Roth, Annika
ORCID: 0000-0002-3376-0968, Lütke, Steffen
ORCID: 0000-0001-6924-7990, Mörgelin, Matthias, Meinberger, Denise
ORCID: 0000-0002-7786-6000, Hermes, Gabriele, Sengle, Gerhard
ORCID: 0000-0003-3932-1242, Koch, Manuel
ORCID: 0000-0002-2962-7814, Drexelius, Marco
ORCID: 0000-0002-5813-2116, Gebauer, Jan
ORCID: 0000-0002-3989-4748, Neundorf, Ines
ORCID: 0000-0001-6450-3991, Elezagic, Dzemal
ORCID: 0000-0003-1041-8470, Paulsson, Mats
ORCID: 0000-0002-6846-857X, Streichert, Thomas
ORCID: 0000-0002-6588-720X and Klatt, Andreas R.
ORCID: 0000-0002-8517-7512
(2025).
Vitamin D-inducible antimicrobial peptide LL-37 binds SARS-CoV-2 Spike and accessory proteins ORF7a and ORF8.
Frontiers in Cellular and Infection Microbiology, 15.
pp. 1-13.
Frontiers.
ISSN 2235-2988
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fcimb-15-1671738.pdf Bereitstellung unter der CC-Lizenz: Creative Commons Attribution. Download (10MB) |
Abstract
[Artikel-Nr. 1671738] Background: The role of vitamin D in Coronavirus Disease 2019 (COVID-19) outcomes remains debated, but emerging evidence suggests it may enhance recovery by strengthening immune responses. Vitamin D upregulates LL-37, an antimicrobial peptide with broad antiviral activity, including potential benefits against SARS-CoV-2. LL-37’s interactions with viral proteins, however, remain incompletely understood. Methods: We investigated LL-37’s interactions with the SARS-CoV-2 Spike glycoprotein and the accessory proteins ORF7a and ORF8 using surface plasmon resonance and negative-stain electron microscopy. These approaches were employed to assess LL-37’s binding capabilities and potential impact on viral infectivity. Results: LL-37 bound multiple domains of the Spike protein and inhibited its interaction with the human angiotensin-converting enzyme 2 (hACE2) receptor in vitro . Up to seven LL-37 molecules were observed surrounding Spike, forming a halo-like structure that may block receptor engagement. LL-37 also bound to ORF7a and ORF8, potentially impairing their ability to disrupt host cell processes. Notably, LL-37’s interaction with ORF7a may prevent degradation of SNAP29, restoring autophagy and promoting viral clearance. Conclusions: LL-37 disrupts key viral-host interactions by binding to Spike, ORF7a, and ORF8, thereby reducing SARS-CoV-2 infectivity. These findings highlight LL-37’s potential as a therapeutic agent in COVID-19 and provide mechanistic insight into its antiviral actions.
| Item Type: | Article |
| Creators: | Creators Email ORCID ORCID Put Code Mörgelin, Matthias UNSPECIFIED UNSPECIFIED UNSPECIFIED Hermes, Gabriele UNSPECIFIED UNSPECIFIED UNSPECIFIED |
| URN: | urn:nbn:de:hbz:38-798830 |
| Identification Number: | 10.3389/fcimb.2025.1671738 |
| Journal or Publication Title: | Frontiers in Cellular and Infection Microbiology |
| Volume: | 15 |
| Page Range: | pp. 1-13 |
| Number of Pages: | 13 |
| Date: | 23 September 2025 |
| Publisher: | Frontiers |
| ISSN: | 2235-2988 |
| Language: | English |
| Faculty: | Central Institutions / Interdisciplinary Research Centers Faculty of Mathematics and Natural Sciences Faculty of Medicine |
| Divisions: | CECAD - Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases Faculty of Mathematics and Natural Sciences > Department of Chemistry > Institute of Biochemistry Faculty of Medicine > Biochemie > Zentrum für Biochemie Faculty of Medicine > Kinder- und Jugendmedizin > Klinik und Poliklinik für Kinder- und Jugendmedizin Faculty of Medicine > Klinische Chemie > Institut für Klinische Chemie Faculty of Medicine > Orthopädie > Klinik und Poliklinik für Orthopädie und Unfallchirurgie Faculty of Medicine > Zahn-, Mund- und Kieferheilkunde > Institut für experimentelle Zahnmedizin und orale muskuloskeletale Biologie Zentrum für Molekulare Medizin |
| Subjects: | Chemistry and allied sciences Life sciences Medical sciences Medicine |
| Uncontrolled Keywords: | Keywords Language SARS-CoV-2 ; COVID-19 ; Spike ; ORF7a ; ORF8 ; LL-37 ; surface plasmon resonance ; vitamin D English |
| ['eprint_fieldname_oa_funders' not defined]: | Publikationsfonds UzK |
| Refereed: | Yes |
| URI: | http://kups.ub.uni-koeln.de/id/eprint/79883 |
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https://orcid.org/0000-0002-3376-0968