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新型乳铁蛋白衍生抗菌肽LF-1抑制……的致龋毒力因子

Novel Lactotransferrin-Derived Antimicrobial Peptide LF-1 Inhibits the Cariogenic Virulence Factors of .

作者信息

Luo Junyuan, Feng Zening, Lyu Xiaohui, Zhang Linglin

机构信息

Department of Endodontics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, College of Stomatology, Shanghai Jiao Tong University, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Key Laboratory of Stomatology, Shanghai Research Institute of Stomatology, No. 639, Zhizaoju Road, Shanghai 200011, China.

Department of Endodontics, Shanghai Stomatological Hospital, Fudan University, No. 356, East Beijing Road, Shanghai 200001, China.

出版信息

Antibiotics (Basel). 2023 Mar 13;12(3):563. doi: 10.3390/antibiotics12030563.

Abstract

We previously developed a novel lactotransferrin-derived antimicrobial peptide, LF-1, with selective antibacterial activity against the characteristic cariogenic bacterium . This study further investigated the effects of LF-1 on the cariogenic virulence factors of and evaluated the changes in virulence-associated enzymes and genes; the viability, acidogenicity, and aciduricity of planktonic ; and initial colonisation and biofilm formation after treatment with LF-1. The method of qRT-PCR was used to evaluate virulence-associated gene expression. LF-1 interfered with the cell viability of within 6 h. LF-1 inhibited the acidogenicity and aciduricity of with reduced lactic acid production and survival in a lethal acidic environment, and inactivated lactate dehydrogenase and FF-ATPase activity. LF-1 decreased surface-adherent within 60 min and inhibited biofilm formation, where scanning electron microscopy and confocal laser scanning microscopy showed reduced extracellular matrix and bacteria. LF-1 downregulates virulence-associated gene expression. LF-1 inhibited the growth and cariogenic virulence factors of in vitro with a reduction in key enzymatic activity and downregulation of virulence-associated gene expression. LF-1 has promising application prospects in the fight against and dental caries.

摘要

我们之前开发了一种新型的乳铁蛋白衍生抗菌肽LF-1,它对典型的致龋菌具有选择性抗菌活性。本研究进一步探究了LF-1对[致龋菌名称未给出]致龋毒力因子的影响,并评估了毒力相关酶和基因的变化;浮游[致龋菌名称未给出]的活力、产酸性和耐酸性;以及用LF-1处理后其初始定植和生物膜形成情况。采用qRT-PCR方法评估[致龋菌名称未给出]毒力相关基因的表达。LF-1在6小时内干扰了[致龋菌名称未给出]的细胞活力。LF-1抑制了[致龋菌名称未给出]的产酸性和耐酸性,乳酸生成减少,在致死性酸性环境中的存活率降低,并使乳酸脱氢酶和FF-ATP酶活性失活。LF-1在60分钟内减少了表面附着的[致龋菌名称未给出],并抑制了[致龋菌名称未给出]生物膜的形成,扫描电子显微镜和共聚焦激光扫描显微镜显示细胞外基质和细菌减少。LF-1下调了[致龋菌名称未给出]毒力相关基因的表达。LF-1在体外抑制了[致龋菌名称未给出]的生长和致龋毒力因子,关键酶活性降低,毒力相关基因表达下调。LF-1在对抗[致龋菌名称未给出]和龋齿方面具有广阔的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bfb/10044700/5f88d67514f7/antibiotics-12-00563-g001.jpg

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