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A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry

Bovine herpesvirus 1 (BoHV-1) is an important pathogen of domestic and wild cattle responsible for major economic losses in dairy and beef industries throughout the world. Inhibition of viral entry plays a crucial role in the control of BoHV-1 infection and aptamers have been reported to inhibit vir...

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Autores principales: Xu, Jian, Zhang, Xixi, Zhou, Shuanghai, Shen, Junjun, Yang, Dawei, Wu, Jing, Li, Xiaoyang, Li, Meiling, Huang, Xiufen, Sealy, Joshua E., Iqbal, Munir, Li, Yongqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603541/
https://www.ncbi.nlm.nih.gov/pubmed/28924154
http://dx.doi.org/10.1038/s41598-017-10070-1
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author Xu, Jian
Zhang, Xixi
Zhou, Shuanghai
Shen, Junjun
Yang, Dawei
Wu, Jing
Li, Xiaoyang
Li, Meiling
Huang, Xiufen
Sealy, Joshua E.
Iqbal, Munir
Li, Yongqing
author_facet Xu, Jian
Zhang, Xixi
Zhou, Shuanghai
Shen, Junjun
Yang, Dawei
Wu, Jing
Li, Xiaoyang
Li, Meiling
Huang, Xiufen
Sealy, Joshua E.
Iqbal, Munir
Li, Yongqing
author_sort Xu, Jian
collection PubMed
description Bovine herpesvirus 1 (BoHV-1) is an important pathogen of domestic and wild cattle responsible for major economic losses in dairy and beef industries throughout the world. Inhibition of viral entry plays a crucial role in the control of BoHV-1 infection and aptamers have been reported to inhibit viral replication. In this study, nine DNA aptamers that target BoHV-1 were generated using systemic evolution of ligands by exponential enrichment. Of the nine candidates, aptamer IBRV-A4 exhibited the highest affinity and specificity for BoHV-1, which bound to BoHV-1 with a Kd value of 3.519 nM and demonstrated the greatest virus binding as shown by fluorescence imaging. The neutralizing ability of aptamer IBRV-A4 was determined using neutralization assays and real time PCR in BoHV-1 infected Madin-darby bovine kidney cells. Virus titration, immunofluorescence and confocal laser scanning microscopy showed virus replication significantly decreased when aptamer IBRV-A4 was added to BoHV-1 infected MDBK cells at 0 and 0.5 hours post-infection, whereas no change was seen when IBRV-A4 was added 2 hours post-infection. This concludes that aptamer IBRV-A4 efficiently inhibits viral entry of BoHV-1 in MDBK cells and is therefore a novel tool for diagnosis and treatment of BoHV-1 infection in cattle.
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spelling pubmed-56035412017-09-20 A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry Xu, Jian Zhang, Xixi Zhou, Shuanghai Shen, Junjun Yang, Dawei Wu, Jing Li, Xiaoyang Li, Meiling Huang, Xiufen Sealy, Joshua E. Iqbal, Munir Li, Yongqing Sci Rep Article Bovine herpesvirus 1 (BoHV-1) is an important pathogen of domestic and wild cattle responsible for major economic losses in dairy and beef industries throughout the world. Inhibition of viral entry plays a crucial role in the control of BoHV-1 infection and aptamers have been reported to inhibit viral replication. In this study, nine DNA aptamers that target BoHV-1 were generated using systemic evolution of ligands by exponential enrichment. Of the nine candidates, aptamer IBRV-A4 exhibited the highest affinity and specificity for BoHV-1, which bound to BoHV-1 with a Kd value of 3.519 nM and demonstrated the greatest virus binding as shown by fluorescence imaging. The neutralizing ability of aptamer IBRV-A4 was determined using neutralization assays and real time PCR in BoHV-1 infected Madin-darby bovine kidney cells. Virus titration, immunofluorescence and confocal laser scanning microscopy showed virus replication significantly decreased when aptamer IBRV-A4 was added to BoHV-1 infected MDBK cells at 0 and 0.5 hours post-infection, whereas no change was seen when IBRV-A4 was added 2 hours post-infection. This concludes that aptamer IBRV-A4 efficiently inhibits viral entry of BoHV-1 in MDBK cells and is therefore a novel tool for diagnosis and treatment of BoHV-1 infection in cattle. Nature Publishing Group UK 2017-09-18 /pmc/articles/PMC5603541/ /pubmed/28924154 http://dx.doi.org/10.1038/s41598-017-10070-1 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
Xu, Jian
Zhang, Xixi
Zhou, Shuanghai
Shen, Junjun
Yang, Dawei
Wu, Jing
Li, Xiaoyang
Li, Meiling
Huang, Xiufen
Sealy, Joshua E.
Iqbal, Munir
Li, Yongqing
A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry
title A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry
title_full A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry
title_fullStr A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry
title_full_unstemmed A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry
title_short A DNA aptamer efficiently inhibits the infectivity of Bovine herpesvirus 1 by blocking viral entry
title_sort dna aptamer efficiently inhibits the infectivity of bovine herpesvirus 1 by blocking viral entry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603541/
https://www.ncbi.nlm.nih.gov/pubmed/28924154
http://dx.doi.org/10.1038/s41598-017-10070-1
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