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表面活性剂在控制动物细胞培养中支原体污染方面的潜在应用。

Potential use of surface-active agents for controlling Mycoplasma contamination in animal cell cultures.

作者信息

Reynolds R K, Hetrick F M

出版信息

Appl Microbiol. 1969 Mar;17(3):405-11. doi: 10.1128/am.17.3.405-411.1969.

Abstract

Seven nonionic detergents, which were determined to be relatively nontoxic to selected animal cell cultures, were tested for their lethal effect on the GDL strain of Mycoplasma hyorhinis. Of the seven detergents tested, five were found to cause complete lysis of the organism in vitro within 24 hr at 37 C. These detergents included Triton WR-1339 and Tweens 20, 40, 60, and 80. When different concentrations of the detergents were tested, Tween 80 was found to be the most effective and Triton WR-1339 the least effective in lysing the mycoplasmata. These same five detergents were used to treat a rat nephroma cell line which was chronically infected with the GDL strain. The mycoplasmata were eliminated from those cultures treated with Triton but they persisted in cultures exposed to the Tween compounds. The Triton-treated cells remained free from infection over a 7-month period, as determined both by cultural methods and fluorescent-antibody staining. The "cure" was effected by treating the cells for either 48 hr with maintenance media containing 1 mg of Triton per ml or for 96 hr with a concentration of 500 mug/ml. Triton was also effective in eliminating the GDL, strain from experimentally infected rat embryo cells after a 48-hr treatment with a concentration of 1 mg/ml. Four other species of Mycoplasma, which were completely lysed by Triton in vitro, were not eliminated from experimentally infected cells by a single treatment with Triton, although the severity of the infection was apparently reduced.

摘要

七种非离子去污剂,经测定对选定的动物细胞培养物相对无毒,对猪鼻支原体GDL菌株的致死作用进行了测试。在所测试的七种去污剂中,发现有五种在37℃下24小时内可在体外使该生物体完全裂解。这些去污剂包括吐温80、吐温20、吐温40、吐温60和曲拉通WR-1339。当测试不同浓度的去污剂时,发现吐温80在裂解支原体方面最有效,而曲拉通WR-1339最无效。同样的这五种去污剂被用于处理长期感染GDL菌株的大鼠肾癌细胞系。用曲拉通处理的培养物中的支原体被清除,但暴露于吐温化合物的培养物中支原体仍然存在。通过培养方法和荧光抗体染色确定,用曲拉通处理的细胞在7个月内一直没有感染。“治愈”是通过用每毫升含1毫克曲拉通的维持培养基处理细胞48小时或用500微克/毫升的浓度处理96小时来实现的。用1毫克/毫升的浓度处理48小时后,曲拉通在从实验感染的大鼠胚胎细胞中清除GDL菌株方面也很有效。另外四种支原体在体外被曲拉通完全裂解,尽管感染的严重程度明显降低,但用曲拉通单次处理并不能从实验感染的细胞中清除它们。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00fd/377702/0c84801fa053/applmicro00003-0083-a.jpg

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