利用多肽纳米颗粒和肽的鸡尾酒疗法治疗变异链球菌。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2024-09-13 Epub Date: 2024-08-19 DOI:10.1021/acsinfecdis.4c00107
Keuna Jeon, Nesha May O Andoy, Delphine Dufour, Jessica Y C Yang, Céline M Lévesque, Ruby May A Sullan
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引用次数: 0

摘要

由变异链球菌生物膜形成的牙菌斑是蛀牙形成的主要因素。虽然抗菌策略已经存在,但抗生素耐药性的风险日益增加,因此有必要采用其他治疗方案。聚塞洛托宁纳米粒子(PSeNPs)最近因其光热特性和广阔的生物医学应用前景而得到认可,为抗菌剂的使用开辟了一条新途径。在这里,我们介绍了一种紫外线引发的 PSeNPs 合成路线,并提高了产量。利用这些 PSeNPs,我们开发出了一种鸡尾酒疗法来降低这种致腔菌的存活率。这种鸡尾酒疗法包括一种针对变异单胞菌的抗菌肽(GH12)、一种能引发变异单胞菌利他细胞死亡的种内能力刺激肽以及激光激活加热的 PSeNPs。肽+PSeNP+激光 "组合能有效抑制突变杆状病毒在浮游生物和生物膜状态下的生长。此外,这种鸡尾酒方法还能有效降低变异沙雷氏菌与白色念珠菌形成的毒性更强的双菌种生物膜的存活率。总之,我们的研究结果加强了多管齐下的治疗策略在复杂的口腔生物膜模型中减少致龋细菌的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cocktail Approach with Polyserotonin Nanoparticles and Peptides for Treatment of <i>Streptococcus mutans</i>.

Cocktail Approach with Polyserotonin Nanoparticles and Peptides for Treatment of Streptococcus mutans.

Dental plaque, formed by a Streptococcus mutans biofilm, is a major contributor to cavity formation. While antimicrobial strategies exist, the growing risk of antibiotic resistance necessitates alternative therapeutic solutions. Polyserotonin nanoparticles (PSeNPs), recently recognized for their photothermal property and promising biomedical applications, open up a new avenue for antimicrobial use. Here, we introduced a UV-initiated synthetic route for PSeNPs with improved yield. Using these PSeNPs, a cocktail treatment to reduce the viability of this cavity-causing bacteria was developed. This cocktail comprises an S. mutans-targeting antimicrobial peptide (GH12), an intraspecies competence-stimulating peptide that triggers altruistic cell death in S. mutans, and laser-activated heating of PSeNPs. The "peptide + PSeNP + laser" combination effectively inhibits S. mutans growth in both planktonic and biofilm states. Moreover, the cocktail approach remains effective in reducing the viability of S. mutans in a more virulent dual-species biofilm with Candida albicans. Overall, our results reinforce the utility of a multipronged therapeutic strategy to reduce cariogenic bacteria in the complex model oral biofilm.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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