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Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles
Human cytomegalovirus (CMV) is a herpesvirus that causes major health problems in neonates as well as in immunocompromised individuals1. At present, a vaccine is not available for CMV infection and the available antiviral drugs suffer from toxicity, poor efficacy and resistance12. Here, we chemicall...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080223/ https://www.ncbi.nlm.nih.gov/pubmed/24989498 http://dx.doi.org/10.1038/srep05550 |
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author | DeRussy, Bernadette M. Aylward, Madeline A. Fan, Zhen Ray, Paresh C. Tandon, Ritesh |
author_facet | DeRussy, Bernadette M. Aylward, Madeline A. Fan, Zhen Ray, Paresh C. Tandon, Ritesh |
author_sort | DeRussy, Bernadette M. |
collection | PubMed |
description | Human cytomegalovirus (CMV) is a herpesvirus that causes major health problems in neonates as well as in immunocompromised individuals1. At present, a vaccine is not available for CMV infection and the available antiviral drugs suffer from toxicity, poor efficacy and resistance12. Here, we chemically conjugated a monoclonal antibody raised against CMV surface glycoprotein (gB) with gold nanoparticles (GNP) and characterized the potential of this gB-GNP conjugate for antiviral activity against CMV. The gB-GNP blocks viral replication, virus-induced cytopathogenic effects and virus spread in cell culture without inducing cytotoxicity. High concentrations of gB-GNP that coat the surface of virus particles block virus entry, whereas lower concentrations block a later stage of virus life cycle. Also, cells treated with gB-GNP gain resistance to CMV infection. In addition, infected cells when bound to gB-GNP can be selectively lysed after exposing them to specific wavelength of laser (nanophotothermolysis). Thus, we have not only designed a potential antiviral strategy that specifically blocks CMV infection at multiple stages of virus life cycle, but we have also characterized a technique that can potentially be useful in eliminating CMV infected cells from donor tissue during transplant or transfusion. |
format | Online Article Text |
id | pubmed-4080223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40802232014-07-09 Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles DeRussy, Bernadette M. Aylward, Madeline A. Fan, Zhen Ray, Paresh C. Tandon, Ritesh Sci Rep Article Human cytomegalovirus (CMV) is a herpesvirus that causes major health problems in neonates as well as in immunocompromised individuals1. At present, a vaccine is not available for CMV infection and the available antiviral drugs suffer from toxicity, poor efficacy and resistance12. Here, we chemically conjugated a monoclonal antibody raised against CMV surface glycoprotein (gB) with gold nanoparticles (GNP) and characterized the potential of this gB-GNP conjugate for antiviral activity against CMV. The gB-GNP blocks viral replication, virus-induced cytopathogenic effects and virus spread in cell culture without inducing cytotoxicity. High concentrations of gB-GNP that coat the surface of virus particles block virus entry, whereas lower concentrations block a later stage of virus life cycle. Also, cells treated with gB-GNP gain resistance to CMV infection. In addition, infected cells when bound to gB-GNP can be selectively lysed after exposing them to specific wavelength of laser (nanophotothermolysis). Thus, we have not only designed a potential antiviral strategy that specifically blocks CMV infection at multiple stages of virus life cycle, but we have also characterized a technique that can potentially be useful in eliminating CMV infected cells from donor tissue during transplant or transfusion. Nature Publishing Group 2014-07-03 /pmc/articles/PMC4080223/ /pubmed/24989498 http://dx.doi.org/10.1038/srep05550 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article DeRussy, Bernadette M. Aylward, Madeline A. Fan, Zhen Ray, Paresh C. Tandon, Ritesh Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles |
title | Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles |
title_full | Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles |
title_fullStr | Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles |
title_full_unstemmed | Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles |
title_short | Inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles |
title_sort | inhibition of cytomegalovirus infection and photothermolysis of infected cells using bioconjugated gold nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080223/ https://www.ncbi.nlm.nih.gov/pubmed/24989498 http://dx.doi.org/10.1038/srep05550 |
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