Dual Antibacterial Activities and Biofilm Eradication of a Marine Peptide-N6NH(2) and Its Analogs against Multidrug-Resistant Aeromonas veronii

文献类型： 外文期刊

第一作者： Li, Ting

作者： Li, Ting;Wang, Zhenlong;Han, Huihui;Teng, Da;Mao, Ruoyu;Hao, Ya;Yang, Na;Wang, Xiumin;Wang, Jianhua;Li, Ting;Wang, Zhenlong;Han, Huihui;Teng, Da;Mao, Ruoyu;Hao, Ya;Yang, Na;Wang, Xiumin;Wang, Jianhua;Wang, Xiumin

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关键词： marine peptide-N6NH(2); non-coded amino acid; Aeromonas veronii; biofilm; antimicrobial activity

期刊名称：INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES （ 影响因子：5.923； 五年影响因子：6.132 ）

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年卷期： 2020 年 21 卷 24 期

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收录情况： SCI

摘要： Aeromonas veronii is one of the main pathogens causing various diseases in humans and animals. It is currently difficult to eradicate drug-resistant A. veronii due to the biofilm formation by conventional antibiotic treatments. In this study, a marine peptide-N6NH(2) and its analogs were generated by introducing Orn or replacing with D-amino acids, Val and Pro; their enzymic stability and antibacterial/antibiofilm ability against multi-drug resistant (MDR) A. veronii ACCC61732 were detected in vitro and in vivo, respectively. The results showed that DN6NH(2) more rapidly killed A. veronii ACCC61732 and had higher stability in trypsin, simulated gastric/intestinal fluid, proteinase K, and mouse serum than the parent peptide-N6NH(2). DN6NH(2) and other analogs significantly improved the ability of N6NH(2) to penetrate the outer membrane of A. veronii ACCC61732. DN6NH(2), N6PNH(2) and V112N6NH(2) protected mice from catheter-associated biofilm infection with MDR A. veronii ACCC61732, superior to N6NH(2) and CIP. DN6NH(2) had more potent efficacy at a dose of 5 mu mol/kg (100% survival) in a mouse peritonitis model than other analogs (50-66.67%) and CIP (83.33%), and it inhibited the bacterial translocation, downregulated pro-inflammatory cytokines, upregulated the anti-inflammatory cytokine, and ameliorated multiple-organ injuries (including the liver, spleen, lung, and kidney). These data suggest that the analogs of N6NH(2) may be a candidate for novel antimicrobial and antibiofilm agents against MDR A. veronii infections.

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