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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
Chong  WangChong Wang1Zhiyuan  WenZhiyuan Wen1Gongxun  ZhongGongxun Zhong1Lei  ShuaiLei Shuai1Chen  WangChen Wang2Qilong  LiuQilong Liu2Chenyu  RenChenyu Ren2金英  葛金英 葛1Xijun  WangXijun Wang1Jinliang  WangJinliang Wang1Renqiang  LiuRenqiang Liu1Xianfeng  ZhangXianfeng Zhang1Yuntao  GuanYuntao Guan1Xijun  HeXijun He1Zhigao  BuZhigao Bu1*
  • 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

The final, formatted version of the article will be published soon.

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

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