Bactericidal activity of mammalian histones is caused by large membrane pore formation

Histones have an important role in eukaryotic innate immunity, wherein histones co-localize with antimicrobial peptides (AMPs). The mechanism of histone cooperation with AMPs and the extent to which histones form pores both remain a mystery. Here, we show that histones form large pores in bacterial membranes that lack lipopolysaccharide (LPS) and that their antimicrobial effect is significantly stronger than that of the clinical AMP polymyxin B. We find that histones and AMPs together produce potent antimicrobial synergy through the formation of 26 nm pores, whereby the pore-forming activity of AMPs on LPS-containing membranes enables histones to enter the periplasmic space and subsequently attack unprotected membranes to create pores. We provide a mechanistic explanation for the long-standing observations of histone antimicrobial activity and demonstrate how antimicrobial synergy arises. The ubiquity of histones and AMPs in innate immunity has significant implications for organismal defense and can be leveraged for novel antibiotic strategies.

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Publication Details

Journal
Cell Reports
Published
2025-05-01
DOI
https://doi.org/10.1016/j.celrep.2025.115658
Citations
1
Primary Topic
Antimicrobial Peptides and Activities
Type
article
Field-Weighted Citation Impact
1.18

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article

Bactericidal activity of mammalian histones is caused by large membrane pore formation

Kumar Perinbam, Michaela Marshall, Jean-Louis Bru, Joseph P. Patterson et al.
1 citations
Cell Reports
Antimicrobial Peptides and Activities
1.18
article

Bactericidal activity of mammalian histones is caused by large membrane pore formation

Kumar Perinbam, Michaela Marshall, Jean-Louis Bru, Joseph P. Patterson, Albert Siryaporn, Serena Abbondante, Steven P. Gross, Katherine McCarthy, Summer J. Kasallis, Paul J. Hurst, Eric Pearlman, Leora Duong, Yonghan Wu, Babu J.N. Reddy
article en
1 citations

Abstract

Histones have an important role in eukaryotic innate immunity, wherein histones co-localize with antimicrobial peptides (AMPs). The mechanism of histone cooperation with AMPs and the extent to which histones form pores both remain a mystery. Here, we show that histones form large pores in bacterial membranes that lack lipopolysaccharide (LPS) and that their antimicrobial effect is significantly stronger than that of the clinical AMP polymyxin B. We find that histones and AMPs together produce potent antimicrobial synergy through the formation of 26 nm pores, whereby the pore-forming activity of AMPs on LPS-containing membranes enables histones to enter the periplasmic space and subsequently attack unprotected membranes to create pores. We provide a mechanistic explanation for the long-standing observations of histone antimicrobial activity and demonstrate how antimicrobial synergy arises. The ubiquity of histones and AMPs in innate immunity has significant implications for organismal defense and can be leveraged for novel antibiotic strategies.

Cell ReportsVol. 44(5)
University of California, Irvine (US)
National Science Foundation, Universität Basel, UC Irvine Materials Research Institute, National Institutes of Health, University of California, Irvine, Materials Research Science and Engineering Center, University of Nebraska, National Institute of Allergy and Infectious Diseases, Division of Materials Research
Openalex Percentile: Top 22%
Antimicrobial Peptides and Activities
1.18
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