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Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs

BACKGROUND: Amblyomma cajennense is the main vector of Rickettsia rickettsii which causes Brazilian spotted fever. This adult tick preferably infests horses and capybaras, but has low host specificity during its immature stages, thus posing a threat to humans and dogs. In this study, the efficacy of...

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Autores principales: Scott, Fabio, Franz, Lilian, Campos, Diefrey Ribeiro, Azevedo, Thaís Ribeiro Correia, Cunha, Daise, Six, Robert H., Maeder, Steven, Cree, Travis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559851/
https://www.ncbi.nlm.nih.gov/pubmed/28814323
http://dx.doi.org/10.1186/s13071-017-2324-0
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author Scott, Fabio
Franz, Lilian
Campos, Diefrey Ribeiro
Azevedo, Thaís Ribeiro Correia
Cunha, Daise
Six, Robert H.
Maeder, Steven
Cree, Travis
author_facet Scott, Fabio
Franz, Lilian
Campos, Diefrey Ribeiro
Azevedo, Thaís Ribeiro Correia
Cunha, Daise
Six, Robert H.
Maeder, Steven
Cree, Travis
author_sort Scott, Fabio
collection PubMed
description BACKGROUND: Amblyomma cajennense is the main vector of Rickettsia rickettsii which causes Brazilian spotted fever. This adult tick preferably infests horses and capybaras, but has low host specificity during its immature stages, thus posing a threat to humans and dogs. In this study, the efficacy of sarolaner (Simparic™/Simparica®, Zoetis) when administered once orally to dogs at 2 mg/kg was evaluated against induced infestations of A. cajennense nymphs for up to 35 days after treatment. METHODS: Based on pretreatment tick counts, 20 dogs were randomly allocated to treatment with sarolaner (Simparic™) dosed at 2 mg/kg of body weight or a placebo on Day 0 of the study. Artificial infestations were performed using laboratory raised A. cajennense nymphs on study days -2, 5, 12, 19, 26 and 33. Efficacy was determined at 48 h post-treatment or post-infestation at each time point relative to the counts for dogs that received placebo. RESULTS: There were no adverse reactions to treatment. A single dose of sarolaner (Simparic™) provided 100% efficacy on study days 2, 7 and 14; and ≥ 99.6% on days 21, 28 and 35. Geometric mean live tick counts for sarolaner were significantly lower than those for placebo on all days (P < 0.0001). CONCLUSIONS: Under the conditions of the present study, sarolaner (Simparic™) administered once orally at 2 mg/kg provided 100% efficacy against existing infestations and ≥ 99.6% efficacy within 48 h against weekly challenges of A. cajennense for at least 35 days after treatment.
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spelling pubmed-55598512017-08-18 Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs Scott, Fabio Franz, Lilian Campos, Diefrey Ribeiro Azevedo, Thaís Ribeiro Correia Cunha, Daise Six, Robert H. Maeder, Steven Cree, Travis Parasit Vectors Research BACKGROUND: Amblyomma cajennense is the main vector of Rickettsia rickettsii which causes Brazilian spotted fever. This adult tick preferably infests horses and capybaras, but has low host specificity during its immature stages, thus posing a threat to humans and dogs. In this study, the efficacy of sarolaner (Simparic™/Simparica®, Zoetis) when administered once orally to dogs at 2 mg/kg was evaluated against induced infestations of A. cajennense nymphs for up to 35 days after treatment. METHODS: Based on pretreatment tick counts, 20 dogs were randomly allocated to treatment with sarolaner (Simparic™) dosed at 2 mg/kg of body weight or a placebo on Day 0 of the study. Artificial infestations were performed using laboratory raised A. cajennense nymphs on study days -2, 5, 12, 19, 26 and 33. Efficacy was determined at 48 h post-treatment or post-infestation at each time point relative to the counts for dogs that received placebo. RESULTS: There were no adverse reactions to treatment. A single dose of sarolaner (Simparic™) provided 100% efficacy on study days 2, 7 and 14; and ≥ 99.6% on days 21, 28 and 35. Geometric mean live tick counts for sarolaner were significantly lower than those for placebo on all days (P < 0.0001). CONCLUSIONS: Under the conditions of the present study, sarolaner (Simparic™) administered once orally at 2 mg/kg provided 100% efficacy against existing infestations and ≥ 99.6% efficacy within 48 h against weekly challenges of A. cajennense for at least 35 days after treatment. BioMed Central 2017-08-17 /pmc/articles/PMC5559851/ /pubmed/28814323 http://dx.doi.org/10.1186/s13071-017-2324-0 Text en © The Author(s). 2017 Open AccessThis 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. 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
Scott, Fabio
Franz, Lilian
Campos, Diefrey Ribeiro
Azevedo, Thaís Ribeiro Correia
Cunha, Daise
Six, Robert H.
Maeder, Steven
Cree, Travis
Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs
title Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs
title_full Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs
title_fullStr Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs
title_full_unstemmed Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs
title_short Efficacy of sarolaner (Simparic™) against induced infestations of Amblyomma cajennense on dogs
title_sort efficacy of sarolaner (simparic™) against induced infestations of amblyomma cajennense on dogs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559851/
https://www.ncbi.nlm.nih.gov/pubmed/28814323
http://dx.doi.org/10.1186/s13071-017-2324-0
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