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Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine

BACKGROUND AND AIM: Equine herpesvirus-1 infection in horses causes a wide range of manifestations affecting the respiratory tract. The virus can cause serious economic losses through sporadic abortion in pregnant mares, perinatal death, respiratory disease in young foals. This study was designed to...

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Autores principales: Warda, Fatma F., Ahmed, Hala El Sawy, Shafik, Nermeen G., Mikhael, Christine A., Abd-ElAziz, Heba M. G., Mohammed, Walaa A., Shosha, Eman A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Veterinary World 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404127/
https://www.ncbi.nlm.nih.gov/pubmed/34475703
http://dx.doi.org/10.14202/vetworld.2021.1815-1821
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author Warda, Fatma F.
Ahmed, Hala El Sawy
Shafik, Nermeen G.
Mikhael, Christine A.
Abd-ElAziz, Heba M. G.
Mohammed, Walaa A.
Shosha, Eman A.
author_facet Warda, Fatma F.
Ahmed, Hala El Sawy
Shafik, Nermeen G.
Mikhael, Christine A.
Abd-ElAziz, Heba M. G.
Mohammed, Walaa A.
Shosha, Eman A.
author_sort Warda, Fatma F.
collection PubMed
description BACKGROUND AND AIM: Equine herpesvirus-1 infection in horses causes a wide range of manifestations affecting the respiratory tract. The virus can cause serious economic losses through sporadic abortion in pregnant mares, perinatal death, respiratory disease in young foals. This study was designed to prepare inactivated equine herpesvirus-1 (EHV-1) vaccine using both 0.005 M binary ethylenimine (BEI) and 0.0006% formaldehyde (FA) to decrease the use of BEI and provide a good immunological response. The efficacy, safety, and duration of immunity of the prepared inactivated EHV-1 vaccine were evaluated. MATERIALS AND METHODS: The prepared FA/BEI-inactivated EHV-1 vaccine was adjuvanted with Alhydrogel and then evaluated by inoculation into guinea pigs, followed by comparison with the commercial inactivated EHV-1 vaccine. These two vaccines were evaluated by testing the safety and immunogenicity in horses classified into two groups. Group A was vaccinated with two doses of the prepared vaccine at a 4-week interval, while Group B was vaccinated with two doses of the commercial vaccine only. Anti-EHV-1 antibodies were detected in horse serum using enzyme-linked immunosorbent assay (ELISA) and virus neutralizing test (VNT). RESULTS: Regarding the time required to inactivate EHV-1 vaccine, this was decreased using 0.005 M BEI and 0.0006% FA from 24 to 8 h. ELISA in Group A horses demonstrated a significant increase in EHV-1 antibody titer at 2 weeks after the booster dose compared with that for the pre-booster one, from 485 to 855 antibody titer, which then peaked at 1240 in the 3(rd) month post-vaccination; after that, it began to decline gradually until the 6(th) month. Meanwhile, in Group B, the ELISA reading increased from 420 to 790 and then peaked at 1215. The VNT mean in Group A increased from 1.1 to 2.5 within 2 weeks after administration of the booster dose, while in Group B it increased from 0.8 to 2.1. Moreover, ELISA in Group A pigs indicated mean antibody titers at the 3(rd) week post-inoculation of 576 for Group A and 554 for Group B. CONCLUSION: The inactivated EHV-1 vaccine, with fewer chemicals, was prepared in a shorter time. It is safe and also more potent to protect horses for up to 6 months against EHV-1 infection than the commercially produced vaccine.
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spelling pubmed-84041272021-09-01 Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine Warda, Fatma F. Ahmed, Hala El Sawy Shafik, Nermeen G. Mikhael, Christine A. Abd-ElAziz, Heba M. G. Mohammed, Walaa A. Shosha, Eman A. Vet World Research Article BACKGROUND AND AIM: Equine herpesvirus-1 infection in horses causes a wide range of manifestations affecting the respiratory tract. The virus can cause serious economic losses through sporadic abortion in pregnant mares, perinatal death, respiratory disease in young foals. This study was designed to prepare inactivated equine herpesvirus-1 (EHV-1) vaccine using both 0.005 M binary ethylenimine (BEI) and 0.0006% formaldehyde (FA) to decrease the use of BEI and provide a good immunological response. The efficacy, safety, and duration of immunity of the prepared inactivated EHV-1 vaccine were evaluated. MATERIALS AND METHODS: The prepared FA/BEI-inactivated EHV-1 vaccine was adjuvanted with Alhydrogel and then evaluated by inoculation into guinea pigs, followed by comparison with the commercial inactivated EHV-1 vaccine. These two vaccines were evaluated by testing the safety and immunogenicity in horses classified into two groups. Group A was vaccinated with two doses of the prepared vaccine at a 4-week interval, while Group B was vaccinated with two doses of the commercial vaccine only. Anti-EHV-1 antibodies were detected in horse serum using enzyme-linked immunosorbent assay (ELISA) and virus neutralizing test (VNT). RESULTS: Regarding the time required to inactivate EHV-1 vaccine, this was decreased using 0.005 M BEI and 0.0006% FA from 24 to 8 h. ELISA in Group A horses demonstrated a significant increase in EHV-1 antibody titer at 2 weeks after the booster dose compared with that for the pre-booster one, from 485 to 855 antibody titer, which then peaked at 1240 in the 3(rd) month post-vaccination; after that, it began to decline gradually until the 6(th) month. Meanwhile, in Group B, the ELISA reading increased from 420 to 790 and then peaked at 1215. The VNT mean in Group A increased from 1.1 to 2.5 within 2 weeks after administration of the booster dose, while in Group B it increased from 0.8 to 2.1. Moreover, ELISA in Group A pigs indicated mean antibody titers at the 3(rd) week post-inoculation of 576 for Group A and 554 for Group B. CONCLUSION: The inactivated EHV-1 vaccine, with fewer chemicals, was prepared in a shorter time. It is safe and also more potent to protect horses for up to 6 months against EHV-1 infection than the commercially produced vaccine. Veterinary World 2021-07 2021-07-15 /pmc/articles/PMC8404127/ /pubmed/34475703 http://dx.doi.org/10.14202/vetworld.2021.1815-1821 Text en Copyright: © Warda, et al. https://creativecommons.org/licenses/by/4.0/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/ (https://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/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Warda, Fatma F.
Ahmed, Hala El Sawy
Shafik, Nermeen G.
Mikhael, Christine A.
Abd-ElAziz, Heba M. G.
Mohammed, Walaa A.
Shosha, Eman A.
Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine
title Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine
title_full Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine
title_fullStr Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine
title_full_unstemmed Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine
title_short Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine
title_sort application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404127/
https://www.ncbi.nlm.nih.gov/pubmed/34475703
http://dx.doi.org/10.14202/vetworld.2021.1815-1821
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