Vet World   Vol.14   July-2021  Article-13

Research Article

Veterinary World, 14(7): 1815-1821

https://doi.org/10.14202/vetworld.2021.1815-1821

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

Fatma F. Warda1, Hala El Sawy Ahmed1, Nermeen G. Shafik2, Christine A. Mikhael2, Heba M. G. Abd-ElAziz2, Walaa A. Mohammed1, and Eman A. Shosha3
1. Agriculture Research Center, Veterinary Serum and Vaccine Research Institute, Abbasia, Cairo, Egypt.
2. Agriculture Research Center, Central Laboratory for Evaluation of Veterinary Biologics, El-Seka-Baida Street, Abbasia, Cairo, Egypt.
3. Department of Microbiology and Immunology, Faculty of Veterinary Medicine, New Valley University, El-Khargia-New Valley governorate, Egypt.

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 3rd month post-vaccination; after that, it began to decline gradually until the 6th 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 3rd 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. Keywords: binary ethylene imine, equine herpesvirus-1, formaldehyde, immunogenicity, inactivated vaccine.

Keywords: binary ethylene imine, equine herpesvirus-1, formaldehyde, immunogenicity, inactivated vaccine.

How to cite this article: Warda FF, Ahmed HE, Shafik NG, Mikhael CA, Abd-ElAziz HMG, Mohammed WA, Shosha EA (2021) Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine, Veterinary World, 14(7): 1815-1821.

Received: 16-02-2021  Accepted: 24-05-2021     Published online: 15-07-2021

Corresponding author: Eman A. Shosha   E-mail: emanshosha25@gmail.com

DOI: 10.14202/vetworld.2021.1815-1821

Copyright: Warda, et al. This article is an open access article 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.