Mycoplasma genitalium was first isolated in 1981, having been cultured from urethral specimens of two men presenting with non-gonococcal urethritis (NGU). M. genitalium belongs to the Mollicutes class, and with a genome of only 580 kilobases in size, is the smallest known self-replicating bacterium.
Although it was initially thought that disease appeared to be limited to the genito-urinary tract, there is some evidence it could potentially cause proctitis. The specialised tip-like structure of M. genitalium enables it to adhere to and invade epithelial cells. Infection may persist for months or years.
The evidence suggests that the majority of people infected with M. genitalium in the genital tract do not develop disease. M. genitalium infection is unequivocally and strongly associated with NGU. Typically, the prevalence of M. genitalium in men with NGU is 10-20% and in male patients with non-chlamydial non-gonococcal urethritis (NCNGU) is 10-35%.
Several studies support an association of M. genitalium infection in cisgender women with post coital bleeding and cervicitis, endometritis and pelvic inflammatory disease (PID).
Signs and symptoms in males:
Complications in males:
The clinical presentation of M. genitalium urethritis is similar to other causes and thus clinical features of acute symptomatic NGU cannot be used to determine the infective aetiology.
Signs and symptoms in females:
Complications in females:
Individuals with cervicitis due to M. genitalium frequently have no symptoms at all. If present, symptoms are nonspecific, with the most common symptom being post-coital bleeding. Clinical signs and symptoms of M. genitalium-associated PID are similar to, and indistinguishable from, PID due to C. trachomatis.
M. genitalium is fastidious and extremely slow growing, thus culture is not useful for diagnosis. Diagnosis should ordinarily be made on NAATs, targeting specific bacterial DNA or RNA targets.
Indications for testing for M. genitalium
Based on symptoms:
Based on risk factors:
Patients should be given a detailed explanation of their condition with particular emphasis on the long-term implications for the health of themselves and their partner(s). This should be reinforced with clear and accurate written information. A patient information leaflet for M. genitalium can be found in the PIL section.
Patients should be advised to abstain from sexual intercourse until 14 days after the start of treatment, and until symptoms have resolved. Where azithromycin has been used this is especially important because of its long half-life, and is likely to reduce the risk of selecting/inducing macrolide resistance if the patient is re-exposed to M. genitalium. We recommend a test of cure (TOC) should be performed in all patients.
Treatment of uncomplicated urogenital infection (urethritis, cervicitis)
Treatment of complicated urogenital infection (PID, epididymo-orchitis)
For alternative regimens, please refer to the full guidelines.
Pregnancy and breastfeeding
A three-day course of azithromycin can be used for uncomplicated M. genitalium infection detected in pregnancy. The use of moxifloxacin in pregnancy is contra-indicated. In women with likely macrolide resistance, or with upper genital tract infection in pregnancy, options are limited. Although doxycycline is considered safe for use in the first trimester by the FDA, the BNF advises against its use in all trimesters. There are no data regarding the use of pristinamycin in pregnancy.
Very low levels of azithromycin are detected in breast milk, and systemic exposure in infants does not exceed that observed when azithromycin is administered for treatment, therefore risk is considered to be low. Doxycycline is excreted into breast milk and is contraindicated in nursing mothers due to the risk of tooth discolouration and effects on bone growth. Use of moxifloxacin is contra-indicated during breastfeeding. Pristinamycin is contraindicated during breastfeeding due to its side effect profile.
Only current partner(s) (including non-regular partners where there is likely to be further sexual contact) should be tested and treated if positive. This is to reduce the risk of re-infection to the index patient. Partners should be given the same antibiotic as the index patient unless there is available resistance information to suggest otherwise.