It is now firmly established that the mollicutes are true eubacteria.
They have evolved regressively (i.e., by genome reduction) from gram-p
ositive bacterial ancestors with a low content of guanine plus cytosin
e in DNA-more specifically, from certain clostridia. Many of their pro
perties, such as small genome size, small number of rRNA operons and t
RNA genes, lack of a cell wall, fastidious growth, and limited metabol
ic activities, are seen as the result of this evolution. Other propert
ies, such as the anaerobiosis of their earliest evolving members (anae
roplasmas and asteroleplasmas), the high adenine-plus-thymine content
of their DNA, their lack of sensitivity to rifampin, and the regulator
y signals for the transcription of their DNA, have been inherited from
their eubacterial ancestors. However, the mollicutes are not simply w
all-less gram-positive bacteria. They have properties of their own. Hi
gh adenine-thymine pressure has resulted in a particular codon usage,
where, for instance, UGA is read as tryptophan and not as stop. These
organisms occupy unique ecological niches and have developed peculiar
systems for pathogenicity, cell adhesion, antigenic variation, and (in
the case of the spiroplasmas) helical morphology and motility. The pu
tative role of certain mollicutes as cofactors in the development of A
IDS may involve their mitogenicity, their superantigenicity, and their
ability to induce cytokines.