Repurposing sunscreen as an antibiotic: zinc-activated avobenzone inhibits methicillin-resistant Staphylococcus aureus

• Published in: Metallomics 2023-09, Vol.15 (9)
• Main Authors: Andrews, Rachel M, Bollar, Gretchen E, Giattina, A Sophia, Dalecki, Alex G, Wallace Jr, John R, Frantz, Leah, Eschliman, Kayla, Covarrubias-Zambrano, Obdulia, Keith, Johnathan D, Duverger, Alexandra, Wagner, Frederic, Wolschendorf, Frank, Bossmann, Stefan H, Birket, Susan E, Kutsch, Olaf
• Format: Article
• Language: English
• Subjects: Animals; Anti-Bacterial Agents - pharmacology; Disease Models, Animal; Drug Repositioning; Humans; Methicillin-Resistant Staphylococcus aureus; Mice; Staphylococcus aureus; Sunscreening Agents - pharmacology; Zinc - pharmacology
• ISSN: 1756-591X; 1756-591X
• DOI: 10.1093/mtomcs/mfad049

Abstract Methicillin-resistant Staphylococcus aureus (MRSA) is a major healthcare concern with associated healthcare costs reaching over ${\$}$1 billion in a single year in the USA. Antibiotic resistance in S. aureus is now observed against last line of defense antibiotics, such as vancomycin, linezolid, and daptomycin. Unfortunately, high throughput drug discovery approaches to identify new antibiotics effective against MRSA have not resulted in much tangible success over the last decades. Previously, we demonstrated the feasibility of an alternative drug discovery approach, the identification of metallo-antibiotics, compounds that gain antibacterial activity only after binding to a transition metal ion and as such are unlikely to be detected in standard drug screens. We now report that avobenzone, the primary active ingredient of most sunscreens, can be activated by zinc to become a potent antibacterial compound against MRSA. Zinc-activated avobenzone (AVB-Zn) potently inhibited a series of clinical MRSA isolates [minimal inhibitory concentration (MIC): 0.62–2.5 µM], without pre-existing resistance and activity without zinc (MIC: >10 µM). AVB-Zn was also active against clinical MRSA isolates that were resistant against the commonly used zinc–salt antibiotic bacitracin. We found AVB-Zn exerted no cytotoxicity on human cell lines and primary cells. Last, we demonstrate AVB-Zn can be deployed therapeutically as lotion preparations, which showed efficacy in a mouse wound model of MRSA infection. AVB-Zn thus demonstrates Zn-activated metallo-antibiotics are a promising avenue for future drug discovery. Graphical Abstract Graphical Abstract Avobenzone (AVB), a common active ingredient in sunscreen, was identified as a zinc-activated antibiotic against methicillin-resistant Staphylococcus aureus (MRSA)using a zinc-dependent screening approach. When translated as a lotion treatment in the presence of zinc, AVB is improves mouse survival in a murine wound infection model.