A novel multiplex qPCR assay for detection of Plasmodium falciparum with histidine-rich protein 2 and 3 (pfhrp2 and pfhrp3) deletions in polyclonal infections.
Antigens, Protozoan
/ genetics
DNA, Protozoan
/ genetics
Diagnostic Tests, Routine
Gene Deletion
Gene Expression
Humans
Kenya
/ epidemiology
Malaria, Falciparum
/ diagnosis
Multiplex Polymerase Chain Reaction
/ methods
Plasmodium falciparum
/ genetics
Protozoan Proteins
/ genetics
Tanzania
/ epidemiology
Travel
United Kingdom
/ epidemiology
Malaria
RDT
pfhrp2
pfldh
qPCR
Journal
EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039
Informations de publication
Date de publication:
May 2020
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
102757Subventions
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.
Références
Sci Rep. 2018 Jul 4;8(1):10097
pubmed: 29973679
PLoS One. 2016 Sep 16;11(9):e0163137
pubmed: 27636709
J Infect Dis. 2017 Jul 1;216(1):36-44
pubmed: 28177502
Malar J. 2014 Jul 22;13:283
pubmed: 25052298
Sci Rep. 2019 Mar 25;9(1):5107
pubmed: 30911048
Malar J. 2017 Mar 6;16(1):105
pubmed: 28264689
Infect Genet Evol. 2018 Aug;62:211-219
pubmed: 29729386
J Infect Dis. 2019 Sep 26;220(9):1444-1452
pubmed: 31249999
PLoS One. 2011;6(7):e22593
pubmed: 21799910
Acta Trop. 2013 Jan;125(1):119-21
pubmed: 23041541
Malar J. 2013 Sep 13;12:320
pubmed: 24028570
Sci Rep. 2017 Nov 7;7(1):14718
pubmed: 29116127
Malar J. 2018 Apr 2;17(1):137
pubmed: 29609602
Sci Rep. 2019 Sep 11;9(1):13107
pubmed: 31511562
Clin Chem. 2009 Apr;55(4):611-22
pubmed: 19246619
Malar J. 2010 Nov 05;9:312
pubmed: 21054863
Biomol Detect Quantif. 2017 Apr 29;12:1-6
pubmed: 28702366
J Clin Microbiol. 2006 Aug;44(8):2773-8
pubmed: 16891491
BMC Res Notes. 2019 Jun 11;12(1):334
pubmed: 31186056
J Infect Dis. 2017 Apr 1;215(7):1156-1166
pubmed: 28329034
Clin Infect Dis. 2019 Aug 30;69(6):1003-1010
pubmed: 30475992
PLoS One. 2010 Jan 25;5(1):e8091
pubmed: 20111602
Emerg Infect Dis. 2018 Mar;24(3):462-470
pubmed: 29460730
EBioMedicine. 2019 Dec;50:14-22
pubmed: 31761619