Enhanced light microscopy visualization of virus particles from Zika virus to filamentous ebolaviruses

Light microscopy is a powerful tool in the detection and analysis of parasites, fungi, and prokaryotes, but has been challenging to use for the detection of individual virus particles. Unlabeled virus particles are too small to be visualized using standard visible light microscopy. Characterization...

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Veröffentlicht in:PloS one 2017-06, Vol.12 (6), p.e0179728-e0179728
Hauptverfasser: Daaboul, George G, Freedman, David S, Scherr, Steven M, Carter, Erik, Rosca, Alexandru, Bernstein, David, Mire, Chad E, Agans, Krystle N, Hoenen, Thomas, Geisbert, Thomas W, Ünlü, M Selim, Connor, John H
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container_title PloS one
container_volume 12
creator Daaboul, George G
Freedman, David S
Scherr, Steven M
Carter, Erik
Rosca, Alexandru
Bernstein, David
Mire, Chad E
Agans, Krystle N
Hoenen, Thomas
Geisbert, Thomas W
Ünlü, M Selim
Connor, John H
description Light microscopy is a powerful tool in the detection and analysis of parasites, fungi, and prokaryotes, but has been challenging to use for the detection of individual virus particles. Unlabeled virus particles are too small to be visualized using standard visible light microscopy. Characterization of virus particles is typically performed using higher resolution approaches such as electron microscopy or atomic force microscopy. These approaches require purification of virions away from their normal millieu, requiring significant levels of expertise, and can only enumerate small numbers of particles per field of view. Here, we utilize a visible light imaging approach called Single Particle Interferometric Reflectance Imaging Sensor (SP-IRIS) that allows automated counting and sizing of thousands of individual virions. Virions are captured directly from complex solutions onto a silicon chip and then detected using a reflectance interference imaging modality. We show that the use of different imaging wavelengths allows the visualization of a multitude of virus particles. Using Violet/UV illumination, the SP-IRIS technique is able to detect individual flavivirus particles (~40 nm), while green light illumination is capable of identifying and discriminating between vesicular stomatitis virus and vaccinia virus (~360 nm). Strikingly, the technology allows the clear identification of filamentous infectious ebolavirus particles and virus-like particles. The ability to differentiate and quantify unlabeled virus particles extends the usefulness of traditional light microscopy and can be embodied in a straightforward benchtop approach allowing widespread applications ranging from rapid detection in biological fluids to analysis of virus-like particles for vaccine development and production.
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subjects Animals
Atomic force microscopy
Binding sites
Biology and Life Sciences
Biomedical engineering
Cell culture
Ebola virus
Ebolavirus - ultrastructure
Electron microscopy
Engineering
Engineering and Technology
Enumeration
Equipment Design
Field of view
Fluids
Fungi
Genomes
Humans
Illumination
Imaging
Immunology
Infectious diseases
Influenza
Interference
Interferometry
Laboratories
Light microscopy
Medical imaging
Medicine and Health Sciences
Microscopy, Electron, Scanning
Microscopy, Interference - instrumentation
Microscopy, Interference - methods
Microscopy, Ultraviolet - instrumentation
Microscopy, Ultraviolet - methods
Molds (Fungi)
Morphology
Nanoparticles
Parasites
Particulates
Prevention
Prokaryotes
Purification
Reflectance
Research and Analysis Methods
Risk factors
Silicon
Sizing
Stomatitis
Vaccine development
Vaccinia virus - ultrastructure
Vector-borne diseases
Vesiculovirus - ultrastructure
Virion - ultrastructure
Virions
Virology
Virus-like particles
Viruses
Visualization
Wavelengths
Zika virus
Zika Virus - ultrastructure
title Enhanced light microscopy visualization of virus particles from Zika virus to filamentous ebolaviruses
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