O'Daly J A, Polanco N
Instituto Venezolano de Investigaciones Científicas, Centre of Microbiology and Cell Biology, Caracas, Venezuela.
Am J Trop Med Hyg. 1990 Jul;43(1):44-51. doi: 10.4269/ajtmh.1990.43.44.
Trypanosoma cruzi epimastigotes changed their pattern of surface proteins when the temperature of growth rose from 30 degrees C to 34 degrees C. Challenge of mice with blood-form trypomastigotes produced high parasitemias when animals were immunized with surface proteins from epimastigotes cultured at 30 degrees C and with Nonidet P-40-extracted epimastigotes pellets cultured at 34 degrees C. However, low parasitemias were recorded after immunization with surface proteins from epimastigotes cultured at 34 degrees C or Nonidet P-40-extracted epimastigotes pellets at 30 degrees C. The lowest parasitemia, together with the longest survival time and absence of immunosuppression, was observed after immunization of mice with the product extracted with non-ionic detergent from epimastigotes grown at 30 degrees C and treated with tosyl-L-lysine-chloromethyl ketone.
当生长温度从30摄氏度升至34摄氏度时,克氏锥虫前鞭毛体的表面蛋白模式发生了变化。用在30摄氏度培养的前鞭毛体表面蛋白以及在34摄氏度培养并用Nonidet P - 40提取的前鞭毛体沉淀对小鼠进行免疫后,再用血液型锥鞭毛体攻击小鼠,会产生高寄生虫血症。然而,用在34摄氏度培养的前鞭毛体表面蛋白或在30摄氏度用Nonidet P - 40提取的前鞭毛体沉淀进行免疫后,记录到的寄生虫血症较低。在用非离子去污剂从在30摄氏度生长并用甲苯磺酰 - L - 赖氨酸 - 氯甲基酮处理的前鞭毛体中提取的产物对小鼠进行免疫后,观察到最低的寄生虫血症,同时伴有最长的存活时间且无免疫抑制现象。