Saouda M, Wu W, Conran P, Boyle M D
Department of Microbiology and Immunology, Medical College of Ohio, Toledo, USA.
J Infect Dis. 2001 Sep 15;184(6):723-31. doi: 10.1086/323083. Epub 2001 Aug 10.
This study compared the pathology and infection pattern of streptococcal pyrogenic exotoxin B-positive (SpeB(+)) and SpeB-negative (SpeB(-)) isogenic variants of an M1 isolate of Streptococcus pyogenes in a mouse skin air sac model. SpeB(+) strains resulted in severe local tissue damage that extended from the epidermis through the subcutaneous layers, whereas isogenic SpeB(-) variants had reduced gross pathology. At the histologic level, differences in necrosis and host responses to each variant were apparent. Injection of purified SpeB alone into a skin air sac failed to induce any significant tissue damage; however, coinjection of the enzyme with either the wild-type or the speB mutant resulted in increased and accelerated tissue necrosis. Surprisingly, coinjection of the enzyme with the spleen-recovered SpeB(-) variant failed to induce a lesion.
本研究在小鼠皮肤气囊模型中比较了化脓性链球菌M1分离株的化脓性链球菌热原性外毒素B阳性(SpeB(+))和SpeB阴性(SpeB(-))同基因变体的病理学和感染模式。SpeB(+)菌株导致严重的局部组织损伤,从表皮延伸至皮下层,而异基因SpeB(-)变体的大体病理学表现较轻。在组织学水平上,各变体在坏死和宿主反应方面存在明显差异。将纯化的SpeB单独注射到皮肤气囊中未能诱导任何显著的组织损伤;然而,将该酶与野生型或speB突变体共同注射会导致组织坏死增加且加速。令人惊讶的是,将该酶与从脾脏恢复的SpeB(-)变体共同注射未能诱导病变。