Assessing the anthelmintic activity of pyrazole-5-carboxamide derivatives against Haemonchus contortus

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Author(s)
Jiao, Yaqing
Preston, Sarah
Song, Hongjian
Jabbar, Abdul
Liu, Yuxiu
Baell, Jonathan
Hofmann, Andreas
Hutchinson, Dana
Wang, Tao
Koehler, Anson V
Fisher, Gillian M
Andrews, Katherine T
Laleu, Benoit
Palmer, Michael J
Burrows, Jeremy N
Wells, Timothy NC
Wang, Qingmin
Gasser, Robin B
Year published
2017
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Background: In this study, we tested five series of pyrazole-5-carboxamide compounds (n = 55) for activity against
parasitic stages of the nematode Haemonchus contortus (barber’s pole worm), one of the most pathogenic parasites
of ruminants.
Methods: In an optimised, whole-organism screening assay, using exsheathed third-stage (xL3) and fourth-stage
(L4) larvae, we measured the inhibition of larval motility and development of H. contortus.
Results: Amongst the 55 compounds, we identified two compounds (designated a-15 and a-17) that reproducibly
inhibit xL3 motility as well as L4 motility and development, with IC50 values ...
View more >Background: In this study, we tested five series of pyrazole-5-carboxamide compounds (n = 55) for activity against parasitic stages of the nematode Haemonchus contortus (barber’s pole worm), one of the most pathogenic parasites of ruminants. Methods: In an optimised, whole-organism screening assay, using exsheathed third-stage (xL3) and fourth-stage (L4) larvae, we measured the inhibition of larval motility and development of H. contortus. Results: Amongst the 55 compounds, we identified two compounds (designated a-15 and a-17) that reproducibly inhibit xL3 motility as well as L4 motility and development, with IC50 values ranging between ~3.4 and 55.6 μM. We studied the effect of these two ‘hit’ compounds on mitochondrial function by measuring oxygen consumption. This assessment showed that xL3s exposed to each of these compounds consumed significantly less oxygen and had less mitochondrial activity than untreated xL3s, which was consistent with specific inhibition of complex I of the respiratory electron transport chain in arthropods. Conclusions: The present findings provide a sound basis for future work, aimed at identifying the targets of compounds a-15 and a-17 and establishing the modes of action of these chemicals in H. contortus.
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View more >Background: In this study, we tested five series of pyrazole-5-carboxamide compounds (n = 55) for activity against parasitic stages of the nematode Haemonchus contortus (barber’s pole worm), one of the most pathogenic parasites of ruminants. Methods: In an optimised, whole-organism screening assay, using exsheathed third-stage (xL3) and fourth-stage (L4) larvae, we measured the inhibition of larval motility and development of H. contortus. Results: Amongst the 55 compounds, we identified two compounds (designated a-15 and a-17) that reproducibly inhibit xL3 motility as well as L4 motility and development, with IC50 values ranging between ~3.4 and 55.6 μM. We studied the effect of these two ‘hit’ compounds on mitochondrial function by measuring oxygen consumption. This assessment showed that xL3s exposed to each of these compounds consumed significantly less oxygen and had less mitochondrial activity than untreated xL3s, which was consistent with specific inhibition of complex I of the respiratory electron transport chain in arthropods. Conclusions: The present findings provide a sound basis for future work, aimed at identifying the targets of compounds a-15 and a-17 and establishing the modes of action of these chemicals in H. contortus.
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Journal Title
Parasites and Vectors
Volume
10
Issue
1
Copyright Statement
© The Author(s) 2017 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Note
Page numbers are not for citation purposes. Instead, this article has the unique article number of 272.
Subject
Medical microbiology
Medical microbiology not elsewhere classified
Health services and systems
Public health