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从人类生殖道分离沙眼衣原体的实验室操作程序。

Laboratory procedures for the isolation of chlamydia trachomatis from the human genital tract.

作者信息

Reeve P, Owen J, Oriel J D

出版信息

J Clin Pathol. 1975 Nov;28(11):910-4. doi: 10.1136/jcp.28.11.910.

Abstract

The technique of isolating Chlamydia trachomatis from the human gential tract by centrifuging clinical specimens on to cell monolayers with subsequent incubation has been improved and simplified. Gentamicin in the media was found to be superior to streptomycin in reducing bacterial contamination of specimens. The infectivity of chlamydial suspensions of laboratory cultured material was significantly reduced by storage at +4 degrees C for more than 48 hours, and by immediate freezing to -70 degrees C. When compared with immediate processing of the specimens, freezing to -70 degrees C was found to reduce the isolation rate of C.trachomatis from men with non-gonococcal urethritis (NGU) by approximately 20%. McCoy cells pretreated with idoxuridine were compared with irradiated McCoy cells for the isolation of C. trachomatis from clinical specimens. There was no significant difference in sensitivity between the two systems, but the former is considerably simpler. The effect of the centrifugal force used for inoculating specimens on to the cell monolayers on the isolation rate of C. trachomatis was studied in groups of men with NGU. Maximal isolation rates were obtained with forces of about 3000 G, which were not significantly raised by further increasing the force used. It is suggested that the isolation of C. trachomatis from the genital tract is now well within the capacity of any laboratory equipped with simple cell culture facilities.

摘要

通过将临床标本离心接种到单层细胞上并随后进行培养,从人类生殖道分离沙眼衣原体的技术已得到改进和简化。研究发现,培养基中的庆大霉素在减少标本细菌污染方面优于链霉素。实验室培养材料的衣原体悬液在4℃储存超过48小时以及立即冷冻至-70℃后,其感染性显著降低。与标本立即处理相比,冷冻至-70℃可使非淋菌性尿道炎(NGU)男性患者沙眼衣原体的分离率降低约20%。将用碘苷预处理的 McCoy 细胞与经辐照的 McCoy 细胞用于从临床标本中分离沙眼衣原体进行比较。两种系统的敏感性无显著差异,但前者要简单得多。在患有NGU的男性组中研究了用于将标本接种到单层细胞上的离心力对沙眼衣原体分离率的影响。使用约3000G的离心力可获得最大分离率,进一步增加离心力并不会显著提高分离率。建议从生殖道分离沙眼衣原体目前对于任何配备简单细胞培养设施的实验室来说都完全可行。

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