Honeysuckle-encoded atypical microRNA2911 directly targets influenza A viruses
Influenza A viruses (IAVs), particularly H1N1, H5N1 and H7N9, pose a substantial threat to public health worldwide. Here, we report that MIR2911, a honeysuckle (HS)-encoded atypical microRNA, directly targets IAVs with a broad spectrum. MIR2911 is highly stable in HS decoction, and continuous drinki...
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creator | Zhou, Zhen Li, Xihan Liu, Jinxiong Dong, Lei Chen, Qun Liu, Jialing Kong, Huihui Zhang, Qianyi Qi, Xian Hou, Dongxia Zhang, Lin Zhang, Guoquan Liu, Yuchen Zhang, Yujing Li, Jing Wang, Jin Chen, Xi Wang, Hua Zhang, Junfeng Chen, Hualan Zen, Ke Zhang, Chen-Yu |
description | Influenza A viruses (IAVs), particularly H1N1, H5N1 and H7N9, pose a substantial threat to public health worldwide. Here, we report that MIR2911, a honeysuckle (HS)-encoded atypical microRNA, directly targets IAVs with a broad spectrum. MIR2911 is highly stable in HS decoction, and continuous drinking or gavage feeding of HS decoction leads to a significant elevation of the MIR2911 level in mouse peripheral blood and lung. Bioinformatics prediction and a luciferase reporter assay showed that MIR2911 could target various IAVs, including H1N1, H5N1 and H7N9. Synthetic MIR2911 significantly inhibited H1N1-encoded
PB2
and
NS1
protein expression, but did not affect mutants in which the MIR2911-binding nucleotide sequences were altered. Synthetic MIR2911, extracted RNA from HS decoction and HS decoction all significantly inhibited H1N1 viral replication and rescued viral infection-induced mouse weight loss, but did not affect infection with a mutant virus in which the MIR2911-binding nucleotide sequences of
PB2
and
NS1
were altered. Importantly, the inhibitory effect of HS decoction on viral replication was abolished by an anti-MIR2911 antagomir, indicating that the physiological concentration of MIR2911 in HS decoction could directly and sufficiently suppress H1N1 viral replication. MIR2911 also inhibited H5N1 and H7N9 viral replication
in vitro
and
in vivo
. Strikingly, administration of MIR2911 or HS decoction dramatically reduced mouse mortality caused by H5N1 infection. Our results demonstrate that MIR2911 is the first active component identified in Traditional Chinese Medicine to directly target various IAVs and may represent a novel type of natural product that effectively suppresses viral infection. |
doi_str_mv | 10.1038/cr.2014.130 |
format | Article |
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PB2
and
NS1
protein expression, but did not affect mutants in which the MIR2911-binding nucleotide sequences were altered. Synthetic MIR2911, extracted RNA from HS decoction and HS decoction all significantly inhibited H1N1 viral replication and rescued viral infection-induced mouse weight loss, but did not affect infection with a mutant virus in which the MIR2911-binding nucleotide sequences of
PB2
and
NS1
were altered. Importantly, the inhibitory effect of HS decoction on viral replication was abolished by an anti-MIR2911 antagomir, indicating that the physiological concentration of MIR2911 in HS decoction could directly and sufficiently suppress H1N1 viral replication. MIR2911 also inhibited H5N1 and H7N9 viral replication
in vitro
and
in vivo
. Strikingly, administration of MIR2911 or HS decoction dramatically reduced mouse mortality caused by H5N1 infection. Our results demonstrate that MIR2911 is the first active component identified in Traditional Chinese Medicine to directly target various IAVs and may represent a novel type of natural product that effectively suppresses viral infection.</description><identifier>ISSN: 1001-0602</identifier><identifier>EISSN: 1748-7838</identifier><identifier>DOI: 10.1038/cr.2014.130</identifier><identifier>PMID: 25287280</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/337/384/331 ; 692/699/255/1578 ; Animals ; Bioinformatics ; Biomedical and Life Sciences ; Cell Biology ; Gene Expression Regulation, Viral ; HEK293 Cells ; Herbal medicine ; Humans ; Influenza A virus - genetics ; Influenza A virus - physiology ; Influenza A Virus, H1N1 Subtype - genetics ; Influenza A Virus, H1N1 Subtype - physiology ; Influenza A Virus, H5N1 Subtype - genetics ; Influenza A Virus, H5N1 Subtype - physiology ; Influenza A Virus, H7N9 Subtype - genetics ; Influenza A Virus, H7N9 Subtype - physiology ; Influenza, Human - therapy ; Influenza, Human - virology ; Life Sciences ; Lonicera - genetics ; Mice ; MicroRNAs - genetics ; MicroRNAs - pharmacokinetics ; MicroRNAs - therapeutic use ; Mutation ; Original ; original-article ; Orthomyxoviridae Infections - therapy ; Orthomyxoviridae Infections - virology ; Public health ; RNA, Plant - genetics ; RNA, Plant - pharmacokinetics ; RNA, Plant - therapeutic use ; Virus Replication</subject><ispartof>Cell research, 2015-01, Vol.25 (1), p.39-49</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Jan 2015</rights><rights>Copyright © 2015 Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences 2015 Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-d47e5722d932d3b21af4140c7ebcdc545917b851cbf291c69fc9a1dfdc250aa63</citedby><cites>FETCH-LOGICAL-c549t-d47e5722d932d3b21af4140c7ebcdc545917b851cbf291c69fc9a1dfdc250aa63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650580/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650580/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25287280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Zhen</creatorcontrib><creatorcontrib>Li, Xihan</creatorcontrib><creatorcontrib>Liu, Jinxiong</creatorcontrib><creatorcontrib>Dong, Lei</creatorcontrib><creatorcontrib>Chen, Qun</creatorcontrib><creatorcontrib>Liu, Jialing</creatorcontrib><creatorcontrib>Kong, Huihui</creatorcontrib><creatorcontrib>Zhang, Qianyi</creatorcontrib><creatorcontrib>Qi, Xian</creatorcontrib><creatorcontrib>Hou, Dongxia</creatorcontrib><creatorcontrib>Zhang, Lin</creatorcontrib><creatorcontrib>Zhang, Guoquan</creatorcontrib><creatorcontrib>Liu, Yuchen</creatorcontrib><creatorcontrib>Zhang, Yujing</creatorcontrib><creatorcontrib>Li, Jing</creatorcontrib><creatorcontrib>Wang, Jin</creatorcontrib><creatorcontrib>Chen, Xi</creatorcontrib><creatorcontrib>Wang, Hua</creatorcontrib><creatorcontrib>Zhang, Junfeng</creatorcontrib><creatorcontrib>Chen, Hualan</creatorcontrib><creatorcontrib>Zen, Ke</creatorcontrib><creatorcontrib>Zhang, Chen-Yu</creatorcontrib><title>Honeysuckle-encoded atypical microRNA2911 directly targets influenza A viruses</title><title>Cell research</title><addtitle>Cell Res</addtitle><addtitle>Cell Res</addtitle><description>Influenza A viruses (IAVs), particularly H1N1, H5N1 and H7N9, pose a substantial threat to public health worldwide. Here, we report that MIR2911, a honeysuckle (HS)-encoded atypical microRNA, directly targets IAVs with a broad spectrum. MIR2911 is highly stable in HS decoction, and continuous drinking or gavage feeding of HS decoction leads to a significant elevation of the MIR2911 level in mouse peripheral blood and lung. Bioinformatics prediction and a luciferase reporter assay showed that MIR2911 could target various IAVs, including H1N1, H5N1 and H7N9. Synthetic MIR2911 significantly inhibited H1N1-encoded
PB2
and
NS1
protein expression, but did not affect mutants in which the MIR2911-binding nucleotide sequences were altered. Synthetic MIR2911, extracted RNA from HS decoction and HS decoction all significantly inhibited H1N1 viral replication and rescued viral infection-induced mouse weight loss, but did not affect infection with a mutant virus in which the MIR2911-binding nucleotide sequences of
PB2
and
NS1
were altered. Importantly, the inhibitory effect of HS decoction on viral replication was abolished by an anti-MIR2911 antagomir, indicating that the physiological concentration of MIR2911 in HS decoction could directly and sufficiently suppress H1N1 viral replication. MIR2911 also inhibited H5N1 and H7N9 viral replication
in vitro
and
in vivo
. Strikingly, administration of MIR2911 or HS decoction dramatically reduced mouse mortality caused by H5N1 infection. Our results demonstrate that MIR2911 is the first active component identified in Traditional Chinese Medicine to directly target various IAVs and may represent a novel type of natural product that effectively suppresses viral infection.</description><subject>631/337/384/331</subject><subject>692/699/255/1578</subject><subject>Animals</subject><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Biology</subject><subject>Gene Expression Regulation, Viral</subject><subject>HEK293 Cells</subject><subject>Herbal medicine</subject><subject>Humans</subject><subject>Influenza A virus - genetics</subject><subject>Influenza A virus - physiology</subject><subject>Influenza A Virus, H1N1 Subtype - genetics</subject><subject>Influenza A Virus, H1N1 Subtype - physiology</subject><subject>Influenza A Virus, H5N1 Subtype - genetics</subject><subject>Influenza A Virus, H5N1 Subtype - physiology</subject><subject>Influenza A Virus, H7N9 Subtype - genetics</subject><subject>Influenza A Virus, H7N9 Subtype - physiology</subject><subject>Influenza, Human - therapy</subject><subject>Influenza, Human - virology</subject><subject>Life Sciences</subject><subject>Lonicera - genetics</subject><subject>Mice</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - pharmacokinetics</subject><subject>MicroRNAs - therapeutic use</subject><subject>Mutation</subject><subject>Original</subject><subject>original-article</subject><subject>Orthomyxoviridae Infections - therapy</subject><subject>Orthomyxoviridae Infections - virology</subject><subject>Public health</subject><subject>RNA, Plant - genetics</subject><subject>RNA, Plant - pharmacokinetics</subject><subject>RNA, Plant - therapeutic use</subject><subject>Virus 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Jialing</creator><creator>Kong, Huihui</creator><creator>Zhang, Qianyi</creator><creator>Qi, Xian</creator><creator>Hou, Dongxia</creator><creator>Zhang, Lin</creator><creator>Zhang, Guoquan</creator><creator>Liu, Yuchen</creator><creator>Zhang, Yujing</creator><creator>Li, Jing</creator><creator>Wang, Jin</creator><creator>Chen, Xi</creator><creator>Wang, Hua</creator><creator>Zhang, Junfeng</creator><creator>Chen, Hualan</creator><creator>Zen, Ke</creator><creator>Zhang, Chen-Yu</creator><general>Nature Publishing Group UK</general><general>Nature Publishing 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atypical microRNA2911 directly targets influenza A viruses</title><author>Zhou, Zhen ; Li, Xihan ; Liu, Jinxiong ; Dong, Lei ; Chen, Qun ; Liu, Jialing ; Kong, Huihui ; Zhang, Qianyi ; Qi, Xian ; Hou, Dongxia ; Zhang, Lin ; Zhang, Guoquan ; Liu, Yuchen ; Zhang, Yujing ; Li, Jing ; Wang, Jin ; Chen, Xi ; Wang, Hua ; Zhang, Junfeng ; Chen, Hualan ; Zen, Ke ; Zhang, Chen-Yu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-d47e5722d932d3b21af4140c7ebcdc545917b851cbf291c69fc9a1dfdc250aa63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>631/337/384/331</topic><topic>692/699/255/1578</topic><topic>Animals</topic><topic>Bioinformatics</topic><topic>Biomedical and Life Sciences</topic><topic>Cell Biology</topic><topic>Gene Expression Regulation, Viral</topic><topic>HEK293 Cells</topic><topic>Herbal medicine</topic><topic>Humans</topic><topic>Influenza A virus - genetics</topic><topic>Influenza A virus - physiology</topic><topic>Influenza A Virus, H1N1 Subtype - genetics</topic><topic>Influenza A Virus, H1N1 Subtype - physiology</topic><topic>Influenza A Virus, H5N1 Subtype - genetics</topic><topic>Influenza A Virus, H5N1 Subtype - physiology</topic><topic>Influenza A Virus, H7N9 Subtype - genetics</topic><topic>Influenza A Virus, H7N9 Subtype - physiology</topic><topic>Influenza, Human - therapy</topic><topic>Influenza, Human - virology</topic><topic>Life Sciences</topic><topic>Lonicera - genetics</topic><topic>Mice</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - pharmacokinetics</topic><topic>MicroRNAs - therapeutic use</topic><topic>Mutation</topic><topic>Original</topic><topic>original-article</topic><topic>Orthomyxoviridae Infections - therapy</topic><topic>Orthomyxoviridae Infections - virology</topic><topic>Public health</topic><topic>RNA, Plant - genetics</topic><topic>RNA, Plant - pharmacokinetics</topic><topic>RNA, Plant 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Jing</au><au>Wang, Jin</au><au>Chen, Xi</au><au>Wang, Hua</au><au>Zhang, Junfeng</au><au>Chen, Hualan</au><au>Zen, Ke</au><au>Zhang, Chen-Yu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Honeysuckle-encoded atypical microRNA2911 directly targets influenza A viruses</atitle><jtitle>Cell research</jtitle><stitle>Cell Res</stitle><addtitle>Cell Res</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>25</volume><issue>1</issue><spage>39</spage><epage>49</epage><pages>39-49</pages><issn>1001-0602</issn><eissn>1748-7838</eissn><abstract>Influenza A viruses (IAVs), particularly H1N1, H5N1 and H7N9, pose a substantial threat to public health worldwide. Here, we report that MIR2911, a honeysuckle (HS)-encoded atypical microRNA, directly targets IAVs with a broad spectrum. MIR2911 is highly stable in HS decoction, and continuous drinking or gavage feeding of HS decoction leads to a significant elevation of the MIR2911 level in mouse peripheral blood and lung. Bioinformatics prediction and a luciferase reporter assay showed that MIR2911 could target various IAVs, including H1N1, H5N1 and H7N9. Synthetic MIR2911 significantly inhibited H1N1-encoded
PB2
and
NS1
protein expression, but did not affect mutants in which the MIR2911-binding nucleotide sequences were altered. Synthetic MIR2911, extracted RNA from HS decoction and HS decoction all significantly inhibited H1N1 viral replication and rescued viral infection-induced mouse weight loss, but did not affect infection with a mutant virus in which the MIR2911-binding nucleotide sequences of
PB2
and
NS1
were altered. Importantly, the inhibitory effect of HS decoction on viral replication was abolished by an anti-MIR2911 antagomir, indicating that the physiological concentration of MIR2911 in HS decoction could directly and sufficiently suppress H1N1 viral replication. MIR2911 also inhibited H5N1 and H7N9 viral replication
in vitro
and
in vivo
. Strikingly, administration of MIR2911 or HS decoction dramatically reduced mouse mortality caused by H5N1 infection. Our results demonstrate that MIR2911 is the first active component identified in Traditional Chinese Medicine to directly target various IAVs and may represent a novel type of natural product that effectively suppresses viral infection.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25287280</pmid><doi>10.1038/cr.2014.130</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Springer Nature - Complete Springer Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | 631/337/384/331 692/699/255/1578 Animals Bioinformatics Biomedical and Life Sciences Cell Biology Gene Expression Regulation, Viral HEK293 Cells Herbal medicine Humans Influenza A virus - genetics Influenza A virus - physiology Influenza A Virus, H1N1 Subtype - genetics Influenza A Virus, H1N1 Subtype - physiology Influenza A Virus, H5N1 Subtype - genetics Influenza A Virus, H5N1 Subtype - physiology Influenza A Virus, H7N9 Subtype - genetics Influenza A Virus, H7N9 Subtype - physiology Influenza, Human - therapy Influenza, Human - virology Life Sciences Lonicera - genetics Mice MicroRNAs - genetics MicroRNAs - pharmacokinetics MicroRNAs - therapeutic use Mutation Original original-article Orthomyxoviridae Infections - therapy Orthomyxoviridae Infections - virology Public health RNA, Plant - genetics RNA, Plant - pharmacokinetics RNA, Plant - therapeutic use Virus Replication |
title | Honeysuckle-encoded atypical microRNA2911 directly targets influenza A viruses |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T19%3A55%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Honeysuckle-encoded%20atypical%20microRNA2911%20directly%20targets%20influenza%20A%20viruses&rft.jtitle=Cell%20research&rft.au=Zhou,%20Zhen&rft.date=2015-01-01&rft.volume=25&rft.issue=1&rft.spage=39&rft.epage=49&rft.pages=39-49&rft.issn=1001-0602&rft.eissn=1748-7838&rft_id=info:doi/10.1038/cr.2014.130&rft_dat=%3Cproquest_pubme%3E3542056761%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1641425123&rft_id=info:pmid/25287280&rfr_iscdi=true |