Type III secretion systems allow Yersinia spp., Salmonella spp.. Shigella s
pp., Bordetella spp., and Pseudomonas aeruginosa and enteropathogenic Esche
richia coli adhering at the surface of a eukaryotic cell to inject bacteria
l proteins across the two bacterial membranes and the eukaryotic cell membr
ane to destroy or subvert the target cell. These systems consist of a secre
tion apparatus, made of similar to 25 proteins, and an array of proteins re
leased by this apparatus. Some of these released proteins are "effectors,"
which are delivered into the cytosol of the target cell, whereas the others
are "translocators," which help the effecters to cross the membrane of the
eukaryotic cell. Most of the effecters act on the cytoskeleton or on intra
cellular-signaling cascades. A protein injected by the enteropathogenic E.
coli serves as a membrane receptor for the docking of the bacterium itself
at the surface of the cell. Type III secretion systems also occur in plant
pathogens where they are involved both in causing disease in susceptible ho
sts and in eliciting the so-called hypersensitive response in resistant or
nonhost plants. They consist of 15-20 Hrp proteins building a secretion app
aratus and two groups of effecters: harpins and avirulence proteins. Harpin
s are presumably secreted in the extracellular compartment, whereas avirule
nce proteins are thought to be targeted into plant cells. Although a cohere
nt picture is clearly emerging, basic questions remain to be answered. In p
articular, little is known about how the type III apparatus fits together t
o deliver proteins in animal cells. It is even more mysterious for plant ce
lls where a thick wall has to be crossed. In spite of these haunting questi
ons, type TIT secretion appears as a fascinating trans-kingdom communicatio
n device.