Hamada S, Koga T, Okahashi N
Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol. 1983 May;254(3):343-51.
A spontaneous mutant of Streptococcus mutans 6715 (serotype g) defective in dextran-induced agglutination ability was isolated. The wild type strain and its mutant were termed as 6715-DP and 6715-DN, respectively. Both strains possessed serotype g antigen, and exerted similar sugar fermentation patterns. Strain 6715-DP was rapidly and strongly agglutinated upon addition of high molecular weight dextran, whereas the mutant strain 6715-DN was not. [14C]Dextran prepared from Leuconostoc mesenteroides dextransucrase and [14C]sucrose bound to fresh or lyophilized 6715-DP cells, but not to the mutant 6715-DN cells. However, both strains adhered to a glass surface in the presence of sucrose. Furthermore, heat-treated (100 degrees C, 10 min) cells of both strains bound cell-free glucosyltransferase, although dextran agglutination ability of strain 6715-DP was destroyed by this treatment, indicating that receptors for dextran and glucosyltransferase were different entities. Furthermore, serotype c, e, and f strains S. mutans did not agglutinate upon addition of dextran, nor did they bind [14C]dextran. However, all these strains and both 6715-DP and 6715-DN strains induced marked dental caries in SPF rats. It is concluded that dextran-induced agglutination ability is not a necessary condition for S. mutans to induce dental caries.
分离出了变形链球菌6715(血清型g)的一种自发突变体,其葡聚糖诱导的凝集能力存在缺陷。野生型菌株及其突变体分别被命名为6715-DP和6715-DN。两种菌株都具有血清型g抗原,并且表现出相似的糖发酵模式。加入高分子量葡聚糖后,6715-DP菌株迅速且强烈地凝集,而突变菌株6715-DN则不会。由肠系膜明串珠菌葡糖基转移酶制备的[14C]葡聚糖和[14C]蔗糖能与新鲜或冻干的6715-DP细胞结合,但不能与突变的6715-DN细胞结合。然而,在蔗糖存在的情况下,两种菌株都能粘附在玻璃表面。此外,两种菌株经热处理(100℃,10分钟)的细胞都能结合无细胞葡糖基转移酶,尽管这种处理破坏了6715-DP菌株的葡聚糖凝集能力,这表明葡聚糖和葡糖基转移酶的受体是不同的实体。此外,血清型c、e和f的变形链球菌菌株在加入葡聚糖后不会凝集,也不结合[14C]葡聚糖。然而,所有这些菌株以及6715-DP和6715-DN菌株在无特定病原体(SPF)大鼠中都能诱发明显的龋齿。得出的结论是,葡聚糖诱导的凝集能力不是变形链球菌诱发龋齿的必要条件。