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New Assay Procedure for Separation of Mycoplasmas from Virus Pools and Tissue Culture Systems

机译:从病毒库和组织培养系统中分离支原体的新测定方法

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摘要

Presence of mycoplasma organisms in tissue culture systems and virus pools was detected by titration of the contaminated material on agarose-suspended BHK21/13S cells. The use of this method permitted isolation of mycoplasmas which could not be detected by standard assay methods. Mycoplasma colonies at concentrations ranging from 104 to 106 colony-forming units/ml in agarose-BHK21/13S media could be distinguished from virus plaques, and the two populations of microorganisms could be easily disassociated either by electron microscopy or by biological methods. All isolated mycoplasmas were identified in growth inhibition tests as belonging to the GDL group. The growth inhibition test on agarose-BHK21/13S cell suspension plates could also be applied directly to those strains which could not be isolated by standard assay procedures.
机译:通过在琼脂糖悬浮的BHK21 / 13S细胞上滴定受污染物质,检测到组织培养系统和病毒库中支原体生物的存在。该方法的使用允许分离支原体,这是标准测定方法无法检测到的。在琼脂糖-BHK21 / 13S培养基中,浓度在10 4 到10 6 菌落形成单位/ ml范围内的支原体菌落可与病毒噬菌斑区分开,并且有两个种群通过电子显微镜或生物方法可以很容易地分离微生物。在生长抑制试验中,所有分离出的支原体均被鉴定为属于GDL组。在琼脂糖-BHK21 / 13S细胞悬浮板上的生长抑制试验也可以直接应用于那些不能通过标准测定方法分离的菌株。

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