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Plasmonic Enhancement of Selective Photonic Virus Inactivation

Femtosecond (fs) pulsed laser irradiation techniques have attracted interest as a photonic approach for the selective inactivation of virus contaminations in biological samples. Conventional pulsed laser approaches require, however, relatively long irradiation times to achieve a significant inactiva...

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Autores principales: Nazari, Mina, Xi, Min, Lerch, Sarah, Alizadeh, M. H., Ettinger, Chelsea, Akiyama, Hisashi, Gillespie, Christopher, Gummuluru, Suryaram, Erramilli, Shyamsunder, Reinhard, Björn M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607298/
https://www.ncbi.nlm.nih.gov/pubmed/28931903
http://dx.doi.org/10.1038/s41598-017-12377-5
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author Nazari, Mina
Xi, Min
Lerch, Sarah
Alizadeh, M. H.
Ettinger, Chelsea
Akiyama, Hisashi
Gillespie, Christopher
Gummuluru, Suryaram
Erramilli, Shyamsunder
Reinhard, Björn M.
author_facet Nazari, Mina
Xi, Min
Lerch, Sarah
Alizadeh, M. H.
Ettinger, Chelsea
Akiyama, Hisashi
Gillespie, Christopher
Gummuluru, Suryaram
Erramilli, Shyamsunder
Reinhard, Björn M.
author_sort Nazari, Mina
collection PubMed
description Femtosecond (fs) pulsed laser irradiation techniques have attracted interest as a photonic approach for the selective inactivation of virus contaminations in biological samples. Conventional pulsed laser approaches require, however, relatively long irradiation times to achieve a significant inactivation of virus. In this study, we investigate the enhancement of the photonic inactivation of Murine Leukemia Virus (MLV) via 805 nm femtosecond pulses through gold nanorods whose localized surface plasmon resonance overlaps with the excitation laser. We report a plasmonically enhanced virus inactivation, with greater than 3.7-log reduction measured by virus infectivity assays. Reliable virus inactivation was obtained for 10 s laser exposure with incident laser powers ≥0.3 W. Importantly, the fs-pulse induced inactivation was selective to the virus and did not induce any measurable damage to co-incubated antibodies. The loss in viral infection was associated with reduced viral fusion, linking the loss in infectivity with a perturbation of the viral envelope. Based on the observations that physical contact between nanorods and virus particles was not required for viral inactivation and that reactive oxygen species (ROS) did not participate in the detected viral inactivation, a model of virus inactivation based on plasmon enhanced shockwave generation is proposed.
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spelling pubmed-56072982017-09-24 Plasmonic Enhancement of Selective Photonic Virus Inactivation Nazari, Mina Xi, Min Lerch, Sarah Alizadeh, M. H. Ettinger, Chelsea Akiyama, Hisashi Gillespie, Christopher Gummuluru, Suryaram Erramilli, Shyamsunder Reinhard, Björn M. Sci Rep Article Femtosecond (fs) pulsed laser irradiation techniques have attracted interest as a photonic approach for the selective inactivation of virus contaminations in biological samples. Conventional pulsed laser approaches require, however, relatively long irradiation times to achieve a significant inactivation of virus. In this study, we investigate the enhancement of the photonic inactivation of Murine Leukemia Virus (MLV) via 805 nm femtosecond pulses through gold nanorods whose localized surface plasmon resonance overlaps with the excitation laser. We report a plasmonically enhanced virus inactivation, with greater than 3.7-log reduction measured by virus infectivity assays. Reliable virus inactivation was obtained for 10 s laser exposure with incident laser powers ≥0.3 W. Importantly, the fs-pulse induced inactivation was selective to the virus and did not induce any measurable damage to co-incubated antibodies. The loss in viral infection was associated with reduced viral fusion, linking the loss in infectivity with a perturbation of the viral envelope. Based on the observations that physical contact between nanorods and virus particles was not required for viral inactivation and that reactive oxygen species (ROS) did not participate in the detected viral inactivation, a model of virus inactivation based on plasmon enhanced shockwave generation is proposed. Nature Publishing Group UK 2017-09-20 /pmc/articles/PMC5607298/ /pubmed/28931903 http://dx.doi.org/10.1038/s41598-017-12377-5 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
Nazari, Mina
Xi, Min
Lerch, Sarah
Alizadeh, M. H.
Ettinger, Chelsea
Akiyama, Hisashi
Gillespie, Christopher
Gummuluru, Suryaram
Erramilli, Shyamsunder
Reinhard, Björn M.
Plasmonic Enhancement of Selective Photonic Virus Inactivation
title Plasmonic Enhancement of Selective Photonic Virus Inactivation
title_full Plasmonic Enhancement of Selective Photonic Virus Inactivation
title_fullStr Plasmonic Enhancement of Selective Photonic Virus Inactivation
title_full_unstemmed Plasmonic Enhancement of Selective Photonic Virus Inactivation
title_short Plasmonic Enhancement of Selective Photonic Virus Inactivation
title_sort plasmonic enhancement of selective photonic virus inactivation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607298/
https://www.ncbi.nlm.nih.gov/pubmed/28931903
http://dx.doi.org/10.1038/s41598-017-12377-5
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