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Computational sensing of herpes simplex virus using a cost-effective on-chip microscope
Caused by the herpes simplex virus (HSV), herpes is a viral infection that is one of the most widespread diseases worldwide. Here we present a computational sensing technique for specific detection of HSV using both viral immuno-specificity and the physical size range of the viruses. This label-free...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501859/ https://www.ncbi.nlm.nih.gov/pubmed/28687769 http://dx.doi.org/10.1038/s41598-017-05124-3 |
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author | Ray, Aniruddha Daloglu, Mustafa Ugur Ho, Joslynn Torres, Avee Mcleod, Euan Ozcan, Aydogan |
author_facet | Ray, Aniruddha Daloglu, Mustafa Ugur Ho, Joslynn Torres, Avee Mcleod, Euan Ozcan, Aydogan |
author_sort | Ray, Aniruddha |
collection | PubMed |
description | Caused by the herpes simplex virus (HSV), herpes is a viral infection that is one of the most widespread diseases worldwide. Here we present a computational sensing technique for specific detection of HSV using both viral immuno-specificity and the physical size range of the viruses. This label-free approach involves a compact and cost-effective holographic on-chip microscope and a surface-functionalized glass substrate prepared to specifically capture the target viruses. To enhance the optical signatures of individual viruses and increase their signal-to-noise ratio, self-assembled polyethylene glycol based nanolenses are rapidly formed around each virus particle captured on the substrate using a portable interface. Holographic shadows of specifically captured viruses that are surrounded by these self-assembled nanolenses are then reconstructed, and the phase image is used for automated quantification of the size of each particle within our large field-of-view, ~30 mm(2). The combination of viral immuno-specificity due to surface functionalization and the physical size measurements enabled by holographic imaging is used to sensitively detect and enumerate HSV particles using our compact and cost-effective platform. This computational sensing technique can find numerous uses in global health related applications in resource-limited environments. |
format | Online Article Text |
id | pubmed-5501859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55018592017-07-10 Computational sensing of herpes simplex virus using a cost-effective on-chip microscope Ray, Aniruddha Daloglu, Mustafa Ugur Ho, Joslynn Torres, Avee Mcleod, Euan Ozcan, Aydogan Sci Rep Article Caused by the herpes simplex virus (HSV), herpes is a viral infection that is one of the most widespread diseases worldwide. Here we present a computational sensing technique for specific detection of HSV using both viral immuno-specificity and the physical size range of the viruses. This label-free approach involves a compact and cost-effective holographic on-chip microscope and a surface-functionalized glass substrate prepared to specifically capture the target viruses. To enhance the optical signatures of individual viruses and increase their signal-to-noise ratio, self-assembled polyethylene glycol based nanolenses are rapidly formed around each virus particle captured on the substrate using a portable interface. Holographic shadows of specifically captured viruses that are surrounded by these self-assembled nanolenses are then reconstructed, and the phase image is used for automated quantification of the size of each particle within our large field-of-view, ~30 mm(2). The combination of viral immuno-specificity due to surface functionalization and the physical size measurements enabled by holographic imaging is used to sensitively detect and enumerate HSV particles using our compact and cost-effective platform. This computational sensing technique can find numerous uses in global health related applications in resource-limited environments. Nature Publishing Group UK 2017-07-07 /pmc/articles/PMC5501859/ /pubmed/28687769 http://dx.doi.org/10.1038/s41598-017-05124-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ray, Aniruddha Daloglu, Mustafa Ugur Ho, Joslynn Torres, Avee Mcleod, Euan Ozcan, Aydogan Computational sensing of herpes simplex virus using a cost-effective on-chip microscope |
title | Computational sensing of herpes simplex virus using a cost-effective on-chip microscope |
title_full | Computational sensing of herpes simplex virus using a cost-effective on-chip microscope |
title_fullStr | Computational sensing of herpes simplex virus using a cost-effective on-chip microscope |
title_full_unstemmed | Computational sensing of herpes simplex virus using a cost-effective on-chip microscope |
title_short | Computational sensing of herpes simplex virus using a cost-effective on-chip microscope |
title_sort | computational sensing of herpes simplex virus using a cost-effective on-chip microscope |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501859/ https://www.ncbi.nlm.nih.gov/pubmed/28687769 http://dx.doi.org/10.1038/s41598-017-05124-3 |
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