Slots J, Gibbons R J
Infect Immun. 1978 Jan;19(1):254-64. doi: 10.1128/iai.19.1.254-264.1978.
This investigation examined the ability of cells of Bacteroides melaninogenicus subsp. asaccharolyticus 381 to adhere to surfaces that might be important for its initial colonization of the mouth and its subsequent colonization in periodontal pockets. Of 48 asaccharolytic strains of B. melaninogenicus, 47 agglutinated human erythrocytes, whereas none of 20 fermentative strains, which included reference cultures of the subspecies intermedius and melaninogenicus, were active. Electron microscopy indicated that both asaccharolytic and fermentative strains possessed pili; hence, the presence of pili did not correlate with the hemagglutinating activities of B. melaninogenicus strains. Both asaccharolytic and fermentative B. melaninogenicus strains suspended in phosphate-buffered saline adhered in high numbers to buccal epithelial cells and to the surfaces of several gram-positive bacteria tested, including Actinomyces viscosus, A. naeslundii, A. israelii, Streptococcus sanguis, and S. mitis. B. melaninogenicus subsp. asaccharolyticus 381 also attached, but in comparatively low numbers, to untreated and to saliva-treated hydroxyapatite. Addition of clarified whole saliva to suspensions of strain 381 almost completely eliminated adherence to buccal epithelial cells and to hydroxyapatite surfaces, but saliva had no detectable effect on attachment to gram-positive plaque bacteria. Both fermentative and nonfermentative strains of B. melaninogenicus also attached in high numbers to crevicular epithelial cells derived from human periodontal pockets, but normal human serum strongly inhibited attachment. Serum also inhibited attachment of strain 381 to saliva- and serum-treated hydroxyapatite, but it had little effect upon attachment to gram-positive bacteria. These observations suggested that salivary and serum components would strongly inhibit the attachment of B. melaninogenicus cells to several oral surfaces, but not to the surfaces of certain gram-positive bacteria commonly present in human dental plaque. This was confirmed by an in vivo experiment in which streptomycin-labeled cells of B. melaninogenicus 381-R were introduced into the mouths of two volunteers. After 10 min, several hundred-fold higher numbers of the organism were recovered from preformed bacterial plaque present on teeth than from clean tooth surfaces or from the buccal mucosa and tongue dorsum. High numbers of B. melaninogenicus cells were also recovered from preformed plaque after 150 min, but virtually no cells of the organism were recovered from the other surfaces studied. These data suggest that the presence of dental plaque containing Actinomyces and other gram-positive bacteria may be essential for the attachment and colonization of B. melaninogenicus cells after their initial introduction into the mouth. Similarly, the presence of subgingival plaque containing gram-positive bacteria may be necessary for its secondary colonization in periodontal pockets.
本研究检测了产黑素类杆菌解糖亚种381的细胞黏附于可能对其在口腔中的初始定植及其随后在牙周袋中定植很重要的表面的能力。在48株产黑素类杆菌解糖菌株中,47株能凝集人红细胞,而20株发酵菌株(包括中间亚种和产黑素亚种的参考培养物)均无此活性。电子显微镜显示,解糖菌株和发酵菌株均有菌毛;因此,菌毛的存在与产黑素类杆菌菌株的血凝活性无关。悬浮于磷酸盐缓冲盐水中的产黑素类杆菌解糖菌株和发酵菌株均大量黏附于颊上皮细胞以及所检测的几种革兰氏阳性菌表面,包括黏性放线菌、内氏放线菌、衣氏放线菌、血链球菌和轻链球菌。产黑素类杆菌解糖亚种381也能黏附,但数量相对较少,黏附于未处理的和经唾液处理的羟基磷灰石。向381菌株悬液中加入澄清的全唾液几乎完全消除了其对颊上皮细胞和羟基磷灰石表面的黏附,但唾液对其黏附于革兰氏阳性菌斑细菌无明显影响。产黑素类杆菌的发酵菌株和非发酵菌株也大量黏附于源自人牙周袋的龈沟上皮细胞,但正常人血清强烈抑制黏附。血清也抑制381菌株对经唾液和血清处理的羟基磷灰石的黏附,但对其黏附于革兰氏阳性菌影响较小。这些观察结果表明,唾液和血清成分会强烈抑制产黑素类杆菌细胞对几种口腔表面的黏附,但不会抑制其对人牙菌斑中常见的某些革兰氏阳性菌表面的黏附。这一点在一项体内实验中得到了证实,该实验将链霉素标记化的产黑素类杆菌381-R细胞引入两名志愿者口腔。10分钟后,从牙齿上预先形成的菌斑中回收的该菌数量比从清洁的牙齿表面、颊黏膜和舌背中回收的数量高出数百倍。150分钟后,从预先形成的菌斑中也回收了大量产黑素类杆菌细胞,但在所研究的其他表面几乎未回收该菌细胞。这些数据表明,含有放线菌和其他革兰氏阳性菌的牙菌斑的存在可能对产黑素类杆菌细胞初次引入口腔后的黏附和定植至关重要。同样,含有革兰氏阳性菌的龈下菌斑的存在可能是其在牙周袋中二次定植所必需的。