Three active efflux systems have been described in Pseudomonas aerugin
osa: namely, MexA-MexB-OprM, MexC-MexD-OprJ, and MexE-MexF-OprN. Each
of these systems consists of 3 proteins, one of which is a broadly-spe
cific transporter able to accommodate a variety of amphiphilic substra
tes. Over-expression of the efflux system, consecutive to mutations in
regulator genes, enhances the resistance levels of the organism (MICs
x 4 to 8-fold) to structurally unrelated antibiotics such as quinolon
es, tetracyclines, chloramphenicol, trimethoprim, and various beta-lac
tams. Therapeutical impact of multidrug resistance remains to be inves
tigated.