A dextrorotatory residues-incorporated bioactive dodecapeptide against enterohemorrhagic Escherichia coli

Ping Zeng, Xuemei Yang, K. Wong, Sheng Chen, Kin-Fai Chan, S. Leung, Lanhua Yi
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Abstract

Aim: This study aims to report an engineered peptide zp39 with favorable bioactivity against enterohemorrhagic Escherichia coli (E. coli, EHEC). Its antibacterial mechanisms and application in a real food system are assessed. Methods: Spatial conformation of synthetic peptide zp39 (GIIAGIIiKIKk-NH2, lowercase letters indicate dextrorotatory amino acids) was predicted by PEPstrMOD and its secondary structure was further determined by circular dichroism (CD) spectroscopy. Then, standard E. coli O157:H7 strain ATCC 43888 was used to evaluate the bioactivity of zp39. A double dilution method was applied to investigate its efficacy in normal broth medium, serum, and highly saline conditions. Its effects on cell membrane permeability and potential were measured by fluorescent assays. Thereafter, morphological changes of E. coli O157:H7 cells were monitored by electron microscopy technologies. Finally, the potential application of zp39 in controlling EHEC in food was tested with spinach juice and the Galleria mellonella larvae model was employed to assess the in vivo efficacy. Results: Peptide zp39 presented an amphiphilic helical structure. It effectively inhibited the growth of E. coli O157:H7 at a concentration of 4 μmol/L in a bactericidal mode. Mechanistic studies revealed that it affected membrane permeability and potential in a dose-dependent manner. Moreover, zp39 maintained satisfactory bioactivity against E. coli O157:H7 even in the presence of 70% serum or 1,000 μmol/L chloride salts. In spinach juice application, > 90% E. coli O157:H7 cells were killed within 2 h after exposure to 64 μmol/L zp39. In vivo study proved that treatment with 64 μmol/L zp39 could effectively boost the survival ratio of infected larvae by 50%. Conclusions: This study depicts a synthetic dodecapeptide that shows the potential application in controlling EHEC. This molecule may be developed into a highly effective antimicrobial agent applied to prevent food contamination and associated infections.
抗肠出血性大肠杆菌的右旋残渣结合生物活性十二肽
目的:本研究旨在报道一种具有良好抗肠出血性大肠杆菌生物活性的工程肽zp39。评价了其抗菌机理及其在实际食品体系中的应用。方法:利用PEPstrMOD预测合成肽zp39 (GIIAGIIiKIKk-NH2,小写字母表示右旋氨基酸)的空间构象,并利用圆二色性(CD)光谱进一步测定其二级结构。然后用标准菌株ATCC 43888评价zp39的生物活性。采用双倍稀释法考察其在正常肉汤培养基、血清和高盐条件下的疗效。用荧光法测定其对细胞膜通透性和电位的影响。随后,用电镜技术监测大肠杆菌O157:H7细胞形态学变化。最后,利用菠菜汁检测zp39在控制食品中肠出血性大肠杆菌中的应用潜力,并采用大mellonera幼虫模型评价其体内效果。结果:肽zp39呈两亲性螺旋结构。在4 μmol/L的浓度下,能有效抑制大肠杆菌O157:H7的生长。机制研究表明,它以剂量依赖的方式影响膜透性和电位。zp39在70%血清或1000 μmol/L氯盐的存在下,对大肠杆菌O157:H7仍保持良好的生物活性。在菠菜汁处理中,64 μmol/L zp39处理后2 h内杀灭大肠杆菌O157:H7细胞的比例大于90%。体内实验证明,64 μmol/L zp39处理可有效提高感染幼虫的存活率50%。结论:本研究描述了一种合成的十二肽,在控制肠出血性大肠杆菌方面具有潜在的应用前景。该分子可发展成为一种高效的抗菌剂,用于预防食品污染和相关感染。
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