Fales W H, Warner J F, Teresa G W
Am J Vet Res. 1977 Apr;38(4):491-5.
A method to demonstrate leukotoxic activity of Fusobacterium necrophorum in vitro is described. Continuous dialysis sac culture system, using reduced liquid medium was used to grow F necrophorum for 7-day periods. The continuous culture dialysis filtrate contained leukotoxic substance(s) which appeared to be less than 10,000 in molecular weight, heat resistant, and stable at 4 C for at least 10 days. Leukotoxic activity was demonstrated in vitro by determining the percentage of macrophages taking up trypan blue dye after these were exposed to a 1:2 solution of continuous culture dialysis filtrate and Eagle's minimal essential medium at 1, 2, 4, and 6 hours. Approximately 90% of these macrophages were destroyed during the 6-hour incubation period.
本文描述了一种在体外证明坏死梭杆菌白细胞毒性活性的方法。使用还原液体培养基的连续透析袋培养系统,将坏死梭杆菌培养7天。连续培养透析滤液中含有白细胞毒性物质,其分子量似乎小于10000,耐热,在4℃下至少稳定10天。通过测定巨噬细胞在暴露于连续培养透析滤液与伊格尔基本培养基1:2溶液1、2、4和6小时后摄取台盼蓝染料的百分比,在体外证明白细胞毒性活性。在6小时的孵育期内,约90%的这些巨噬细胞被破坏。