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Florfenicol induces early embryonic death in eggs collected from treated hens
BACKGROUND: Florfenicol, a commonly used veterinary antibiotic, was reported to have caused a severe drop in egg hatchability following its off-label use on a broiler breeder farm in South Africa. According to the pharmacovigilance report, hatchability dropped by 80 % for up to a week following a fi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538914/ https://www.ncbi.nlm.nih.gov/pubmed/26282556 http://dx.doi.org/10.1186/s12917-015-0536-0 |
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author | AL-Shahrani, S. Naidoo, V. |
author_facet | AL-Shahrani, S. Naidoo, V. |
author_sort | AL-Shahrani, S. |
collection | PubMed |
description | BACKGROUND: Florfenicol, a commonly used veterinary antibiotic, was reported to have caused a severe drop in egg hatchability following its off-label use on a broiler breeder farm in South Africa. According to the pharmacovigilance report, hatchability dropped by 80 % for up to a week following a five day course at 10 mg/kg (both males and females treated metaphylactically) to manage an Escherichia coli infection. While mammalian toxicity studies indicate the potential for early embryonic death in utero or testicular damage, no literature is available on the avian toxicity of florfenicol. For this study we investigated the effects of florfenicol at various doses from 10 to 90 mg/kg on the egg hatchability in a breeder flock we kept and established under controlled conditions, with the same cockerels and hens being exposed in a phased manner. RESULTS: Following five days of oral exposure, no toxic signs were evident in any of the cockerels or hens treated at doses up to 90 mg/kg. Treatment of only the cockerels had no effect on egg hatchability, while treatment of only the hens at doses of 60 and 90 mg/kg resulted in decreased hatchability of 0 % in comparison to 70 % of the control as early 24 h after treatment. In all cases, decreased hatchability was associated with embryonic death at 5 days of development. The toxic effects of florfenicol were completely reversible with comparable hatchability being present by day 4 post-treatment withdrawal. Toxicity correlated with total egg florfenicol concentrations with an LC(50) of 1.07 μg/g. CONCLUSION: Florfenicol appears to be toxic to the developing chick embryo at around day 5 of incubation, in the absence of related toxicity in the hen or cockerel. |
format | Online Article Text |
id | pubmed-4538914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45389142015-08-18 Florfenicol induces early embryonic death in eggs collected from treated hens AL-Shahrani, S. Naidoo, V. BMC Vet Res Research Article BACKGROUND: Florfenicol, a commonly used veterinary antibiotic, was reported to have caused a severe drop in egg hatchability following its off-label use on a broiler breeder farm in South Africa. According to the pharmacovigilance report, hatchability dropped by 80 % for up to a week following a five day course at 10 mg/kg (both males and females treated metaphylactically) to manage an Escherichia coli infection. While mammalian toxicity studies indicate the potential for early embryonic death in utero or testicular damage, no literature is available on the avian toxicity of florfenicol. For this study we investigated the effects of florfenicol at various doses from 10 to 90 mg/kg on the egg hatchability in a breeder flock we kept and established under controlled conditions, with the same cockerels and hens being exposed in a phased manner. RESULTS: Following five days of oral exposure, no toxic signs were evident in any of the cockerels or hens treated at doses up to 90 mg/kg. Treatment of only the cockerels had no effect on egg hatchability, while treatment of only the hens at doses of 60 and 90 mg/kg resulted in decreased hatchability of 0 % in comparison to 70 % of the control as early 24 h after treatment. In all cases, decreased hatchability was associated with embryonic death at 5 days of development. The toxic effects of florfenicol were completely reversible with comparable hatchability being present by day 4 post-treatment withdrawal. Toxicity correlated with total egg florfenicol concentrations with an LC(50) of 1.07 μg/g. CONCLUSION: Florfenicol appears to be toxic to the developing chick embryo at around day 5 of incubation, in the absence of related toxicity in the hen or cockerel. BioMed Central 2015-08-18 /pmc/articles/PMC4538914/ /pubmed/26282556 http://dx.doi.org/10.1186/s12917-015-0536-0 Text en © AL-Shahrani and Naidoo. 2015 Open Access This 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 Article AL-Shahrani, S. Naidoo, V. Florfenicol induces early embryonic death in eggs collected from treated hens |
title | Florfenicol induces early embryonic death in eggs collected from treated hens |
title_full | Florfenicol induces early embryonic death in eggs collected from treated hens |
title_fullStr | Florfenicol induces early embryonic death in eggs collected from treated hens |
title_full_unstemmed | Florfenicol induces early embryonic death in eggs collected from treated hens |
title_short | Florfenicol induces early embryonic death in eggs collected from treated hens |
title_sort | florfenicol induces early embryonic death in eggs collected from treated hens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538914/ https://www.ncbi.nlm.nih.gov/pubmed/26282556 http://dx.doi.org/10.1186/s12917-015-0536-0 |
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