Sela S, Marouni M J, Perry R, Barzilai A
Department of Human Microbiology, Sackler school of Medicine, Tel-Aviv University, Ramat Aviv, Israel.
FEMS Microbiol Lett. 2000 Dec 15;193(2):187-93. doi: 10.1111/j.1574-6968.2000.tb09422.x.
Lipoteichoic acid (LTA) is thought to play a role in the interactions between Streptococcus pyogenes and host cells. We have examined the effect of exogenous LTA on the adherence and entry of S. pyogenes JRS4 strain into HEp-2 epithelial cells. LTA markedly inhibited bacterial entry in a concentration-dependent manner, up to 250 microg ml(-1). In contrast, LTA had only a slight inhibitory effect on adherence. LTA also inhibited the entry but not adherence of Salmonella typhimurium strain into HEp-2 cells. Binding experiments showed a dose-dependent binding of LTA to cells up to 10 microg ml(-1). Confocal laser microscopy imaging and analysis revealed that LTA was internalized by the epithelial cells and colocalized with F-actin. These results might imply that, following binding, exogenous LTA enters HEp-2 cells and exerts a cytotoxic effect that interferes with bacterial internalization. A possible target for LTA activity might be the actin cytoskeleton, which is known to be essential for bacterial uptake.
脂磷壁酸(LTA)被认为在化脓性链球菌与宿主细胞的相互作用中发挥作用。我们研究了外源性LTA对化脓性链球菌JRS4菌株黏附并进入HEp-2上皮细胞的影响。LTA以浓度依赖的方式显著抑制细菌进入,最高可达250μg/ml。相比之下,LTA对黏附只有轻微的抑制作用。LTA也抑制鼠伤寒沙门氏菌菌株进入HEp-2细胞,但不影响其黏附。结合实验表明,LTA与细胞的结合呈剂量依赖性,最高可达10μg/ml。共聚焦激光显微镜成像和分析显示,LTA被上皮细胞内化并与F-肌动蛋白共定位。这些结果可能意味着,结合后外源性LTA进入HEp-2细胞并发挥细胞毒性作用,干扰细菌内化。LTA活性的一个可能靶点可能是肌动蛋白细胞骨架,已知其对细菌摄取至关重要。