Stokes G V
Infect Immun. 1973 Feb;7(2):173-7. doi: 10.1128/iai.7.2.173-177.1973.
L cells (mouse fibroblasts), uninfected and infected with Chlamydia psittaci (meningopneumonitis strain), were labeled with (14)C-amino acids, and their membranous organelles were separated by isopycnic equilibrium centrifugation of whole cell homogenates on discontinuous sucrose density gradients. Incorporation of labeled amino acids into host and parasitic proteins was differentiated on the basis of susceptibility to cycloheximide. Twenty hours after infection with C. psittaci, incorporation of newly synthesized proteins into the internal membranes of L cells was almost completely inhibited, and internal membranes made prior to infection were altered or destroyed. The unit membrane that at all times surrounds the cytoplasmic vacuole containing the multiplying chlamydiae was made by the host from membranes or membrane precursors present before infection. No proteins synthesized by C. psittaci became associated with host cell membranes. Destruction or modification of the internal membranes of the host cell may be an integral part of the chlamydial developmental cycle.
用(14)C - 氨基酸标记未感染和感染了鹦鹉热衣原体(脑膜肺炎菌株)的L细胞(小鼠成纤维细胞),并通过在不连续蔗糖密度梯度上对全细胞匀浆进行等密度平衡离心来分离其膜性细胞器。根据对环己酰亚胺的敏感性区分标记氨基酸掺入宿主蛋白和寄生蛋白的情况。感染鹦鹉热衣原体20小时后,新合成的蛋白质掺入L细胞内膜的过程几乎完全受到抑制,感染前形成的内膜发生改变或被破坏。始终包围着含有正在繁殖的衣原体的细胞质空泡的单位膜是由宿主利用感染前存在的膜或膜前体形成。鹦鹉热衣原体合成的蛋白质未与宿主细胞膜结合。宿主细胞内膜的破坏或修饰可能是衣原体发育周期的一个组成部分。