{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,7]],"date-time":"2026-09-07T12:32:33Z","timestamp":1788784353869,"version":"build-2803163510"},"reference-count":54,"publisher":"Oxford University Press (OUP)","issue":"1","license":[{"start":{"date-parts":[[2025,7,28]],"date-time":"2025-07-28T00:00:00Z","timestamp":1753660800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"funder":[{"name":"UAB CF Research and Translation Core Center","award":["P30DK072482"],"award-info":[{"award-number":["P30DK072482"]}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["HL149944"],"award-info":[{"award-number":["HL149944"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000897","name":"Cystic Fibrosis Foundation","doi-asserted-by":"publisher","award":["Harrod19IO"],"award-info":[{"award-number":["Harrod19IO"]}],"id":[{"id":"10.13039\/100000897","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Immunologic Diseases and Basic Immunology","award":["5T32AI007051-54"],"award-info":[{"award-number":["5T32AI007051-54"]}]},{"name":"Immunologic Diseases and Basic Immunology","award":["1F31AI183758-01"],"award-info":[{"award-number":["1F31AI183758-01"]}]}],"content-domain":{"domain":["www.atsjournals.org"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,1,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Streptococcus pneumoniae (Spn) infection secondary to influenza A virus (IAV) frequently leads to an increase in morbidity and mortality of IAV. Our recent work establishes that IAV infection disrupts bacterial host defense in the lung epithelium through loss of cystic fibrosis transmembrane conductance regulator protein (CFTR) function, causing an acidification of the airway surface liquid (ASL) and subsequently increasing susceptibility to Spn. Infection with IAV and other respiratory pathogens causes a robust endoplasmic reticulum (ER) stress response. However, the role of this acute ER stress response in predisposing the airway epithelium to susceptibility to bacterial infections remains unknown. Using a primary differentiated human bronchial airway epithelial cell (HBEC) culture system, we found that both IAV-induced ER stress and ER stress alone increased susceptibility to Spn in the airway epithelium and led to a loss of CFTR activity, subsequently causing a disruption in the rheostatic properties of the ASL. Importantly, in HBECs without functional CFTR, modulation of ER stress in the presence and absence of IAV has no effect on susceptibility to Spn. Restoration of ASL pH after ER stress in HBECs with functional CFTR reduces Spn, suggesting that ER stress increases susceptibility to bacterial infection by disrupting CFTR and causing an acidification of the ASL. Here, we demonstrate a clear role for ER stress in disruption of both the airway epithelium and bacterial host defense mechanisms during respiratory viral infection.<\/jats:p>\n                  <jats:p>Clinical trial registered with www.clinicaltrials.gov (NCT04164212).<\/jats:p>","DOI":"10.1165\/rcmb.2025-0141oc","type":"journal-article","created":{"date-parts":[[2025,7,28]],"date-time":"2025-07-28T20:06:04Z","timestamp":1753733164000},"page":"40-51","update-policy":"https:\/\/doi.org\/10.1164\/crossmarkpolicies","source":"Crossref","is-referenced-by-count":4,"title":["Endoplasmic Reticulum Stress Disrupts the Airway Epithelium and Reduces Host Defense during Influenza A Virus Infection"],"prefix":"10.1093","volume":"74","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1987-3560","authenticated-orcid":false,"given":"Erin Y","family":"Earnhardt","sequence":"first","affiliation":[{"name":"Department of Anesthesiology and Perioperative 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