cGAS-STING Signaling Regulates Initial Innate Control of Cytomegalovirus Infection
Several innate sensing pathways contribute to the control of early cytomegalovirus (CMV) infection, leading to a multiphasic type I interferon (IFN-I) response that limits viral replication and promotes host defenses. Toll-like receptor (TLR)-dependent pathways induce IFN-I production in CMV-infecte...
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description | Several innate sensing pathways contribute to the control of early cytomegalovirus (CMV) infection, leading to a multiphasic type I interferon (IFN-I) response that limits viral replication and promotes host defenses. Toll-like receptor (TLR)-dependent pathways induce IFN-I production in CMV-infected plasmacytoid dendritic cells; however, the initial burst of IFN-I that occurs within the first few hours in vivo is TLR independent and emanates from stromal cells. Here we show that primary human endothelial cells mount robust IFN-I responses to human CMV that are dependent upon cyclic GMP-AMP synthase (cGAS), STING, and interferon regulatory factor 3 (IRF3) signaling. Disruption of STING expression in endothelial cells by clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 revealed that it is essential for the induction of IFN-I and restriction of CMV replication. Consistently, STING was necessary to mount the first phase of IFN-I production and curb CMV replication in infected mice. Thus, DNA sensing through STING is critical for primary detection of both human and mouse CMV in nonhematopoietic cells and drives the initial wave of IFN-I that is key for controlling early viral replication
.
Cytomegalovirus (CMV) is one of the most common viral pathogens, with the majority of people contracting the virus in their lifetime. Although acute infection is mostly asymptomatic in healthy persons, significant pathology is observed in immunocompromised individuals, and chronic CMV infection may exacerbate a myriad of inflammatory conditions. Here we show that primary human endothelial cells mount robust IFN-I responses against CMV via a cGAS/STING/IRF3 pathway. Disruption of STING expression by CRISPRs revealed an essential role in eliciting IFN-I responses and restricting CMV replication. Consistently, in mice, STING is necessary for the first phase of IFN-I production that limits early CMV replication. Our results demonstrate a pivotal role for the cGAS-STING pathway in the initial detection of CMV infection. |
doi_str_mv | 10.1128/JVI.01040-16 |
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.
Cytomegalovirus (CMV) is one of the most common viral pathogens, with the majority of people contracting the virus in their lifetime. Although acute infection is mostly asymptomatic in healthy persons, significant pathology is observed in immunocompromised individuals, and chronic CMV infection may exacerbate a myriad of inflammatory conditions. Here we show that primary human endothelial cells mount robust IFN-I responses against CMV via a cGAS/STING/IRF3 pathway. Disruption of STING expression by CRISPRs revealed an essential role in eliciting IFN-I responses and restricting CMV replication. Consistently, in mice, STING is necessary for the first phase of IFN-I production that limits early CMV replication. Our results demonstrate a pivotal role for the cGAS-STING pathway in the initial detection of CMV infection.</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/JVI.01040-16</identifier><identifier>PMID: 27334590</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animals ; Cellular Response to Infection ; Cytomegalovirus ; Cytomegalovirus Infections - immunology ; Disease Models, Animal ; Endothelial Cells - immunology ; Endothelial Cells - virology ; Human cytomegalovirus ; Human Umbilical Vein Endothelial Cells ; Humans ; Immunity, Innate ; Interferon Regulatory Factor-3 - metabolism ; Interferon Type I - metabolism ; Membrane Proteins - metabolism ; Mice, Inbred C57BL ; Murine cytomegalovirus ; Nucleotidyltransferases - metabolism ; Signal Transduction</subject><ispartof>Journal of virology, 2016-09, Vol.90 (17), p.7789-7797</ispartof><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved. 2016 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-39d6a4a16eff0d5aceee2bea3e38ffbe549381a8e03141b0a6e3a7410fef37b53</citedby><cites>FETCH-LOGICAL-c460t-39d6a4a16eff0d5aceee2bea3e38ffbe549381a8e03141b0a6e3a7410fef37b53</cites><orcidid>0000-0003-3876-6741</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988162/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988162/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27334590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lio, Chan-Wang J</creatorcontrib><creatorcontrib>McDonald, Bryan</creatorcontrib><creatorcontrib>Takahashi, Mariko</creatorcontrib><creatorcontrib>Dhanwani, Rekha</creatorcontrib><creatorcontrib>Sharma, Nikita</creatorcontrib><creatorcontrib>Huang, Jenny</creatorcontrib><creatorcontrib>Pham, Elise</creatorcontrib><creatorcontrib>Benedict, Chris A</creatorcontrib><creatorcontrib>Sharma, Sonia</creatorcontrib><title>cGAS-STING Signaling Regulates Initial Innate Control of Cytomegalovirus Infection</title><title>Journal of virology</title><addtitle>J Virol</addtitle><description>Several innate sensing pathways contribute to the control of early cytomegalovirus (CMV) infection, leading to a multiphasic type I interferon (IFN-I) response that limits viral replication and promotes host defenses. Toll-like receptor (TLR)-dependent pathways induce IFN-I production in CMV-infected plasmacytoid dendritic cells; however, the initial burst of IFN-I that occurs within the first few hours in vivo is TLR independent and emanates from stromal cells. Here we show that primary human endothelial cells mount robust IFN-I responses to human CMV that are dependent upon cyclic GMP-AMP synthase (cGAS), STING, and interferon regulatory factor 3 (IRF3) signaling. Disruption of STING expression in endothelial cells by clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 revealed that it is essential for the induction of IFN-I and restriction of CMV replication. Consistently, STING was necessary to mount the first phase of IFN-I production and curb CMV replication in infected mice. Thus, DNA sensing through STING is critical for primary detection of both human and mouse CMV in nonhematopoietic cells and drives the initial wave of IFN-I that is key for controlling early viral replication
.
Cytomegalovirus (CMV) is one of the most common viral pathogens, with the majority of people contracting the virus in their lifetime. Although acute infection is mostly asymptomatic in healthy persons, significant pathology is observed in immunocompromised individuals, and chronic CMV infection may exacerbate a myriad of inflammatory conditions. Here we show that primary human endothelial cells mount robust IFN-I responses against CMV via a cGAS/STING/IRF3 pathway. Disruption of STING expression by CRISPRs revealed an essential role in eliciting IFN-I responses and restricting CMV replication. Consistently, in mice, STING is necessary for the first phase of IFN-I production that limits early CMV replication. Our results demonstrate a pivotal role for the cGAS-STING pathway in the initial detection of CMV infection.</description><subject>Animals</subject><subject>Cellular Response to Infection</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus Infections - immunology</subject><subject>Disease Models, Animal</subject><subject>Endothelial Cells - immunology</subject><subject>Endothelial Cells - virology</subject><subject>Human cytomegalovirus</subject><subject>Human Umbilical Vein Endothelial Cells</subject><subject>Humans</subject><subject>Immunity, Innate</subject><subject>Interferon Regulatory Factor-3 - metabolism</subject><subject>Interferon Type I - metabolism</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice, Inbred C57BL</subject><subject>Murine cytomegalovirus</subject><subject>Nucleotidyltransferases - metabolism</subject><subject>Signal Transduction</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1LJDEQhoOs6Kx687z0cQ-2VnXSmeQiyODOjoiCo-ItpHsqvZFMRzvdgv9-20_c256Koh5e3uJhbB_hELFQR2e3i0NAEJCj3GATBK3yskTxjU0AiiIvubrbZt9TugdAIaTYYtvFlHNRapiwq3p-ssyX14uLebb0TWuDb5vsipoh2J5Stmh9720YZzvu2Sy2fRdDFl02e-7jmhob4pPvhhfSUd372O6yTWdDor33ucNufp1ez37n55fzxezkPK-FhD7neiWtsCjJOViVtiaioiLLiSvnKiqF5gqtIuAosAIridupQHDk-LQq-Q47fst9GKo1rWoaq9lgHjq_tt2zidabfy-t_2Oa-GSEVgplMQb8fA_o4uNAqTdrn2oKwbYUh2RQFVONsuT6P9DRhdYg1YgevKF1F1PqyH02QjAvxsxozLwaMyhH_MfXLz7hD0X8L8FvkmU</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Lio, Chan-Wang J</creator><creator>McDonald, Bryan</creator><creator>Takahashi, Mariko</creator><creator>Dhanwani, Rekha</creator><creator>Sharma, Nikita</creator><creator>Huang, Jenny</creator><creator>Pham, Elise</creator><creator>Benedict, Chris A</creator><creator>Sharma, Sonia</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U9</scope><scope>H94</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3876-6741</orcidid></search><sort><creationdate>20160901</creationdate><title>cGAS-STING Signaling Regulates Initial Innate Control of Cytomegalovirus Infection</title><author>Lio, Chan-Wang J ; McDonald, Bryan ; Takahashi, Mariko ; Dhanwani, Rekha ; Sharma, Nikita ; Huang, Jenny ; Pham, Elise ; Benedict, Chris A ; Sharma, Sonia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-39d6a4a16eff0d5aceee2bea3e38ffbe549381a8e03141b0a6e3a7410fef37b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Cellular Response to Infection</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus Infections - immunology</topic><topic>Disease Models, Animal</topic><topic>Endothelial Cells - immunology</topic><topic>Endothelial Cells - virology</topic><topic>Human cytomegalovirus</topic><topic>Human Umbilical Vein Endothelial Cells</topic><topic>Humans</topic><topic>Immunity, Innate</topic><topic>Interferon Regulatory Factor-3 - metabolism</topic><topic>Interferon Type I - metabolism</topic><topic>Membrane Proteins - metabolism</topic><topic>Mice, Inbred C57BL</topic><topic>Murine cytomegalovirus</topic><topic>Nucleotidyltransferases - metabolism</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lio, Chan-Wang J</creatorcontrib><creatorcontrib>McDonald, Bryan</creatorcontrib><creatorcontrib>Takahashi, Mariko</creatorcontrib><creatorcontrib>Dhanwani, Rekha</creatorcontrib><creatorcontrib>Sharma, Nikita</creatorcontrib><creatorcontrib>Huang, Jenny</creatorcontrib><creatorcontrib>Pham, Elise</creatorcontrib><creatorcontrib>Benedict, Chris A</creatorcontrib><creatorcontrib>Sharma, Sonia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lio, Chan-Wang J</au><au>McDonald, Bryan</au><au>Takahashi, Mariko</au><au>Dhanwani, Rekha</au><au>Sharma, Nikita</au><au>Huang, Jenny</au><au>Pham, Elise</au><au>Benedict, Chris A</au><au>Sharma, Sonia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>cGAS-STING Signaling Regulates Initial Innate Control of Cytomegalovirus Infection</atitle><jtitle>Journal of virology</jtitle><addtitle>J Virol</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>90</volume><issue>17</issue><spage>7789</spage><epage>7797</epage><pages>7789-7797</pages><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>Several innate sensing pathways contribute to the control of early cytomegalovirus (CMV) infection, leading to a multiphasic type I interferon (IFN-I) response that limits viral replication and promotes host defenses. Toll-like receptor (TLR)-dependent pathways induce IFN-I production in CMV-infected plasmacytoid dendritic cells; however, the initial burst of IFN-I that occurs within the first few hours in vivo is TLR independent and emanates from stromal cells. Here we show that primary human endothelial cells mount robust IFN-I responses to human CMV that are dependent upon cyclic GMP-AMP synthase (cGAS), STING, and interferon regulatory factor 3 (IRF3) signaling. Disruption of STING expression in endothelial cells by clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 revealed that it is essential for the induction of IFN-I and restriction of CMV replication. Consistently, STING was necessary to mount the first phase of IFN-I production and curb CMV replication in infected mice. Thus, DNA sensing through STING is critical for primary detection of both human and mouse CMV in nonhematopoietic cells and drives the initial wave of IFN-I that is key for controlling early viral replication
.
Cytomegalovirus (CMV) is one of the most common viral pathogens, with the majority of people contracting the virus in their lifetime. Although acute infection is mostly asymptomatic in healthy persons, significant pathology is observed in immunocompromised individuals, and chronic CMV infection may exacerbate a myriad of inflammatory conditions. Here we show that primary human endothelial cells mount robust IFN-I responses against CMV via a cGAS/STING/IRF3 pathway. Disruption of STING expression by CRISPRs revealed an essential role in eliciting IFN-I responses and restricting CMV replication. Consistently, in mice, STING is necessary for the first phase of IFN-I production that limits early CMV replication. Our results demonstrate a pivotal role for the cGAS-STING pathway in the initial detection of CMV infection.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>27334590</pmid><doi>10.1128/JVI.01040-16</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3876-6741</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cellular Response to Infection Cytomegalovirus Cytomegalovirus Infections - immunology Disease Models, Animal Endothelial Cells - immunology Endothelial Cells - virology Human cytomegalovirus Human Umbilical Vein Endothelial Cells Humans Immunity, Innate Interferon Regulatory Factor-3 - metabolism Interferon Type I - metabolism Membrane Proteins - metabolism Mice, Inbred C57BL Murine cytomegalovirus Nucleotidyltransferases - metabolism Signal Transduction |
title | cGAS-STING Signaling Regulates Initial Innate Control of Cytomegalovirus Infection |
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