Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using Dielectrophoresis

Human African trypanosomiasis (HAT), also known as sleeping sickness, is a vector-borne neglected tropical disease endemic to rural sub-Saharan Africa. Current methods of early detection in the affected rural communities generally begin with general screening using the card agglutination test for tr...

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Main Authors: Devin Keck, Callie Stuart, Josie Duncan, Emily Gullette, Rodrigo Martinez-Duarte
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Micromachines
Subjects:
Online Access:https://www.mdpi.com/2072-666X/11/6/625
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author Devin Keck
Callie Stuart
Josie Duncan
Emily Gullette
Rodrigo Martinez-Duarte
author_facet Devin Keck
Callie Stuart
Josie Duncan
Emily Gullette
Rodrigo Martinez-Duarte
author_sort Devin Keck
collection DOAJ
description Human African trypanosomiasis (HAT), also known as sleeping sickness, is a vector-borne neglected tropical disease endemic to rural sub-Saharan Africa. Current methods of early detection in the affected rural communities generally begin with general screening using the card agglutination test for trypanosomiasis (CATT), a serological test. However, the gold standard for confirmation of trypanosomiasis remains the direct observation of the causative parasite, <i>Trypanosoma brucei</i>. Here, we present the use of dielectrophoresis (DEP) to enrich <i>T. brucei</i> parasites in specific locations to facilitate their identification in a future diagnostic assay. DEP refers to physical movement that can be selectively induced on the parasites when exposing them to electric field gradients of specific magnitude, phase and frequency. The long-term goal of our work is to use DEP to selectively trap and enrich <i>T. brucei</i> in specific locations while eluting all other cells in a sample. This would allow for a diagnostic test that enables the user to characterize the presence of parasites in specific locations determined <i>a priori</i> instead of relying on scanning a sample. In the work presented here, we report the characterization of the conditions that lead to high enrichment, 780% in 50 s, of the parasite in specific locations using an array of titanium microelectrodes.
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spelling doaj.art-cdba393716914372b063f392cd13ae332023-11-20T05:04:28ZengMDPI AGMicromachines2072-666X2020-06-0111662510.3390/mi11060625Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using DielectrophoresisDevin Keck0Callie Stuart1Josie Duncan2Emily Gullette3Rodrigo Martinez-Duarte4Multiscale Manufacturing Laboratory, Department of Mechanical Engineering, Clemson University, Clemson, SC 29634, USAMultiscale Manufacturing Laboratory, Department of Mechanical Engineering, Clemson University, Clemson, SC 29634, USAMultiscale Manufacturing Laboratory, Department of Mechanical Engineering, Clemson University, Clemson, SC 29634, USAMultiscale Manufacturing Laboratory, Department of Mechanical Engineering, Clemson University, Clemson, SC 29634, USAMultiscale Manufacturing Laboratory, Department of Mechanical Engineering, Clemson University, Clemson, SC 29634, USAHuman African trypanosomiasis (HAT), also known as sleeping sickness, is a vector-borne neglected tropical disease endemic to rural sub-Saharan Africa. Current methods of early detection in the affected rural communities generally begin with general screening using the card agglutination test for trypanosomiasis (CATT), a serological test. However, the gold standard for confirmation of trypanosomiasis remains the direct observation of the causative parasite, <i>Trypanosoma brucei</i>. Here, we present the use of dielectrophoresis (DEP) to enrich <i>T. brucei</i> parasites in specific locations to facilitate their identification in a future diagnostic assay. DEP refers to physical movement that can be selectively induced on the parasites when exposing them to electric field gradients of specific magnitude, phase and frequency. The long-term goal of our work is to use DEP to selectively trap and enrich <i>T. brucei</i> in specific locations while eluting all other cells in a sample. This would allow for a diagnostic test that enables the user to characterize the presence of parasites in specific locations determined <i>a priori</i> instead of relying on scanning a sample. In the work presented here, we report the characterization of the conditions that lead to high enrichment, 780% in 50 s, of the parasite in specific locations using an array of titanium microelectrodes.https://www.mdpi.com/2072-666X/11/6/625sleeping sicknessHuman African trypanosomiasistrypanosomatitaniumdielectrophoresis
spellingShingle Devin Keck
Callie Stuart
Josie Duncan
Emily Gullette
Rodrigo Martinez-Duarte
Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using Dielectrophoresis
Micromachines
sleeping sickness
Human African trypanosomiasis
trypanosoma
titanium
dielectrophoresis
title Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using Dielectrophoresis
title_full Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using Dielectrophoresis
title_fullStr Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using Dielectrophoresis
title_full_unstemmed Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using Dielectrophoresis
title_short Highly Localized Enrichment of <i>Trypanosoma brucei</i> Parasites Using Dielectrophoresis
title_sort highly localized enrichment of i trypanosoma brucei i parasites using dielectrophoresis
topic sleeping sickness
Human African trypanosomiasis
trypanosoma
titanium
dielectrophoresis
url https://www.mdpi.com/2072-666X/11/6/625
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