Fully automated point-of-care differential diagnosis of acute febrile illness.

<h4>Background</h4>In this work, a platform was developed and tested to allow to detect a variety of candidate viral, bacterial and parasitic pathogens, for acute fever of unknown origin. The platform is based on a centrifugal microfluidic cartridge, the LabDisk ("FeverDisk" fo...

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Main Authors: Sebastian Hin, Benjamin Lopez-Jimena, Mohammed Bakheit, Vanessa Klein, Seamus Stack, Cheikh Fall, Amadou Sall, Khalid Enan, Mohamed Mustafa, Liz Gillies, Viorel Rusu, Sven Goethel, Nils Paust, Roland Zengerle, Sieghard Frischmann, Manfred Weidmann, Konstantinos Mitsakakis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-02-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://doi.org/10.1371/journal.pntd.0009177
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spelling doaj-bc4d38e4f63249c587951b10be519b902021-06-25T04:32:15ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352021-02-01152e000917710.1371/journal.pntd.0009177Fully automated point-of-care differential diagnosis of acute febrile illness.Sebastian HinBenjamin Lopez-JimenaMohammed BakheitVanessa KleinSeamus StackCheikh FallAmadou SallKhalid EnanMohamed MustafaLiz GilliesViorel RusuSven GoethelNils PaustRoland ZengerleSieghard FrischmannManfred WeidmannKonstantinos Mitsakakis<h4>Background</h4>In this work, a platform was developed and tested to allow to detect a variety of candidate viral, bacterial and parasitic pathogens, for acute fever of unknown origin. The platform is based on a centrifugal microfluidic cartridge, the LabDisk ("FeverDisk" for the specific application), which integrates all necessary reagents for sample-to-answer analysis and is processed by a compact, point-of-care compatible device.<h4>Methodology/principal findings</h4>A sample volume of 200 μL per FeverDisk was used. In situ extraction with pre-stored reagents was achieved by bind-wash-elute chemistry and magnetic particles. Enzymes for the loop-mediated isothermal amplification (LAMP) were pre-stored in lyopellet form providing stability and independence from the cold chain. The total time to result from sample inlet to read out was 2 h. The proof-of-principle was demonstrated in three small-scale feasibility studies: in Dakar, Senegal and Khartoum, Sudan we tested biobanked samples using 29 and 9 disks, respectively; in Reinfeld, Germany we tested spiked samples and analyzed the limit of detection using three bacteria simultaneously spiked in whole blood using 15 disks. Overall during the three studies, the FeverDisk detected dengue virus (different serotypes), chikungunya virus, Plasmodium falciparum, Salmonella enterica Typhi, Salmonella enterica Paratyphi A and Streptococcus pneumoniae.<h4>Conclusions/significance</h4>The FeverDisk proved to be universally applicable as it successfully detected all different types of pathogens as single or co-infections, while it also managed to define the serotype of un-serotyped dengue samples. Thirty-eight FeverDisks at the two African sites provided 59 assay results, out of which 51 (86.4%) were confirmed with reference assay results. The results provide a promising outlook for future implementation of the platform in larger prospective clinical studies for defining its clinical sensitivity and specificity. The technology aims to provide multi-target diagnosis of the origins of fever, which will help fight lethal diseases and the incessant rise of antimicrobial resistance.https://doi.org/10.1371/journal.pntd.0009177
collection DOAJ
language English
format Article
sources DOAJ
author Sebastian Hin
Benjamin Lopez-Jimena
Mohammed Bakheit
Vanessa Klein
Seamus Stack
Cheikh Fall
Amadou Sall
Khalid Enan
Mohamed Mustafa
Liz Gillies
Viorel Rusu
Sven Goethel
Nils Paust
Roland Zengerle
Sieghard Frischmann
Manfred Weidmann
Konstantinos Mitsakakis
spellingShingle Sebastian Hin
Benjamin Lopez-Jimena
Mohammed Bakheit
Vanessa Klein
Seamus Stack
Cheikh Fall
Amadou Sall
Khalid Enan
Mohamed Mustafa
Liz Gillies
Viorel Rusu
Sven Goethel
Nils Paust
Roland Zengerle
Sieghard Frischmann
Manfred Weidmann
Konstantinos Mitsakakis
Fully automated point-of-care differential diagnosis of acute febrile illness.
PLoS Neglected Tropical Diseases
author_facet Sebastian Hin
Benjamin Lopez-Jimena
Mohammed Bakheit
Vanessa Klein
Seamus Stack
Cheikh Fall
Amadou Sall
Khalid Enan
Mohamed Mustafa
Liz Gillies
Viorel Rusu
Sven Goethel
Nils Paust
Roland Zengerle
Sieghard Frischmann
Manfred Weidmann
Konstantinos Mitsakakis
author_sort Sebastian Hin
title Fully automated point-of-care differential diagnosis of acute febrile illness.
title_short Fully automated point-of-care differential diagnosis of acute febrile illness.
title_full Fully automated point-of-care differential diagnosis of acute febrile illness.
title_fullStr Fully automated point-of-care differential diagnosis of acute febrile illness.
title_full_unstemmed Fully automated point-of-care differential diagnosis of acute febrile illness.
title_sort fully automated point-of-care differential diagnosis of acute febrile illness.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2021-02-01
description <h4>Background</h4>In this work, a platform was developed and tested to allow to detect a variety of candidate viral, bacterial and parasitic pathogens, for acute fever of unknown origin. The platform is based on a centrifugal microfluidic cartridge, the LabDisk ("FeverDisk" for the specific application), which integrates all necessary reagents for sample-to-answer analysis and is processed by a compact, point-of-care compatible device.<h4>Methodology/principal findings</h4>A sample volume of 200 μL per FeverDisk was used. In situ extraction with pre-stored reagents was achieved by bind-wash-elute chemistry and magnetic particles. Enzymes for the loop-mediated isothermal amplification (LAMP) were pre-stored in lyopellet form providing stability and independence from the cold chain. The total time to result from sample inlet to read out was 2 h. The proof-of-principle was demonstrated in three small-scale feasibility studies: in Dakar, Senegal and Khartoum, Sudan we tested biobanked samples using 29 and 9 disks, respectively; in Reinfeld, Germany we tested spiked samples and analyzed the limit of detection using three bacteria simultaneously spiked in whole blood using 15 disks. Overall during the three studies, the FeverDisk detected dengue virus (different serotypes), chikungunya virus, Plasmodium falciparum, Salmonella enterica Typhi, Salmonella enterica Paratyphi A and Streptococcus pneumoniae.<h4>Conclusions/significance</h4>The FeverDisk proved to be universally applicable as it successfully detected all different types of pathogens as single or co-infections, while it also managed to define the serotype of un-serotyped dengue samples. Thirty-eight FeverDisks at the two African sites provided 59 assay results, out of which 51 (86.4%) were confirmed with reference assay results. The results provide a promising outlook for future implementation of the platform in larger prospective clinical studies for defining its clinical sensitivity and specificity. The technology aims to provide multi-target diagnosis of the origins of fever, which will help fight lethal diseases and the incessant rise of antimicrobial resistance.
url https://doi.org/10.1371/journal.pntd.0009177
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