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Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies

BACKGROUND: Antibiotic treatment of horses with strangles is reported to impair the development of immunity to subsequent exposure to Streptococcus equi ssp equi (S. equi). However, apart from a single clinical report, evidence‐based studies for this hypothesis are lacking. HYPOTHESIS/OBJECTIVE: To...

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Autores principales: Pringle, John, Storm, Emma, Waller, Andrew, Riihimäki, Miia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979097/
https://www.ncbi.nlm.nih.gov/pubmed/31769122
http://dx.doi.org/10.1111/jvim.15668
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author Pringle, John
Storm, Emma
Waller, Andrew
Riihimäki, Miia
author_facet Pringle, John
Storm, Emma
Waller, Andrew
Riihimäki, Miia
author_sort Pringle, John
collection PubMed
description BACKGROUND: Antibiotic treatment of horses with strangles is reported to impair the development of immunity to subsequent exposure to Streptococcus equi ssp equi (S. equi). However, apart from a single clinical report, evidence‐based studies for this hypothesis are lacking. HYPOTHESIS/OBJECTIVE: To determine whether penicillin treatment during clinical strangles influences the development or persistence of seropositivity to S. equi‐specific antibodies. ANIMALS: A natural outbreak of strangles with 100% morbidity in 41 unvaccinated mature Icelandic horses. METHODS: A prospective longitudinal study of acute clinical strangles from onset through full recovery approximately 10 months after the index case. Horses were monitored clinically 6 times for S. equi, as well as serologically for antibodies to antigens A and C of S. equi using an enhanced indirect ELISA. Seven horses received penicillin within 11 days of onset of fever (Group 1), 5 between 16 and 22 days after onset of fever (Group 2), and the remainder (Group 3, n = 29) received no antibiotics during clinical disease. The proportions of seropositive horses in each group were compared using an extension of Fisher's exact test with P < .05 as the level of significance. RESULTS: Although all horses were seropositive to S. equi within 2 months of the index case, significantly fewer horses treated early (Group 1) remained seropositive by 4 to 6 months (P = .04 and .02, respectively). CONCLUSIONS AND CLINICAL IMPORTANCE: Findings support earlier suggestions that penicillin administered during acute strangles can interfere with persistence of humoral immunity to S. equi.
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spelling pubmed-69790972020-01-28 Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies Pringle, John Storm, Emma Waller, Andrew Riihimäki, Miia J Vet Intern Med EQUID BACKGROUND: Antibiotic treatment of horses with strangles is reported to impair the development of immunity to subsequent exposure to Streptococcus equi ssp equi (S. equi). However, apart from a single clinical report, evidence‐based studies for this hypothesis are lacking. HYPOTHESIS/OBJECTIVE: To determine whether penicillin treatment during clinical strangles influences the development or persistence of seropositivity to S. equi‐specific antibodies. ANIMALS: A natural outbreak of strangles with 100% morbidity in 41 unvaccinated mature Icelandic horses. METHODS: A prospective longitudinal study of acute clinical strangles from onset through full recovery approximately 10 months after the index case. Horses were monitored clinically 6 times for S. equi, as well as serologically for antibodies to antigens A and C of S. equi using an enhanced indirect ELISA. Seven horses received penicillin within 11 days of onset of fever (Group 1), 5 between 16 and 22 days after onset of fever (Group 2), and the remainder (Group 3, n = 29) received no antibiotics during clinical disease. The proportions of seropositive horses in each group were compared using an extension of Fisher's exact test with P < .05 as the level of significance. RESULTS: Although all horses were seropositive to S. equi within 2 months of the index case, significantly fewer horses treated early (Group 1) remained seropositive by 4 to 6 months (P = .04 and .02, respectively). CONCLUSIONS AND CLINICAL IMPORTANCE: Findings support earlier suggestions that penicillin administered during acute strangles can interfere with persistence of humoral immunity to S. equi. John Wiley & Sons, Inc. 2019-11-26 2020 /pmc/articles/PMC6979097/ /pubmed/31769122 http://dx.doi.org/10.1111/jvim.15668 Text en © 2019 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. 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 EQUID
Pringle, John
Storm, Emma
Waller, Andrew
Riihimäki, Miia
Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies
title Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies
title_full Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies
title_fullStr Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies
title_full_unstemmed Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies
title_short Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi‐specific antibodies
title_sort influence of penicillin treatment of horses with strangles on seropositivity to streptococcus equi ssp. equi‐specific antibodies
topic EQUID
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979097/
https://www.ncbi.nlm.nih.gov/pubmed/31769122
http://dx.doi.org/10.1111/jvim.15668
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