# Multiplexed polypeptide-based hybrid bacterial clusters by tailoring the conjugation for synergistic treatment of infected wounds

**Authors:** Jiang Xiao, Zhongquan Song, Xiangdong Lai, Xiangyang Zhang, Xiaohui Liu, Hui Jiang, Minjie Li, Xuemei Wang

PMC · DOI: 10.1016/j.mtbio.2025.102040 · Materials Today Bio · 2025-07-01

## TL;DR

This paper introduces a new method to create hybrid bacterial clusters that can treat infected wounds by combining antibacterial and anti-inflammatory properties.

## Contribution

The novel contribution is the development of a biomimetic polypeptide-based hybrid bacterial cluster using tailored conjugation methods for synergistic wound treatment.

## Key findings

- The hybrid bacterial clusters effectively regulate macrophage polarization to M2 type.
- The clusters enhance local drug concentration for multifunctional bacterial killing.
- The method shows excellent antibacterial, anti-inflammatory, and healing effects in mice.

## Abstract

Drug-resistant bacterial infections and excessive inflammation pose serious challenges to wound healing. Currently, biomaterial-assisted antibacterial therapies demonstrate excellent therapeutic potential by enriching antibacterial agents at the site of infection and combining the advantages of multiple therapeutic agents. Here, inspired by bacterial aggregation behaviors in living organisms that regulate host physiological activities, a biomimetic polypeptide-based hybrid bacterial cluster is reported for treatment of infected wounds (PTS-UGT). Specifically, hybrid bacteria (UGT) were first constructed by a method of stepwise biological self-assembly with Staphylococcus epidermidis (SE) bacterial surface growth of gold and silver particles (UG) and polyphenolization of gold and silver particles. Subsequently, under the inducement of borate-diphenol coordination interactions and multiple hydrogen bonding, UGT was assembled with the side-chain boronic-acid-modified antibacterial polypeptide tobramycin (PTS) to form biomimetic hybrid bacterial clusters (PTS-UGT) by tailoring the conjugation methods. These clusters integrate the multiplexing and aggregation enhancement functions of bio-self-assembled gold, silver, polyphenol particles, bacterial immunomodulatory components and antibacterial polypeptides, which can effectively regulate the polarization of macrophages to M2 type and enhance the local effective drug concentration for multifunctional bacterial killing, thereby showing excellent antibacterial, anti-inflammatory and healing effects on infected wounds in mice, providing new ideas for the development of biomaterial-assisted antibacterial therapy.

Inspired by the close influence of bacterial spatial aggregation on host-microbe interactions, the multiplexed polypeptide-based hybrid bacterial cluster (PTS-UGT) with antibacterial and anti-inflammatory efficacy was constructed through a straightforward method of stepwise biological self-assembly and tailoring the conjugation based on boric acid-polyphenol-metal ion interaction for synergistic treatment of infected wounds.Image 1

•Drawing inspiration from the close influence of bacterial spatial aggregation on host-microbe interactions, the polypeptide-based hybrid bacterial cluster (PTS-UGT) was designed for synergistic treatment of infected wounds.•The bacteria cluster (PTS-UGT) was constructed through a straightforward method of stepwise biological self-assembly of Staphylococcus epidermidis and tailoring the conjugation based on boric acid-polyphenol-metal ion interaction.•This study proposed a strategy of engineering hybrid commensal bacteria with multiplexing and aggregation-enhancing functions for antibacterial and anti-inflammatory.

Drawing inspiration from the close influence of bacterial spatial aggregation on host-microbe interactions, the polypeptide-based hybrid bacterial cluster (PTS-UGT) was designed for synergistic treatment of infected wounds.

The bacteria cluster (PTS-UGT) was constructed through a straightforward method of stepwise biological self-assembly of Staphylococcus epidermidis and tailoring the conjugation based on boric acid-polyphenol-metal ion interaction.

This study proposed a strategy of engineering hybrid commensal bacteria with multiplexing and aggregation-enhancing functions for antibacterial and anti-inflammatory.

## Linked entities

- **Chemicals:** tobramycin (PubChem CID 36294)
- **Species:** Staphylococcus epidermidis (taxon 1282)

## Full-text entities

- **Diseases:** PTS (MESH:C535325), bacterial infections (MESH:D001424), inflammation (MESH:D007249), infection (MESH:D007239), infected wounds (MESH:D014946)
- **Chemicals:** hydrogen (MESH:D006859), polyphenol (MESH:D059808), diphenol (-), gold (MESH:D006046), silver (MESH:D012834), tobramycin (MESH:D014031), borate (MESH:D001881), boronic-acid (MESH:D001897), PTS (MESH:D010984)
- **Species:** Staphylococcus epidermidis (species) [taxon 1282], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12269884/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC12269884/full.md

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Source: https://tomesphere.com/paper/PMC12269884