tetherin/CD317/BST-2对仙台病毒和尼帕病毒病毒样颗粒释放的抑制作用,但对腮腺炎病毒无抑制作用。

Q4 Medicine
Weng-Sheng Kong, Takashi Irie, Asuka Yoshida, Ryoko Kawabata, Takahiro Kadoi, Takemasa Sakaguchi
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引用次数: 0

摘要

Tetherin(也称为BST-2或CD317)最近被确定为一种有效的ifn诱导的抗病毒蛋白,可抑制感染细胞中多种包膜病毒颗粒的释放。对一些包膜病毒(包括逆转录病毒、丝状病毒和沙粒病毒)的抗病毒活性进行了研究。在这里,我们表明tetherin也能够阻断由仙台病毒基质蛋白驱动的病毒样颗粒(vlp)的释放。结合tetherin对尼帕病毒VLP释放的抑制作用,这些结果表明副粘病毒可能被添加到易受tetherin抑制的病毒列表中。Tetherin与尼帕病毒基质蛋白共定位并在细胞中积累,表明它存在于颗粒组装位点,或被募集到颗粒组装位点。然而,应该指出的是,tetherin对副粘病毒腮腺炎vlp的释放无效,这表明某些包膜病毒可能对tetherin的活性不敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of virus-like particle release of Sendai virus and Nipah virus, but not that of mumps virus, by tetherin/CD317/BST-2.

Tetherin (also known as BST-2 or CD317) has recently been identified as a potent IFN-induced anti-viral protein that inhibits the release of diverse enveloped virus particles from infected cells. The anti-viral activity of tetherin on a number of enveloped viruses, including retroviruses, filoviruses and arenaviruses, has been examined. Here, we show that tetherin is also capable of blocking the release of virus-like particles (VLPs) driven by the matrix protein of Sendai virus. Together with inhibition of Nipah virus VLP release by tetherin, these results indicate that paramyxoviruses are to be added to the list of viruses that are susceptible to tetherin inhibition. Tetherin co-localized with Nipah virus matrix proteins and accumulated in cells, indicating that it is present at, or recruited to, sites of particle assembly. It should be noted, however, that tetherin was not effective against the release of paramyxovirus mumps VLPs, indicating that certain enveloped viruses may not be sensitive to tetherin activity.

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来源期刊
Hiroshima journal of medical sciences
Hiroshima journal of medical sciences Medicine-Medicine (all)
CiteScore
0.30
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