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没食子儿茶素没食子酸酯通过抑制伪狂犬病病毒复制周期中的进入和释放阶段来抑制其复制。

Gallocatechin Gallate Inhibits the Replication of Pseudorabies Virus via Suppressing the Entry and Release Stages in Its Replication Cycle.

作者信息

Bo Zongyi, Zhu Jinjin, Guo Mengjiao, Zhang Chengcheng, Cao Yongzhong, Zhang Xiaorong, Wu Yantao

机构信息

Joint International Research Laboratory of Agriculture and Agri-Product Safety, The Ministry of Education of China, Yangzhou University, Yangzhou 225009, China.

Jiangsu Co-Innovation Center for the Prevention of Animal Infectious Disease and Zoonoses, College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.

出版信息

Vet Sci. 2023 Mar 1;10(3):189. doi: 10.3390/vetsci10030189.

Abstract

The pseudorabies virus is a widespread swine pathogen that has caused significant economic losses to the global pig industry. Due to the emergence of PRV variant strains in recent years, vaccines cannot provide complete protection against the infection of PRV. Therefore, the research on antiviral compounds is of great importance for PRV treatment. In this study, an EGFP-labeled PRV was used to screen anti-PRV compounds from 86 natural product extracts. Gallocatechin gallate was found to efficiently inhibit the replication of PRV with a half-maximal inhibitory concentration (IC) of 0.41 μM. In addition, it was found that gallocatechin gallate was unable to directly inactivate PRV and had no effect on the attachment stage of PRV. However, it was found that gallocatechin gallate significantly suppressed the viral entry stage. Furthermore, it was found that the release stage of PRV was also significantly suppressed by gallocatechin gallate. Together, this study found that gallocatechin gallate could efficiently inhibit the replication of PRV by suppressing the entry and release stages of PRV, which will contribute to the development of a new therapeutic strategy against PRV infection.

摘要

伪狂犬病病毒是一种广泛传播的猪病原体,给全球养猪业造成了重大经济损失。由于近年来伪狂犬病病毒变异株的出现,疫苗无法提供针对伪狂犬病病毒感染的完全保护。因此,对抗病毒化合物的研究对于伪狂犬病病毒的治疗至关重要。在本研究中,使用一种绿色荧光蛋白标记的伪狂犬病病毒从86种天然产物提取物中筛选抗伪狂犬病病毒化合物。发现表没食子儿茶素没食子酸酯能有效抑制伪狂犬病病毒的复制,半数抑制浓度(IC)为0.41μM。此外,发现表没食子儿茶素没食子酸酯不能直接使伪狂犬病病毒失活,并且对伪狂犬病病毒的附着阶段没有影响。然而,发现表没食子儿茶素没食子酸酯显著抑制病毒进入阶段。此外,发现表没食子儿茶素没食子酸酯也显著抑制伪狂犬病病毒的释放阶段。总之,本研究发现表没食子儿茶素没食子酸酯可通过抑制伪狂犬病病毒的进入和释放阶段有效抑制其复制,这将有助于开发针对伪狂犬病病毒感染的新治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/250f/10059259/510826b86c3e/vetsci-10-00189-g001.jpg

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