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Test ID: MHRP    
Mycoplasma hominis, Molecular Detection, PCR

Useful For Suggests clinical disorders or settings where the test may be helpful

Rapid, sensitive, and specific identification of Mycoplasma hominis from synovial fluid, genitourinary, reproductive, and lower respiratory sources

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Mycoplasma hominis causes septic arthritis and postpartum fever, and has been associated with pelvic inflammatory disease and bacterial vaginosis. Culture isolation is laborious, requiring a high degree of technical skill and taking several days. PCR detection is sensitive, specific, and provides same-day results. The described PCR assay has replaced conventional culture for Mycoplasma hominis at Mayo Medical Laboratories.

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Not applicable

Interpretation Provides information to assist in interpretation of the test results

A positive PCR result for the presence of a specific sequence found within the Mycoplasma hominis tuf gene indicates the presence of Mycoplasma hominis DNA in the specimen.


A negative PCR result indicates the absence of detectable Mycoplasma hominis DNA in the specimen, but does not rule-out infection as false-negative results may occur due to the following; inhibition of PCR, sequence variability underlying the primers and/or probes, or the presence of Mycoplasma hominis in quantities less than the limit of detection of the assay.

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Interfering substances may affect the accuracy of this assay; results should always be interpreted in conjunction with clinical and epidemiological findings.


This test does not detect other mycoplasmas or ureaplasmas (including Mycoplasma pneumoniae, a common cause of community acquired pneumonia).

Supportive Data

This assay was clinically validated in a blinded manner using 292 archived specimens submitted for Mycoplasma hominis culture, 281 of which were in M4, M5, or Universal Transport Media (UTM). The specimens consisted of 251 genitourinary, 32 reproductive fluids or tissues, and 9 respiratory specimens. Compared to culture, PCR had 90.7% (39/43) sensitivity and 99.2% (245/247) specificity (p=0.41). Discordant results on the archived specimens (n=6) were tested by PCR by Dr. Kathleen A. Stellrecht at the Albany Medical Center (J Clin Microbiol 2004;42:1528-1533). Dr. Stellrecht found both of the PCR-positive/culture-negative specimens to be PCR positive, and 3 of 4 specimens that were PCR negative/culture positive to be PCR negative. The limit of detection of the assay is 100 targets/mcL for all validated sources. Additional whole organism spiking studies (at the limit of detection of the assay) were performed using 30 or more of each of the following: genitourinary swabs, respiratory specimens, genitourinary fluid, reproductive tissue/fluid and synovial fluid. All results (except for 6) were as expected.

Clinical Reference Provides recommendations for further in-depth reading of a clinical nature

1. Waites KB, Taylor-Robinson D: Mycoplasma and Ureaplasma. In Manual of Clinical Microbiology. Tenth edition. Edited by J Versalovic. ASM Press, Washington, DC, 2011

2. Stellrecht KA, Woron AM, Mishrik NG, Venezia RA: Comparison of multiplex PCR assay with culture detection of genital mycoplasmas. J Clin Microbiol 2004;42:1528-1533

3. Kenny GE: Genital mycoplasmas: Mycoplasma genitalium, Mycoplasma hominis, and Ureaplasma species. In Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases. Edited by GL Mandell, RG Douglas, JE Bennett. Churchill Livingstone, New York, 2008

4. Yoshida T, Maeda SI, Deguchi T, et al: Rapid detection of Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma parvum, and Ureaplasma urealyticum organisms in genitourinary samples by PCR-microtiter plate hybridization assay. J Clin Microbiol 2003;41:1850-1855

5. Cunningham SA, Shannon SK, Rosenblatt J, Patel R: Comparison of culture and rapid polymerase chain reaction detection of Mycoplasma hominis, Ureaplasma urealyticum and Ureaplasma parvum from genitourinary specimens. 48th Annual Infectious Diseases Society of America Meeting, 2010

6.Cunningham SA, Mandrekar JN, Rosenblatt JE, Patel R:  Rapid PCR Detection of Mycoplasma hominis, Ureaplasma urealyticum, and Ureaplasma parvum. International Journal of Bacteriology 2013;vol 2013:1-7