Edmondson Diane G, Norris Steven J
Department of Pathology and Laboratory Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas.
Department of Microbiology and Molecular Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas.
Curr Protoc. 2021 Feb;1(2):e44. doi: 10.1002/cpz1.44.
For over a century, investigation of Treponema pallidum subsp. pallidum, the spiral-shaped bacterium that causes syphilis, was hindered by an inability to culture the organism in vitro. A recent breakthrough has enabled continuous in vitro growth of this organism in co-culture with mammalian tissue culture cells. This article contains the protocols needed to culture T. pallidum in the standard laboratory environment. In addition, protocols for growing and maintaining the required tissue culture cells, for generating isogenic strains by limiting dilution, and for quantitating T. pallidum by darkfield microscopy are included. © 2021 Wiley Periodicals LLC. Basic Protocol 1: In vitro cultivation of Treponema pallidum Basic Protocol 2: Generation of isogenic strains Support Protocol 1: Alternate harvest procedure Support Protocol 2: Culture of Sf1Ep cells Support Protocol 3: Assessment of T. pallidum number and viability.
一个多世纪以来,梅毒螺旋体亚种苍白密螺旋体(引起梅毒的螺旋状细菌)的研究因无法在体外培养该生物体而受阻。最近的一项突破使得这种生物体能够在与哺乳动物组织培养细胞的共培养中在体外持续生长。本文包含在标准实验室环境中培养梅毒螺旋体所需的方案。此外,还包括培养和维持所需组织培养细胞、通过有限稀释产生同基因菌株以及通过暗视野显微镜对梅毒螺旋体进行定量的方案。© 2021 威利期刊有限责任公司。基本方案 1:梅毒螺旋体的体外培养 基本方案 2:同基因菌株的产生 支持方案 1:替代收获程序 支持方案 2:Sf1Ep 细胞的培养 支持方案 3:梅毒螺旋体数量和活力的评估。