4.8 Article

Evaluating the Performance of Malaria Genetics for Inferring Changes in Transmission Intensity Using Transmission Modeling

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 38, Issue 1, Pages 274-289

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msaa225

Keywords

malaria; genetics; surveillance; modeling

Funding

  1. Wellcome Trust PhD Studentships [109312/Z/15/Z, 105272/Z/14/Z]
  2. Bill and Melinda Gates Foundation
  3. UK Royal Society Dorothy Hodgkin fellowship
  4. Medical Research Council
  5. Department for International Development
  6. Division of Malaria Control, Ministry of Public Health and Sanitation through DFID through the WHO Kenya Country Office
  7. National Institute of General Medical Sciences [U54GM088558]
  8. UK Medical Research Council (MRC)
  9. UK Department for International Development (DFID)
  10. European Union
  11. Wellcome [103602, 212176]
  12. Skills Development Fellowship
  13. MRC [MR/R015600/1] Funding Source: UKRI

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Significant progress has been made in global malaria control, but innovative tools are needed for continued progress. Research on using genetic sequencing to simulate malaria parasite genetics found that superinfection significantly affects genetic diversity. Parasite genetics could serve as a surveillance tool for malaria, but patient metadata is essential for accuracy.
Substantial progress has been made globally to control malaria, however there is a growing need for innovative new tools to ensure continued progress. One approach is to harness genetic sequencing and accompanying methodological approaches as have been used in the control of other infectious diseases. However, to utilize these methodologies for malaria, we first need to extend the methods to capture the complex interactions between parasites, human and vector hosts, and environment, which all impact the level of genetic diversity and relatedness of malaria parasites. We develop an individual-based transmission model to simulate malaria parasite genetics parameterized using estimated relationships between complexity of infection and age from five regions in Uganda and Kenya. We predict that cotransmission and superinfection contribute equally to within-host parasite genetic diversity at 11.5% PCR prevalence, above which superinfections dominate. Finally, we characterize the predictive power of six metrics of parasite genetics for detecting changes in transmission intensity, before grouping them in an ensemble statistical model. The model predicted malaria prevalence with a mean absolute error of 0.055. Different assumptions about the availability of sample metadata were considered, with the most accurate predictions of malaria prevalence made when the clinical status and age of sampled individuals is known. Parasite genetics may provide a novel surveillance tool for estimating the prevalence of malaria in areas in which prevalence surveys are not feasible. However, the findings presented here reinforce the need for patient metadata to be recorded and made available within all future attempts to use parasite genetics for surveillance.

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