Gram‐Negative Bacteria Targeting AIE Photosensitizer for Selective Photodynamic Killing of <i>Vibrio vulnificus</i>

ABSTRACT Vibrio vulnificus is a highly virulent Gram‐negative bacterium exhibiting extensive resistance to various antibiotics, presenting significant challenges for efficient and selective eradication. Recently, photosensitizer (PS)‐based photodynamic therapy has emerged as an effective strategy against bacteria and biofilms. However, traditional PS struggles to penetrate the unique membrane structure of Gram‐negative bacteria such as V. vulnificus , while avoiding traversal of the membrane barrier of eukaryotic cells. To address this issue, herein, a PS named BDTP with aggregation‐induced emission properties was developed. BDTP can specifically target the DNA of V. vulnificus , but integrate into the cell membrane, preventing damage to the contents in eukaryotic cells due to its hydrophilic/lipophilic “Y‐shaped” structural characteristics. In dark conditions, BDTP functions as an antibiotic, inhibiting bacterial proliferation. Upon white light stimulation, BDTP can induce phototoxic damage to the DNA of V. vulnificus and effectively inhibit/clear V. vulnificus biofilms. Additionally, the eukaryotic cell membrane barrier significantly reduces PS‐induced damage to its nucleic acids. This strategy significantly promotes the healing of infected wounds in V. vulnificus ‐infected mice. Our work introduces the first PS targeting V. vulnificus ‐associated infections, demonstrating efficacy both in vitro and in vivo.

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Aggregate
Published
2024-11-26
DOI
https://doi.org/10.1002/agt2.709
Citations
9
Primary Topic
Vibrio bacteria research studies
Type
article
Field-Weighted Citation Impact
5.56

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article

Gram‐Negative Bacteria Targeting AIE Photosensitizer for Selective Photodynamic Killing of Vibrio vulnificus

Hangshu Xin, Kang‐Nan Wang, Simin Sun, Zong‐Wan Mao et al.
9 citations
Aggregate
Vibrio bacteria research studies
5.56
article

Gram‐Negative Bacteria Targeting AIE Photosensitizer for Selective Photodynamic Killing of Vibrio vulnificus

Hangshu Xin, Kang‐Nan Wang, Simin Sun, Zong‐Wan Mao, Yuying Wang, Wenjin Wang, Qiang Lin, Bing Liu
article en
9 citations

Abstract

ABSTRACT Vibrio vulnificus is a highly virulent Gram‐negative bacterium exhibiting extensive resistance to various antibiotics, presenting significant challenges for efficient and selective eradication. Recently, photosensitizer (PS)‐based photodynamic therapy has emerged as an effective strategy against bacteria and biofilms. However, traditional PS struggles to penetrate the unique membrane structure of Gram‐negative bacteria such as V. vulnificus , while avoiding traversal of the membrane barrier of eukaryotic cells. To address this issue, herein, a PS named BDTP with aggregation‐induced emission properties was developed. BDTP can specifically target the DNA of V. vulnificus , but integrate into the cell membrane, preventing damage to the contents in eukaryotic cells due to its hydrophilic/lipophilic “Y‐shaped” structural characteristics. In dark conditions, BDTP functions as an antibiotic, inhibiting bacterial proliferation. Upon white light stimulation, BDTP can induce phototoxic damage to the DNA of V. vulnificus and effectively inhibit/clear V. vulnificus biofilms. Additionally, the eukaryotic cell membrane barrier significantly reduces PS‐induced damage to its nucleic acids. This strategy significantly promotes the healing of infected wounds in V. vulnificus ‐infected mice. Our work introduces the first PS targeting V. vulnificus ‐associated infections, demonstrating efficacy both in vitro and in vivo.

AggregateVol. 6(3)
Shandong University (CN), Sun Yat-sen University (CN), Chinese University of Hong Kong, Shenzhen (CN), State Key Laboratory of Crystal Materials, Ocean University of China (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Natural Science Foundation of Shandong Province, National Key Research and Development Program of China
Openalex Percentile: Top 4%
Vibrio bacteria research studies
5.56
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