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16 results for “Sindbis virus”
Supplementary Material: Fluorescent Protein‐Tagged Sindbis Virus E2 Glycoprotein Allows Single Particle Analysis of Virus Budding from Live Cells
<p>Supplementary Videos for <em>Viruses</em> <strong>2015</strong>, <em>7</em>(12), 6182-6199; doi:10.3390/v7122926, http://www.mdpi.com/1999-4915/7/12/2926:</p> <p><strong>Video S1A</strong> BHK cells infected with mCherry-E2 virus at 3 h p.i. Glycoprotein containing vesicles are transported to the PM from where individual virions bud out. White arrow point to budding virions. Overall amount of glycoproteins present on the PM and the number of virus particles budding out are relatively reduced compared to the late stage of infection. Images were acquired at a rate of 0.99 fps and 75 frames were acquired. Video was generated using these images and played at a rate of 5 fps. Image acquisition time is shown as Time: hour: minute: second: millisecond (h:min:sec:msec ) and the scale bar represents 10 μm.</p> <p><strong>Video S1B </strong>Enlarged area of video S1A showing budding virus particles from PM. White arrow indicates single particle post-budding moving away from the cell. Images were acquired at a rate of 0.99 fps and 75 frames were acquired. Video was generated using these images and played at a rate of 5 fps. Image acquisition time is shown as Time: hour: minute: second: millisecond (h:min:sec:msec ) and the scale bar represents 10 μm.</p> <p><strong>Video S2A</strong> Virus budding and single particle movement associated with filopodial extensions observed from mCherry-E2 virus-infected BHK cells at 6 h p.i. Glycoprotein containing vesicle transport to the PM is also observed. Budded virions travel along the periphery of filopodia and are released from filopodial extensions to the surrounding media. Image acquisition was at a rate of 1 fps and 285 frames were acquired. Movie was generated using these images and played at a rate of 7 fps. Image acquisition time is shown as Time: h:min:sec:msec and the scale bar represents 10 μm.</p> <p><strong>Video S2B</strong> Enlarged area of video S2A showing budding virus particles from filopodia. White arrow indicates virus budding from filopodial extensions. Images were acquired at a rate of 1 fps and the acquired 285 frames were used to generate the video at a rate of 7 fps. Image acquisition time is shown as Time: h:min:sec:msec and the scale bar represents 10 μm.</p> <p><strong>Video S3</strong> BHK cells transfected with RNA from a non-budding cdE2 mutant <sub>416</sub>CC<sub>417</sub>/A2 mCherry-E2 virus. This non-budding mutant is unable to release fluorescent virus particles from the infected cells. The video shows the absence of fluorescent virus particle budding from the PM at 6 h post transfection even though the PM and filopodial extensions contain mCherry-E2. Despite the transport of glycoproteins to the PM, no fluorescent particles were released into the media. Yellow arrows point toward filopodial extensions. For the video, 304 images were acquired at a rate of 0.98 fps and the video was generated using the acquired images at a rate of 7 fps. Image acquisition time is shown as Time: h:min:sec:msec and the scale bar represents 10 μm.</p> <p><strong>Video S4</strong> BHK cells transfected with RNA from an E1 Fusion loop (G91D) mutant of mCherry-E2 virus at 6 h post transfection. This non-fusing mutant produces fluorescent virus particles at a slower rate compared to WT that are unable to fuse after entering a new cell. White arrow points to fluorescent particles that are releasing into the media from filopodial extensions. Yellow arrow represents a fluorescent particle that had entered an adjacent un-transfected cell. A total of 149 images were acquired at a rate of 0.98 fps. Video was generated using these images at a rate of 7 fps. Image acquisition time is shown as Time: h:min:sec:msec and the scale bar represents 10 μm.</p> <p> </p> <p><strong>Video S5A</strong> Glycoprotein E2 (mCherry-E2; red) colocalizing with Golgi stain (green) in BHK cells infected with mCherry-E2 virus and stained with BODIPY FL C5 ceramide at 5 h p.i. and imaged at 6 h p.i. Glycoprotein-containing red vesicles originate from Golgi as evidenced from the colocalization of red and green and these vesicles display anterograde transport to the PM and the virus particles are released by budding from the PM. Fluorescent particles are also seen budding from filopodial extensions (white arrows). Images were acquired at a rate of 0.13 fps for 295 seconds. Video was generated using these acquired images at a rate of 5 fps. Image acquisition time is shown as Time: h:min:sec:msec and the scale bar represents 10 μm.</p> <p><strong>Video S5B</strong> An enlarged area of the video S5A near the white arrow showing movement of particles on filopodial extensions between two cells. Movie was played at a rate of 5 fps. Image acquisition time is shown as Time: h:min:sec:msec and the scale bar represents 10 μm.</p> <p> </p> <p> </p>
Data from: Predicting spatial patterns of Sindbis virus (SINV) infection risk in Finland using vector, host and environmental data
Open the record for dataset details and reuse information.
Detection of small RNAs generated during early infection of human HEK 293 cells by the alphavirus Sindbis virus
GEO Series GSE46254. Homo sapiens. 3 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Host derivation of Sindbis virus influences mammalian type 1 interferon response to infection
GEO Series GSE234344. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
Cross-species comparative analysis of Dicer proteins during Sindbis virus infection
GEO Series GSE62934. Homo sapiens; Sindbis virus; Drosophila melanogaster. 11 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Transcriptome analysis of tumors isolated from ovarian cancer tumor bearing mice treated with Sindbis Virus vectors and untreated controls
GEO Series GSE216750. Mus musculus. 15 samples. Type: Expression profiling by high throughput sequencing.
Targeted NGS on artificial microRNAs expressed by a pool of heterogeneous Sindbis viruses
GEO Series GSE197271. Sindbis virus. 21 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Sindbis virus induces the production of a novel class of endogenous siRNAs in Aedes aegypti mosquitoes
GEO Series GSE35161. Aedes aegypti. 3 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Viral small RNAs in Sindbis virus-infected mammalian cells
GEO Series GSE48831. Chlorocebus aethiops; Homo sapiens. 10 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Transcriptome sequencing data sets for mice brain infected with Sindbis virus and treated with glucosylceramide synthase inhibitor
GEO Series GSE171912. Mus musculus. 15 samples. Type: Expression profiling by high throughput sequencing.
Expression profile of adult Drosophila melanogaster expressing a self-replicating RNA of Sindbis virus
GEO Series GSE42726. Drosophila melanogaster. 12 samples. Type: Expression profiling by array.
Small RNA sequencing of mock treated or Sindbis virus-infected wild type and RNaseIII knockout cells
GEO Series GSE98135. Homo sapiens. 4 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Transcriptome analysis of T cells from mice immunized with Sindbis Virus Spike and/or aOX40
GEO Series GSE176203. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing.
Identification of Interactions between Sindbis Virus Capsid Protein and Cytoplasmic vRNA as Novel Virulence Determinants
GEO Series GSE99879. Sindbis virus; Homo sapiens. 5 samples. Type: Other.
The Identification and Characterization of Sindbis Virus RNA:Host Protein Interactions
GEO Series GSE103693. Homo sapiens. 5 samples. Type: Other; Genome binding/occupancy profiling by high throughput sequencing.
N6-Methyladenosine reader YTHDF3 regulate Sindbis virus release by incomplete selective autophagy flux maintenance through SQSTM1
GEO Series GSE280392. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
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