病毒噬菌体治疗牙周病的应用:来自过去的未来机会

L. Viganó, Matteo Fanuli, C. Casu
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引用次数: 0

摘要

抑制细胞膜合成的药物(如青霉素和头孢菌素);干扰微生物细胞膜、影响渗透性的制剂(例如一些抗真菌制剂);通过影响30S或50S亚核糖体单元功能来抑制蛋白质合成的药物(如四环素类、大环内酯类和克林霉素)阻断微生物重要代谢阶段的药物(例如磺酰胺类)。干扰核酸合成的药物(如甲硝唑和喹诺酮类药物)。抗微生物耐药性可分为3类:内在耐药性、突变耐药性和获得性耐药性。对特定抗生素产生的内在耐药性是微生物特有的自然特征。例如,一些口腔细菌,如许多链球菌,缺乏转化和处理活性形式的甲硝唑非活性代谢产物所需的硝基还原酶,因此不受药物影响。突变耐药性是由于自发的染色体突变而产生的,这种突变会产生对药物具有耐药性的基因修饰的细菌繁殖。最后,获得性耐药性是从另一种微生物获得编码抗生素耐药性的遗传元素。这个过程可以通过转导、转化或结合来进行。噬菌体在细菌的口腔微生态失调中发挥着关键作用,即使在存在抗性物种的情况下也是如此。这个以前被忽视的想法正在成为关于口腔生物膜复杂结构的最可靠的假设之一。噬菌体疗法可以用于大多数感染,因为噬菌体几乎存在于所有种类的细菌中。口腔是微生物最密集的栖息地之一,包括约60亿个细菌。2-4这些细菌和唾液是口腔微生物群的主要组成部分,它们可能有害,但也在免疫系统中发挥有益和必要的作用。这些细菌已经进化为在牙齿表面、牙龈上皮和口腔中生存。细菌聚集成称为生物膜的复杂群落。在口腔生物膜内
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Use of viral phage-therapy in periodontal disease: animminent future chance coming from the past
Agents that inhibit the synthesis of cell membrane (eg penicillin and cephalosporin); Agents that interfere with the cell membrane of the microorganism, influencing the permeability (for example some antimycotic agents); Agents that inhibit protein synthesis by influencing 30S or 50S sub-ribosomal units functions (e.g. tetracyclines, macrolides and clindamycin) Agents that block important metabolic phases of microorganisms (for example in sulfonamides). Agents that interfere with nucleic acid synthesis (eg. metronidazole and quinolones). Antimicrobial resistance can be classified into 3 groups: intrinsic, mutational and acquired resistance. Intrinsic resistance developed to a specific antibiotic is a peculiar natural feature of the microorganism. For example, some oral bacteria, such many streptococci, lack in nitroreductase needed for converting and processing metronidazole inactive metabolites in their active form and therefore are not affected by the drug. Mutational resistance occurs due to a spontaneous chromosomal mutation that produces a g en tically modiified bacterial popuplation that is resist ant to the drug. Finally, the acquired resistance is an acquisition from another microorganism of a genetic element that codes for antibiotic resistance. This process can take place by transduction, transformation or conjugation. Phages can play a key role in bacteria in oral dysbiosis even in the presence of resistant species. This previously ignored idea is becoming one of the most reliable hypotheses on the complex structures of oral biofilm. Bacteriophage therapy can be developed for most infections because bacteriophages are present in almost all species of bacteria. The oral cavity is one of the most densely populated habitats of microorganisms and includes about 6 billion bacteria.2–4 These bacteria together with saliva are the main components of oral microbioma, they can be harmful, but they also play beneficial and necessary role in the immune system. These bacteria have evolved to survive on the surface of the tooth, on the gingival epithelium and in the oral cavity. Bacteria aggregate into complex communities called biofilms. Within the oral biofilm the
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