The requirement for novel classes of antibiotics to combat the emergence of
resistant and multi-resistant bacteria has coincided with the completion s
equencing of a number of bacterial genomes. The in silico analysis of these
genomes coupled with innovative genetic manipulation has already led to th
e identification of conserved essential (either in vitro or in vivo, depend
ing on the methodology) genes that are potential targets for antibacterial
research. New technologies, made possible by access to the genomic sequence
s, are capable of simultaneously quantifying almost the entire complement o
f gene products synthesised by bacterial cells. These technologies are open
ing up the way for the analysis of expression patterns elicited in cells in
response to changes in their environment. The integration of these technol
ogies into the drug discovery process is still in its infancy and the poten
tial wealth of information, some of it already available, has yet to be ful
ly realised.