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解脲脲原体的分组与分型

[Grouping and typing of Ureaplasma urealyticum].

作者信息

Kong F, Zhu X, Zhou J

机构信息

Department of Dermatology, First Hospital, Beijing Medical University.

出版信息

Zhonghua Yi Xue Za Zhi. 1996 Feb;76(2):138-40.

PMID:8758449
Abstract

OBJECTIVE

To construct the molecular biological methods to group and type Ureaplasma urealyticum.

METHOD

Polymerase chain reaction was used to detect and group the 14 standard serotypes of Ureaplasma urealyticum. 272 urogenital tract clinical samples were detected and grouped. Random amplified polymorphic deoxyribose nucleic acid was used to study and compare Ureaplasma urealyticum serotypes 1, 3, 6, 14, 8, 10, 11.

RESULTS

Detected by the polymerase chain reaction, group 1 had 403 bp amplified fragments, and group 2 had 448 bp amplified fragments. 272 urogenital tract clinical samples were detected. 72 cases were positive for ureaplasma urealyticum, 69 were positive for group 1, and 3 were positive for group 2. Random amplified polymorphic deoxyribose nucleic acid was used and gene fingerprinting maps of ureaplasma urealyticum serotypes 1, 3, 6, 14, 8, 10, 11 were constructed.

CONCLUSIONS

Ureaplasma urealyticum grouping method was constructed by polymerase chain reaction. Among the urogenital tract clinical samples positive for Ureaplasma urealyticum, group 1 was more common to be positive. Random amplified polymorphic deoxyribose nucleic acid can be used as typing method of Ureaplasma urealyticum.

摘要

目的

构建解脲脲原体分组和分型的分子生物学方法。

方法

采用聚合酶链反应检测和解脲脲原体的14种标准血清型进行分组。对272份泌尿生殖道临床样本进行检测和分组。采用随机扩增多态性脱氧核糖核酸对解脲脲原体血清型1、3、6、14、8、10、11进行研究和比较。

结果

通过聚合酶链反应检测,第1组有403bp扩增片段,第2组有448bp扩增片段。对272份泌尿生殖道临床样本进行检测。72例解脲脲原体阳性,其中第1组阳性69例,第2组阳性3例。采用随机扩增多态性脱氧核糖核酸构建了解脲脲原体血清型1、3、6、14、8、10、11的基因指纹图谱。

结论

采用聚合酶链反应构建了解脲脲原体分组方法。在解脲脲原体阳性的泌尿生殖道临床样本中,第1组阳性更为常见。随机扩增多态性脱氧核糖核酸可作为解脲脲原体的分型方法。

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