微生物学
生物膜
酶
沙门氏菌
背景(考古学)
蜡螟
体内
聚磷酸盐
生物
化学
激酶
抗生素
细菌
多药耐受
生物化学
脾脏
体外
抗药性
蛋白激酶A
金黄色葡萄球菌
抗生素耐药性
肠沙门氏菌
结肠炎
蛋白激酶C
作者
Shufang Li,Hongfa Lv,Shuai Yuan,Jiazhang Qiu,Xuming Deng,Qiaoling Zhang,Jianfeng Wang
出处
期刊:Phytomedicine
[Elsevier BV]
日期:2025-09-23
卷期号:148: 157278-157278
标识
DOI:10.1016/j.phymed.2025.157278
摘要
value of 17 μg/mL based on enzyme inhibition assays. DAP was found to inhibit bacterial motility, biofilm formation and stress resistance while also exhibiting the cellular protective effects against Salmonella infection. Molecular dynamics simulations and fluorescence quenching assays confirmed a direct interaction between DAP and PPK, specifically targeting the L590 and I41 amino acid residues, altering its conformational stability. In vivo studies using the Galleria mellonella model and a murine colitis model showed that DAP significantly improved survival rates by 60% and reduced bacterial burden in the liver, spleen and colon. Furthermore, the therapeutic effects of DAP were confirmed in a S. Pullorum infection model, further highlighting its potential as a novel therapeutic agent. Collectively, our findings suggest that targeting PPK with DAP may provide a promising strategy for treating Salmonella infections, especially in the context of increasing antibiotic resistance.
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