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Intrinsic multiplication rate variation and plasticity of human blood stage malaria parasites.
Stewart, Lindsay B; Diaz-Ingelmo, Ofelia; Claessens, Antoine; Abugri, James; Pearson, Richard D; Goncalves, Sonia; Drury, Eleanor; Kwiatkowski, Dominic P; Awandare, Gordon A; Conway, David J.
Affiliation
  • Stewart LB; Department of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London, WC1E 7HT, UK.
  • Diaz-Ingelmo O; Department of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London, WC1E 7HT, UK.
  • Claessens A; Department of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London, WC1E 7HT, UK.
  • Abugri J; LPHI, MIVEGEC, INSERM, CNRS, IRD, University of Montpellier, 34095, Montpellier, Cedex 5, France.
  • Pearson RD; Department of Applied Chemistry and Biochemistry, Faculty of Applied Sciences, University for Development Studies, Tamale, Ghana.
  • Goncalves S; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP) and Department of Biochemistry, Cell and Molecular Biology, University of Ghana, Legon, Accra, Ghana.
  • Drury E; MRC Centre for Genomics and Global Health, Big Data Institute, University of Oxford, Oxford, OX3 7BN, UK.
  • Kwiatkowski DP; Wellcome Sanger Institute, Cambridge, CB10 1SA, UK.
  • Awandare GA; Wellcome Sanger Institute, Cambridge, CB10 1SA, UK.
  • Conway DJ; Wellcome Sanger Institute, Cambridge, CB10 1SA, UK.
Commun Biol ; 3(1): 624, 2020 10 28.
Article in En | MEDLINE | ID: mdl-33116247
ABSTRACT
Pathogen multiplication rate is theoretically an important determinant of virulence, although often poorly understood and difficult to measure accurately. We show intrinsic asexual blood stage multiplication rate variation of the major human malaria parasite Plasmodium falciparum to be associated with blood-stage infection intensity in patients. A panel of clinical isolates from a highly endemic West African population was analysed repeatedly during five months of continuous laboratory culture, showing a range of exponential multiplication rates at all timepoints tested, mean rates increasing over time. All isolates had different genome sequences, many containing within-isolate diversity that decreased over time in culture, but increases in multiplication rates were not primarily attributable to genomic selection. New mutants, including premature stop codons emerging in a few isolates, did not attain sufficiently high frequencies to substantially affect overall multiplication rates. Significantly, multiplication rate variation among the isolates at each of the assayed culture timepoints robustly correlated with parasite levels seen in patients at clinical presentation, indicating innate parasite control of multiplication rate that contributes to virulence.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmodium falciparum / Malaria, Falciparum Limits: Humans Country/Region as subject: Africa Language: En Journal: Commun Biol Year: 2020 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmodium falciparum / Malaria, Falciparum Limits: Humans Country/Region as subject: Africa Language: En Journal: Commun Biol Year: 2020 Type: Article Affiliation country: United kingdom