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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Veröffentlicht in:Journal of virology 2016-09, Vol.90 (17), p.7789-7797
Hauptverfasser: Lio, Chan-Wang J, McDonald, Bryan, Takahashi, Mariko, Dhanwani, Rekha, Sharma, Nikita, Huang, Jenny, Pham, Elise, Benedict, Chris A, Sharma, Sonia
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container_end_page 7797
container_issue 17
container_start_page 7789
container_title Journal of virology
container_volume 90
creator Lio, Chan-Wang J
McDonald, Bryan
Takahashi, Mariko
Dhanwani, Rekha
Sharma, Nikita
Huang, Jenny
Pham, Elise
Benedict, Chris A
Sharma, Sonia
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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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. 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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. 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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
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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