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通过调节(刺激或抑制)未刺激的小鼠脾细胞的胸苷掺入来检测支原体污染。

Detection of mycoplasma contamination through modulation (stimulation or inhibition) of thymidine incorporation by unstimulated mouse spleen cells.

作者信息

Alzani R, Rossi R, Cozzi E, Trizio D, Marcucci F

机构信息

Department of Immunology, Farmitalia Carlo Erba, Nerviano, Italy.

出版信息

J Immunol Methods. 1992 Jul 31;152(1):35-42. doi: 10.1016/0022-1759(92)90086-9.

Abstract

In the present report we describe a rapid and sensitive assay for mycoplasma detection in cell cultures. The assay is based on the ability of contaminated culture supernatants to modulate [3H]TdR incorporation by unstimulated mouse splenocytes. Several mycoplasma species (Mycoplasma orale, culturable and non-culturable strains of Mycoplasma hyorhinis) inhibited [3H]TdR incorporation and permitted the detection of some contaminated cell cultures that would otherwise have escaped detection in assays measuring [3H]TdR incorporation by mitogen-stimulated splenocytes. On the other hand, several other mycoplasma species (Mycoplasma arginini, Mycoplasma hominis) strongly enhanced [3H]TdR incorporation by unstimulated splenocytes. This enhancement was optimally detectable on day 2 after initiation of the cultures. The sensitivity of the assay was determined for a mycoplasma species (culturable M. hyorhinis) that inhibited as well as for one (M. arginini) that enhanced [3H]TdR incorporation. In both cases, the sensitivity was such that 1-3 x 10(2) mycoplasma colony-forming units (CFU) could be detected.

摘要

在本报告中,我们描述了一种用于检测细胞培养物中支原体的快速灵敏检测方法。该检测方法基于受污染的培养上清液调节未刺激的小鼠脾细胞掺入[3H]TdR的能力。几种支原体(口腔支原体、猪鼻支原体的可培养和不可培养菌株)抑制了[3H]TdR的掺入,并能检测出一些在通过丝裂原刺激的脾细胞掺入[3H]TdR的检测中原本会漏检的受污染细胞培养物。另一方面,其他几种支原体(精氨酸支原体、人型支原体)强烈增强了未刺激脾细胞掺入[3H]TdR的能力。这种增强在培养开始后第2天最易检测到。针对抑制[3H]TdR掺入的一种支原体(可培养的猪鼻支原体)以及增强[3H]TdR掺入的一种支原体(精氨酸支原体)测定了该检测方法的灵敏度。在这两种情况下,灵敏度都能检测到1 - 3×10(2)个支原体集落形成单位(CFU)。

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