Radhakrishnan Megha Periyappilly, Suryaletha Karthika, Joseph Iype, George Sanil, Thomas Sabu
Cholera & Biofilm Research Laboratory, Pathogen Biology Group, Rajiv Gandhi Centre for Biotechnology, Govt. of India, Trivandrum, 695 014, Kerala, India.
Interdisciplinary Biology, Rajiv Gandhi Centre for Biotechnology, Trivandrum, 695 014, Kerala, India.
Protein Pept Lett. 2023;30(10):795-805. doi: 10.2174/0109298665266332231001115508.
Brevinin2 HYba5 (Peptide 29) is a novel cationic peptide identified from an endemic frog, . and are troublesome biofilm-forming pathogens associated with nosocomial and community-acquired infections and contribute to the severity of infections associated with implanted devices and chronic wounds. Co-existence of both pathogens in biofilm mode contributes to an increased antibiotic resistance, treatment failure and hence persistent disease burden. Identifying a novel and stable, less toxic compound targeting multispecies biofilm with a lower probability of acquiring resistance in comparison to antibiotics is highly warranted.
Evaluate the activity of Brevinin2 HYba5 against and mixed biofilm.
The anti-biofilm activity of peptide 29 was tested by Crystal violet assay, Confocal laser scanning Microscopy (CLSM) and MTT Assay. Cytotoxicity of the peptide was tested in RBC and L929 fibroblast cell line. Biofilm inhibitory activity of the peptide was evaluated at different temperatures, pH, serum and plasma concentrations. The antibiofilm potential of the peptide was tested against polymicrobial biofilm by Fluorescent hybridisation (FISH) and plate counting on HiCrome UTI Agar media.
The peptide 29 could inhibit biofilm formation of and individually as well as in polymicrobial biofilm at 75 μM concentration. The peptide maintained its antibiofilm potential at different temperatures, serum and plasma concentrations. Activity of the peptide was high at acidic and neutral pH but found to get reduced towards alkaline pH. The peptide is nonhemolytic and does not exhibit significant cytotoxicity against the L929 fibroblast cell line (92.80% cell viability).
The biofilm inhibition property makes peptide 29 a promising candidate for the management of and biofilm, especially in catheter-associated devices to prevent the initial colonization and thus can ease the burden of pathogenic biofilm-associated infections.
Brevinin2 HYba5(肽29)是从一种本地青蛙中鉴定出的新型阳离子肽。金黄色葡萄球菌和大肠杆菌是与医院感染和社区获得性感染相关的麻烦的生物膜形成病原体,并且会加重与植入设备和慢性伤口相关的感染的严重程度。这两种病原体以生物膜模式共存会导致抗生素耐药性增加、治疗失败,从而导致持续的疾病负担。因此,非常有必要鉴定一种新型、稳定、低毒的化合物,该化合物靶向多物种生物膜,与抗生素相比获得耐药性的可能性更低。
评估Brevinin2 HYba针对金黄色葡萄球菌和大肠杆菌混合生物膜的活性。
通过结晶紫测定法、共聚焦激光扫描显微镜(CLSM)和MTT测定法测试肽29的抗生物膜活性。在红细胞和L929成纤维细胞系中测试该肽的细胞毒性。在不同温度、pH值、血清和血浆浓度下评估该肽的生物膜抑制活性。通过荧光原位杂交(FISH)和在HiCrome UTI琼脂培养基上进行平板计数,测试该肽对多微生物生物膜的抗生物膜潜力。
肽29在75μM浓度下可以单独抑制金黄色葡萄球菌和大肠杆菌的生物膜形成,以及多微生物生物膜的形成。该肽在不同温度、血清和血浆浓度下均保持其抗生物膜潜力。该肽在酸性和中性pH值下活性较高,但在碱性pH值下活性降低。该肽无溶血作用,并且对L929成纤维细胞系没有显著的细胞毒性(细胞活力为92.80%)。
生物膜抑制特性使肽29成为治疗金黄色葡萄球菌和大肠杆菌生物膜的有前景的候选药物,尤其是在与导管相关的设备中,以防止初始定植,从而可以减轻致病性生物膜相关感染的负担。