Rosendal S, Valdivieso-Garcia A
Appl Environ Microbiol. 1981 Apr;41(4):1000-2. doi: 10.1128/aem.41.4.1000-1002.1981.
Samples of liquid mycoplasma cultures were mixed with equal part of a 0.01% solution of acridine orange and placed on agar plates. The number of fluorescing organisms per field was counted in an epifluorescence microscope at an X 1,000 magnification. When the number of fluorescing organisms per field was related to the number of colony-forming units per milliliter during the growth cycle, highly significant correlation was found in cultures with greater than or equal to 10(6) colony-forming units per ml during the exponential growth phase. The counts were weakly correlated during the stationary phase and not correlated during the death phase. This technique provides a mean to enumerate mycoplasmas in liquid cultures.
将液体支原体培养物样本与等份的0.01%吖啶橙溶液混合,然后置于琼脂平板上。在落射荧光显微镜下以1000倍放大倍数计数每个视野中发荧光的生物体数量。当将每个视野中发荧光的生物体数量与生长周期中每毫升菌落形成单位的数量相关联时,发现在指数生长期每毫升菌落形成单位大于或等于10⁶的培养物中存在高度显著的相关性。在稳定期计数的相关性较弱,在死亡期则无相关性。该技术提供了一种对液体培养物中的支原体进行计数的方法。