Mycoplasmas are the smallest free living microorganisms with the small
est genome. The G+C content is in general low (25-33%) and the coding
capacity is about 600 proteins. Mycoplasma species are phylogeneticall
y related, they use the genetic codon UGA for tryptophan, and show rap
id evolution, with a high rate of divergence. The genomes of Mycoplasm
a genitalium and Mycoplasma pneumoniae have been fully sequenced. Stri
king features of the M. genitalium sequencing project are the presence
of a high number of membrane proteins with no resemblance to previous
ly sequenced genes and the presence of repeated fragments of the gene
encoding the tip-localized 140 kDa adhesin (MgPa). Many Myco- plasma s
pecies display a high frequency of antigenic variation, both as phase
and size variation of individual antigens. Mycoplasma hominis isolates
are known to be antigenic heterogeneous, as reflected in the reactivi
ty with monoclonal antibodies (MAbs). The genetics of the antigenic va
riation has been studied for three different surface exposed antigens:
P120, Lmp, and P50/Vaa, The gene encoding P120 had a hyper-variable r
egion in the N-terminal region. In addition, a second gene with homolo
gy to p120 was identified. The gene encoding Lmp, a 135 kDa protein is
repeated and both genes are translated and both contain internal repe
ated sequences. Deletion mutants in the Imp gene were obtained by cult
ivation of M. hominis PG21 with MAb 552 specific for the repeated part
of Lmp. One of the Imp genes had deletions of from four to eight repe
ats. The other gene was left unaltered. The genes encoding P50/Vaa sho
w a different form of variability where domains of the genes seem to b
e exchangeable. The genomic maps of five M. hominis strains showed tha
t even though the size of the genomes varied the position of the diffe
rent genes were in general conserved.