Falkler W A, Smoot C N, Mongiello J R
Arch Oral Biol. 1982;27(7):553-9. doi: 10.1016/0003-9969(82)90069-3.
The characteristic haemagglutination (HA) caused by Fusobacterium nucleatum strains was used for measuring their attachment to oral epithelial, gingival fibroblast and white blood cells. Whole cells and sonicated preparations of oral F. nucleatum strains VPI No. 4355, 10197 and ATCC No. 10953 haemagglutinated human and sheep red blood cells. Sonicated preparations of the organisms were tested for HA activity before and after absorption with human cells. Buccal epithelial, gingival fibroblast and white blood cells bound the HA-active fragments, as observed by: (1) decrease in the HA activity of the sonicated preparation after absorption, (2) increase in HA activity of the cells used for absorption, (3) presence of microbial fragments on the cells after absorption detected by fluorescent antibody. The HA-active fragments were released from the cells by EDTA; furthermore, galactose but not glucose inhibited the attachment of F. nucleatum to human cells. The role of cell binding in colonization by the organisms and in immune-stimulated damage to host cells is important.
具核梭杆菌菌株引起的特征性血凝反应(HA)被用于测定其对口腔上皮细胞、牙龈成纤维细胞和白细胞的黏附情况。口腔具核梭杆菌菌株VPI No. 4355、10197以及ATCC No. 10953的全细胞和超声破碎制剂能够凝集人和绵羊的红细胞。在用人细胞吸附前后,对这些微生物的超声破碎制剂进行了HA活性检测。观察发现,颊黏膜上皮细胞、牙龈成纤维细胞和白细胞能够结合HA活性片段,依据如下:(1)吸附后超声破碎制剂的HA活性降低;(2)用于吸附的细胞的HA活性增加;(3)通过荧光抗体检测发现吸附后细胞上存在微生物片段。HA活性片段可被EDTA从细胞上释放出来;此外,半乳糖而非葡萄糖能够抑制具核梭杆菌对人细胞的黏附。细胞黏附在该微生物的定植以及免疫刺激对宿主细胞造成的损伤中所起的作用至关重要。