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Detection and biovar discrimination of Ureaplasma urealyticum by real-time PCR

Cited 64 time in Web of Science Cited 70 time in Scopus
Authors

Yi, Jongyoun; Yoon, Bo Hyun; Kim, Eui-Chong

Issue Date
2005-07-12
Publisher
Elsevier
Citation
Mol Cell Probes. 2005 Aug;19(4):255-60.
Keywords
AllelesFemaleHumansPolymerase Chain Reaction/*methodsUreaplasma urealyticum/*classification/genetics/*isolation & purificationBacterial Typing Techniques
Abstract
Prenatal intrauterine infection has been recognized as an important cause of premature birth, and Ureaplasma urealyticum is one of the commonest pathogens. U. urealyticum consists of 14 serovars that can be divided into two biovars (parvo and T960), and the pathogenicity of U. urealyticum may be different according to the biovar. To detect U. urealyticum and determine its biovar simultaneously, we developed a real-time polymerase chain reaction (PCR) assay targeting urease gene. The real-time PCR biovar-typed two reference strains and 42 culture isolates of U. urealyticum as correctly as conventional PCR with direct sequencing. Subsequently, 87 clinical specimens (amniotic fluid, cord blood, vaginal swab) were tested for culture, conventional PCR, and real-time PCR. When compared with conventional PCR, sensitivity and specificity of real-time PCR were 89.5 and 98.5%, respectively, and those of culture were 47.4 and 100%, respectively. Of 18 clinical specimens that were found positive and biovar-typed by real-time PCR, parvo biovar was 66.7% and T960 biovar was 33.3%. This real-time PCR assay can be useful for the simultaneous detection and biovar discrimination of U. urealyticum in clinical specimens. Further study to quantify U. urealyticum would be facilitated on the basis of this method.
ISSN
0890-8508 (Print)
Language
English
URI
https://hdl.handle.net/10371/13443
DOI
https://doi.org/10.1016/j.mcp.2005.04.002
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