Folmsbee Martha, Howard Glenn, McAlister Morven
Pall Corporation, 25 Harbor Park Dr., Port Washington, NY 11050, USA.
Biologicals. 2010 Mar;38(2):214-7. doi: 10.1016/j.biologicals.2009.11.001. Epub 2010 Feb 9.
Careful media filtration prior to use is an important part of a mycoplasma contamination prevention program. This study was conducted to increase our knowledge of factors that influence efficient filtration of mycoplasma. The cell size of Acholeplasma laidlawii was measured after culture in various nutritional conditions using scanning electron microscopy. The maximum cell size changed, but the minimum cell size remained virtually unchanged and all tested nutritional conditions resulted in a population of cells smaller than 0.2 microm. Culture in Tryptic Soy Broth (TSB) resulted in an apparent increase in the percentage of very small cells which was not reflected in increased penetration of non-retentive 0.2 microm rated filters. A. laidlawii cultured in selected media formulations was used to challenge 0.2 microm rated filters using mycoplasma broth base as the carrier fluid. We used 0.2 microm rated filters as an analytical tool because A. laidlawii is known to penetrate 0.2 microm filters and the degrees of penetration can be compared. Culture of A. laidlawii in TSB resulted in cells that did not penetrate 0.2 microm rated filters to the same degree as cells cultured in other media such as mycoplasma broth or in TSB supplemented with 10% horse serum.
使用前进行仔细的介质过滤是支原体污染预防计划的重要组成部分。本研究旨在增加我们对影响支原体高效过滤因素的了解。使用扫描电子显微镜在各种营养条件下培养后,测量了莱氏无胆甾原体的细胞大小。最大细胞大小发生了变化,但最小细胞大小几乎保持不变,并且所有测试的营养条件下产生的细胞群体均小于0.2微米。在胰蛋白胨大豆肉汤(TSB)中培养导致非常小的细胞百分比明显增加,但这并未反映在0.2微米额定孔径的非保留型过滤器的穿透增加上。使用支原体肉汤基础液作为载液,将在选定培养基配方中培养的莱氏无胆甾原体用于挑战0.2微米额定孔径的过滤器。我们使用0.2微米额定孔径的过滤器作为分析工具,因为已知莱氏无胆甾原体可穿透0.2微米的过滤器,并且可以比较穿透程度。在TSB中培养莱氏无胆甾原体产生的细胞穿透0.2微米额定孔径过滤器的程度与在其他培养基(如支原体肉汤或补充有10%马血清的TSB)中培养的细胞不同。