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在常规尿液定量培养程序中使用点滴接种法和胱氨酸-乳糖-缺电解质培养基。

Use of droplet plating method and cystine-lactose-lactng electrolyte-deficient medium in routine quantitative urine culturing procedure.

作者信息

Neblett T R

出版信息

J Clin Microbiol. 1976 Sep;4(3):296-305. doi: 10.1128/jcm.4.3.296-305.1976.

Abstract

Droplet plating of 0.01 ml of 10(-2) dilutions of mixed sonically treated urines onto cystine-lactose electrolyte-deficient agar permits formation of discrete, easily counted colonies within a small circumscribed area without interference by Proteus overswarm. Each colony is considered as arising from a single viable cell. The single dilution permits precise reproducible quantitation of urine bacteria population within the range 10(4) to 10(6) cells/ml of sample. Droplet-plated counts were found to be consistently (approximately) double those determined by standard pour plate quantitation. The method requires only inexpensive readily available materials and has been performed routinely in a large-volume clinical laboratory for several years.

摘要

将0.01 ml经超声处理的混合尿液10⁻²稀释液滴加在胱氨酸 - 乳糖电解质缺乏琼脂上,可在小的限定区域内形成离散的、易于计数的菌落,而不受变形杆菌过度生长的干扰。每个菌落被认为是由单个活细胞产生的。单次稀释可在每毫升样品10⁴至10⁶个细胞的范围内对尿液细菌数量进行精确的、可重复的定量。发现滴加平板计数始终(大约)是标准倾注平板定量法测定值的两倍。该方法仅需要廉价且易于获得的材料,并且已经在一个大容量临床实验室中常规进行了数年。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6e7/274453/346eb4513d52/jcm00218-0117-a.jpg

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