Dale J B, Baird R W, Courtney H S, Hasty D L, Bronze M S
VA Medical Center, Memphis, TN 38104.
J Infect Dis. 1994 Feb;169(2):319-23. doi: 10.1093/infdis/169.2.319.
Previous studies have shown that lipoteichoic acid (LTA) of group A streptococci plays a central role in the adherence of these organisms to epithelial cells. In this study, intranasal instillation of purified LTA but not deacylated LTA in mice blocked colonization and prevented death after intranasal challenge infection with group A streptococci. Bacteria pretreated with rabbit antisera against LTA also failed to colonize or infect mice after intranasal challenge. In vitro studies showed that LTA and M protein inhibited adherence of type 24 streptococci to mouse pharyngeal cells. Passive intranasal administration of purified type 24 M protein protected mice from death after challenge infection with type 24 streptococci but had no significant effect on pharyngeal colonization. Surface LTA and M protein may mediate adherence of streptococci to mouse pharyngeal cells, and blocking adherence with LTA prevents colonization and infection in this animal model.
先前的研究表明,A 组链球菌的脂磷壁酸(LTA)在这些微生物与上皮细胞的黏附中起核心作用。在本研究中,给小鼠鼻内滴注纯化的 LTA 而非去酰化的 LTA,可阻止 A 组链球菌鼻内攻击感染后的定植并预防死亡。用抗 LTA 的兔抗血清预处理的细菌在鼻内攻击后也无法在小鼠体内定植或感染。体外研究表明,LTA 和 M 蛋白可抑制 24 型链球菌对小鼠咽部细胞的黏附。鼻内被动给予纯化的 24 型 M 蛋白可保护小鼠免受 24 型链球菌攻击感染后的死亡,但对咽部定植无显著影响。表面 LTA 和 M 蛋白可能介导链球菌与小鼠咽部细胞的黏附,并且在该动物模型中用 LTA 阻断黏附可防止定植和感染。