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Interaction of inflammatory cells and oral microorganisms. VIII. Detection of leukotoxic activity of a plaque-derived gram-negative microorganism.

机译:炎症细胞与口腔微生物的相互作用。八。检测噬斑来源的革兰氏阴性微生物的白细胞毒性活性。

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摘要

In the present study we identified a gram-negative anaerobic rod referred to as Y4 which was cytotoxic for human polymorphonuclear leukocytes. Y4 was isolated from dental plaque of a patient with juvenile periodontitis and presented most of the taxonomic characteristics of Actinobacillus species. Under experimental conditions, viable Y4 were cytotoxic for human peripheral blood polymorphonuclear leukocytes in serum-free cultures. Cytotoxicity was dependent on bacterial concentrations and was enhanced in the presence of a fresh or heat-inactivated (56 degrees C, 30 min) autologous serum. Leukotoxicity was independent of phagocytosis. Y4 leukotoxic effect was abolished when bacteria were heat treated (56 degrees C, 30 min) or when incubations were carried out at 4 degrees C instead of at 37 degrees C. The leukotoxicity was monitored by electron microscopy and biochemically by measuring lactate dehydrogenase indicator of cell viability. No cytotoxic effects of Y4 on human mononuclear cells, chicken fibroblasts, or mouse macrophages were detected under the conditions studied. Polymorphonuclear leukocytes may play an important role in the host defense against bacteria in periodontal disease. The cytotoxic effect of Y4 for polymorphonuclear leukocytes presented in this study is the first report of a direct offensive microbial vector in a plaque-derived microorganism and may prove to be relevant in the pathogenesis of juvenile periodontitis.
机译:在本研究中,我们鉴定出了一种称为Y4的革兰氏阴性厌氧棒,它对人多形核白细胞具有细胞毒性。从幼年牙周炎患者的牙菌斑中分离出Y4,并显示了放线杆菌属物种的大多数分类学特征。在实验条件下,活的Y4对无血清培养物中人外周血多形核白细胞具有细胞毒性。细胞毒性取决于细菌的浓度,并在新鲜或热灭活(56摄氏度,30分钟)自体血清的存在下增强。白细胞毒性与吞噬作用无关。当细菌经过热处理(56摄氏度,30分钟)或在4摄氏度而不是37摄氏度进行温育时,Y4的白细胞毒性作用消失。白细胞毒性通过电子显微镜和生化测定法检测乳酸脱氢酶指示剂进行监测。细胞活力。在所研究的条件下,未检测到Y4对人单核细胞,鸡成纤维细胞或小鼠巨噬细胞的细胞毒性作用。多形核白细胞可能在牙周疾病的宿主防御细菌中起重要作用。在这项研究中,Y4对多形核白细胞的细胞毒性作用是斑块来源的微生物中直接进攻性微生物载体的首次报道,可能被证明与青少年牙周炎的发病机制有关。

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