A digital microscope for the diagnosis of Plasmodium falciparum and Plasmodium vivax, including P. falciparum with hrp2/hrp3 deletion.


Journal

PLOS global public health
ISSN: 2767-3375
Titre abrégé: PLOS Glob Public Health
Pays: United States
ID NLM: 9918283779606676

Informations de publication

Date de publication:
2024
Historique:
received: 13 12 2023
accepted: 18 03 2024
medline: 20 5 2024
pubmed: 20 5 2024
entrez: 20 5 2024
Statut: epublish

Résumé

Sensitive and accurate malaria diagnosis is required for case management to accelerate control efforts. Diagnosis is particularly challenging where multiple Plasmodium species are endemic, and where P. falciparum hrp2/3 deletions are frequent. The Noul miLab is a fully automated portable digital microscope that prepares a blood film from a droplet of blood, followed by staining and detection of parasites by an algorithm. Infected red blood cells are displayed on the screen of the instrument. Time-to-result is approximately 20 minutes, with less than two minutes hands-on time. We evaluated the miLab among 659 suspected malaria patients in Gondar, Ethiopia, where P. falciparum and P. vivax are endemic, and the frequency of hrp2/3 deletions is high, and 991 patients in Ghana, where P. falciparum transmission is intense. Across both countries combined, the sensitivity of the miLab for P. falciparum was 94.3% at densities >200 parasites/μL by qPCR, and 83% at densities >20 parasites/μL. The miLab was more sensitive than local microscopy, and comparable to RDT. In Ethiopia, the miLab diagnosed 51/52 (98.1%) of P. falciparum infections with hrp2 deletion at densities >20 parasites/μL. Specificity of the miLab was 94.0%. For P. vivax diagnosis in Ethiopia, the sensitivity of the miLab was 97.0% at densities >200 parasites/μL (RDT: 76.8%, microscopy: 67.0%), 93.9% at densities >20 parasites/μL, and specificity was 97.6%. In Ethiopia, where P. falciparum and P. vivax were frequent, the miLab assigned the wrong species to 15/195 mono-infections at densities >20 parasites/μL by qPCR, and identified only 5/18 mixed-species infections correctly. In conclusion, the miLab was more sensitive than microscopy and thus is a valuable addition to the toolkit for malaria diagnosis, particularly for areas with high frequencies of hrp2/3 deletions.

Identifiants

pubmed: 38768243
doi: 10.1371/journal.pgph.0003091
pii: PGPH-D-23-02507
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0003091

Informations de copyright

Copyright: © 2024 Ewnetu et al. 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 author and source are credited.

Déclaration de conflit d'intérêts

This work was funded by Noul Inc, the developer of the miLab digital microscope. Noul Inc. holds all intellectual property of the miLab device. Noul awarded grants to the University of Notre Dame for CK to conduct the research. Noul also provided funding to LMC Projects for LC to conduct research, and to WL and YE to compensate them for expenses related to the research, including per diem payments. None of the authors holds any intellectual property rights in the miLab device, or shares of Noul. The authors have discussed the results with Noul throughout the project, and taken the joint decision to publish. It was the sole responsibility of the corresponding author to ensure all data is accurate, and that data interpretation is correct. The relationship between the authors and Noul did not alter their adherence to PLOS policies on sharing data and materials. There are no patents, products in development or marketed products associated with this research to declare. All commercial affiliations for all authors are included in the manuscript.

Auteurs

Yalemwork Ewnetu (Y)

Department of Medical Biotechnology, Institute of Biotechnology, University of Gondar, Gondar, Ethiopia.
University of Gondar Comprehensive Specialized Hospital, Gondar, Ethiopia.

Kingsley Badu (K)

Department of Theoretical and Applied Biology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Lise Carlier (L)

LMC Projects, Amsterdam, The Netherlands.

Claudia A Vera-Arias (CA)

Department of Biological Sciences & Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.

Emma V Troth (EV)

Department of Biological Sciences & Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.

Abdul-Hakim Mutala (AH)

Department of Theoretical and Applied Biology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Stephen Opoku Afriyie (SO)

Department of Theoretical and Applied Biology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Thomas Kwame Addison (TK)

Department of Theoretical and Applied Biology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Nega Berhane (N)

Department of Medical Biotechnology, Institute of Biotechnology, University of Gondar, Gondar, Ethiopia.

Wossenseged Lemma (W)

Department of Medical Parasitology, School of Biomedical and Laboratory Sciences, Collage of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.

Cristian Koepfli (C)

Department of Biological Sciences & Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.

Classifications MeSH