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犬发热伴血小板减少综合征病毒疫苗的研发。

Vaccine Development for Severe Fever with Thrombocytopenia Syndrome Virus in Dogs.

机构信息

Bio-Safety Research Institute and College of Veterinary Medicine, Jeonbuk National University, Iksan, 54531, Republic of Korea.

Korea Zoonosis Research Institute, Jeonbuk National University, Iksan, 54531, Republic of Korea.

出版信息

J Microbiol. 2024 Apr;62(4):327-335. doi: 10.1007/s12275-024-00119-y. Epub 2024 Apr 18.

Abstract

Severe fever with thrombocytopenia syndrome (SFTS) is a life-threatening viral zoonosis. The causative agent of this disease is the Dabie bandavirus, which is usually known as the SFTS virus (SFTSV). Although the role of vertebrates in SFTSV transmission to humans remains uncertain, some reports have suggested that dogs could potentially transmit SFTSV to humans. Consequently, preventive measures against SFTSV in dogs are urgently needed. In the present study, dogs were immunized three times at two-week intervals with formaldehyde-inactivated SFTSV with two types of adjuvants. SFTSV (KCD46) was injected into all dogs two weeks after the final immunization. Control dogs showed viremia from 2 to 4 days post infection (dpi), and displayed white pulp atrophy in the spleen, along with a high level of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling assay (TUNEL) positive area. However, the inactivated SFTSV vaccine groups exhibited rare pathological changes and significantly reduced TUNEL positive areas in the spleen. Furthermore, SFTSV viral loads were not detected at any of the tested dpi. Our results indicate that both adjuvants can be safely used in combination with an inactivated SFTSV formulation to induce strong neutralizing antibodies. Inactivated SFTSV vaccines effectively prevent pathogenicity and viremia in dogs infected with SFTSV. In conclusion, our study highlighted the potential of inactivated SFTSV vaccination for SFTSV control in dogs.

摘要

严重发热伴血小板减少综合征(SFTS)是一种危及生命的病毒性人畜共患病。该病的病原体是大别山病毒,通常被称为 SFTS 病毒(SFTSV)。尽管脊椎动物在 SFTSV 向人类传播中的作用仍不确定,但有一些报告表明,狗可能将 SFTSV 传播给人类。因此,迫切需要针对狗的 SFTSV 预防措施。在本研究中,用两种佐剂将甲醛灭活的 SFTSV 三次免疫狗,间隔两周。所有狗在最后一次免疫后两周都接种了 SFTSV(KCD46)。对照狗在感染后 2 至 4 天出现病毒血症,脾脏白髓萎缩,并出现高水平的末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记检测(TUNEL)阳性区。然而,灭活的 SFTSV 疫苗组脾脏的病理变化很少,TUNEL 阳性区显著减少。此外,在任何测试的 dpi 都未检测到 SFTSV 病毒载量。我们的结果表明,两种佐剂都可以安全地与灭活的 SFTSV 制剂联合使用,以诱导强烈的中和抗体。灭活的 SFTSV 疫苗可有效预防 SFTSV 感染狗的致病性和病毒血症。总之,我们的研究强调了灭活 SFTSV 疫苗在控制狗 SFTSV 方面的潜力。

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