Fitzgerald T J, Miller J N, Sykes J A
Infect Immun. 1975 May;11(5):1141-6. doi: 10.1128/iai.11.5.1141-1146.1975.
The interaction of Treponema pallidum (Nichols strain) with cultured cells was investigated under aerobic conditions. Cell monolayers derived from rabbit testicular tissue extended the survival of treponemes as indicated by active motility. Large numbers of organisms rapidly attached to cultured cells. Within 3 h, one to twelve actively motile treponemes were attached to 25 to 50% of the cells. In addition, T. pallidum attained intracellularity as early as 30 min after inoculation of the cell monolayers. In sharp contrast, T. phagedenis biotype Reiter and T. denticola did not attach and did not enter cultured cells. Most importantly, intracellular and/or attached T. pallidum retained virulence for at least 24 h. Similar observations of attachment and retention of virulence were detected with ME-180, a cell line derived from a human cervical carcinoma. Preliminary studies with superoxide dismutase indicated that this enzyme prolonged treponemal motility and retention of virulence in the presence of cultured cells. These data provide guidelines for further investigations of in vitro cultivation of T. pallidum.
在有氧条件下研究了梅毒螺旋体(Nichols株)与培养细胞的相互作用。源自兔睾丸组织的细胞单层延长了螺旋体的存活时间,表现为活跃的运动性。大量的螺旋体迅速附着于培养细胞。在3小时内,25%至50%的细胞附着有一至十二条活跃运动的螺旋体。此外,在接种细胞单层后30分钟,梅毒螺旋体就已进入细胞内。与之形成鲜明对比的是,Reiter噬菌体型梅毒螺旋体和齿垢密螺旋体不附着也不进入培养细胞。最重要的是,细胞内和/或附着的梅毒螺旋体至少在24小时内保持毒力。用人宫颈癌来源的细胞系ME-180也检测到了类似的附着和毒力保留现象。超氧化物歧化酶的初步研究表明,在有培养细胞存在的情况下,该酶可延长螺旋体的运动性和毒力保留时间。这些数据为梅毒螺旋体体外培养的进一步研究提供了指导。