{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T18:03:57Z","timestamp":1785434637440,"version":"3.56.0"},"reference-count":79,"publisher":"American Society for Microbiology","issue":"5","license":[{"start":{"date-parts":[[2026,5,13]],"date-time":"2026-05-13T00:00:00Z","timestamp":1778630400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,5,13]],"date-time":"2026-05-13T00:00:00Z","timestamp":1778630400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["mBio"],"published-print":{"date-parts":[[2026,5,13]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>Human parainfluenza viruses (HPIVs) cause significant respiratory illnesses including croup and pneumonia. HPIV infection begins with fusion of viral and host cell membranes, driven by the coordinated actions of the attachment (HN) and fusion (F) glycoproteins, which together form the fusion\/entry complex. We have described fusion inhibitory peptides that are derived from the heptad repeat (HRC) domain of the F glycoprotein and have potent antiviral activity against HPIV3 and other paramyxoviruses. These peptides inhibit fusion by binding to the transiently exposed N-terminal heptad repeat (HRN) segments of the F prehairpin intermediate and preventing the six-helix bundle (6HB) formation that is required for the membrane fusion process. We report viral variants that escape inhibition by an HRC-derived \u03b1\/\u03b2-peptide of HPIV3 through an HN mutation that enhances HN\u2019s activation of F and a mutation in F\u2019s HRN domain that destabilizes the 6HB. The F HRN domain bearing the alteration shows reduced \u03b1-helicity relative to the wild-type HRN and forms an assembly with the HRC domain that is destabilized relative to the wild-type 6HB. This viral variant is not resistant to an HRC-derived \u03b1-peptide inhibitor that forms a more stable 6HB relative to the HRC-derived \u03b1\/\u03b2-peptide. The emergence of this variant suggests that improved inhibitor potency against HPIV3 could be achieved by increasing the stability of the \u03b1\/\u03b2-peptide\/HRN 6HB. The unique mutation in F that reduces sensitivity to inhibitor also compromises viral fitness in a human airway model and impairs viral infection, presumably as a result of diminished post-fusion state stability.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>IMPORTANCE<\/jats:title>\n                    <jats:p>\n                      Human parainfluenza viruses (HPIVs) are major causes of lower respiratory tract disease, including croup and pneumonia. Viral entry is initiated when the viral receptor binding protein engages its host receptor and activates the viral fusion (F) protein. The F protein then undergoes an essential refolding process, inserting into the host membrane and collapsing into a stable six-helix bundle (6HB) structure to drive membrane fusion. This step is a promising target for antiviral peptides, which can block infection by preventing the formation of the 6HB structure. Here, we examined an HPIV variant that emerged under selection pressure from such a prototype antiviral peptide. A single mutation in F destabilized the 6HB and disrupted refolding, enabling viral spread in the presence of the antiviral peptide. However, this adaptation within a highly conserved region imposed a substantial fitness cost in the airway, underscoring the critical constraints on fusion protein function during infection\n                      <jats:italic toggle=\"yes\">in vivo<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1128\/mbio.02741-25","type":"journal-article","created":{"date-parts":[[2026,4,14]],"date-time":"2026-04-14T13:00:11Z","timestamp":1776171611000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["A fusion protein\u2019s weak link: functional constraints revealed by inhibitory peptide interaction with the parainfluenza fusion 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