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Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis

BACKGROUND: Equine herpesvirus‐5 is commonly isolated from the lungs of horses with EMPF, suggesting an etiological link. Valacyclovir is used empirically to treat EMPF; however, no data is available concerning its impact on EHV‐5 viral kinetics. OBJECTIVES: To determine the effect of oral administr...

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Autores principales: Easton‐Jones, Charlotte A., Madigan, John E., Barnum, Samantha, Maxwell, Lara K., Taylor, Sandra D., Arnesen, Terry, Pusterla, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189341/
https://www.ncbi.nlm.nih.gov/pubmed/30221792
http://dx.doi.org/10.1111/jvim.15230
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author Easton‐Jones, Charlotte A.
Madigan, John E.
Barnum, Samantha
Maxwell, Lara K.
Taylor, Sandra D.
Arnesen, Terry
Pusterla, Nicola
author_facet Easton‐Jones, Charlotte A.
Madigan, John E.
Barnum, Samantha
Maxwell, Lara K.
Taylor, Sandra D.
Arnesen, Terry
Pusterla, Nicola
author_sort Easton‐Jones, Charlotte A.
collection PubMed
description BACKGROUND: Equine herpesvirus‐5 is commonly isolated from the lungs of horses with EMPF, suggesting an etiological link. Valacyclovir is used empirically to treat EMPF; however, no data is available concerning its impact on EHV‐5 viral kinetics. OBJECTIVES: To determine the effect of oral administration of valacyclovir on EHV‐5 viral load measured by qPCR in blood, nasal secretions (NS) and BALF in horses with EMPF. ANIMALS: Six horses diagnosed with EMPF. METHODS: A prospective clinical trial was performed. Horses received 10 days of PO administered valacyclovir (loading dose 30 mg/kg, maintenance dose 20 mg/kg). Blood, NS, and BALF were collected for EHV‐5 viral kinetics analyses during treatment. Blood and NS were collected every other day. BALF was collected on day 0 and day 10. RESULTS: There was no statistical difference in median EHV‐5 viral load between day 0 and day 10 for all samples tested. In blood median EHV‐5 viral load was 7676 (range 575‐39 781) on day 0 and 6822 (range 1136‐18 635) glycoprotein B (gB) gene copies per million cells on day 10. For NS median EHV‐5 viral load was 2.944 × 10(6) (range 184 691‐3.394 × 10(9)) on day 0 and 8.803 × 10(6) (range 251 186‐9.868 × 10(8)) gB gene copies per million cells on day 10. For BALF median EHV‐5 viral load was 59,842 (range 61‐315 655) on day 0 and 185 083 (range 3562‐542 417) gB gene copies per million cells on day 10. CONCLUSIONS AND CLINICAL IMPORTANCE: Valacyclovir might not be an effective short‐term antiviral treatment but efficacy in treatment of EMPF is unknown.
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spelling pubmed-61893412018-10-22 Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis Easton‐Jones, Charlotte A. Madigan, John E. Barnum, Samantha Maxwell, Lara K. Taylor, Sandra D. Arnesen, Terry Pusterla, Nicola J Vet Intern Med EQUID BACKGROUND: Equine herpesvirus‐5 is commonly isolated from the lungs of horses with EMPF, suggesting an etiological link. Valacyclovir is used empirically to treat EMPF; however, no data is available concerning its impact on EHV‐5 viral kinetics. OBJECTIVES: To determine the effect of oral administration of valacyclovir on EHV‐5 viral load measured by qPCR in blood, nasal secretions (NS) and BALF in horses with EMPF. ANIMALS: Six horses diagnosed with EMPF. METHODS: A prospective clinical trial was performed. Horses received 10 days of PO administered valacyclovir (loading dose 30 mg/kg, maintenance dose 20 mg/kg). Blood, NS, and BALF were collected for EHV‐5 viral kinetics analyses during treatment. Blood and NS were collected every other day. BALF was collected on day 0 and day 10. RESULTS: There was no statistical difference in median EHV‐5 viral load between day 0 and day 10 for all samples tested. In blood median EHV‐5 viral load was 7676 (range 575‐39 781) on day 0 and 6822 (range 1136‐18 635) glycoprotein B (gB) gene copies per million cells on day 10. For NS median EHV‐5 viral load was 2.944 × 10(6) (range 184 691‐3.394 × 10(9)) on day 0 and 8.803 × 10(6) (range 251 186‐9.868 × 10(8)) gB gene copies per million cells on day 10. For BALF median EHV‐5 viral load was 59,842 (range 61‐315 655) on day 0 and 185 083 (range 3562‐542 417) gB gene copies per million cells on day 10. CONCLUSIONS AND CLINICAL IMPORTANCE: Valacyclovir might not be an effective short‐term antiviral treatment but efficacy in treatment of EMPF is unknown. John Wiley & Sons, Inc. 2018-09-17 2018 /pmc/articles/PMC6189341/ /pubmed/30221792 http://dx.doi.org/10.1111/jvim.15230 Text en © 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
Easton‐Jones, Charlotte A.
Madigan, John E.
Barnum, Samantha
Maxwell, Lara K.
Taylor, Sandra D.
Arnesen, Terry
Pusterla, Nicola
Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis
title Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis
title_full Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis
title_fullStr Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis
title_full_unstemmed Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis
title_short Effect of valacyclovir on EHV‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis
title_sort effect of valacyclovir on ehv‐5 viral kinetics in horses with equine multinodular pulmonary fibrosis
topic EQUID
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189341/
https://www.ncbi.nlm.nih.gov/pubmed/30221792
http://dx.doi.org/10.1111/jvim.15230
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