

Outcomes: None.

Results: No differences between the two species were identified by a detailed comparison of parasite morphology (N=9, N=8, respectively) and sex ratio (N=5, N=4) in archived blood films. The geometric mean latency period in P ovale wallikeri was 40.6 days (95% CI 28.9 to 57.0), whereas that for P ovale curtisi was more than twice as long at 85.7 days (95% CI 66.1 to 111.1; p=0.002). Further, the proportion of ovale malaria sensu lato which occurred in patients reporting chemoprophylaxis use was higher than for Plasmodium falciparum (OR 7.56; p<0.0001) or P vivax (OR 1.82; p<0.0001).

Conclusions: These findings provide the first difference of epidemiological significance observed between the two parasites which cause ovale malaria, and suggest that control measures aimed at P falciparum may not be adequate for reducing the burden of malaria caused by P ovale curtisi and P ovale wallikeri.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657643PMC
http://dx.doi.org/10.1136/bmjopen-2013-002711DOI Listing

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