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工程化的食菌蛭弧菌可增强抗生素渗透并消除生物膜。

Engineered Bdellovibrio bacteriovorus enhances antibiotic penetration and biofilm eradication.

作者信息

Tang Ying, Chen Yang, Qi Yong-Dan, Yan Hui-Yi, Peng Wen-An, Wang Yu-Qiang, Huang Qian-Xiao, Liu Xin-Hua, Ye Jing-Jie, Yu Yun, Zhang Xian-Zheng, Huang Cui

机构信息

State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University. Wuhan 430079, PR China.

Key Laboratory of Biomedical Polymers of Ministry of Education & Department of Chemistry, Wuhan University, Wuhan 430072, PR China.

出版信息

J Control Release. 2025 Apr 10;380:283-296. doi: 10.1016/j.jconrel.2025.01.075. Epub 2025 Feb 6.

DOI:10.1016/j.jconrel.2025.01.075
PMID:39894266
Abstract

Biofilms increase bacterial resistance to antibiotics, as conventional antibiotic doses are often ineffective at penetrating the biofilm matrix to eliminate bacteria. Recent research has shown that the Gram-negative predator bacterium Bdellovibrio bacteriovorus can penetrate Gram-positive bacterial biofilms during its predation phase and benefit from them without direct predation. Here, based on the penetration ability of B. bacteriovorus, we constructed antibiotic-loaded liposome-engineered B. bacteriovorus as a drug delivery strategy for biofilm-related diseases. As a "living antibiotic," B. bacteriovorus can prey on Gram-negative bacteria, penetrate biofilms, and disrupt their dense structure. During this process, the rapid movement of B. bacteriovorus enhances the delivery of antibiotic-loaded liposomes into the biofilm, promoting efficient antibiotic release and improving biofilm eradication. Our findings demonstrate that this engineered living antibiotic strategy significantly improves the control and removal of bacterial biofilms, accelerates the elimination of dental plaque, promotes wound healing, and holds promise as a novel platform for treating biofilm-related infections.

摘要

生物膜会增加细菌对抗生素的耐药性,因为传统抗生素剂量往往无法有效穿透生物膜基质以消灭细菌。最近的研究表明,革兰氏阴性捕食细菌食菌蛭弧菌在其捕食阶段可以穿透革兰氏阳性细菌生物膜,并在不进行直接捕食的情况下从中受益。在此,基于食菌蛭弧菌的穿透能力,我们构建了负载抗生素的脂质体工程化食菌蛭弧菌,作为一种针对生物膜相关疾病的药物递送策略。作为一种“活抗生素”,食菌蛭弧菌可以捕食革兰氏阴性细菌,穿透生物膜,并破坏其致密结构。在此过程中,食菌蛭弧菌的快速移动增强了负载抗生素的脂质体向生物膜中的递送,促进了抗生素的有效释放并改善了生物膜的根除效果。我们的研究结果表明,这种工程化活抗生素策略显著改善了对细菌生物膜的控制和清除,加速了牙菌斑的消除,促进了伤口愈合,并有望成为治疗生物膜相关感染的新型平台。

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