马尔堡病毒利用 Rab11 介导的内细胞途径产生病毒粒子。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2024-09-03 Epub Date: 2024-07-30 DOI:10.1128/spectrum.00269-24
Wakako Furuyama, Kento Yamada, Miako Sakaguchi, Andrea Marzi, Asuka Nanbo
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引用次数: 0

摘要

丝状病毒产生的病毒颗粒具有特征性的丝状形态。主要的病毒基质蛋白VP40被运输到质膜上,促进病毒颗粒的形成和随后的病毒排出。在本研究中,我们评估了小 GTP 酶 Rab11 介导的内细胞途径在马尔堡病毒(MARV)颗粒形成和出芽中的作用。虽然 Rab11 主要定位于核周区域,但它在瞬时表达 MARV VP40 的细胞的胞质中却表现出更弥散的分布。Rab11 与 MARV 样颗粒结合在一起。表达显性阴性形式的 Rab11 和敲除 Rab11 会减少细胞外围的 VP40 片段数量。此外,下调 Rab11 可适度减少 MARV 样颗粒和真实 MARV 的释放。我们进一步证实,VP40会诱导微管网络向细胞外围分布,而这在一定程度上与Rab11有关。微管的解聚减少了 VP40 在细胞外围的聚集,同时也减少了病毒颗粒的形成。VP40 与微管的主要成分α-微管蛋白有物理相互作用,但与 Rab11 没有相互作用。综上所述,这些结果表明 VP40 与微管发生了部分相互作用,促进了微管向细胞外周的分布,从而将瞬时拴系的 Rab11 阳性囊泡运往细胞表面。由于我们之前证明了 Rab11 在埃博拉病毒颗粒形成过程中的作用,本文的研究结果表明丝状病毒一般会利用囊泡贩运机制来实现病毒颗粒的正常形成和随后的排出。包括马尔堡病毒和埃博拉病毒在内的丝状病毒会产生独特的丝状病毒颗粒。虽然众所周知这些病毒的主要病毒基质蛋白 VP40 会被运输到细胞表面并促进病毒颗粒的产生,但相关分子机制的细节仍不清楚。为了填补这一知识空白,我们研究了小 GTP 酶 Rab11 介导的内细胞途径在这一过程中的作用。我们的研究结果表明,马尔堡病毒利用 Rab11 介导的囊泡牵引途径,以微管网络依赖的方式释放病毒样颗粒和真病毒。此前的研究结果表明,Rab11 也参与了埃博拉病毒颗粒的产生。总之,这些数据表明,丝状病毒一般可能会劫持依赖微管的囊泡运输机制,以进行富有成效的复制。因此,这一途径是开发泛丝状病毒疗法的潜在目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Marburg virus exploits the Rab11-mediated endocytic pathway in viral-particle production.

Filoviruses produce viral particles with characteristic filamentous morphology. The major viral matrix protein, VP40, is trafficked to the plasma membrane and promotes viral particle formation and subsequent viral egress. In the present study, we assessed the role of the small GTPase Rab11-mediated endocytic pathway in Marburg virus (MARV) particle formation and budding. Although Rab11 was predominantly localized in the perinuclear region, it exhibited a more diffuse distribution in the cytoplasm of cells transiently expressing MARV VP40. Rab11 was incorporated into MARV-like particles. Expression of the dominant-negative form of Rab11 and knockdown of Rab11 decreased the amount of VP40 fractions in the cell periphery. Moreover, downregulation of Rab11 moderately reduced the release of MARV-like particles and authentic MARV. We further demonstrated that VP40 induces the distribution of the microtubule network toward the cell periphery, which was partly associated with Rab11. Depolymerization of microtubules reduced the accumulation of VP40 in the cell periphery along with viral particle formation. VP40 physically interacted with α-tubulin, a major component of microtubules, but not with Rab11. Taken together, these results suggested that VP40 partly interacts with microtubules and facilitates their distribution toward the cell periphery, leading to the trafficking of transiently tethering Rab11-positive vesicles toward the cell surface. As we previously demonstrated the role of Rab11 in the formation of Ebola virus particles, the results here suggest that filoviruses in general exploit the vesicle-trafficking machinery for proper virus-particle formation and subsequent egress. These pathways may be a potential target for the development of pan-filovirus therapeutics.IMPORTANCEFiloviruses, including Marburg and Ebola viruses, produce distinct filamentous viral particles. Although it is well known that the major viral matrix protein of these viruses, VP40, is trafficked to the cell surface and promotes viral particle production, details regarding the associated molecular mechanisms remain unclear. To address this knowledge gap, we investigated the role of the small GTPase Rab11-mediated endocytic pathway in this process. Our findings revealed that Marburg virus exploits the Rab11-mediated vesicle-trafficking pathway for the release of virus-like particles and authentic virions in a microtubule network-dependent manner. Previous findings demonstrated that Rab11 is also involved in Ebola virus-particle production. Taken together, these data suggest that filoviruses, in general, may hijack the microtubule-dependent vesicle-trafficking machinery for productive replication. Therefore, this pathway presents as a potential target for the development of pan-filovirus therapeutics.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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