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聚合酶链反应检测与支原体IST 2检测及培养法用于检测解脲脲原体和人型支原体感染的比较

[Comparison of polymerase chain reaction assay and Mycoplasma IST 2 test with culture for detection of infections caused by Ureaplasma urealyticum and Mycoplasma hominis].

作者信息

Rastawicki Waldemar, Kalota Hanna, Jagielski Marek, Gierczyński Rafał

机构信息

Zakład Bakteriologii PZH w Warszawie.

出版信息

Med Dosw Mikrobiol. 2004;56(1):99-108.

Abstract

The polymerase chain reaction (PCR) technique and commercial Mycoplasma IST 2 test were compared with culture for the detection of U. urealyticum and M. hominis in 173 clinical samples obtained from patients without clinical symptoms from genito-urinary tract. The presence of U. urealyticum was diagnosed by culture in 24 samples, by PCR in 33 samples and by Mycoplasma IST 2 test in 39 samples. The presence of M. hominis was diagnosed in 26 samples only by Mycoplasma IST 2 test--culture and PCR were negative. The study showed the excellent sensitivity (100%) and good specificity (appropriately 94.0% and 90.0%) for U. urealyticum in PCR and Mycoplasma IST 2 test. The discrepancy of results obtained in Mycoplasma IST 2 test and culture as well as in PCR may suggest the over sensitivity of the commercial test for detection of M. hominis.

摘要

对173份取自无泌尿生殖道临床症状患者的临床样本,采用聚合酶链反应(PCR)技术和商业化的支原体IST 2检测法,与培养法进行比较,以检测解脲脲原体和人型支原体。通过培养法在24份样本中诊断出解脲脲原体,通过PCR法在33份样本中诊断出解脲脲原体,通过支原体IST 2检测法在39份样本中诊断出解脲脲原体。仅通过支原体IST 2检测法在26份样本中诊断出人型支原体——培养法和PCR法均为阴性。该研究表明,PCR法和支原体IST 2检测法对解脲脲原体具有出色的敏感性(100%)和良好的特异性(分别约为94.0%和90.0%)。支原体IST 2检测法与培养法以及PCR法所得结果的差异可能表明,该商业化检测法人型支原体检测的敏感性过高。

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