Abstract

The microscopic examination of Giemsa-stained thin and/or thick blood films (Giemsa microscopy) is the standard method of malaria diagnosis. However, the results of the diagnosis significantly depend on the skills of clinical technicians. Furthermore, sample preparation and analysis are laborious and time-consuming. Therefore, in this study, we investigated if a commercially available fluorescent cell counter, LUNA-FL, was useful for the detection of Plasmodium parasite and the estimation of parasitemia. Whole blood samples from uninfected persons, spiked with P. falciparum-infected erythrocytes, were analysed. Most of the leucocytes and platelets were removed from whole blood samples with SiO2-nanofiber filters set on spin columns. The filtered samples were stained with acridine orange, and automatic detection, as well as counting of erythrocytes and parasites, were performed using LUNA-FL. Whole blood, with various levels of parasites, was analysed by Giemsa microscopy or with LUNA-FL to estimate parasitemia, and a comparative analysis was performed. The coefficient determination value of the regression line was high (R2 = 0.98), indicating that accurate quantitative parasite detection could be performed using LUNA-FL. LUNA-FL has a low running cost; it is compact, fast, and easy to operate, and may therefore be useful for point-of-care testing in the endemic areas.

Highlights

  • The World Health Organization (WHO) recommends that all suspected malaria cases should have a parasite-based diagnosis, by either a microscopic analysis with Giemsa-stained blood films (Giemsa microscopy) or a rapid diagnosis test (RDT), prior to treatment with artemisinin-based combination therapy (ACT) [1]

  • In order to perform highly sensitive and quantitative malaria diagnosis, some devices, that can detect fluorescent nuclear-stained parasites in infected erythrocytes by forming a monolayer on microchambers or a microplate [11,12,13,14], or by using flow cytometers [15], have been developed. These devices have a microscope with a digital camera or a charge-coupled device camera for the detection of erythrocytes and/or labelled parasites, and they may be unsuitable for point-of-care testing (POCT) except in hospitals located in urban areas

  • The blood sample (10 μ L4) wof a10s applied to Chamber B (Figure 1A), and the chamber was set to the “Fluorescent Image Analysis” Amuotdoem(aFtiigcucreell1cBobu)n. tAinltghwouitghhbtrhigehdte-fifaeuldltiemxapgoessucraentibmeepfeorrfothrme ecdouunstiinnggLoUf NleuAc-oFcLy.tTehs eiseLryetvherlo5c,ytthees wexeproescuoruenttiemdeifnotrhpeabrarisgithet-dfieetledctiimonagweass, assetthtoeyLewveerle1n2ofot rstgarieneendfwluiothretshceenncuec.lTeahresetxapinos(Fuirgeutrime 1eBfao)r

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Summary

Introduction

The World Health Organization (WHO) recommends that all suspected malaria cases should have a parasite-based diagnosis, by either a microscopic analysis with Giemsa-stained blood films (Giemsa microscopy) or a rapid diagnosis test (RDT), prior to treatment with artemisinin-based combination therapy (ACT) [1]. In order to perform highly sensitive and quantitative malaria diagnosis, some devices, that can detect fluorescent nuclear-stained parasites in infected erythrocytes by forming a monolayer on microchambers or a microplate [11,12,13,14], or by using flow cytometers [15], have been developed. These devices have a microscope with a digital camera or a charge-coupled device camera for the detection of erythrocytes and/or labelled parasites, and they may be unsuitable for POCT except in hospitals located in urban areas. Rapid, easy-to-operate, and accurate quantitative malaria detection was possible using LUNA-FL, suggesting that malaria diagnosis can be performed in endemic countries using the device

Parasite Culture
Preparation of Spin Columns
Detection of Parasite-Infected Erythrocytes Using LUNA-FL
Protocol for Detection of Parasite Using LUNA-FL
Detection of Parasites Using LUNA-FL
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