肠道病毒D68囊体的形成和稳定性需要酸性体
Ganna Galitska1, Alagie Jassey1, Michael A Wagner1
1Department of Microbiology and Immunology, University of Maryland School of Medicine, 685 W. Baltimore St, Baltimore, MD 21201, USA.
bioRxiv : the preprint server for biology
|July 3, 2023
概括
肠道病毒D68需要特定的器官酸化才能形成囊. 抑制这一过程会破坏病毒的复制,并导致细胞变化,与脊髓灰质炎病毒不同.
科学领域:
- 病毒学 病毒学
- 细胞生物学 细胞生物学
背景情况:
- 肠道病毒D68 (EV-D68) 是一种与急性软骨髓炎 (AFM) 相关的皮科纳病毒.
- 了解EV-D68的致病性是有限的,通常依赖于脊髓灰质炎病毒模型.
- 低pH值促进了脊髓灰质炎病毒囊的成熟,但对EV-D68的要求不太了解.
研究的目的:
- 为了研究在EV-D68感染中隔间酸化的作用.
- 为了确定受pH影响的EV-D68复制的关键阶段.
- 描述与受损酸化相关的细胞变化.
主要方法:
- 主体细胞感染了EV-D68.8.
- 在特定的时间点抑制隔间酸化.
- 显微镜观察病毒复制器官和囊形成.
- 病毒RNA复制和病毒组合的分析.
主要成果:
- 在3-4hpi窗口 ("过渡点") 中抑制隔间酸化导致了EV-D68囊形成和维护的缺陷.
- 这种抑制导致病毒复制器官在核附近聚集.
- 酸性化对于从RNA复制过渡到virion组装至关重要.
结论:
- 与脊髓灰质炎病毒相比,EV-D68具有不同的酸化要求.
- 隔间酸化是EV-D68病毒生产中的一个关键的,时间敏感的步骤.
- 结果揭示了对EV-D68复制动态和潜在治疗点的新见解.
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