MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factors
Abstract Background Human enterovirus 71 (EV-A71) is a non-enveloped virus that has a single stranded positive sense RNA genome. In a previous study, we showed that miR-876-5p upregulation was observed in the serum of patients with severe EV-A71 infection. Micro-876-5p (miR-876-5p) is a circulating...
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doaj-d567b531fc364ab788c60e5049c702f32021-02-07T12:26:41ZengBMCVirology Journal1743-422X2020-02-0117111110.1186/s12985-020-1284-8MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factorsPeng Xu0Hwa Xu1Hsu Sheng Cheng2Han-Hsiang Chan3Robert Y. L. Wang4Xiangyang No.1 People’s Hospital and Hubei University of MedicineCollege of Resources and Environment Qingdao Agricultural UnviersityGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung UniversityGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung UniversityDepartment of Biomedical Sciences, College of Medicine, Chang Gung UniversityAbstract Background Human enterovirus 71 (EV-A71) is a non-enveloped virus that has a single stranded positive sense RNA genome. In a previous study, we showed that miR-876-5p upregulation was observed in the serum of patients with severe EV-A71 infection. Micro-876-5p (miR-876-5p) is a circulating miRNA that can be identified to modulate EV-A71 infections through both in vitro and in vivo studies. However, the regulatory mechanisms that involve miR-876-5p in the EV-A71 infection cycle remain unclear. Methods We demonstrated that miR-876-5p facilitated EV-A71 replication and expression by overexpression and knocking-down of miR-876-5p through the transfection of miR-876-5p plasmid and miR-876-5p inhibitor. Although miR-876-5p suppressed CREB5 expression, luciferase reporter assay confirmed this. We also evaluated the role of miR-876-5p in the EV-A71 infection cycle by CREB5 mediated by transfection with an anti-miR-876-5P inhibitor or in combination with an si-CREB5 plasmid. Results MicroR-876-5p was upregulated in EV-A71-infected neuroblastoma cells. Overexpression of miR-876-5p or knockdown of cyclic-AMP responsive element binding protein 5 (CREB5) promoted EV-A71 replication. The downregulation of miR-876-5p inhibited the accumulation of viral RNA and the production of viral proteins. Interestingly, CREB5 overexpression also suppressed EV-A71 replication. Our in vitro studies reveal that miR-876-5p directly targets CREB5. Finally, downregulation of CREB5 protein abated the inhibitory effect of anti-miR-876-5p and induced inhibitory effect of EV-A71 replication. Conclusions Our results suggest that intracellular miR-876-5p promotes EV-A71 replication indirectly by targeting the host CREB5 protein.https://doi.org/10.1186/s12985-020-1284-8Enterovirus A71microRNA-876-5pCREB5Antiviral protein |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Peng Xu Hwa Xu Hsu Sheng Cheng Han-Hsiang Chan Robert Y. L. Wang |
spellingShingle |
Peng Xu Hwa Xu Hsu Sheng Cheng Han-Hsiang Chan Robert Y. L. Wang MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factors Virology Journal Enterovirus A71 microRNA-876-5p CREB5 Antiviral protein |
author_facet |
Peng Xu Hwa Xu Hsu Sheng Cheng Han-Hsiang Chan Robert Y. L. Wang |
author_sort |
Peng Xu |
title |
MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factors |
title_short |
MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factors |
title_full |
MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factors |
title_fullStr |
MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factors |
title_full_unstemmed |
MicroRNA 876-5p modulates EV-A71 replication through downregulation of host antiviral factors |
title_sort |
microrna 876-5p modulates ev-a71 replication through downregulation of host antiviral factors |
publisher |
BMC |
series |
Virology Journal |
issn |
1743-422X |
publishDate |
2020-02-01 |
description |
Abstract Background Human enterovirus 71 (EV-A71) is a non-enveloped virus that has a single stranded positive sense RNA genome. In a previous study, we showed that miR-876-5p upregulation was observed in the serum of patients with severe EV-A71 infection. Micro-876-5p (miR-876-5p) is a circulating miRNA that can be identified to modulate EV-A71 infections through both in vitro and in vivo studies. However, the regulatory mechanisms that involve miR-876-5p in the EV-A71 infection cycle remain unclear. Methods We demonstrated that miR-876-5p facilitated EV-A71 replication and expression by overexpression and knocking-down of miR-876-5p through the transfection of miR-876-5p plasmid and miR-876-5p inhibitor. Although miR-876-5p suppressed CREB5 expression, luciferase reporter assay confirmed this. We also evaluated the role of miR-876-5p in the EV-A71 infection cycle by CREB5 mediated by transfection with an anti-miR-876-5P inhibitor or in combination with an si-CREB5 plasmid. Results MicroR-876-5p was upregulated in EV-A71-infected neuroblastoma cells. Overexpression of miR-876-5p or knockdown of cyclic-AMP responsive element binding protein 5 (CREB5) promoted EV-A71 replication. The downregulation of miR-876-5p inhibited the accumulation of viral RNA and the production of viral proteins. Interestingly, CREB5 overexpression also suppressed EV-A71 replication. Our in vitro studies reveal that miR-876-5p directly targets CREB5. Finally, downregulation of CREB5 protein abated the inhibitory effect of anti-miR-876-5p and induced inhibitory effect of EV-A71 replication. Conclusions Our results suggest that intracellular miR-876-5p promotes EV-A71 replication indirectly by targeting the host CREB5 protein. |
topic |
Enterovirus A71 microRNA-876-5p CREB5 Antiviral protein |
url |
https://doi.org/10.1186/s12985-020-1284-8 |
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