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Published in: Malaria Journal 1/2019

Open Access 01-12-2019 | Chloroquin | Methodology

Application of the automated haematology analyzer XN-30 for discovery and development of anti-malarial drugs

Authors: Takahiro Tougan, Yuji Toya, Kinya Uchihashi, Toshihiro Horii

Published in: Malaria Journal | Issue 1/2019

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Abstract

Background

The erythrocytic stage of Plasmodium falciparum parasites in humans is clinically important, as the parasites at this growth stage causes malarial symptoms. Most of the currently available anti-malarial drugs target this stage, but the emergence and spread of parasites resistant to anti-malarial drugs are a major challenge to global eradication efforts; therefore, the development of novel medicines is urgently required. In this study, the in vitro anti-malarial activity of five current anti-malarial drugs (artemisinin, atovaquone, chloroquine, mefloquine, and pyrimethamine) and 400 compounds from the Pathogen Box provided by the Medicines for Malaria Venture on P. falciparum parasites was characterized using the XN-30 analyzer. Furthermore, the outcomes obtained using the analyser were classified according to the parasitaemias of total and each developmental stages.

Results

The growth inhibition rate and the half-maximal (50%) inhibitory concentration (IC50) of the five current anti-malarial drugs were calculated from the parasitaemia detected using the XN-30 analyzer. Respective strains and drugs presented strongly fitted sigmoidal curves, and the median SD at all tested concentrations was 1.6, suggesting that the variation in values measured with the analyser was acceptably low for the comparison of drug efficacy. Furthermore, the anti-malarial activity of the 400 compounds from the Pathogen Box was tested, and 141 drugs were found to be effective. In addition, the efficacy was classified into 4 types (Type I, parasites were arrested or killed without DNA replication; Type II, parasites were arrested or killed similar to Type I, and the parasitaemia was apparently decreased; Type III, parasites progressed to trophozoite without sufficient DNA replication; and Type IV, parasites were arrested at late trophozoite or schizont after DNA replication).

Conclusion

The current study demonstrates that the XN-30 analyzer objectively, reproducibly, and easily evaluated and characterized the anti-malarial efficacy of various compounds. The results indicate the potential of the XN-30 analyzer as a powerful tool for drug discovery and development in addition to its use as an important diagnostic tool.
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Literature
2.
go back to reference Fidock DA, Rosenthal PJ, Croft SL, Brun R, Nwaka S. Antimalarial drug discovery: efficacy models for compound screening. Nat Rev Drug Discov. 2004;3:509–20.CrossRef Fidock DA, Rosenthal PJ, Croft SL, Brun R, Nwaka S. Antimalarial drug discovery: efficacy models for compound screening. Nat Rev Drug Discov. 2004;3:509–20.CrossRef
3.
go back to reference McClure NS, Day T. A theoretical examination of the relative importance of evolution management and drug development for managing resistance. Proc Biol Sci. 2014;281:20141861.CrossRef McClure NS, Day T. A theoretical examination of the relative importance of evolution management and drug development for managing resistance. Proc Biol Sci. 2014;281:20141861.CrossRef
4.
go back to reference Hamaguchi Y, Yoshida T, Suzuki Y, Okazaki T, Uchihashi K, Wada A. Overview of malaria detection technology achieved with automated hematology analyzer XN-30. Sysmex J Int. 2017;27:1–6. Hamaguchi Y, Yoshida T, Suzuki Y, Okazaki T, Uchihashi K, Wada A. Overview of malaria detection technology achieved with automated hematology analyzer XN-30. Sysmex J Int. 2017;27:1–6.
5.
go back to reference Tougan T, Suzuki Y, Itagaki S, Izuka M, Toya Y, Uchihashi K, et al. An automated haematology analyzer XN-30 distinguishes developmental stages of falciparum malaria parasite cultured in vitro. Malar J. 2018;17:59.CrossRef Tougan T, Suzuki Y, Itagaki S, Izuka M, Toya Y, Uchihashi K, et al. An automated haematology analyzer XN-30 distinguishes developmental stages of falciparum malaria parasite cultured in vitro. Malar J. 2018;17:59.CrossRef
6.
go back to reference Tougan T, Suzuki Y, Izuka M, Aono K, Okazaki T, Toya Y, et al. Application of the automated haematology analyzer XN-30 in an experimental rodent model of malaria. Malar J. 2018;17:165.CrossRef Tougan T, Suzuki Y, Izuka M, Aono K, Okazaki T, Toya Y, et al. Application of the automated haematology analyzer XN-30 in an experimental rodent model of malaria. Malar J. 2018;17:165.CrossRef
8.
go back to reference Trager W, Jensen JB. Human malaria parasites in continuous culture. Science. 1976;193:673–5.CrossRef Trager W, Jensen JB. Human malaria parasites in continuous culture. Science. 1976;193:673–5.CrossRef
9.
go back to reference Lambros C, Vanderberg JP. Synchronization of Plasmodium falciparum erythrocytic stages in culture. J Parasitol. 1979;65:418–20.CrossRef Lambros C, Vanderberg JP. Synchronization of Plasmodium falciparum erythrocytic stages in culture. J Parasitol. 1979;65:418–20.CrossRef
11.
go back to reference Zhang JH, Chung TD, Oldenburg KR. A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J Biomol Screen. 1999;4:67–73.CrossRef Zhang JH, Chung TD, Oldenburg KR. A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J Biomol Screen. 1999;4:67–73.CrossRef
12.
go back to reference Powell DJ, Hertzberg RP, Macarrόn R. Design and implementation of high-throughput screening assays. Methods Mol Biol. 2016;1439:1–32.CrossRef Powell DJ, Hertzberg RP, Macarrόn R. Design and implementation of high-throughput screening assays. Methods Mol Biol. 2016;1439:1–32.CrossRef
13.
go back to reference Peterson DS, Milhous WK, Wellems TE. Molecular basis of differential resistance to cycloguanil and pyrimethamine in Plasmodium falciparum malaria. Proc Natl Acad Sci USA. 1990;87:3018–22.CrossRef Peterson DS, Milhous WK, Wellems TE. Molecular basis of differential resistance to cycloguanil and pyrimethamine in Plasmodium falciparum malaria. Proc Natl Acad Sci USA. 1990;87:3018–22.CrossRef
14.
go back to reference Baniecki ML, Wirth DF, Clardy J. High-throughput Plasmodium falciparum growth assay for malaria drug discovery. Antimicrob Agents Chemother. 2007;51:716–23.CrossRef Baniecki ML, Wirth DF, Clardy J. High-throughput Plasmodium falciparum growth assay for malaria drug discovery. Antimicrob Agents Chemother. 2007;51:716–23.CrossRef
15.
go back to reference Allison JL, O’Brien RL, Hahn FE. DNA: reaction with chloroquine. Science. 1965;149:1111–3.CrossRef Allison JL, O’Brien RL, Hahn FE. DNA: reaction with chloroquine. Science. 1965;149:1111–3.CrossRef
16.
go back to reference Cohen SN, Yielding KL. Inhibition of DNA and RNA polymerase reactions by chloroquine. Proc Natl Acad Sci USA. 1965;54:521–7.CrossRef Cohen SN, Yielding KL. Inhibition of DNA and RNA polymerase reactions by chloroquine. Proc Natl Acad Sci USA. 1965;54:521–7.CrossRef
17.
go back to reference Hahn FE, O’Brien RL, Ciak J, Allison JL, Olenick JG. Studies on modes of action of chloroquine, quinacrine, and quinine and on chloroquine resistance. Mil Med. 1966;131(Suppl):1071–89.CrossRef Hahn FE, O’Brien RL, Ciak J, Allison JL, Olenick JG. Studies on modes of action of chloroquine, quinacrine, and quinine and on chloroquine resistance. Mil Med. 1966;131(Suppl):1071–89.CrossRef
18.
go back to reference O’Brien RL, Olenick JG, Hahn FE. Reactions of quinine, chloroquine, and quinacrine with DNA and their effects on the DNA and RNA polymerase reactions. Proc Natl Acad Sci USA. 1966;55:1511–7.CrossRef O’Brien RL, Olenick JG, Hahn FE. Reactions of quinine, chloroquine, and quinacrine with DNA and their effects on the DNA and RNA polymerase reactions. Proc Natl Acad Sci USA. 1966;55:1511–7.CrossRef
19.
go back to reference Tong JX, Chandramohanadas R, Tan KS. High-content screening of the Medicines for Malaria Venture Pathogen Box for Plasmodium falciparum digestive vacuole-disrupting molecules reveals valuable starting points for drug discovery. Antimicrob Agents Chemother. 2018;62:e02031.CrossRef Tong JX, Chandramohanadas R, Tan KS. High-content screening of the Medicines for Malaria Venture Pathogen Box for Plasmodium falciparum digestive vacuole-disrupting molecules reveals valuable starting points for drug discovery. Antimicrob Agents Chemother. 2018;62:e02031.CrossRef
20.
go back to reference Dennis ASM, Rosling JEO, Lehane AM, Kirk K. Diverse antimalarials from whole-cell phenotypic screens disrupt malaria parasite ion and volume homeostasis. Sci Rep. 2018;8:8795.CrossRef Dennis ASM, Rosling JEO, Lehane AM, Kirk K. Diverse antimalarials from whole-cell phenotypic screens disrupt malaria parasite ion and volume homeostasis. Sci Rep. 2018;8:8795.CrossRef
Metadata
Title
Application of the automated haematology analyzer XN-30 for discovery and development of anti-malarial drugs
Authors
Takahiro Tougan
Yuji Toya
Kinya Uchihashi
Toshihiro Horii
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Malaria Journal / Issue 1/2019
Electronic ISSN: 1475-2875
DOI
https://doi.org/10.1186/s12936-019-2642-0

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