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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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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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0179728</identifier><identifier>PMID: 28651016</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>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</subject><ispartof>PloS one, 2017-06, Vol.12 (6), p.e0179728-e0179728</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Daaboul et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Daaboul et al 2017 Daaboul et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-e5e049939508b155cf5b554c70d5d8b8fa29cfc5176ecf4e767d25f7624d4b8a3</citedby><cites>FETCH-LOGICAL-c692t-e5e049939508b155cf5b554c70d5d8b8fa29cfc5176ecf4e767d25f7624d4b8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484481/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484481/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28651016$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Daaboul, George G</creatorcontrib><creatorcontrib>Freedman, David S</creatorcontrib><creatorcontrib>Scherr, Steven M</creatorcontrib><creatorcontrib>Carter, Erik</creatorcontrib><creatorcontrib>Rosca, Alexandru</creatorcontrib><creatorcontrib>Bernstein, David</creatorcontrib><creatorcontrib>Mire, Chad E</creatorcontrib><creatorcontrib>Agans, Krystle N</creatorcontrib><creatorcontrib>Hoenen, Thomas</creatorcontrib><creatorcontrib>Geisbert, Thomas W</creatorcontrib><creatorcontrib>Ünlü, M Selim</creatorcontrib><creatorcontrib>Connor, John H</creatorcontrib><title>Enhanced light microscopy visualization of virus particles from Zika virus to filamentous ebolaviruses</title><title>PloS one</title><addtitle>PLoS One</addtitle><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.</description><subject>Animals</subject><subject>Atomic force microscopy</subject><subject>Binding sites</subject><subject>Biology and Life Sciences</subject><subject>Biomedical engineering</subject><subject>Cell culture</subject><subject>Ebola virus</subject><subject>Ebolavirus - ultrastructure</subject><subject>Electron microscopy</subject><subject>Engineering</subject><subject>Engineering and Technology</subject><subject>Enumeration</subject><subject>Equipment Design</subject><subject>Field of view</subject><subject>Fluids</subject><subject>Fungi</subject><subject>Genomes</subject><subject>Humans</subject><subject>Illumination</subject><subject>Imaging</subject><subject>Immunology</subject><subject>Infectious diseases</subject><subject>Influenza</subject><subject>Interference</subject><subject>Interferometry</subject><subject>Laboratories</subject><subject>Light microscopy</subject><subject>Medical imaging</subject><subject>Medicine and Health Sciences</subject><subject>Microscopy, Electron, Scanning</subject><subject>Microscopy, Interference - 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recordid | cdi_plos_journals_1913783357 |
source | MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS) |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T10%3A40%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Enhanced%20light%20microscopy%20visualization%20of%20virus%20particles%20from%20Zika%20virus%20to%20filamentous%20ebolaviruses&rft.jtitle=PloS%20one&rft.au=Daaboul,%20George%20G&rft.date=2017-06-26&rft.volume=12&rft.issue=6&rft.spage=e0179728&rft.epage=e0179728&rft.pages=e0179728-e0179728&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0179728&rft_dat=%3Cgale_plos_%3EA497001829%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1913783357&rft_id=info:pmid/28651016&rft_galeid=A497001829&rft_doaj_id=oai_doaj_org_article_0b055bddd4854c9ea81244a60424d765&rfr_iscdi=true |