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从临床标本中分离和鉴定解脲脲原体的适当技术和培养基的意义。

Significance of appropriate techniques and media for isolation and identification of Ureaplasma urealyticum from clinical specimens.

作者信息

Kundsin R B, Parreno A, Poulin S

出版信息

J Clin Microbiol. 1978 Oct;8(4):445-53. doi: 10.1128/jcm.8.4.445-453.1978.

Abstract

Controversy over the association of Ureaplasma urealyticum with reproductive failure may be due to methods used to isolate the microorganism. U. urealyticum isolations from clinical material should be done simultaneously in broth and on Shepard's differential agar medium (A7) containing manganese sulfate. Urine sediments result in a 9% (P = 0.0002) higher rate of isolation than than cervical and urethral swabs. Primary isolations may not display standard textbook morphology. Isolated colonies may be present, but brown streaks in cervical mucus or a coalescent haze around epithelial cells in urine sediment may also be seen in areas of concentrated growth. The broth and agar media used, method of incubation, type of specimen, and method of storing specimens before culture are all factors which influence the recovery of U. urealyticum.

摘要

解脲脲原体与生殖功能衰竭之间关联存在争议,可能是由于分离该微生物所采用的方法。从临床材料中分离解脲脲原体应同时在肉汤培养基和含有硫酸锰的谢泼德鉴别琼脂培养基(A7)上进行。尿液沉淀物的分离率比宫颈和尿道拭子高9%(P = 0.0002)。初次分离可能不会呈现标准教科书描述的形态。可能会出现分离的菌落,但在宫颈黏液中的棕色条纹或尿液沉淀物中上皮细胞周围的融合性薄雾在生长密集区域也可能可见。所使用的肉汤和琼脂培养基、培养方法、标本类型以及培养前标本的储存方法都是影响解脲脲原体回收率的因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4919/275269/dd9e72136e85/jcm00195-0108-a.jpg

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