变形链球菌的蓝光光抑制:潜在的发色团和机制

Sherif A. Mohamad, Ian L. Megson, Alistair H. Kean
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引用次数: 0

摘要

直接应用蓝光(λ = 400-500 nm)提供了一种很有前途的抗菌方式,其作用是通过活性氧的产生介导的。卟啉是细菌合成血红素所必需的有机化合物,被认为是细菌中主要的蓝光发色团,对蓝光的敏感性至关重要。然而,变形链球菌-龋齿的主要致病物种-已经显示出对蓝光的易感性,尽管据报道缺乏血红素合成途径,这就提出了一个问题,即这种易感性是如何介导的。变形链球菌缺乏含血红素的细胞色素来进行完全的有氧呼吸,而主要依靠黄素腺嘌呤二核苷酸酶进行氧依赖性代谢。本文综述了蓝光对变形链球菌抑制作用的潜在靶发色团及其机制。许多报道支持这样的观点,即血红素合成途径被阻断的细菌仍然具有在适当条件下能够产生卟啉和血红素蛋白的遗传前因。蓝光被黄素吸收,因此,黄素酶也代表潜在的发色团。综上所述,根据体外生长和代谢条件,变形链球菌体内存在不止一种蓝光发色团。为了优化蓝光抗菌作用的临床应用,未来的研究应集中在体内模型和临床试验上。
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Blue light photoinhibition of Streptococcus mutans: potential chromophores and mechanisms
Abstract The direct application of blue light (λ = 400–500 nm) provides a promising antimicrobial modality, the effects of which are mediated through generation of reactive oxygen species. Porphyrins are organic compounds essential for bacterial synthesis of heme and are understood to be the main blue light chromophores within bacteria, which are critical to the sensitivity to blue light. However, Streptococcus mutans — the principal etiological species of dental caries — has shown susceptibility towards blue light despite reportedly lacking heme synthesis pathways, raising a question as to how this susceptibility is mediated. S. mutans lacks heme-containing cytochromes for full aerobic respiration, instead relying mainly on flavin adenine dinucleotide enzymes for oxygen-dependent metabolism. This review article investigates the potential target chromophores and mechanisms underpinning the inhibitory effects of blue light in S. mutans . Multiple reports support the proposition that bacteria with blocked heme synthetic pathways still possess the genetic antecedents capable of generating porphyrins and heme proteins under appropriate conditions. Blue light is absorbed by flavins, and hence, the flavoenzymes also represent potential chromophores. In conclusion, depending on in-vitro growth and metabolic conditions, there is more than one blue light chromophore within S. mutans . To optimise clinical application of blue light-induced antimicrobial effects, future investigations should focus on in-vivo models and clinical trials.
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