Elucidating the complex and dynamic host-microbe interactions during infect
ion requires, among other things, detailed knowledge of microbial gene expr
ession in vivo. Recently, advances in fluorescence and bioluminescence dete
ction techniques, as well as recombinase-based in vivo expression technolog
y, have rendered monitoring virulence gene expression in vivo a feasible ta
sk. These techniques have been adapted by several laboratories to study the
spatial and temporal patterns of virulence gene expression by organisms su
ch as Salmonella typhimurium, Listeria monocytogenes, Yersinia entercolitic
a and Vibrio cholerae during infection of tissue culture or animal models o
f infection.