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PCR-Based Identification of Oral Streptococcal Species.基于聚合酶链反应的口腔链球菌种类鉴定
Int J Dent. 2016;2016:3465163. doi: 10.1155/2016/3465163. Epub 2016 Sep 14.
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Identification of novel cyclic lipopeptides from a positional scanning combinatorial library with enhanced antibacterial and antibiofilm activities.从具有增强抗菌和抗生物膜活性的位置扫描组合文库中鉴定新型环脂肽。
Eur J Med Chem. 2016 Jan 27;108:354-363. doi: 10.1016/j.ejmech.2015.11.032. Epub 2015 Nov 30.
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High-level iron mitigates fusaricidin-induced membrane damage and reduces membrane fluidity leading to enhanced drug resistance in Bacillus subtilis.高浓度铁减轻了枯草芽孢杆菌中杀镰孢菌素诱导的膜损伤并降低了膜流动性,从而增强了耐药性。
J Basic Microbiol. 2016 May;56(5):502-9. doi: 10.1002/jobm.201500291. Epub 2015 Oct 15.
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Precision-guided antimicrobial peptide as a targeted modulator of human microbial ecology.精准导向抗菌肽作为人类微生物生态的靶向调节剂。
Proc Natl Acad Sci U S A. 2015 Jun 16;112(24):7569-74. doi: 10.1073/pnas.1506207112. Epub 2015 Jun 1.
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The formation of Streptococcus mutans persisters induced by the quorum-sensing peptide pheromone is affected by the LexA regulator.群体感应肽信息素诱导的变形链球菌持留菌的形成受LexA调节因子的影响。
J Bacteriol. 2015 Mar;197(6):1083-94. doi: 10.1128/JB.02496-14. Epub 2015 Jan 12.
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Antibiotic development challenges: the various mechanisms of action of antimicrobial peptides and of bacterial resistance.抗生素研发挑战:抗菌肽的多种作用机制与细菌耐药性
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Triclosan/copolymer containing toothpastes for oral health.含三氯生/共聚物的口腔护理牙膏。
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In vitro and in vivo activities of novel cyclic lipopeptides against staphylococcal biofilms.新型环脂肽对葡萄球菌生物膜的体外和体内活性
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10
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一种新型合成环脂肽对致龋变形链球菌UA159的抗菌及抗生物膜活性

Antibacterial and Antibiofilm Activities of a Novel Synthetic Cyclic Lipopeptide against Cariogenic Streptococcus mutans UA159.

作者信息

Min Kyung R, Galvis Adriana, Williams Brandon, Rayala Ramanjaneyulu, Cudic Predrag, Ajdic Dragana

机构信息

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.

出版信息

Antimicrob Agents Chemother. 2017 Jul 25;61(8). doi: 10.1128/AAC.00776-17. Print 2017 Aug.

DOI:10.1128/AAC.00776-17
PMID:28533236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5527655/
Abstract

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.

摘要

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。