ABPs: diffusible antibacterial toxins secreted by and active against diverse gram-positive bacteria

ABSTRACT Competition between organisms is a ubiquitous feature of life on Earth and a major driver of evolutionary innovation. As Earth’s most diverse and abundant organisms, bacteria employ numerous strategies to inhibit the growth of competitors, ranging from the production of diffusible antibiotic metabolites to the secretion of sophisticated protein toxins. Although secreted antibacterial protein toxins have been extensively studied in gram-negative bacteria, analogous systems employed by gram-positive organisms remain comparatively poorly understood. Recent work has shed light on a widespread family of secreted protein toxins associated with co-secreted serine proteases that likely mediate interbacterial competition among gram-positive species. These systems, termed a nti b acterial p rotein (ABP) systems, consist of a secreted polymorphic t oxin (AbpT), a co-secreted serine p rotease (AbpP), and a cytoplasmic i mmunity protein (AbpI). Following proteolytic processing, ABP toxins inhibit the growth of a remarkably diverse range of gram-positive bacteria spanning the phyla Bacillota and Actinomycetota. Existing evidence suggests that these proteins combine the properties of cationic antimicrobial peptides with those of classical polymorphic antibacterial toxins, potentially enabling toxin delivery into distantly related bacteria. In this review, we summarize the current understanding of the organization, mechanisms, and ecology of ABP systems; discuss major outstanding questions regarding toxin import and native biological function; and highlight opportunities for future mechanistic and biotechnological investigation in this emerging field.

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Publication Details

Journal
Infection and Immunity
Published
2026-07-22
DOI
https://doi.org/10.1128/iai.00297-26
Primary Topic
Biochemical and Structural Characterization
Type
article
Field-Weighted Citation Impact
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article

ABPs: diffusible antibacterial toxins secreted by and active against diverse gram-positive bacteria

John C. Whitney, Jake Colautti, Joshua J. Woodward, Daniel Mwangi
Infection and Immunity
Biochemical and Structural Characterization
article

ABPs: diffusible antibacterial toxins secreted by and active against diverse gram-positive bacteria

John C. Whitney, Jake Colautti, Joshua J. Woodward, Daniel Mwangi
article en

Abstract

ABSTRACT Competition between organisms is a ubiquitous feature of life on Earth and a major driver of evolutionary innovation. As Earth’s most diverse and abundant organisms, bacteria employ numerous strategies to inhibit the growth of competitors, ranging from the production of diffusible antibiotic metabolites to the secretion of sophisticated protein toxins. Although secreted antibacterial protein toxins have been extensively studied in gram-negative bacteria, analogous systems employed by gram-positive organisms remain comparatively poorly understood. Recent work has shed light on a widespread family of secreted protein toxins associated with co-secreted serine proteases that likely mediate interbacterial competition among gram-positive species. These systems, termed a nti b acterial p rotein (ABP) systems, consist of a secreted polymorphic t oxin (AbpT), a co-secreted serine p rotease (AbpP), and a cytoplasmic i mmunity protein (AbpI). Following proteolytic processing, ABP toxins inhibit the growth of a remarkably diverse range of gram-positive bacteria spanning the phyla Bacillota and Actinomycetota. Existing evidence suggests that these proteins combine the properties of cationic antimicrobial peptides with those of classical polymorphic antibacterial toxins, potentially enabling toxin delivery into distantly related bacteria. In this review, we summarize the current understanding of the organization, mechanisms, and ecology of ABP systems; discuss major outstanding questions regarding toxin import and native biological function; and highlight opportunities for future mechanistic and biotechnological investigation in this emerging field.

Infection and Immunity
University of Washington (US), Center for Discovery (US), McMaster University (CA)
Industry, innovation and infrastructure
Openalex Percentile: Top 14%
Biochemical and Structural Characterization
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