{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:31:19Z","timestamp":1787016679188,"version":"build-2736575974"},"reference-count":61,"publisher":"American Society for Microbiology","issue":"11","license":[{"start":{"date-parts":[[2018,6,1]],"date-time":"2018-06-01T00:00:00Z","timestamp":1527811200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/100000060","name":"HHS | NIH | National Institute of Allergy and Infectious Diseases","doi-asserted-by":"publisher","award":["AI062885"],"award-info":[{"award-number":["AI062885"]}],"id":[{"id":"10.13039\/100000060","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000001","name":"National Science Foundation","doi-asserted-by":"publisher","award":["DMS-1361411"],"award-info":[{"award-number":["DMS-1361411"]}],"id":[{"id":"10.13039\/100000001","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100006108","name":"HHS | NIH | National Center for Advancing Translational Sciences","doi-asserted-by":"publisher","award":["UL1TR001439"],"award-info":[{"award-number":["UL1TR001439"]}],"id":[{"id":"10.13039\/100006108","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Virol"],"published-print":{"date-parts":[[2018,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    Lower respiratory tract infection with respiratory syncytial virus (RSV) produces profound inflammation. Despite an understanding of the role of adaptive immunity in RSV infection, the identity of the major sentinel cells initially triggering inflammation is controversial. Here we evaluate the role of nonciliated secretoglobin (\n                    <jats:italic>Scgb1a1<\/jats:italic>\n                    )-expressing bronchiolar epithelial cells in RSV infection. Mice expressing a tamoxifen (TMX)-inducible Cre recombinase-estrogen receptor fusion protein (CreERTM) knocked into the\n                    <jats:italic>Scgb1a1<\/jats:italic>\n                    locus were crossed with mice that harbor a\n                    <jats:italic>RelA<\/jats:italic>\n                    conditional allele (\n                    <jats:italic>\n                      RelA\n                      <jats:sup>fl<\/jats:sup>\n                    <\/jats:italic>\n                    ), with loxP sites flanking exons 5 to 8 of the Rel homology domain. The\n                    <jats:italic>Scgb1a1<\/jats:italic>\n                    <jats:sup>CreERTM\/+<\/jats:sup>\n                    \u00d7 RelA\n                    <jats:sup>fl\/fl<\/jats:sup>\n                    mouse is a\n                    <jats:italic>RelA<\/jats:italic>\n                    conditional knockout (RelA\n                    <jats:sup>CKO<\/jats:sup>\n                    ) of a nonciliated epithelial cell population enriched in the small bronchioles. TMX-treated RelA\n                    <jats:sup>CKO<\/jats:sup>\n                    mice have reduced pulmonary neutrophilic infiltration and impaired expression and secretion of NF-\u03baB-dependent cytokines in response to RSV. In addition, RelA\n                    <jats:sup>CKO<\/jats:sup>\n                    mice had reduced expression levels of interferon (IFN) regulatory factor 1\/7 (IRF1\/7) and retinoic acid-inducible gene I (RIG-I), components of the mucosal IFN positive-feedback loop. We demonstrate that RSV replication induces RelA to complex with bromodomain-containing protein 4 (BRD4), a cofactor required for RNA polymerase II (Pol II) phosphorylation, activating the atypical histone acetyltransferase (HAT) activity of BRD4 required for phospho-Ser2 Pol II formation, histone H3K122 acetylation, and cytokine secretion\n                    <jats:italic>in vitro<\/jats:italic>\n                    and\n                    <jats:italic>in vivo<\/jats:italic>\n                    . TMX-treated RelA\n                    <jats:sup>CKO<\/jats:sup>\n                    mice have less weight loss and reduced airway obstruction\/hyperreactivity yet similar levels of IFN-\u03b3 production despite higher levels of virus production. These data indicate that the nonciliated\n                    <jats:italic>Scgb1a1<\/jats:italic>\n                    -expressing epithelium is a major innate sensor for restricting RSV infection by mediating neutrophilic inflammation and chemokine and mucosal IFN production via the RelA-BRD4 pathway.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>IMPORTANCE<\/jats:bold>\n                    RSV infection is the most common cause of infant hospitalizations in the United States, resulting in 2.1 million children annually requiring medical attention. RSV primarily infects nasal epithelial cells, spreading distally to produce severe lower respiratory tract infections. Our study examines the role of a nonciliated respiratory epithelial cell population in RSV infection. We genetically engineered a mouse that can be selectively depleted of the NF-\u03baB\/RelA transcription factor in this subset of epithelial cells. These mice show an impaired activation of the bromodomain-containing protein 4 (BRD4) coactivator, resulting in reduced cytokine expression and neutrophilic inflammation. During the course of RSV infection, epithelial RelA-depleted mice have reduced disease scores and airway hyperreactivity yet increased levels of virus replication. We conclude that RelA-BRD4 signaling in nonciliated bronchiolar epithelial cells mediates neutrophilic airway inflammation and disease severity. This complex is an attractive target to reduce the severity of infection.\n                  <\/jats:p>","DOI":"10.1128\/jvi.00441-18","type":"journal-article","created":{"date-parts":[[2018,3,23]],"date-time":"2018-03-23T06:52:48Z","timestamp":1521787968000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":48,"title":["Central Role of the NF-\u03baB Pathway in the\n                    <i>Scgb1a1<\/i>\n                    -Expressing Epithelium in Mediating Respiratory Syncytial Virus-Induced Airway Inflammation"],"prefix":"10.1128","volume":"92","author":[{"given":"Bing","family":"Tian","sequence":"first","affiliation":[{"name":"Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA"},{"name":"Sealy Center for Molecular Medicine, University of Texas Medical Branch, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jun","family":"Yang","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA"},{"name":"Sealy Center for Molecular Medicine, University of Texas Medical Branch, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yingxin","family":"Zhao","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA"},{"name":"Sealy Center for Molecular Medicine, University of Texas Medical Branch, Galveston, Texas, USA"},{"name":"Institute for Translational Sciences, University of Texas Medical Branch, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Teodora","family":"Ivanciuc","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, University of Texas Medical Branch, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hong","family":"Sun","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maki","family":"Wakamiya","sequence":"additional","affiliation":[{"name":"Institute for Translational Sciences, University of Texas Medical Branch, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Roberto P.","family":"Garofalo","sequence":"additional","affiliation":[{"name":"Sealy Center for Molecular Medicine, University of Texas Medical Branch, Galveston, Texas, USA"},{"name":"Department of Pediatrics, University of Texas Medical Branch, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Allan R.","family":"Brasier","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, School of Medicine and Public Health, University of Wisconsin\u2014Madison, Madison, Wisconsin, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_2_2_2","volume-title":"Respiratory syncytial virus","author":"Collins PL","year":"2001","unstructured":"Collins PL, Chanock RM, Murphy RR. 2001. 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