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An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes

Parasitic nematodes infect hundreds of millions of people and farmed livestock. Further, plant parasitic nematodes result in major crop damage. The pipeline of therapeutic compounds is limited and parasite resistance to the existing anthelmintic compounds is a global threat. We have developed an INV...

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Autores principales: Partridge, Frederick A., Brown, Anwen E., Buckingham, Steven D., Willis, Nicky J., Wynne, Graham M., Forman, Ruth, Else, Kathryn J., Morrison, Alison A., Matthews, Jacqueline B., Russell, Angela J., Lomas, David A., Sattelle, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734697/
https://www.ncbi.nlm.nih.gov/pubmed/29223747
http://dx.doi.org/10.1016/j.ijpddr.2017.11.004
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author Partridge, Frederick A.
Brown, Anwen E.
Buckingham, Steven D.
Willis, Nicky J.
Wynne, Graham M.
Forman, Ruth
Else, Kathryn J.
Morrison, Alison A.
Matthews, Jacqueline B.
Russell, Angela J.
Lomas, David A.
Sattelle, David B.
author_facet Partridge, Frederick A.
Brown, Anwen E.
Buckingham, Steven D.
Willis, Nicky J.
Wynne, Graham M.
Forman, Ruth
Else, Kathryn J.
Morrison, Alison A.
Matthews, Jacqueline B.
Russell, Angela J.
Lomas, David A.
Sattelle, David B.
author_sort Partridge, Frederick A.
collection PubMed
description Parasitic nematodes infect hundreds of millions of people and farmed livestock. Further, plant parasitic nematodes result in major crop damage. The pipeline of therapeutic compounds is limited and parasite resistance to the existing anthelmintic compounds is a global threat. We have developed an INVertebrate Automated Phenotyping Platform (INVAPP) for high-throughput, plate-based chemical screening, and an algorithm (Paragon) which allows screening for compounds that have an effect on motility and development of parasitic worms. We have validated its utility by determining the efficacy of a panel of known anthelmintics against model and parasitic nematodes: Caenorhabditis elegans, Haemonchus contortus, Teladorsagia circumcincta, and Trichuris muris. We then applied the system to screen the Pathogen Box chemical library in a blinded fashion and identified compounds already known to have anthelmintic or anti-parasitic activity, including tolfenpyrad, auranofin, and mebendazole; and 14 compounds previously undescribed as anthelmintics, including benzoxaborole and isoxazole chemotypes. This system offers an effective, high-throughput system for the discovery of novel anthelmintics.
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spelling pubmed-57346972017-12-21 An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes Partridge, Frederick A. Brown, Anwen E. Buckingham, Steven D. Willis, Nicky J. Wynne, Graham M. Forman, Ruth Else, Kathryn J. Morrison, Alison A. Matthews, Jacqueline B. Russell, Angela J. Lomas, David A. Sattelle, David B. Int J Parasitol Drugs Drug Resist Article Parasitic nematodes infect hundreds of millions of people and farmed livestock. Further, plant parasitic nematodes result in major crop damage. The pipeline of therapeutic compounds is limited and parasite resistance to the existing anthelmintic compounds is a global threat. We have developed an INVertebrate Automated Phenotyping Platform (INVAPP) for high-throughput, plate-based chemical screening, and an algorithm (Paragon) which allows screening for compounds that have an effect on motility and development of parasitic worms. We have validated its utility by determining the efficacy of a panel of known anthelmintics against model and parasitic nematodes: Caenorhabditis elegans, Haemonchus contortus, Teladorsagia circumcincta, and Trichuris muris. We then applied the system to screen the Pathogen Box chemical library in a blinded fashion and identified compounds already known to have anthelmintic or anti-parasitic activity, including tolfenpyrad, auranofin, and mebendazole; and 14 compounds previously undescribed as anthelmintics, including benzoxaborole and isoxazole chemotypes. This system offers an effective, high-throughput system for the discovery of novel anthelmintics. Elsevier 2017-12-02 /pmc/articles/PMC5734697/ /pubmed/29223747 http://dx.doi.org/10.1016/j.ijpddr.2017.11.004 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Partridge, Frederick A.
Brown, Anwen E.
Buckingham, Steven D.
Willis, Nicky J.
Wynne, Graham M.
Forman, Ruth
Else, Kathryn J.
Morrison, Alison A.
Matthews, Jacqueline B.
Russell, Angela J.
Lomas, David A.
Sattelle, David B.
An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes
title An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes
title_full An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes
title_fullStr An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes
title_full_unstemmed An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes
title_short An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes
title_sort automated high-throughput system for phenotypic screening of chemical libraries on c. elegans and parasitic nematodes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734697/
https://www.ncbi.nlm.nih.gov/pubmed/29223747
http://dx.doi.org/10.1016/j.ijpddr.2017.11.004
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