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Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines
The genus Flavivirus contains more than 70 single-stranded, positive-sense arthropod-borne RNA viruses. Some flaviviruses are particularly medically important to humans and other vertebrates including dengue virus (DENV), West Nile virus, and yellow fever virus. These viruses are transmitted to vert...
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/PMC5537255/ https://www.ncbi.nlm.nih.gov/pubmed/28761113 http://dx.doi.org/10.1038/s41598-017-07279-5 |
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author | Zhang, Guangmei Asad, Sultan Khromykh, Alexander A. Asgari, Sassan |
author_facet | Zhang, Guangmei Asad, Sultan Khromykh, Alexander A. Asgari, Sassan |
author_sort | Zhang, Guangmei |
collection | PubMed |
description | The genus Flavivirus contains more than 70 single-stranded, positive-sense arthropod-borne RNA viruses. Some flaviviruses are particularly medically important to humans and other vertebrates including dengue virus (DENV), West Nile virus, and yellow fever virus. These viruses are transmitted to vertebrates by mosquitoes and other arthropod species. Mosquitoes are also infected by insect-specific flaviviruses (ISFs) that do not appear to be infective to vertebrates. Cell fusing agent virus (CFAV) was the first described ISF, which was discovered in an Aedes aegypti cell culture. We found that while CFAV infection could be significantly reduced by application of RNAi against the NS5 gene, removal of the treatment led to quick restoration of CFAV replication. Interestingly, we found that CFAV infection significantly enhanced replication of DENV, and vice versa, DENV infection significantly enhanced replication of CFAV in mosquito cells. We have shown that CFAV infection leads to increase in the expression of ribonuclease kappa (RNASEK), which is known to promote infection of viruses that rely on endocytosis and pH-dependent entry. Knockdown of RNASEK by dsRNA resulted in reduced DENV replication. Thus, increased expression of RNASEK induced by CFAV is likely to contribute to enhanced DENV replication in CFAV-infected cells. |
format | Online Article Text |
id | pubmed-5537255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55372552017-08-03 Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines Zhang, Guangmei Asad, Sultan Khromykh, Alexander A. Asgari, Sassan Sci Rep Article The genus Flavivirus contains more than 70 single-stranded, positive-sense arthropod-borne RNA viruses. Some flaviviruses are particularly medically important to humans and other vertebrates including dengue virus (DENV), West Nile virus, and yellow fever virus. These viruses are transmitted to vertebrates by mosquitoes and other arthropod species. Mosquitoes are also infected by insect-specific flaviviruses (ISFs) that do not appear to be infective to vertebrates. Cell fusing agent virus (CFAV) was the first described ISF, which was discovered in an Aedes aegypti cell culture. We found that while CFAV infection could be significantly reduced by application of RNAi against the NS5 gene, removal of the treatment led to quick restoration of CFAV replication. Interestingly, we found that CFAV infection significantly enhanced replication of DENV, and vice versa, DENV infection significantly enhanced replication of CFAV in mosquito cells. We have shown that CFAV infection leads to increase in the expression of ribonuclease kappa (RNASEK), which is known to promote infection of viruses that rely on endocytosis and pH-dependent entry. Knockdown of RNASEK by dsRNA resulted in reduced DENV replication. Thus, increased expression of RNASEK induced by CFAV is likely to contribute to enhanced DENV replication in CFAV-infected cells. Nature Publishing Group UK 2017-07-31 /pmc/articles/PMC5537255/ /pubmed/28761113 http://dx.doi.org/10.1038/s41598-017-07279-5 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 Zhang, Guangmei Asad, Sultan Khromykh, Alexander A. Asgari, Sassan Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines |
title | Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines |
title_full | Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines |
title_fullStr | Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines |
title_full_unstemmed | Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines |
title_short | Cell fusing agent virus and dengue virus mutually interact in Aedes aegypti cell lines |
title_sort | cell fusing agent virus and dengue virus mutually interact in aedes aegypti cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537255/ https://www.ncbi.nlm.nih.gov/pubmed/28761113 http://dx.doi.org/10.1038/s41598-017-07279-5 |
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