Genetic Profiling of Plasmodium ovale wallikeri Relapses With Microsatellite Markers and Whole-Genome Sequencing

J Infect Dis. 2023 Oct 18;228(8):1089-1098. doi: 10.1093/infdis/jiad216.

Abstract

Like Plasmodium vivax, both Plasmodium ovale curtisi and Plasmodium ovale wallikeri have the ability to cause relapse in humans, defined as recurring asexual parasitemia originating from liver-dormant forms subsequent to a primary infection. Here, we investigated relapse patterns in P ovale wallikeri infections from a cohort of travelers who were exposed to the parasite in sub-Saharan Africa and then experienced relapses after their return to France. Using a novel set of 8 highly polymorphic microsatellite markers, we genotyped 15 P ovale wallikeri relapses. For most relapses, the paired primary and relapse infections were highly genetically related (with 12 being homologous), an observation that was confirmed by whole-genome sequencing for the 4 relapses we further studied. This is, to our knowledge, the first genetic evidence of relapses in P ovale spp.

Keywords: Plasmodium ovale wallikeri; WGS; microsatellites; relapses; sWGA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Malaria* / parasitology
  • Microsatellite Repeats / genetics
  • Plasmodium ovale* / genetics
  • Plasmodium vivax / genetics
  • Recurrence