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A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment

Dogs are the reservoir host of zoonotic visceral leishmaniasis (VL) caused by Leishmania infantum (Kinetoplastida: Trypanosomatidae). Both subclinically‐infected and sick animals can be infectious to competent phlebotomine vectors. The degree and duration of insecticidal efficacy of an oral dose of...

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Autores principales: Bongiorno, G., Meyer, L., Evans, A., Lekouch, N., Bianchi, R., Khoury, C., Chiummo, R., Thomas, E., Gradoni, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318609/
https://www.ncbi.nlm.nih.gov/pubmed/31769060
http://dx.doi.org/10.1111/mve.12420
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author Bongiorno, G.
Meyer, L.
Evans, A.
Lekouch, N.
Bianchi, R.
Khoury, C.
Chiummo, R.
Thomas, E.
Gradoni, L.
author_facet Bongiorno, G.
Meyer, L.
Evans, A.
Lekouch, N.
Bianchi, R.
Khoury, C.
Chiummo, R.
Thomas, E.
Gradoni, L.
author_sort Bongiorno, G.
collection PubMed
description Dogs are the reservoir host of zoonotic visceral leishmaniasis (VL) caused by Leishmania infantum (Kinetoplastida: Trypanosomatidae). Both subclinically‐infected and sick animals can be infectious to competent phlebotomine vectors. The degree and duration of insecticidal efficacy of an oral dose of fluralaner (Bravecto®; Merck Animal Health) was determined in dogs exposed to bites of Phlebotomus perniciosus (Diptera: Psychodidae), a main Mediterranean vector of VL. Twelve dogs allocated to two groups of six animals each were included in a parallel‐group designed, negative‐controlled, randomized, blinded, single‐centre efficacy study. Group 2 was treated with fluralaner on day 0, and sand‐fly exposure of both groups was performed on days 1, 28 and 84. Viability of blood‐fed females was assessed up to 96 h after exposure and efficacy was measured as the survival rate of specimens fed on Group 2 versus those fed on Group 1. A mortality of 100% was recorded at 24 h in females fed on Group 2 at both days 1 and 28. Significant insecticidal efficacy was still observed on day 84, with > 50% mortality recorded by 48 h post blood meal in Group 2. Fluralaner treatment of dogs represents a promising and affordable method for reducing the pool of infected vectors in endemic settings of zoonotic VL.
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spelling pubmed-73186092020-06-29 A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment Bongiorno, G. Meyer, L. Evans, A. Lekouch, N. Bianchi, R. Khoury, C. Chiummo, R. Thomas, E. Gradoni, L. Med Vet Entomol Short Communications Dogs are the reservoir host of zoonotic visceral leishmaniasis (VL) caused by Leishmania infantum (Kinetoplastida: Trypanosomatidae). Both subclinically‐infected and sick animals can be infectious to competent phlebotomine vectors. The degree and duration of insecticidal efficacy of an oral dose of fluralaner (Bravecto®; Merck Animal Health) was determined in dogs exposed to bites of Phlebotomus perniciosus (Diptera: Psychodidae), a main Mediterranean vector of VL. Twelve dogs allocated to two groups of six animals each were included in a parallel‐group designed, negative‐controlled, randomized, blinded, single‐centre efficacy study. Group 2 was treated with fluralaner on day 0, and sand‐fly exposure of both groups was performed on days 1, 28 and 84. Viability of blood‐fed females was assessed up to 96 h after exposure and efficacy was measured as the survival rate of specimens fed on Group 2 versus those fed on Group 1. A mortality of 100% was recorded at 24 h in females fed on Group 2 at both days 1 and 28. Significant insecticidal efficacy was still observed on day 84, with > 50% mortality recorded by 48 h post blood meal in Group 2. Fluralaner treatment of dogs represents a promising and affordable method for reducing the pool of infected vectors in endemic settings of zoonotic VL. Blackwell Publishing Ltd 2019-11-26 2020-06 /pmc/articles/PMC7318609/ /pubmed/31769060 http://dx.doi.org/10.1111/mve.12420 Text en © 2019 The Authors. Medical and Veterinary Entomology published by John Wiley & Sons Ltd on behalf of Royal Entomological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communications
Bongiorno, G.
Meyer, L.
Evans, A.
Lekouch, N.
Bianchi, R.
Khoury, C.
Chiummo, R.
Thomas, E.
Gradoni, L.
A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment
title A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment
title_full A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment
title_fullStr A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment
title_full_unstemmed A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment
title_short A single oral dose of fluralaner (Bravecto®) in dogs rapidly kills 100% of blood‐fed Phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment
title_sort single oral dose of fluralaner (bravecto®) in dogs rapidly kills 100% of blood‐fed phlebotomus perniciosus, a main visceral leishmaniasis vector, for at least 1 month after treatment
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318609/
https://www.ncbi.nlm.nih.gov/pubmed/31769060
http://dx.doi.org/10.1111/mve.12420
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