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|Title: ||Evaluation of transcription mediated amplification and polymerase chain reaction assays for detection of mycoplasma genitalium in urine specimens of men with urethritis|
|Authors: ||Ramoncha, Magdeline Raesibe|
|Advisors: ||Le Roux, M C|
|Keywords: ||Mycoplasma genitalium|
Human mycoplasma species
|Issue Date: ||2010|
|Publisher: ||University of Limpopo (Medunsa Campus)|
|Abstract: ||Mycoplasma genitalium, a human mycoplasma species has been established as a cause of
nongonococcal urethritis (NGU) in men, particularly in Chlamydia trachomatis-negative
patients. It was also shown to play a role in cervicitis and pelvic inflammatory disease (PID) in
women. Due to difficulty in culturing, and the lack of routine molecular diagnostic tests, many
M. genitalium infections are undetected.
The purpose of this study was to evaluate three nucleic acid amplification tests (NAATs) i.e. a
recently developed Gen-Probe research only transcription mediated amplification (TMA) assay,
a conventional polymerase chain reaction (PCR) assay and a real-time PCR (q-PCR) assay for
the detection of M. genitalium in urine specimens of men with symptoms of urethritis. To
evaluate the three assays, 300 urine specimens were collected between June 2007 and July 2008
from sexually active male patients presenting with discharge (N=94) and/or burning on
micturition (N=206) to a private medical practitioner in Silverton, Pretoria. A specimen was
considered positive by extension of the gold standard i.e. if any two of the three assays were
positive. This was used to calculate the sensitivity and specificity of each method.
TMA detected M. genitalium in 62 (21%), PCR in 43 (14%) and q-PCR in 48 (16%) of the 300
patients. The sensitivities of the assays were 100% (TMA), 92% (q-PCR) and 78% (PCR), with
specificities of 90% (TMA), 95% (q-PCR) and 97% (PCR). The sensitivity of the TMA assay
was higher than that of the q-PCR and PCR assays. The lower sensitivity obtained by the q-PCR
assay might have been due to inhibition and limitations in the amount of the DNA template.
However, the q-PCR assay was easy to perform as it combines amplification and detection thus
eliminating further handling of PCR products. The PCR, although with a higher specificity, was
the least desirable in terms of testing time and problems with subjectivity when reading agarose
We concluded that the Gen-Probe TMA assay is a highly sensitive method for detection of M.
genitalium in urine specimens of men. The use of Gen-Probe TMA and the q-PCR assay, will
increase the detection of M. genitalium in clinical specimens at this catchment area.|
|Description: ||Thesis (MSc (Med)(Microbiology))--University of Limpopo (Medunsa Campus), 2010.|
|Appears in Collections:||Theses and Dissertations (Biochemistry)|
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