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Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States

BACKGROUND: Infection by 2 or more protozoa is linked with increased severity of disease in marine mammals with protozoan encephalitis. HYPOTHESIS/OBJECTIVES: To assess whether horses with equine protozoal myeloencephalitis (EPM) caused by Sarcocystis neurona also have evidence of infection with Neo...

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Autores principales: Schale, Sarah, Howe, Daniel, Yeargan, Michelle, Morrow, Jennifer K., Graves, Amy, Johnson, Amy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980325/
https://www.ncbi.nlm.nih.gov/pubmed/29633348
http://dx.doi.org/10.1111/jvim.15127
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author Schale, Sarah
Howe, Daniel
Yeargan, Michelle
Morrow, Jennifer K.
Graves, Amy
Johnson, Amy L.
author_facet Schale, Sarah
Howe, Daniel
Yeargan, Michelle
Morrow, Jennifer K.
Graves, Amy
Johnson, Amy L.
author_sort Schale, Sarah
collection PubMed
description BACKGROUND: Infection by 2 or more protozoa is linked with increased severity of disease in marine mammals with protozoan encephalitis. HYPOTHESIS/OBJECTIVES: To assess whether horses with equine protozoal myeloencephalitis (EPM) caused by Sarcocystis neurona also have evidence of infection with Neospora hughesi or Toxoplasma gondii. We hypothesized that horses with EPM would be more likely than horses with cervical vertebral stenotic myelopathy (CVSM) to be positive for antibodies to multiple protozoan parasites. ANIMALS: One hundred one horses with neurologic disease: 49 with EPM and 52 with CVSM. METHODS: Case review. Archived serum and cerebrospinal fluid (CSF) from 101 horses were examined. Inclusion criteria included neurologic disease, antemortem or postmortem diagnosis of EPM or CVSM, and availability of serological results or archived samples for testing. Additional testing for antibodies was performed on serum for T. gondii, as well as serum and CSF for N. hughesi. RESULTS: Horses with EPM were more likely than horses with CVSM to have positive immunologic results for S. neurona on serum (95.9% versus 76.9%, P = .0058), CSF (98.0% versus 44.2%, P < .00001), and serum : CSF titer ratio (91.8% versus 0%, P < .00001). Positive results for Neospora and Toxoplasma were uncommon, with total seroprevalence rates of 12.9% and 14.9%, respectively. The proportions of EPM cases testing positive for Neospora and Toxoplasma (16% and 12%) were not different from the proportions of CVSM cases testing positive (10% and 17%, P = .31 and .47, respectively). CONCLUSION: Results do not indicate an important role for protozoal coinfection in EPM in the eastern United States.
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spelling pubmed-59803252018-06-06 Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States Schale, Sarah Howe, Daniel Yeargan, Michelle Morrow, Jennifer K. Graves, Amy Johnson, Amy L. J Vet Intern Med EQUID BACKGROUND: Infection by 2 or more protozoa is linked with increased severity of disease in marine mammals with protozoan encephalitis. HYPOTHESIS/OBJECTIVES: To assess whether horses with equine protozoal myeloencephalitis (EPM) caused by Sarcocystis neurona also have evidence of infection with Neospora hughesi or Toxoplasma gondii. We hypothesized that horses with EPM would be more likely than horses with cervical vertebral stenotic myelopathy (CVSM) to be positive for antibodies to multiple protozoan parasites. ANIMALS: One hundred one horses with neurologic disease: 49 with EPM and 52 with CVSM. METHODS: Case review. Archived serum and cerebrospinal fluid (CSF) from 101 horses were examined. Inclusion criteria included neurologic disease, antemortem or postmortem diagnosis of EPM or CVSM, and availability of serological results or archived samples for testing. Additional testing for antibodies was performed on serum for T. gondii, as well as serum and CSF for N. hughesi. RESULTS: Horses with EPM were more likely than horses with CVSM to have positive immunologic results for S. neurona on serum (95.9% versus 76.9%, P = .0058), CSF (98.0% versus 44.2%, P < .00001), and serum : CSF titer ratio (91.8% versus 0%, P < .00001). Positive results for Neospora and Toxoplasma were uncommon, with total seroprevalence rates of 12.9% and 14.9%, respectively. The proportions of EPM cases testing positive for Neospora and Toxoplasma (16% and 12%) were not different from the proportions of CVSM cases testing positive (10% and 17%, P = .31 and .47, respectively). CONCLUSION: Results do not indicate an important role for protozoal coinfection in EPM in the eastern United States. John Wiley and Sons Inc. 2018-04-10 2018 /pmc/articles/PMC5980325/ /pubmed/29633348 http://dx.doi.org/10.1111/jvim.15127 Text en Copyright © 2018 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-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle EQUID
Schale, Sarah
Howe, Daniel
Yeargan, Michelle
Morrow, Jennifer K.
Graves, Amy
Johnson, Amy L.
Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States
title Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States
title_full Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States
title_fullStr Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States
title_full_unstemmed Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States
title_short Protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern United States
title_sort protozoal coinfection in horses with equine protozoal myeloencephalitis in the eastern united states
topic EQUID
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980325/
https://www.ncbi.nlm.nih.gov/pubmed/29633348
http://dx.doi.org/10.1111/jvim.15127
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