# An integrated multi-omic approach for discovery and dereplication of bioactive microbial natural products

**Authors:** Negero Gemeda Negeri, Duong Duc Anh Nguyen, Michael Michael, Emma Kenshole, Calum Walsh, Louise M. Judd, Liam K. R. Sharkey, Weiguang Zeng, Timothy P. Stinear, Marion Herisse, Chuan Huang, Max J. Cryle, Sacha J. Pidot

PMC · DOI: 10.1099/mgen.0.001552 · Microbial Genomics · 2025-10-28

## TL;DR

This study uses a new method to isolate and identify antibiotic-producing bacteria from soil, uncovering new bioactive compounds and improving antibiotic discovery.

## Contribution

The novel use of diffusion chambers and integration of bioactivity screening, mass spectrometry, and genomics enhances antibiotic discovery from uncultivable soil bacteria.

## Key findings

- 1,218 bacterial isolates from 61 genera were recovered using diffusion chambers.
- 16% of isolates showed antibiotic activity against E. coli or S. aureus, including multidrug-resistant strains.
- MS and genomics identified known and new antibiotics like actinomycin D, nigericin, and streptothricin.

## Abstract

Soil bacteria are a major source of clinically useful antibiotics, yet the majority of soil-dwelling micro-organisms remain uncultivable by standard laboratory methods. To access this untapped microbial diversity, we employed microbial diffusion chambers to isolate bacteria from ten Australian soil samples. A total of 1,218 bacterial isolates were recovered, representing a diverse collection spanning 61 genera from 32 families, covering the major known phyla of soil bacteria. Antibiotic activity screening revealed that 16% of isolates inhibited the growth of at least 1 of Escherichia coli or Staphylococcus aureus, with 120 isolates displaying activity against multidrug-resistant pathogens including methicillin-resistant S. aureus and vancomycin-resistant Enterococcus faecium. Mass spectrometry-based dereplication using GNPS identified known antibiotics in 33% of bioactive strains, including actinomycin D, nonactins and valinomycin. Genomic analysis confirmed the presence of corresponding biosynthetic gene clusters, while targeted analysis of selected strains uncovered production of additional antibiotics such as nigericin and streptothricin that were not initially detected by MS. Our results demonstrate that diffusion chambers enhance bacterial recovery from soil and show the benefits of a combined pipeline including bioactivity screening, MS and genomics for effective antibiotic dereplication and discovery.

## Linked entities

- **Chemicals:** actinomycin D (PubChem CID 457193), valinomycin (PubChem CID 5649), nigericin (PubChem CID 34230), streptothricin (PubChem CID 475825)
- **Species:** Escherichia coli (taxon 562), Staphylococcus aureus (taxon 1280), Enterococcus faecium (taxon 1352)

## Full-text entities

- **Chemicals:** streptothricin (MESH:D013309), nonactins (MESH:C050476), nigericin (MESH:D009550), vancomycin (MESH:D014640), valinomycin (MESH:D014634), actinomycin D (MESH:D003609), methicillin (MESH:D008712)
- **Species:** Enterococcus faecium (species) [taxon 1352], Staphylococcus aureus (species) [taxon 1280], Escherichia coli (E. coli, species) [taxon 562], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12560952/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12560952/full.md

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Source: https://tomesphere.com/paper/PMC12560952