衣原体和生殖支原体在蔗糖磷酸盐缓冲液和脲酶颜色试验培养基中转运的回收。

Health laboratory science Pub Date : 1977-01-01
T F Smith, L A Weed, G R Pettersen, J W Segura
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引用次数: 0

摘要

将75例尿道炎男性尿道拭子提取到磷酸胰蛋白酶肉汤中,等量分装到含有磷酸蔗糖缓冲液(2SP)和脲酶颜色试验培养基(U-9)的小瓶中。培养基中未发现抗生素。运输至实验室后,分别在McCoy细胞培养液和琼脂培养基中接种沙眼衣原体和解脲原体,评估其恢复情况。与U-9培养液相比,2SP培养液中沙眼原体的检出率(17比12,P = 0.03)显著高于U-9培养液中沙眼原体的检出率(P < 0.01)。两种培养基对解脲脲菌的分离率与人支原体的分离率无显著差异。采用参比菌株检测4℃时沙眼衣原体和realyticum的灭活率。沙眼衣原体在2SP和U-9培养基中的失活情况相似,但在2SP培养基中包涵体的数量始终较大。相反,在两种培养基中,解脲菌的菌落形成单位的数量实际上在24小时内都有所增加。结果表明,2SP是沙眼衣原体和生殖道支原体联合回收的最佳培养基。使用一种运输介质,因此一次拭子培养对医生和实验室都有明显的节省时间和费用的优点,对病人来说,它将消除进行多次培养可能带来的不适。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recovery of Chlamydia and Genital Mycoplasma transported in sucrose phosphate buffer and urease color test medium.

Urethral swabs from 75 males with urethritis were extracted into tryptose phosphate broth and then equal aliquots were dispensed into vials containing sucrose phosphate buffer (2SP) and urease color test medium (U-9). No antibiotics were present in the media. After transport to the laboratory, the recovery of Chlamydia trachomatis and Ureaplasma urealyticum was evaluated after inoculation into McCoy's cell cultures and agar medium, respectively. C. trachomatis was recovered from significantly more patients (17 versus 12, P = 0.03) with higher inclusion counts (P less than 0.01) in specimens transported in 2SP as compared with those in U-9 medium. No significant differences between the isolation rate of U. urealyticum and that of Mycoplasma hominis were found with the two media. The rate of inactivation of C. trachomatis and U. realyticum at 4 C was examined by means of reference strains. The inactivation of C. trachomatis was similar in both 2SP and U-9 media, but the number of inclusions was consistently greater in the 2SP medium. In contrast, the number of colony-forming units of U. urealyticum actually increased over a 24-hour period in both media. We conclude that 2SP is the best medium for the combined recovery of C. trachomatis and genital Mycoplasma. The use of one transport medium and hence a single swab culture has the obvious advantages of saving time and expense for both physician and laboratory, and for the patient it will eliminate the possible discomfort of having multiple cultures taken.

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