Mycoplasma genitalium, discovered almost 20 years ago, is one of 14 mycopla
smas of human origin and is found predominantly in the genital tract, being
sexually transmitted. It is mainly flask-shaped, and the MgPa protein of t
he narrow terminal portion 6 instrumental in its attachment to eukaryotic c
ell surfaces. The terminal structure may also be involved in the gliding mo
vement of M genitalium. It metabolises glucose but not arginine or urea and
is susceptible to broad-spectrum antibiotics in a manner similar to M pneu
moniae. The M genitalium genome, the smallest known for a self-replicating
organism, namely 580 Kb, was the first to be fully sequenced. All the propo
sed open reading frames of the genome are contained in the M pneumoniae gen
ome, with the latter containing other specific genes. In addition, the MgPa
adhesin gene of M genitalium has considerable sequence homology with the P
1 adhesin gene of M pneumoniae. Apart from adhesion, invasion of eukaryotic
cells by M genitalium has been demonstrated, entrance being mediated appar
ently by the terminal structure; intracellular location may promote chronic
infection and enhance pathogenicity. Thus, apart from acute nongonococcal
urethritis, M genitalium is associated with the chronic disease. M genitali
um, lacking all the genes for amino acid synthesis, requires an exogenous s
upply and this probably accounts for the difficulty of primary cultural iso
lation. Reliable detection is made routinely by means of the polymerase cha
in reaction (PCR), primers and probes fcr which are detailed, although PCR
technology in combination with cell culture and mycoplasmal medium has resu
lted in some isolates.