The reduction of exogenous ferric iron by Listeria monocytogenes, a Gr
am-positive food-borne pathogen, was investigated. Using an assay inco
rporating the ferrous iron chelator ferrozine, we showed that intact c
ells of L. monocytogenes, when exposed to ferric iron, were able to ra
pidly reduce and solubilize the iron to the ferrous form. Reduction oc
curred only after direct contact between the bacteria and the iron sou
rce. A number of different ferric iron chelates, including transferrin
and lactoferrin-bound iron, haemoglobin, ferritin, and iron complexed
to siderophores, could be reduced. The ferric reductase activity was
expressed by both reference strains and clinical isolates of L. monocy
togenes and by all other species of Listeria, although significant qua
ntitative differences were observed. In L. monocytogenes, the expressi
on of ferric reductase was not affected by the growth phase of the bac
teria nor by the presence or absence of iron in the growth medium. How
ever, expression was greatly reduced in bacteria grown anaerobically a
nd when cultured in media of reduced pH. In addition, bacteria grown a
t a cold temperature displayed greater ferric reductase activity than
cells grown at higher temperatures. A surface-associated ferric reduct
ase system may be one component of a general iron scavenging mechanism
which can be used by Listeria growing in a variety of environments.