In vitro and in silico Evaluation of the Anti-Biofilm Activity of Histatin 5 against Streptococcus mutans

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-03-26 DOI:10.1007/s10989-024-10601-1
Shiva Golshani, Aida Iraji, Zeinab Kadkhoda, Alireza Vatanara
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Abstract

Dental caries is a prevalent and costly disease throughout the world. Streptococcus mutans is widely recognized as one of the key contributing factors in the development of dental caries. Major virulence factors associated with the cariogenicity of S. mutans include adhesion, formation biofilm, acidogenicity and acidurity. Histatin 5, a salivary antimicrobial peptide, exhibited therapeutic effects in the oral cavity. The aim of this study was to evaluate the potential anti-biofilm effects of histatin 5 against S. mutans via in vitro and in silico approaches. Also, the impact of histatin 5 on acidogenicity and acidurity was accessed. The resazurin microdilution method was used to evaluate the anti-biofilm and anti-adhesive activity. Furthermore, molecular docking was carried out to identify the crucial structural features of histatin 5 in binding to glucansucrase enzyme of S. mutans, which is involved in biofilm formation. The findings showed that histatin 5 considerably inhibited the biofilm formation of S. mutans in a dose-dependent manner and could potentially limit the acidogenicity and acidurity of S. mutans. The results of confocal laser scanning microscopy indicated the inhibitory effects of histatin 5 on biofilm formation of S. mutans cells. Moreover, histatin 5 displayed a favorable interaction with glucansucrase, which suggests that it could potentially act as an inhibitor for this enzyme. These findings suggest that histatin 5 could be a promising candidate for the development of a new efficient therapeutic agent for the prevention and treatment of dental caries.

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对组蛋白 5 对抗变异链球菌生物膜活性的体外和硅学评估
龋齿是一种在全世界普遍存在且代价高昂的疾病。人们普遍认为,变异链球菌是导致龋齿发生的关键因素之一。与变异链球菌致龋性相关的主要毒力因素包括粘附性、生物膜的形成、致酸性和酸纯度。组织蛋白 5 是一种唾液抗菌肽,对口腔有治疗作用。本研究的目的是通过体外和硅学方法,评估组蛋白 5 对突变杆状病毒的潜在抗生物膜作用。此外,还研究了组蛋白 5 对致酸性和酸纯度的影响。此外,还采用利马嗪微稀释法评估了组蛋白 5 的抗生物膜和抗粘附活性。此外,研究人员还进行了分子对接,以确定组蛋白 5 与突变杆状病毒葡聚糖琥珀酸酶结合的关键结构特征,该酶参与生物膜的形成。研究结果表明,组蛋白 5 能以剂量依赖的方式显著抑制突变杆状病毒生物膜的形成,并有可能限制突变杆状病毒的致酸性和酸纯度。激光共聚焦扫描显微镜的结果表明,组蛋白5对突变杆状病毒细胞生物膜的形成具有抑制作用。此外,组蛋白5还与葡聚糖琥珀酸酶发生了良好的相互作用,这表明组蛋白5有可能成为该酶的抑制剂。这些研究结果表明,组蛋白 5 有可能成为开发预防和治疗龋齿的新型高效治疗剂的候选物质。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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