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Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus

BACKGROUND: Topical permethrin treatment is known to prevent feeding of sandflies on dogs. This study investigated the anti-feeding efficacy and the immediate insecticidal efficacy (knock-down effect) of topical treatment of dogs with a new commercially available combination of indoxacarb and permet...

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Autores principales: Frenais, Régis, Flochlay-Sigognault, Annie, Milon-Harnois, Gaëlle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030270/
https://www.ncbi.nlm.nih.gov/pubmed/24886557
http://dx.doi.org/10.1186/1756-3305-7-217
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author Frenais, Régis
Flochlay-Sigognault, Annie
Milon-Harnois, Gaëlle
author_facet Frenais, Régis
Flochlay-Sigognault, Annie
Milon-Harnois, Gaëlle
author_sort Frenais, Régis
collection PubMed
description BACKGROUND: Topical permethrin treatment is known to prevent feeding of sandflies on dogs. This study investigated the anti-feeding efficacy and the immediate insecticidal efficacy (knock-down effect) of topical treatment of dogs with a new commercially available combination of indoxacarb and permethrin (Activyl(®) Tick Plus), compared with a negative control. METHODS: Sedated dogs were individually exposed to unfed female sandflies in a darkened chamber for one hour 2, 7, 14, 21 and 29 days after treatment. Mean fly feeding and survival rates in the two groups after one hour of exposure were used to calculate the anti-feeding efficacy and the knock-down effect, respectively. RESULTS: On Days 2, 7, 14, 21 and 29 post treatment, the anti-feeding efficacy was 99, 98, 96, 88 and 84% based on geometric means. The mean number of fed sandflies in the treated group was significantly lower than in the control group mean at every evaluation time point. The knock-down effect, measured at one hour after exposure of the flies to treated dogs, was 32, 27, 9, 0 and 4% based on geometric means, at the same time points. The number of dead flies was significantly higher in the treated group on Days 2 and 7 post-treatment. No adverse effects of treatment were observed at any time during the study. CONCLUSIONS: Activyl(®) Tick Plus treatment of dogs provided a high anti-feeding efficacy against Phlebotomus perniciosus from 2 to 21 days post treatment, with continuing significant anti-feeding to 29 days post-treatment, and was well tolerated. Some knock-down effect following one hour of exposure of flies to treated dogs was observed in the first week after treatment.
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spelling pubmed-40302702014-06-06 Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus Frenais, Régis Flochlay-Sigognault, Annie Milon-Harnois, Gaëlle Parasit Vectors Research BACKGROUND: Topical permethrin treatment is known to prevent feeding of sandflies on dogs. This study investigated the anti-feeding efficacy and the immediate insecticidal efficacy (knock-down effect) of topical treatment of dogs with a new commercially available combination of indoxacarb and permethrin (Activyl(®) Tick Plus), compared with a negative control. METHODS: Sedated dogs were individually exposed to unfed female sandflies in a darkened chamber for one hour 2, 7, 14, 21 and 29 days after treatment. Mean fly feeding and survival rates in the two groups after one hour of exposure were used to calculate the anti-feeding efficacy and the knock-down effect, respectively. RESULTS: On Days 2, 7, 14, 21 and 29 post treatment, the anti-feeding efficacy was 99, 98, 96, 88 and 84% based on geometric means. The mean number of fed sandflies in the treated group was significantly lower than in the control group mean at every evaluation time point. The knock-down effect, measured at one hour after exposure of the flies to treated dogs, was 32, 27, 9, 0 and 4% based on geometric means, at the same time points. The number of dead flies was significantly higher in the treated group on Days 2 and 7 post-treatment. No adverse effects of treatment were observed at any time during the study. CONCLUSIONS: Activyl(®) Tick Plus treatment of dogs provided a high anti-feeding efficacy against Phlebotomus perniciosus from 2 to 21 days post treatment, with continuing significant anti-feeding to 29 days post-treatment, and was well tolerated. Some knock-down effect following one hour of exposure of flies to treated dogs was observed in the first week after treatment. BioMed Central 2014-05-09 /pmc/articles/PMC4030270/ /pubmed/24886557 http://dx.doi.org/10.1186/1756-3305-7-217 Text en Copyright © 2014 Frenais et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Frenais, Régis
Flochlay-Sigognault, Annie
Milon-Harnois, Gaëlle
Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus
title Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus
title_full Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus
title_fullStr Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus
title_full_unstemmed Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus
title_short Anti-feeding efficacy of Activyl(®) Tick Plus topical treatment of dogs against Phlebotomus perniciosus
title_sort anti-feeding efficacy of activyl(®) tick plus topical treatment of dogs against phlebotomus perniciosus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030270/
https://www.ncbi.nlm.nih.gov/pubmed/24886557
http://dx.doi.org/10.1186/1756-3305-7-217
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