Screening and identification of antimicrobial peptides from the gut microbiome of cockroach Blattella germanica

被引:0
作者
Chen, Sizhe [1 ,4 ,5 ]
Qi, Huitang [1 ]
Zhu, Xingzhuo [3 ]
Liu, Tianxiang [2 ]
Fan, Yuting [1 ]
Su, Qi [4 ,5 ]
Gong, Qiuyu [3 ]
Jia, Cangzhi [2 ]
Liu, Tian [1 ]
机构
[1] Dalian Univ Technol, Sch Bioengn, MOE Key Lab Biointelligent Mfg, Dalian 116024, Liaoning, Peoples R China
[2] Dalian Maritime Univ, Sch Sci, Dalian 116026, Peoples R China
[3] Xiaan Jiaotong Univ, Affiliated Hosp 1, Dept Thorac Surg, Xian 710061, Peoples R China
[4] Microbiota I Ctr Mag, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China
来源
MICROBIOME | 2024年 / 12卷 / 01期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Antimicrobial peptides; Deep learning tool; <italic>Blattella germanica</italic>; Gut microbiome; In vivo activity; RESISTANCE; EVOLUTION; PROTEIN;
D O I
10.1186/s40168-024-01985-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BackgroundThe overuse of antibiotics has led to lethal multi-antibiotic-resistant microorganisms around the globe, with restricted availability of novel antibiotics. Compared to conventional antibiotics, evolutionarily originated antimicrobial peptides (AMPs) are promising alternatives to address these issues. The gut microbiome of Blattella germanica represents a previously untapped resource of naturally evolving AMPs for developing antimicrobial agents.ResultsUsing the in-house designed tool "AMPidentifier," AMP candidates were mined from the gut microbiome of B. germanica, and their activities were validated both in vitro and in vivo. Among filtered candidates, AMP1, derived from the symbiotic microorganism Blattabacterium cuenoti, demonstrated broad-spectrum antibacterial activity, low cytotoxicity towards mammalian cells, and a lack of hemolytic effects. Mechanistic studies revealed that AMP1 rapidly permeates the bacterial cell and accumulates intracellularly, resulting in a gradual and mild depolarization of the cell membrane during the initial incubation period, suggesting minimal direct impact on membrane integrity. Furthermore, observations from fluorescence microscopy and scanning electron microscopy indicated abnormalities in bacterial binary fission and compromised cell structure. These findings led to the hypothesis that AMP1 may inhibit bacterial cell wall synthesis. Furthermore, AMP1 showed potent antibacterial and wound healing effects in mice, with comparable performances of vancomycin.ConclusionsThis study exemplifies an interdisciplinary approach to screening safe and effective AMPs from natural biological tissues, and our identified AMP 1 holds promising potential for clinical application.Graphical AbstractBfzw53yZZxeQJxRuWThBYFVideo Abstract
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页数:18
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