In Vitro Antibacterial Activity of a Novel Acid-Activated Antimicrobial Peptide against Streptococcus mutans.

IF 1.9 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Haixing Lin, Runhong Zhou, Minna Zhang, Ruifeng Huang, Cuiqiong Fan, Shaofen Zhou, Jingnan Qiu, Jian He
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引用次数: 0

Abstract

Background: Dental caries is an oral disease associated with infection by microbial biofilm. The metabolic activity of cariogenic bacteria results in a pH decrease in the plaque biofilm, causing tooth demineralization. This acidic environment favors the growth of cariogenic bacteria that are highly resistant to strong acids, which, in turn, produce more acid resulting in a further decrease in the pH of the plaque biofilm. Therefore, the strategy of utilizing the acidic dental plaque microenvironment to prevent and treat dental caries has become a hot research topic in recent years, such as the development of pH-sensitive drug delivery systems.

Aims: Design of a new acid-activated antibacterial peptide.

Objectives: To design and synthesis an acid targeted antimicrobial peptide with the GWHHFFHFFHFF sequence.

Methods: Minimum inhibitory concentration (MIC) and minimum bacterial concentration (MBC) testing confirmed its antibacterial activity. Propidium iodide (PI) staining was used to detect nucleic acid leakage. Determination of anti-biofilm activity by biofilm inhibition assay. A phototoxicity study confirmed the phototoxicity of PPIX-P12.

Results: MIC and MBC testing confirmed that P12 possessed acid-activated anti-Streptococcus mutans activity. Bactericidal kinetic experiments and propidium iodide (PI) staining experiments showed that P12 killed planktonic S. mutans UA159 cells leading to the leakage of nucleic acids in the acidic medium. Moreover, P12 showed acid-activated anti-biofilms at the early and mature biofilm stages. P12 was conjugated with the phototherapeutic agent protoporphyrin IX (PpIX) to construct the protoporphyrin derivative PpIX-P12. In vitro experiments revealed that PpIX-P12 displayed better antibacterial activity in pH 5.5 medium than in pH 7.2 medium.

Conclusion: In conclusion, we designed an acid-activated AMP, which had no antimicrobial activity at neutral pH, but had antimicrobial activity at an acidic pH.

新型酸激活抗菌肽对变异链球菌的体外抗菌活性
背景:龋齿是一种与微生物生物膜感染有关的口腔疾病:龋齿是一种与微生物生物膜感染有关的口腔疾病。致龋菌的新陈代谢活动导致牙菌斑生物膜的 pH 值降低,造成牙齿脱矿。这种酸性环境有利于对强酸有很强抵抗力的致龋细菌的生长,反过来又会产生更多的酸,导致牙菌斑生物膜的 pH 值进一步下降。因此,利用酸性牙菌斑微环境预防和治疗龋齿的策略已成为近年来的研究热点,如开发 pH 值敏感的给药系统:设计并合成一种具有 GWHHFFHFFHFF 序列的酸靶向抗菌肽:最小抑菌浓度(MIC)和最小细菌浓度(MBC)测试证实了其抗菌活性。碘化丙啶(PI)染色用于检测核酸泄漏。通过生物膜抑制试验确定抗生物膜活性。光毒性研究证实了 PPIX-P12 的光毒性:MIC和MBC测试证实P12具有酸激活抗变异链球菌活性。杀菌动力学实验和碘化丙啶(PI)染色实验表明,P12 能杀死浮游的变异链球菌 UA159 细胞,导致酸性培养基中核酸的泄漏。此外,P12 在生物膜的早期和成熟阶段都表现出酸激活抗生物膜作用。P12 与光治疗剂原卟啉 IX(PpIX)共轭,构建了原卟啉衍生物 PpIX-P12。体外实验显示,PpIX-P12 在 pH 值为 5.5 的培养基中比在 pH 值为 7.2 的培养基中显示出更好的抗菌活性:总之,我们设计了一种酸激活的 AMP,它在中性 pH 值下没有抗菌活性,但在酸性 pH 值下具有抗菌活性。
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来源期刊
Current protein & peptide science
Current protein & peptide science 生物-生化与分子生物学
CiteScore
5.20
自引率
0.00%
发文量
73
审稿时长
6 months
期刊介绍: Current Protein & Peptide Science publishes full-length/mini review articles on specific aspects involving proteins, peptides, and interactions between the enzymes, the binding interactions of hormones and their receptors; the properties of transcription factors and other molecules that regulate gene expression; the reactions leading to the immune response; the process of signal transduction; the structure and function of proteins involved in the cytoskeleton and molecular motors; the properties of membrane channels and transporters; and the generation and storage of metabolic energy. In addition, reviews of experimental studies of protein folding and design are given special emphasis. Manuscripts submitted to Current Protein and Peptide Science should cover a field by discussing research from the leading laboratories in a field and should pose questions for future studies. Original papers, research articles and letter articles/short communications are not considered for publication in Current Protein & Peptide Science.
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