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Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication
Aleutian mink disease (AMD), which is caused by Aleutian mink disease virus (AMDV), is an important contagious disease for which no effective vaccine is yet available. AMD causes major economic losses for mink farmers globally and threatens some carnivores such as skunks, genets, foxes and raccoons....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907208/ https://www.ncbi.nlm.nih.gov/pubmed/33633317 http://dx.doi.org/10.1038/s41598-021-84223-8 |
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author | Lu, Taofeng Zhang, Hui Zhou, Jie Ma, Qin Yan, Wenzhuo Zhao, Lili Wu, Shuguang Chen, Hongyan |
author_facet | Lu, Taofeng Zhang, Hui Zhou, Jie Ma, Qin Yan, Wenzhuo Zhao, Lili Wu, Shuguang Chen, Hongyan |
author_sort | Lu, Taofeng |
collection | PubMed |
description | Aleutian mink disease (AMD), which is caused by Aleutian mink disease virus (AMDV), is an important contagious disease for which no effective vaccine is yet available. AMD causes major economic losses for mink farmers globally and threatens some carnivores such as skunks, genets, foxes and raccoons. Aptamers have exciting potential for the diagnosis and/or treatment of infectious viral diseases, including AMD. Using a magnetic beads-based systemic evolution of ligands by exponential enrichment (SELEX) approach, we have developed aptamers with activity against AMDV after 10 rounds of selection. After incubation with the ADVa012 aptamer (4 μM) for 48 h, the concentration of AMDV in the supernatant of infected cells was 47% lower than in the supernatant of untreated cells, whereas a random library of aptamers has no effect. The half-life of ADVa012 was ~ 32 h, which is significantly longer than that of other aptamers. Sequences and three dimensions structural modeling of selected aptamers indicated that they fold into similar stem-loop structures, which may be a preferred structure for binding to the target protein. The ADVa012 aptamer was shown to have an effective and long-lasting inhibitory effect on viral production in vitro. |
format | Online Article Text |
id | pubmed-7907208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79072082021-02-26 Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication Lu, Taofeng Zhang, Hui Zhou, Jie Ma, Qin Yan, Wenzhuo Zhao, Lili Wu, Shuguang Chen, Hongyan Sci Rep Article Aleutian mink disease (AMD), which is caused by Aleutian mink disease virus (AMDV), is an important contagious disease for which no effective vaccine is yet available. AMD causes major economic losses for mink farmers globally and threatens some carnivores such as skunks, genets, foxes and raccoons. Aptamers have exciting potential for the diagnosis and/or treatment of infectious viral diseases, including AMD. Using a magnetic beads-based systemic evolution of ligands by exponential enrichment (SELEX) approach, we have developed aptamers with activity against AMDV after 10 rounds of selection. After incubation with the ADVa012 aptamer (4 μM) for 48 h, the concentration of AMDV in the supernatant of infected cells was 47% lower than in the supernatant of untreated cells, whereas a random library of aptamers has no effect. The half-life of ADVa012 was ~ 32 h, which is significantly longer than that of other aptamers. Sequences and three dimensions structural modeling of selected aptamers indicated that they fold into similar stem-loop structures, which may be a preferred structure for binding to the target protein. The ADVa012 aptamer was shown to have an effective and long-lasting inhibitory effect on viral production in vitro. Nature Publishing Group UK 2021-02-25 /pmc/articles/PMC7907208/ /pubmed/33633317 http://dx.doi.org/10.1038/s41598-021-84223-8 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lu, Taofeng Zhang, Hui Zhou, Jie Ma, Qin Yan, Wenzhuo Zhao, Lili Wu, Shuguang Chen, Hongyan Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication |
title | Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication |
title_full | Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication |
title_fullStr | Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication |
title_full_unstemmed | Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication |
title_short | Aptamer-targeting of Aleutian mink disease virus (AMDV) can be an effective strategy to inhibit virus replication |
title_sort | aptamer-targeting of aleutian mink disease virus (amdv) can be an effective strategy to inhibit virus replication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907208/ https://www.ncbi.nlm.nih.gov/pubmed/33633317 http://dx.doi.org/10.1038/s41598-021-84223-8 |
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