AllTheBacteria: a community resource empowers biology and discovers novel peptide antibiotics

Journal: bioRxiv
Published Date:

Abstract

Public microbial genomes encode an immense record of biological diversity, evolution and molecular function, but much of this information remains difficult to reuse because raw sequencing data are not uniformly assembled, quality controlled, annotated or searchable at scale. Here we present AllTheBacteria, an open, community-built resource that transforms public bacterial short-read whole-genome sequencing reads into a uniformly processed discovery platform. The current analysed release contains 2,440,377 high-quality bacterial and archaeal genomes from 11,273 species, together with standardized taxonomic assignments, genome annotations, antimicrobial resistance calls, antiphage-defence annotations, protein structure predictions and AI-ready sequence tables. We show that this infrastructure enables applications that would otherwise be impractical, from global sequence search and outbreak contextualization to pangenome method development, antimicrobial resistance reservoir mapping and antiphage-defence ecology. As a stringent experimental demonstration, we mined 3,919,096 encrypted peptide fragments from AllTheBacteria proteomes using our deep learning model APEX 1.1, identifying 1,867 candidates with predicted antimicrobial activity. We synthesized 24 representative peptides and tested them against 20 clinically relevant bacterial strains, including antibiotic-resistant pathogens. Multiple peptides showed low-micromolar activity, membrane-responsive conformational transitions and selective envelope perturbation. A lead molecule, ATB20, reduced Acinetobacter baumannii burden in a murine skin abscess model with efficacy comparable to polymyxin B and no overt toxicity. Together, these results establish AllTheBacteria as both a foundational community resource for microbiology and a renewable engine for AI-guided antimicrobial discovery.

Authors

  • Hunt
  • M.; Torres
  • M. D. T.; Alikhan
  • N.-F.; Anderson
  • D.; Andreani
  • M. L.; Blom
  • J.; Bouras
  • G.; Brinkman
  • F.; Carroll
  • L. M.; Croxen
  • M. A.; Floto
  • A.; Hall
  • M. B.; Hawkey
  • J.; Horsfield
  • S. T.; Jia
  • B.; Lacey
  • J. A.; Lee
  • H.-S.; Lima
  • L.; MacAlasdair
  • N.; Mallawaarachchi
  • S.; Matlock
  • W.; Moustafa
  • A. M.; Petit
  • R.; Raghuram
  • V.; Ramnath
  • V.; Russell
  • M. J.; Sanderson
  • T.; Saratto
  • T.; Schwengers
  • O.; Seemann
  • T.; Shaw
  • L. P.; Shen
  • W.; Thomson
  • N.; Tonkin-Hill
  • G.; Toussaint
  • J.; Viet
  • T. L.; Wachsmann
  • J. v.; Wan
  • F.; Weimann
  • A.; Wheatley
  • R. M.; Wiatrak
  • M.; Xie
  • O.; Fuente-Nunez
  • C. d.

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