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应用支原体属特异性聚合酶链反应监测支原体感染的衣原体菌株的去污情况。

Application of a Mycoplasma group-specific PCR for monitoring decontamination of Mycoplasma-infected Chlamydia sp. strains.

作者信息

Ossewaarde J M, de Vries A, Bestebroer T, Angulo A F

机构信息

Research Laboratory for Infectious Diseases, National Institute of Public Health and Environmental Hygiene, Bilthoven, The Netherlands.

出版信息

Appl Environ Microbiol. 1996 Feb;62(2):328-31. doi: 10.1128/aem.62.2.328-331.1996.

Abstract

Mycoplasma contamination of biological materials remains a major problem. Most contaminations are caused by the use of Mycoplasma-contaminated cell lines. We adapted a Mycoplasma group-specific PCR to detect Mycoplasma contamination in cell lines and demonstrate its use in monitoring decontamination procedures with Mycoplasma-contaminated suspensions of Chlamydia spp. Three different methods were investigated: the use of Mycoplasma-specific antiserum in cell culture, physical separation by the combined use of enzymatic treatment and differential centrifugation, and the use of detergents. With these methods only incubation with Triton X-100 resulted in decontamination of Mycoplasma-contaminated suspensions of several laboratory strains of Chlamydia pneumoniae, C. pecorum, and C. trachomatis. Only one C. pneumoniae strain, UZG-1, was sensitive to Triton X-100 treatment. Since 39 of 40 throat swabs from patients with symptoms of an upper respiratory tract infection had positive reactions in the Mycoplasma group-specific PCR, this procedure could also have clinical significance in attempts to propagate C. pneumoniae strains from clinical specimens.

摘要

生物材料的支原体污染仍然是一个主要问题。大多数污染是由使用受支原体污染的细胞系引起的。我们采用了一种支原体属特异性PCR来检测细胞系中的支原体污染,并展示其在监测衣原体属支原体污染悬液的去污程序中的应用。研究了三种不同的方法:在细胞培养中使用支原体特异性抗血清、通过酶处理和差速离心相结合进行物理分离以及使用去污剂。使用这些方法,只有用Triton X-100孵育能使几种肺炎衣原体、猪衣原体和沙眼衣原体实验室菌株的支原体污染悬液去污。只有一株肺炎衣原体菌株UZG-1对Triton X-100处理敏感。由于40例有上呼吸道感染症状患者的咽喉拭子中有39份在支原体属特异性PCR中呈阳性反应,该程序在从临床标本中培养肺炎衣原体菌株的尝试中也可能具有临床意义。

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