Brecher S M, van Houte J, Hammond B F
Infect Immun. 1978 Nov;22(2):603-14. doi: 10.1128/iai.22.2.603-614.1978.
Germfree rats fed a high-sucrose diet were inoculated with Actinomyces viscosus strain T14-Vi (virulent) or T14-Av (avirulent). The mean recovery of strain T14-Vi from six extracted finely ground molars of rats sacrificed after 90 days was 1.1 x 10(8) colony-forming units (CFU). The mean recovery of strain T14-Av was 5.7 x 10(7) CFU, which was significantly less. Strain T14-Vi caused severe alveolar bone loss, but only minimal bone loss occurred in rats infected with strain T14-Av. Scanning electron microscopy of teeth of germfree rats revealed that strain T14-Vi colonized in the fissures as well as on tooth surface areas near the gingiva; strain T14-Av also colonized in fissures but was unable to colonize the teeth near the gingiva. In studies with conventional rats fed a high-sucrose diet, streptomycin-resistant strain T14-Vi colonized on the teeth of all rats inoculated with in the order of 10(8) or 10(7) CFU and on the teeth of about half of the rats inoculated with 10(6) or 10(5) CFU. In contrast, streptomycin-resistant strain T14-Av could not be detected on the teeth of any of the rats in groups similarly inoculated. In vitro "resting" cells of both strains suspended in conventional or germfree rat saliva survived to comparable degrees. [(3)H]thymidine-labeled T14-Vi cells adhered well to hydroxyapatite (HA) beads and to HA beads pretreated with saliva obtained from germfree or conventional rats. In contrast, T14-Av cells adhered less well than did T14-Vi cells to HA, whereas their adherence to saliva-coated HA was negligible. Transmission electron microscopy of negatively stained T14-Vi and T14-Av cells repeatedly passed in 1% phosphotungstic acid revealed fibrils on cells of both strains. T14-Av cells were covered by large amounts of extracellular material which was presumably heteropolysaccharide; little extracellular material was present on the surface of T14-Vi cells. T14-Vi cells had a relatively low affinity for the heteropolysaccharide synthesized by strain T14-Av. Other evidence also suggested that this polysaccharide had a relatively low affinity for saliva-coated HA. Collectively, the evidence indicates that the difference in periodontopathic potential between strains T14-Vi and T14-Av results from their different abilities to colonize teeth. This difference is probably due to the lower adherence of T14-Av cells to teeth rather than to their ability to grow in the mouth. The low affinity of T14-Av cells for tooth surfaces may be due, in part, to the presence of large amounts of cell-surface-associated polysaccharide.
给无菌大鼠喂食高糖饮食后,用粘性放线菌T14 - Vi菌株(有毒力)或T14 - Av菌株(无毒力)进行接种。在90天后处死的大鼠的六颗精细研磨的磨牙中,T14 - Vi菌株的平均回收量为1.1×10⁸ 菌落形成单位(CFU)。T14 - Av菌株的平均回收量为5.7×10⁷ CFU,明显较少。T14 - Vi菌株导致严重的牙槽骨丧失,但感染T14 - Av菌株的大鼠仅发生极少的骨丧失。对无菌大鼠牙齿的扫描电子显微镜检查显示,T14 - Vi菌株在裂隙以及牙龈附近的牙齿表面区域定植;T14 - Av菌株也在裂隙中定植,但无法在牙龈附近的牙齿上定植。在对喂食高糖饮食的常规大鼠的研究中,抗链霉素的T14 - Vi菌株在所有接种10⁸ 或10⁷ CFU的大鼠牙齿上以及大约一半接种10⁶ 或10⁵ CFU的大鼠牙齿上定植。相比之下,在同样接种的组中,任何大鼠的牙齿上都未检测到抗链霉素的T14 - Av菌株。悬浮在常规或无菌大鼠唾液中的两种菌株的体外“静止”细胞存活程度相当。[³H]胸腺嘧啶核苷标记的T14 - Vi细胞与羟基磷灰石(HA)珠以及用无菌或常规大鼠唾液预处理的HA珠粘附良好。相比之下,T14 - Av细胞与HA的粘附不如T14 - Vi细胞,而它们对唾液包被的HA的粘附可忽略不计。对在1%磷钨酸中反复传代的负染T14 - Vi和T14 - Av细胞的透射电子显微镜检查显示,两种菌株的细胞上都有纤丝。T14 - Av细胞被大量可能是杂多糖的细胞外物质覆盖;T14 - Vi细胞表面几乎没有细胞外物质。T14 - Vi细胞对T14 - Av菌株合成的杂多糖亲和力相对较低。其他证据也表明,这种多糖对唾液包被的HA亲和力相对较低。总体而言,证据表明T14 - Vi和T14 - Av菌株在牙周致病潜力上的差异源于它们在牙齿上定植能力的不同。这种差异可能是由于T14 - Av细胞对牙齿的粘附性较低,而不是它们在口腔中生长的能力。T14 - Av细胞对牙齿表面的低亲和力可能部分归因于大量与细胞表面相关的多糖的存在。