Nishioka K, Nakano T, Hirao N, Asada Y
Department of Dermatology, Kansai Medical University, Fumizonocho, Moriguchishi, Osaka 570, Japan.
J Dermatol. 1977 Feb;4(1):13-8. doi: 10.1111/j.1346-8138.1977.tb01005.x.
Exfoliatin, an exotoxin produced by phage group 2 staphylococci, was separated and was analyzed. The toxin was separated in a single peak by Sephadex G-100 gel filtration and subsequent DEAE Sephadex chromatography. By acrylamide gel disc electrophoresis this single peak was found to contain 2 components both of which posessed exfoliative activity and the same antigenic properties. Their molecular weight, however, differed; the major component had a molecular weight of 30,000 and the minor component had 27,000. The toxin was stable when heated at 60 degrees C for 40 minutes, and labile at 100 degrees C for 20 minutes. The toxin was immunogenic to mice and produced antibody which could be transmitted to neonatal mice to neutralize exfoliative activity of the toxin. Innoculation of the bacteria caused the production of antibodies against both exfoliatin and alpha-hemolysin in mice. The antibodies were also transmitted to neonatal mice to neutralize the exfoliative activity of exfoliatin.
表皮剥脱毒素是由噬菌体Ⅱ群葡萄球菌产生的一种外毒素,已被分离并进行了分析。通过葡聚糖G - 100凝胶过滤和随后的二乙氨基乙基葡聚糖柱层析,该毒素被分离成单一峰。通过聚丙烯酰胺凝胶圆盘电泳发现,这个单一峰含有两种成分,二者均具有表皮剥脱活性和相同的抗原特性。然而,它们的分子量不同;主要成分的分子量为30,000,次要成分的分子量为27,000。该毒素在60℃加热40分钟时稳定,在100℃加热20分钟时不稳定。该毒素对小鼠具有免疫原性,并产生抗体,该抗体可传递给新生小鼠以中和毒素的表皮剥脱活性。接种该细菌可使小鼠产生针对表皮剥脱毒素和α - 溶血素的抗体。这些抗体也可传递给新生小鼠以中和表皮剥脱毒素的表皮剥脱活性。