Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>

In the present study, we established a practical and cost-effective high throughput screening assay, which relies on the measurement of the motility of <i>Caenorhabditis elegans</i> by infrared light-interference. Using this assay, we screened 14,400 small molecules from the “HitFinder”...

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Main Authors: Aya C. Taki, Joseph J. Byrne, Peter R. Boag, Abdul Jabbar, Robin B. Gasser
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/14/4156
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spelling doaj-ec99f61d08e24752b82da337c6cc792c2021-07-23T13:56:16ZengMDPI AGMolecules1420-30492021-07-01264156415610.3390/molecules26144156Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>Aya C. Taki0Joseph J. Byrne1Peter R. Boag2Abdul Jabbar3Robin B. Gasser4Department of Veterinary Biosciences, Faculty of Veterinary and Agricultural Sciences, Melbourne Veterinary School, The University of Melbourne, Parkville, VIC 3010, AustraliaDepartment of Veterinary Biosciences, Faculty of Veterinary and Agricultural Sciences, Melbourne Veterinary School, The University of Melbourne, Parkville, VIC 3010, AustraliaDepartment of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, AustraliaDepartment of Veterinary Biosciences, Faculty of Veterinary and Agricultural Sciences, Melbourne Veterinary School, The University of Melbourne, Parkville, VIC 3010, AustraliaDepartment of Veterinary Biosciences, Faculty of Veterinary and Agricultural Sciences, Melbourne Veterinary School, The University of Melbourne, Parkville, VIC 3010, AustraliaIn the present study, we established a practical and cost-effective high throughput screening assay, which relies on the measurement of the motility of <i>Caenorhabditis elegans</i> by infrared light-interference. Using this assay, we screened 14,400 small molecules from the “HitFinder” library (Maybridge), achieving a hit rate of 0.3%. We identified small molecules that reproducibly inhibited the motility of <i>C. elegans</i> (young adults) and assessed dose relationships for a subset of compounds. Future work will critically evaluate the potential of some of these hits as candidates for subsequent optimisation or repurposing as nematocides or nematostats. This high throughput screening assay has the advantage over many previous assays in that it is cost- and time-effective to carry out and achieves a markedly higher throughput (~10,000 compounds per week); therefore, it is suited to the screening of libraries of tens to hundreds of thousands of compounds for subsequent evaluation and development. The present phenotypic whole-worm assay should be readily adaptable to a range of socioeconomically important parasitic nematodes of humans and animals, depending on their dimensions and motility characteristics in vitro, for the discovery of new anthelmintic candidates. This focus is particularly important, given the widespread problems associated with drug resistance in many parasitic worms of livestock animals globally.https://www.mdpi.com/1420-3049/26/14/4156high throughput screening<i>Caenorhabditis elegans</i>phenotypic screenmotilityinfrared light-interferenceanthelmintic
collection DOAJ
language English
format Article
sources DOAJ
author Aya C. Taki
Joseph J. Byrne
Peter R. Boag
Abdul Jabbar
Robin B. Gasser
spellingShingle Aya C. Taki
Joseph J. Byrne
Peter R. Boag
Abdul Jabbar
Robin B. Gasser
Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>
Molecules
high throughput screening
<i>Caenorhabditis elegans</i>
phenotypic screen
motility
infrared light-interference
anthelmintic
author_facet Aya C. Taki
Joseph J. Byrne
Peter R. Boag
Abdul Jabbar
Robin B. Gasser
author_sort Aya C. Taki
title Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>
title_short Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>
title_full Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>
title_fullStr Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>
title_full_unstemmed Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against <i>Caenorhabditis elegans</i>
title_sort practical high-throughput method to screen compounds for anthelmintic activity against <i>caenorhabditis elegans</i>
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2021-07-01
description In the present study, we established a practical and cost-effective high throughput screening assay, which relies on the measurement of the motility of <i>Caenorhabditis elegans</i> by infrared light-interference. Using this assay, we screened 14,400 small molecules from the “HitFinder” library (Maybridge), achieving a hit rate of 0.3%. We identified small molecules that reproducibly inhibited the motility of <i>C. elegans</i> (young adults) and assessed dose relationships for a subset of compounds. Future work will critically evaluate the potential of some of these hits as candidates for subsequent optimisation or repurposing as nematocides or nematostats. This high throughput screening assay has the advantage over many previous assays in that it is cost- and time-effective to carry out and achieves a markedly higher throughput (~10,000 compounds per week); therefore, it is suited to the screening of libraries of tens to hundreds of thousands of compounds for subsequent evaluation and development. The present phenotypic whole-worm assay should be readily adaptable to a range of socioeconomically important parasitic nematodes of humans and animals, depending on their dimensions and motility characteristics in vitro, for the discovery of new anthelmintic candidates. This focus is particularly important, given the widespread problems associated with drug resistance in many parasitic worms of livestock animals globally.
topic high throughput screening
<i>Caenorhabditis elegans</i>
phenotypic screen
motility
infrared light-interference
anthelmintic
url https://www.mdpi.com/1420-3049/26/14/4156
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