TY - JOUR
T1 - An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes
AU - Partridge, Frederick A
AU - Brown, Anwen E
AU - Buckingham, Steven D
AU - Willis, Nicky J
AU - Wynne, Graham M
AU - Forman, Ruth
AU - Else, Kathryn J
AU - Morrison, Alison A
AU - Matthews, Jacqueline B
AU - Russell, Angela J
AU - Lomas, David A
AU - Sattelle, David B
N1 - Copyright © 2017 The Authors. Published by Elsevier Ltd.. All rights reserved.
PY - 2018/4
Y1 - 2018/4
N2 - 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.
AB - 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.
U2 - 10.1016/j.ijpddr.2017.11.004
DO - 10.1016/j.ijpddr.2017.11.004
M3 - Article
C2 - 29223747
SN - 2211-3207
VL - 8
SP - 8
EP - 21
JO - International journal for parasitology. Drugs and drug resistance
JF - International journal for parasitology. Drugs and drug resistance
IS - 1
ER -