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P-glycoproteins play a role in ivermectin resistance in cyathostomins()

Anthelmintic resistance is a global problem that threatens sustainable control of the equine gastrointestinal cyathostomins (Phylum Nematoda; Superfamily Strongyloidea). Of the three novel anthelmintic classes that have reached the veterinary market in the last decade, none are currently licenced in...

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Autores principales: Peachey, L.E., Pinchbeck, G.L., Matthews, J.B., Burden, F.A., Lespine, A., von Samson-Himmelstjerna, G., Krücken, J., Hodgkinson, J.E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681340/
https://www.ncbi.nlm.nih.gov/pubmed/29121562
http://dx.doi.org/10.1016/j.ijpddr.2017.10.006
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author Peachey, L.E.
Pinchbeck, G.L.
Matthews, J.B.
Burden, F.A.
Lespine, A.
von Samson-Himmelstjerna, G.
Krücken, J.
Hodgkinson, J.E.
author_facet Peachey, L.E.
Pinchbeck, G.L.
Matthews, J.B.
Burden, F.A.
Lespine, A.
von Samson-Himmelstjerna, G.
Krücken, J.
Hodgkinson, J.E.
author_sort Peachey, L.E.
collection PubMed
description Anthelmintic resistance is a global problem that threatens sustainable control of the equine gastrointestinal cyathostomins (Phylum Nematoda; Superfamily Strongyloidea). Of the three novel anthelmintic classes that have reached the veterinary market in the last decade, none are currently licenced in horses, hence current control regimens focus on prolonging the useful lifespan of licenced anthelmintics. This approach would be facilitated by knowledge of the resistance mechanisms to the most widely used anthelmintics, the macrocyclic lactones (ML). There are no data regarding resistance mechanisms to MLs in cyathostomins, although in other parasitic nematodes, the ABC transporters, P-glycoproteins (P-gps), have been implicated in playing an important role. Here, we tested the hypothesis that P-gps are, at least in part, responsible for reduced sensitivity to the ML ivermectin (IVM) in cyathostomins; first, by measuring transcript levels of pgp-9 in IVM resistant versus IVM sensitive third stage larvae (L3) pre-and post-IVM exposure in vitro. We then tested the effect of a range of P-gp inhibitors on the effect of IVM against the same populations of L3 using the in vitro larval development test (LDT) and larval migration inhibition test (LMIT). We demonstrated that, not only was pgp-9 transcription significantly increased in IVM resistant compared to IVM sensitive L3 after anthelmintic exposure (p < 0.001), but inhibition of P-gp activity significantly increased sensitivity of the larvae to IVM in vitro, an effect only observed in the IVM resistant larvae in the LMIT. These data strongly implicate a role for P-gps in IVM resistance in cyathostomins. Importantly, this raises the possibility that P-gp inhibitor-IVM combination treatments might be used in vivo to increase the effectiveness of IVM against cyathostomins in Equidae.
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spelling pubmed-56813402017-11-20 P-glycoproteins play a role in ivermectin resistance in cyathostomins() Peachey, L.E. Pinchbeck, G.L. Matthews, J.B. Burden, F.A. Lespine, A. von Samson-Himmelstjerna, G. Krücken, J. Hodgkinson, J.E. Int J Parasitol Drugs Drug Resist Article Anthelmintic resistance is a global problem that threatens sustainable control of the equine gastrointestinal cyathostomins (Phylum Nematoda; Superfamily Strongyloidea). Of the three novel anthelmintic classes that have reached the veterinary market in the last decade, none are currently licenced in horses, hence current control regimens focus on prolonging the useful lifespan of licenced anthelmintics. This approach would be facilitated by knowledge of the resistance mechanisms to the most widely used anthelmintics, the macrocyclic lactones (ML). There are no data regarding resistance mechanisms to MLs in cyathostomins, although in other parasitic nematodes, the ABC transporters, P-glycoproteins (P-gps), have been implicated in playing an important role. Here, we tested the hypothesis that P-gps are, at least in part, responsible for reduced sensitivity to the ML ivermectin (IVM) in cyathostomins; first, by measuring transcript levels of pgp-9 in IVM resistant versus IVM sensitive third stage larvae (L3) pre-and post-IVM exposure in vitro. We then tested the effect of a range of P-gp inhibitors on the effect of IVM against the same populations of L3 using the in vitro larval development test (LDT) and larval migration inhibition test (LMIT). We demonstrated that, not only was pgp-9 transcription significantly increased in IVM resistant compared to IVM sensitive L3 after anthelmintic exposure (p < 0.001), but inhibition of P-gp activity significantly increased sensitivity of the larvae to IVM in vitro, an effect only observed in the IVM resistant larvae in the LMIT. These data strongly implicate a role for P-gps in IVM resistance in cyathostomins. Importantly, this raises the possibility that P-gp inhibitor-IVM combination treatments might be used in vivo to increase the effectiveness of IVM against cyathostomins in Equidae. Elsevier 2017-10-25 /pmc/articles/PMC5681340/ /pubmed/29121562 http://dx.doi.org/10.1016/j.ijpddr.2017.10.006 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
Peachey, L.E.
Pinchbeck, G.L.
Matthews, J.B.
Burden, F.A.
Lespine, A.
von Samson-Himmelstjerna, G.
Krücken, J.
Hodgkinson, J.E.
P-glycoproteins play a role in ivermectin resistance in cyathostomins()
title P-glycoproteins play a role in ivermectin resistance in cyathostomins()
title_full P-glycoproteins play a role in ivermectin resistance in cyathostomins()
title_fullStr P-glycoproteins play a role in ivermectin resistance in cyathostomins()
title_full_unstemmed P-glycoproteins play a role in ivermectin resistance in cyathostomins()
title_short P-glycoproteins play a role in ivermectin resistance in cyathostomins()
title_sort p-glycoproteins play a role in ivermectin resistance in cyathostomins()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681340/
https://www.ncbi.nlm.nih.gov/pubmed/29121562
http://dx.doi.org/10.1016/j.ijpddr.2017.10.006
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