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本文引用的文献

1
Mapping in vitro local material properties of intact and disrupted virions at high resolution using multi-harmonic atomic force microscopy.采用多谐原子力显微镜高分辨率测绘完整和破碎病毒的体外局部材料特性。
Nanoscale. 2013 Jun 7;5(11):4729-36. doi: 10.1039/c3nr34088k. Epub 2013 Apr 18.
2
Mechanical properties of viruses analyzed by atomic force microscopy: a virological perspective.原子力显微镜分析病毒的力学性质:病毒学视角。
Virus Res. 2012 Sep;168(1-2):1-22. doi: 10.1016/j.virusres.2012.06.008. Epub 2012 Jun 15.
3
Identification of common biological pathways and drug targets across multiple respiratory viruses based on human host gene expression analysis.基于人类宿主基因表达分析鉴定多种呼吸道病毒的常见生物途径和药物靶点。
PLoS One. 2012;7(3):e33174. doi: 10.1371/journal.pone.0033174. Epub 2012 Mar 14.
4
Targeting RSV with vaccines and small molecule drugs.利用疫苗和小分子药物针对呼吸道合胞病毒(RSV)
Infect Disord Drug Targets. 2012 Apr;12(2):110-28. doi: 10.2174/187152612800100143.
5
Resolving structure and mechanical properties at the nanoscale of viruses with frequency modulation atomic force microscopy.利用调频原子力显微镜解析病毒的纳米级结构和力学性质。
PLoS One. 2012;7(1):e30204. doi: 10.1371/journal.pone.0030204. Epub 2012 Jan 25.
6
Respiratory syncytial virus infection and immunity.呼吸道合胞病毒感染与免疫。
Rev Med Virol. 2012 Jul;22(4):230-44. doi: 10.1002/rmv.1704. Epub 2012 Jan 31.
7
Localization and force analysis at the single virus particle level using atomic force microscopy.基于原子力显微镜的单病毒颗粒水平的定位和力分析。
Biochem Biophys Res Commun. 2012 Jan 6;417(1):109-15. doi: 10.1016/j.bbrc.2011.11.065. Epub 2011 Nov 22.
8
Respiratory syncytial virus induces host RNA stress granules to facilitate viral replication.呼吸道合胞病毒诱导宿主 RNA 应激颗粒促进病毒复制。
J Virol. 2010 Dec;84(23):12274-84. doi: 10.1128/JVI.00260-10. Epub 2010 Sep 15.
9
Activity investigation of pinostrobin towards herpes simplex virus-1 as determined by atomic force microscopy.原子力显微镜研究松脂素对单纯疱疹病毒-1 的作用。
Phytomedicine. 2011 Jan 15;18(2-3):110-8. doi: 10.1016/j.phymed.2010.07.001. Epub 2010 Aug 23.
10
Atomic force microscopy investigation of the giant mimivirus.原子力显微镜研究巨型拟病毒。
Virology. 2010 Aug 15;404(1):127-37. doi: 10.1016/j.virol.2010.05.007.

原子力显微镜观察呼吸道合胞病毒感染 HEp-2 细胞的过程。

Atomic force microscopic investigation of respiratory syncytial virus infection in HEp-2 cells.

机构信息

Center for NanoBiotechnology Research, Alabama State University, Montgomery, Alabama 36101, U.S.A.

出版信息

J Microsc. 2014 Jan;253(1):31-41. doi: 10.1111/jmi.12095. Epub 2013 Nov 19.

DOI:10.1111/jmi.12095
PMID:24251370
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4090083/
Abstract

Respiratory syncytial virus (RSV) primarily causes bronchiolitis and pneumonia in infants. In spite of intense research, no safe and effective vaccine has been developed yet. For understanding its pathogenesis and development of anti-RSV drugs/therapeutics, it is indispensable to study the RSV-host interaction. Although, there are limited studies using electron microscopy to elucidate the infection process of RSV, to our knowledge, no study has reported the morphological impact of RSV infection using atomic force microscopy. We report the cytoplasmic and nuclear changes in human epidermoid cell line type 2 using atomic force microscopy. Human epidermoid cell line type 2 cells, grown on cover slips, were infected with RSV and fixed after various time periods, processed and observed for morphological changes using atomic force microscopy. RSV infected cells showed loss of membrane integrity, with degeneration in the cellular content and cytoskeleton. Nuclear membrane was disintegrated and nuclear volume was decreased. The chromatin of the RSV infected cells was condensed, progressing towards degeneration via pyknosis and apoptosis. Membrane protrusions of ~150-200 nm diameter were observed on RSV infected cells after 6 h, suggestive of prospective RSV budding sites. To our knowledge, this is the first study of RSV infection process using atomic force microscopy. Such morphological studies could help explore viral infection process aiding the development of anti-RSV therapies.

摘要

呼吸道合胞病毒(RSV)主要导致婴儿细支气管炎和肺炎。尽管进行了深入的研究,但尚未开发出安全有效的疫苗。为了了解其发病机制和抗 RSV 药物/疗法的发展,研究 RSV-宿主相互作用是必不可少的。尽管使用电子显微镜阐明 RSV 的感染过程的研究有限,但据我们所知,尚无研究使用原子力显微镜报告 RSV 感染的形态影响。我们使用原子力显微镜报告了人表皮细胞系 2 型的细胞质和核变化。将人表皮细胞系 2 型细胞在盖玻片上生长,用 RSV 感染,然后在不同时间段固定,使用原子力显微镜处理和观察形态变化。RSV 感染的细胞显示出膜完整性丧失,细胞内容物和细胞骨架退化。核膜破裂,核体积减小。RSV 感染细胞的染色质浓缩,通过固缩和凋亡逐渐退化。在感染 RSV 6 小时后,在 RSV 感染的细胞上观察到直径约为 150-200nm 的膜突起,提示可能是 RSV 的出芽部位。据我们所知,这是使用原子力显微镜研究 RSV 感染过程的首次研究。这种形态学研究可以帮助探索病毒感染过程,有助于开发抗 RSV 疗法。