Dendritic cells (DC) are potent antigen-presenting cells that play a crucia
l role in initiation and modulation of specific immune responses. Various p
athogens like viruses or bacteria are able to persist inside DC. In this st
udy we investigated the ability of the Gram-Negative bacteria Salmonella ty
phimurium and Escherichia coli to infect DC. DC isolated from peripheral bl
ood of healthy donors were infected with wildtype S. typhimurium and a nonp
athogenic E. coli stool isolate. Association of bacteria with DC was assess
ed by labeling of the bacteria with green fluorescent protein. Both Gram-ne
gative bacteria were associated with DC as evidenced by microscopy and flow
cytometry. The intracellular location could be confirmed by lysis of DC an
d subsequent determination of colony-forming units on agar plates, which sh
owed a rapid decline in viable Gram-negative bacteria 6 h after infection,
being by far more pronounced for E. coli than for S. typhimurium. Testing t
he stimulation of T cells by infected versus uninfected but otherwise ident
ically treated human immature DC in a mitogen-dependent T cell proliferatio
n assay, we found that S. typhimurium, but not E. coli exhibited a suppress
ive effect on T cell stimulation, being most significant on days 3-5 after
infection. Thus, suppression of dendritic cell function was associated with
an enteropathogenic bacterium, S. typhimurium, which can cause severe form
s of enteritis. The bacteria with normally mild or no gastric symptoms, E.
coli, had no influence on stimulation of T cells by DC.