Wikström M B, Dahlén G, Linde A
J Clin Microbiol. 1983 May;17(5):759-67. doi: 10.1128/jcm.17.5.759-767.1983.
Samples were taken from blood accumulated in dental alveoli after surgical removal of mandibular third molars, from subgingival plaque of teeth with advanced periodontal destructions, from teeth with infected necrotic pulps, and from subjects suffering from angular cheilitis. Of the microorganisms subcultured from these samples, 116 strains were assayed for enzymes degrading fibrinogen and fibrin. Enzymes degrading fibrinogen were assayed with the thin-layer enzyme assay cultivation technique. This assay involves the cultivation of microorganisms on culture agars applied over fibrinogen-coated polystyrene surfaces. Enzymes degrading fibrin were assayed with both a plate assay and a tube assay, in which fibrin was mixed with a microbial culture medium. Microorganisms degrading fibrinogen or fibrin or both were isolated from all sampling sites. Activity was mainly detected in strains of Actinomyces, Bacteroides, Fusobacterium, Peptococcus, Propionibacterium, and Staphylococcus aureus. Most Fusobacterium strains degraded fibrinogen only. Enzymes degrading fibrinogen as well as enzymes degrading fibrin via activation of plasminogen were revealed in strains of Clostridium, S. aureus, and Streptococcus pyogenes. It was generally found that fibrinogen was degraded by more strains than was fibrin, which indicates that different proteases may be involved.
样本取自下颌第三磨牙手术拔除后牙槽内积聚的血液、晚期牙周破坏牙齿的龈下菌斑、感染坏死牙髓的牙齿以及患口角炎的受试者。从这些样本中传代培养的微生物中,检测了116株降解纤维蛋白原和纤维蛋白的酶。采用薄层酶法培养技术检测降解纤维蛋白原的酶。该检测方法包括在涂有纤维蛋白原的聚苯乙烯表面的培养基上培养微生物。采用平板法和试管法检测降解纤维蛋白的酶,即将纤维蛋白与微生物培养基混合。从所有采样部位均分离出降解纤维蛋白原或纤维蛋白或两者的微生物。活性主要在放线菌、拟杆菌、梭杆菌、消化球菌、丙酸杆菌和金黄色葡萄球菌菌株中检测到。大多数梭杆菌菌株仅降解纤维蛋白原。在梭菌、金黄色葡萄球菌和化脓性链球菌菌株中发现了降解纤维蛋白原的酶以及通过激活纤溶酶原降解纤维蛋白的酶。一般发现,降解纤维蛋白原的菌株比降解纤维蛋白的菌株多,这表明可能涉及不同的蛋白酶。