Skip to main content


  • Oral presentation
  • Open Access

Dynamics of P. vivax clones in a cohort of children with or without primaquine treatment at baseline

  • 1, 2,
  • 3, 4,
  • 1, 2,
  • 3, 5,
  • 4,
  • 1, 2,
  • 4,
  • 1, 2,
  • 3, 6 and
  • 1, 2
Malaria Journal201413 (Suppl 1) :O24

  • Published:


  • Placebo
  • Blood Sample
  • Infectious Disease
  • Lower Risk
  • Placebo Recipient

P. vivax was detected by PCR in 45% of children aged 5-10 years from our study area in Papua New Guinea (PNG). 504 children were randomized into 2 arms according to Primaquine (PQ) treatment or not at baseline and actively and passively followed for 9 months. We genotyped all P. vivax infections, the majority of these being multi-clone infections. All blood samples positive for P. vivax by qPCR were tested for gametocyte carriage by targeting pvs25 transcripts. Primaquine reduced the risk of P. vivax infections by 80%. The multiplicity of infection and the density of asexual P. vivax stages were not significantly different in both treatment arms. The number of new clones (force of blood-stage infection) was 2.38 ± 0.17 per person per year-at-risk in the PQ-arm compared to 8.04 ± 0.41 in the Placebo arm (P < 0.05). The duration of infections did not differ between the treatment arms, with 73 days [95% CI: 33-849] and 68 days [95% CI: 40-247] in the PQ or Placebo arm, respectively. Detectability of P. vivax clones was low with 0.26 ± 0.06 and 0.24 ± 0.04 in the PQ and Placebo arms. PQ-treated children had a 75% lower risk of carrying gametocytes compared to Placebo recipients. P. vivax positive children in both arms were equally likely to show gametocyte positivity. We conclude that P. vivax relapses contribute significantly to the high burden of P. vivax infection and transmission in PNG. All other infection dynamics parameters were consistent between treatment arms and apparent relapses behave like new infections.

Authors’ Affiliations

Swiss Tropical and Public Health Institute, Basel, Switzerland
University of Basel, Basel, Switzerland
Walter and Eliza Hall Institute, Parkville, Australia
PNG Institute of Medical Research, Madang & Maprik, Papua New Guinea
Department of Medical Biology, University of Melbourne, Victoria, Australia
Centre de Recerca en Salut Internacional de Barcelona (CRESIB), Barcelona, Spain


© Wampfler et al; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate. Please note that comments may be removed without notice if they are flagged by another user or do not comply with our community guidelines.