International Journal of Infectious Diseases (Jul 2021)

Failure of rapid diagnostic tests in Plasmodium falciparum malaria cases among travelers to the UK and Ireland: Identification and characterisation of the parasites

  • Debbie Nolder,
  • Lindsay Stewart,
  • Julie Tucker,
  • Amy Ibrahim,
  • Adam Gray,
  • Tumena Corrah,
  • Carmel Gallagher,
  • Laurence John,
  • Edel O’Brien,
  • Dinesh Aggarwal,
  • Ernest Diez Benavente,
  • Donelly van Schalkwyk,
  • Gisela Henriques,
  • Nuno Sepúlveda,
  • Susana Campino,
  • Peter Chiodini,
  • Colin Sutherland,
  • Khalid B. Beshir

Journal volume & issue
Vol. 108
pp. 137 – 144

Abstract

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Objectives: Our objective was to systematically investigate false-negative histidine-rich protein 2 rapid diagnostic tests (HRP2-RDT) in imported Plasmodium falciparum malaria cases from travelers to the UK and the Republic of Ireland (RoI). Methods: Five imported malaria cases in travellers returning to the UK and RoI from East Africa were reported to the PHE Malaria Reference Laboratory as negative according to histidine-rich protein (HRP2)-RDT. The cases were systematically investigated using microscopic, RDT, molecular, genomic, and in in vitro approaches. Results: In each case, HRP2-RDT was negative, whereas microscopy confirmed the presence of P. falciparum. Further analysis revealed that the genes encoding HRP2 and HRP3 were deleted in three of the five cases. Whole-genome sequencing in one of these isolates confirmed deletions in P. falciparum chromosomes 8 and 13. Our study produced evidence that the fourth case, which had high parasitemia at clinical presentation, was a rare example of antigen saturation (‘prozone-like effect’), leading to a false negative in the HRP2-RDT, while the fifth case was due to low parasitemia. Conclusions: False-negative HRP2-RDT results with P. falciparum are concerning. Our findings emphasise the necessity of supporting the interpretation of RDT results with microscopy, in conjunction with clinical observations, and sets out a systematic approach to identifying parasites carrying pfhrp2 and pfhrp3 deletions.

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