First report of closantel treatment failure against Fasciola hepatica in cattle

Control of Fasciola hepatica infection in livestock is based on annual treatment using flukicides such as triclabendazole, albendazole and closantel. However, triclabendazole resistant F. hepatica populations are emerging worldwide and resistance is emerging to albendazole, whereas it has until now...

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Main Authors: Adam Novobilský, Johan Höglund
Format: Article
Language:English
Published: Elsevier 2015-12-01
Series:International Journal for Parasitology: Drugs and Drug Resistance
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211320715300075
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spelling doaj-7c3b4a360ac94cf089bff55afaef27172020-11-24T21:47:24ZengElsevierInternational Journal for Parasitology: Drugs and Drug Resistance2211-32072015-12-015317217710.1016/j.ijpddr.2015.07.003First report of closantel treatment failure against Fasciola hepatica in cattleAdam NovobilskýJohan HöglundControl of Fasciola hepatica infection in livestock is based on annual treatment using flukicides such as triclabendazole, albendazole and closantel. However, triclabendazole resistant F. hepatica populations are emerging worldwide and resistance is emerging to albendazole, whereas it has until now never been described for closantel. In Sweden, a topical formulation containing a combination of closantel and ivermectin (Closamectin Pour On) has been registered for use in cattle only since 2011. This study evaluated the efficacy of closantel against F. hepatica in naturally infected beef cattle using both coproantigen and faecal egg count reduction tests. Faecal egg counts (FEC) and coproantigen ELISA examinations were conducted in February 2014 in three beef cattle herds (A, B, C) in south-western Sweden. On each farm, 10 F. hepatica coproantigen-positive and F. hepatica egg-positive animals were allocated after 12–16 weeks of housing into groups and treated topically with a minimum of 20 mg closantel per kg body weight. Faecal samples were collected from selected animals on 0, 7 and 21 day post-treatment (PT). Based on FEC, closantel efficacy 21 days PT was 72% (95% CI: 65–77%) and 97% (95% CI: 95–98%) on farms A and B, respectively. No FEC reduction at all was observed on farm C. In total, 4, 1 and 6 animals remained coproantigen-positive at 21 days PT on farms A, B and C, respectively. Closantel treatment failure was confirmed on two of the farms. As the animals were housed 12–16 weeks before treatment and thereafter during the entire study, failure due to the presence of juvenile flukes was excluded. Although the cause of closantel failure currently remains unclear, development of resistance or/and absorption failure of topical administration should be considered. To our knowledge, this is the first report of closantel treatment failure against F. hepatica in cattle.http://www.sciencedirect.com/science/article/pii/S2211320715300075ClosantelCoproantigen ELISAFaecal egg countFlukicideLiver flukePour-onResistance
collection DOAJ
language English
format Article
sources DOAJ
author Adam Novobilský
Johan Höglund
spellingShingle Adam Novobilský
Johan Höglund
First report of closantel treatment failure against Fasciola hepatica in cattle
International Journal for Parasitology: Drugs and Drug Resistance
Closantel
Coproantigen ELISA
Faecal egg count
Flukicide
Liver fluke
Pour-on
Resistance
author_facet Adam Novobilský
Johan Höglund
author_sort Adam Novobilský
title First report of closantel treatment failure against Fasciola hepatica in cattle
title_short First report of closantel treatment failure against Fasciola hepatica in cattle
title_full First report of closantel treatment failure against Fasciola hepatica in cattle
title_fullStr First report of closantel treatment failure against Fasciola hepatica in cattle
title_full_unstemmed First report of closantel treatment failure against Fasciola hepatica in cattle
title_sort first report of closantel treatment failure against fasciola hepatica in cattle
publisher Elsevier
series International Journal for Parasitology: Drugs and Drug Resistance
issn 2211-3207
publishDate 2015-12-01
description Control of Fasciola hepatica infection in livestock is based on annual treatment using flukicides such as triclabendazole, albendazole and closantel. However, triclabendazole resistant F. hepatica populations are emerging worldwide and resistance is emerging to albendazole, whereas it has until now never been described for closantel. In Sweden, a topical formulation containing a combination of closantel and ivermectin (Closamectin Pour On) has been registered for use in cattle only since 2011. This study evaluated the efficacy of closantel against F. hepatica in naturally infected beef cattle using both coproantigen and faecal egg count reduction tests. Faecal egg counts (FEC) and coproantigen ELISA examinations were conducted in February 2014 in three beef cattle herds (A, B, C) in south-western Sweden. On each farm, 10 F. hepatica coproantigen-positive and F. hepatica egg-positive animals were allocated after 12–16 weeks of housing into groups and treated topically with a minimum of 20 mg closantel per kg body weight. Faecal samples were collected from selected animals on 0, 7 and 21 day post-treatment (PT). Based on FEC, closantel efficacy 21 days PT was 72% (95% CI: 65–77%) and 97% (95% CI: 95–98%) on farms A and B, respectively. No FEC reduction at all was observed on farm C. In total, 4, 1 and 6 animals remained coproantigen-positive at 21 days PT on farms A, B and C, respectively. Closantel treatment failure was confirmed on two of the farms. As the animals were housed 12–16 weeks before treatment and thereafter during the entire study, failure due to the presence of juvenile flukes was excluded. Although the cause of closantel failure currently remains unclear, development of resistance or/and absorption failure of topical administration should be considered. To our knowledge, this is the first report of closantel treatment failure against F. hepatica in cattle.
topic Closantel
Coproantigen ELISA
Faecal egg count
Flukicide
Liver fluke
Pour-on
Resistance
url http://www.sciencedirect.com/science/article/pii/S2211320715300075
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