ORIGINAL RESEARCH article
Front. Cell. Infect. Microbiol.
Sec. Microbial Vaccines
This article is part of the Research TopicVaccine and Infectious Disease InformaticsView all 9 articles
Evaluation of the protective efficacy of a recombinant adenovirus-vectored SARS-CoV-2 vaccine candidate for veterinary use
Provisionally accepted- 1National High Containment Laboratory for Animal Diseases Control and Prevention, Chinese Academy of Agricultural Sciences Harbin Veterinary Research Institute State Key Laboratory for Animal Disease Control and Prevention, Harbin, China
- 2Chinese Academy of Agricultural Sciences Harbin Veterinary Research Institute State Key Laboratory for Animal Disease Control and Prevention, Harbin, China
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Since 2019, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has posed a global health threat. Its high transmissibility and cross-species infectivity have disrupted public health systems and worldwide economies, with companion and agricultural animals, like cats and minks, showing high susceptibility. This study evaluated rAd5-S6P, a recombinant vaccine using an adenovirus type 5 vector expressing a modified SARS-CoV-2 spike protein, in murine, feline, and mink models. Results demonstrated that rAd5-S6P elicited a robust humoral immune response when administered via intramuscular, intranasal, and oral routes, which conferred complete protection in mice. In feline and mink models, immunization with rAd-S6P resulted in significantly reduced viral shedding after high-dose SARS-CoV-2 challenge, and no infectious virus was detected in any of the examined organs of minks. Collectively, rAd5-S6P exhibited protective efficacy across species, supporting its translational potential as a veterinary vaccine. These findings provide critical evidence for animal vaccination strategies to control SARS-CoV-2 circulation and reduce zoonotic transmission risks.
Keywords: Veterinary vaccine, SARS-CoV-2, adenovirus vector, protective efficacy, Animal Models
Received: 27 Sep 2025; Accepted: 27 Nov 2025.
Copyright: © 2025 Wang, Wen, Zhong, Shuai, Wang, Liu, Ren, 葛, Wang, Wang, Liu, Zhang, Guan, He and Bu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Zhigao Bu
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
