Min Kyung R, Galvis Adriana, Williams Brandon, Rayala Ramanjaneyulu, Cudic Predrag, Ajdic Dragana
Department of Dermatology and Cutaneous Surgery, Miller School of Medicine, University of Miami, Miami, Florida, USA.
Department of Chemistry and Biochemistry, Center for Molecular Biology and Biotechnology, Florida Atlantic University, Jupiter, Florida, USA.
Antimicrob Agents Chemother. 2017 Jul 25;61(8). doi: 10.1128/AAC.00776-17. Print 2017 Aug.
Despite continuous efforts to control cariogenic dental biofilms, very few effective antimicrobial treatments exist. In this study, we characterized the activity of the novel synthetic cyclic lipopeptide 4 (CLP-4), derived from fusaricidin, against the cariogenic pathogen UA159. We determined CLP-4's MIC, minimum bactericidal concentration (MBC), and spontaneous resistance frequency, and we performed time-kill assays. Additionally, we assessed CLP-4's potential to inhibit biofilm formation and eradicate preformed biofilms. Our results demonstrate that CLP-4 has strong antibacterial activity and is a potent bactericidal agent with low spontaneous resistance frequency. At a low concentration of 5 μg/ml, CLP-4 completely inhibited UA159 biofilm formation, and at 50 μg/ml, it reduced the viability of established biofilms by >99.99%. We also assessed CLP-4's cytotoxicity and stability against proteolytic digestion. CLP-4 withstood trypsin or chymotrypsin digestion even after treatment for 24 h, and our toxicity studies showed that CLP-4 effective concentrations had negligible effects on hemolysis and the viability of human oral fibroblasts. In summary, our findings showed that CLP-4 is a potent antibacterial and antibiofilm agent with remarkable stability and low nonspecific cytotoxicity. Hence, CLP-4 is a promising novel antimicrobial peptide with potential for clinical application in the prevention and treatment of dental caries.
尽管人们不断努力控制致龋性牙菌斑生物膜,但有效的抗菌治疗方法却非常少。在本研究中,我们对源自镰刀菌素的新型合成环脂肽4(CLP - 4)对致龋病原体UA159的活性进行了表征。我们测定了CLP - 4的最低抑菌浓度(MIC)、最低杀菌浓度(MBC)和自发耐药频率,并进行了时间 - 杀菌试验。此外,我们评估了CLP - 4抑制生物膜形成和根除已形成生物膜的潜力。我们的结果表明,CLP - 4具有很强的抗菌活性,是一种自发耐药频率低的强效杀菌剂。在5μg/ml的低浓度下,CLP - 4完全抑制了UA159生物膜的形成,在50μg/ml时,它使已形成生物膜的活力降低了>99.99%。我们还评估了CLP - 4的细胞毒性和对蛋白水解消化的稳定性。即使经过24小时的处理,CLP - 4仍能抵抗胰蛋白酶或糜蛋白酶的消化,我们的毒性研究表明,CLP - 4的有效浓度对溶血和人牙龈成纤维细胞的活力影响可忽略不计。总之,我们的研究结果表明,CLP - 4是一种强效的抗菌和抗生物膜剂,具有显著的稳定性和低非特异性细胞毒性。因此,CLP - 4是一种有前景的新型抗菌肽,在预防和治疗龋齿方面具有临床应用潜力。