A novel multiplex qPCR assay for detection of Plasmodium falciparum with histidine-rich protein 2 and 3 (pfhrp2 and pfhrp3) deletions in polyclonal infections.


Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
May 2020
Historique:
received: 22 02 2020
revised: 13 03 2020
accepted: 30 03 2020
pubmed: 14 5 2020
medline: 2 4 2021
entrez: 14 5 2020
Statut: ppublish

Résumé

Many health facilities in malaria endemic countries are dependent on Rapid diagnostic tests (RDTs) for diagnosis and some National Health Service (NHS) hospitals without expert microscopists rely on them for diagnosis out of hours. The emergence of P. falciparum lacking the gene encoding histidine-rich protein 2 and 3 (HRP2 and HRP3) and escaping RDT detection threatens progress in malaria control and elimination. Currently, confirmation of RDT negative due to the deletion of pfhrp2 and pfhrp3, which encodes a cross-reactive protein isoform, requires a series of PCR assays. These tests have different limits of detection and many laboratories have reported difficulty in confirming the absence of the deletions with certainty. We developed and validated a novel and rapid multiplex real time quantitative (qPCR) assay to detect pfhrp2, pfhrp3, confirmatory parasite and human reference genes simultaneously. We also applied the assay to detect pfhrp2 and pfhrp3 deletion in 462 field samples from different endemic countries and UK travellers. The qPCR assay demonstrated diagnostic sensitivity of 100% (n = 19, 95% CI= (82.3%; 100%)) and diagnostic specificity of 100% (n = 31; 95% CI= (88.8%; 100%)) in detecting pfhrp2 and pfhrp3 deletions. In addition, the assay estimates P. falciparum parasite density and accurately detects pfhrp2 and pfhrp3 deletions masked in polyclonal infections. We report pfhrp2 and pfhrp3 deletions in parasite isolates from Kenya, Tanzania and in UK travellers. The new qPCR is easily scalable to routine surveillance studies in countries where P. falciparum parasites lacking pfhrp2 and pfhrp3 are a threat to malaria control.

Sections du résumé

BACKGROUND BACKGROUND
Many health facilities in malaria endemic countries are dependent on Rapid diagnostic tests (RDTs) for diagnosis and some National Health Service (NHS) hospitals without expert microscopists rely on them for diagnosis out of hours. The emergence of P. falciparum lacking the gene encoding histidine-rich protein 2 and 3 (HRP2 and HRP3) and escaping RDT detection threatens progress in malaria control and elimination. Currently, confirmation of RDT negative due to the deletion of pfhrp2 and pfhrp3, which encodes a cross-reactive protein isoform, requires a series of PCR assays. These tests have different limits of detection and many laboratories have reported difficulty in confirming the absence of the deletions with certainty.
METHODS METHODS
We developed and validated a novel and rapid multiplex real time quantitative (qPCR) assay to detect pfhrp2, pfhrp3, confirmatory parasite and human reference genes simultaneously. We also applied the assay to detect pfhrp2 and pfhrp3 deletion in 462 field samples from different endemic countries and UK travellers.
RESULTS RESULTS
The qPCR assay demonstrated diagnostic sensitivity of 100% (n = 19, 95% CI= (82.3%; 100%)) and diagnostic specificity of 100% (n = 31; 95% CI= (88.8%; 100%)) in detecting pfhrp2 and pfhrp3 deletions. In addition, the assay estimates P. falciparum parasite density and accurately detects pfhrp2 and pfhrp3 deletions masked in polyclonal infections. We report pfhrp2 and pfhrp3 deletions in parasite isolates from Kenya, Tanzania and in UK travellers.
INTERPRETATION CONCLUSIONS
The new qPCR is easily scalable to routine surveillance studies in countries where P. falciparum parasites lacking pfhrp2 and pfhrp3 are a threat to malaria control.

Identifiants

pubmed: 32403083
pii: S2352-3964(20)30132-8
doi: 10.1016/j.ebiom.2020.102757
pmc: PMC7218259
pii:
doi:

Substances chimiques

Antigens, Protozoan 0
DNA, Protozoan 0
HRP-2 antigen, Plasmodium falciparum 0
HRP3 protein, Plasmodium falciparum 0
Protozoan Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102757

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : R01 AI121558
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest JBP reports non-financial support in the form of in-kind donation of laboratory testing and reagents from Abbott Laboratories for studies of viral hepatitis and financial support from the World Health Organization. Other authors declare no conflict of interest.

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Auteurs

Lynn Grignard (L)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom.

Debbie Nolder (D)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom; PHE Malaria Reference Laboratory, London School of Hygiene & Tropical Medicine, United Kingdom.

Nuno Sepúlveda (N)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom; Centre of Statistics and Applications of University of Lisbon, Portugal.

Araia Berhane (A)

Communicable Diseases Control Division, Ministry of Health, Eritrea.

Selam Mihreteab (S)

Communicable Diseases Control Division, Ministry of Health, Eritrea.

Robert Kaaya (R)

Kilimanjaro Christian Medical University College, Tanzania.

Jody Phelan (J)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom.

Kara Moser (K)

University of North Carolina at Chapel Hill, United States.

Donelly A van Schalkwyk (DA)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom.

Susana Campino (S)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom.

Jonathan B Parr (JB)

University of North Carolina at Chapel Hill, United States.

Jonathan J Juliano (JJ)

University of North Carolina at Chapel Hill, United States.

Peter Chiodini (P)

PHE Malaria Reference Laboratory, London School of Hygiene & Tropical Medicine, United Kingdom; UCL Hospital for Tropical Diseases, United Kingdom.

Jane Cunningham (J)

World Health Organization, Geneva, Switzerland.

Colin J Sutherland (CJ)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom.

Chris Drakeley (C)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom.

Khalid B Beshir (KB)

Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, United Kingdom. Electronic address: Khalid.Beshir@lshtm.ac.uk.

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Classifications MeSH