(HOME)
Subject: Iron and bacteria
______________
J Clin Invest 61: 1428-40 (1978)[78194498]
The critical role of iron in host-bacterial interactions.
S. M. Payne & R. A. Finkelstein
The ability of potential pathogens to acquire iron in a host is an
important determinant of both their virulence and the nature of the
infection produced. Virulent gram-negative bacteria are capable of
acquiring sufficient iron from the host because their virulence (for
chick embryos) is unaffected by exogenous iron. Avirulent mutants
which are apparently limited in their ability to acquire iron could be
isolated from the virulent strains. The lethality of these mutants was
significantly enhanced by exogenous iron. Reduction of the relatively
high serum iron saturation of chick embryos (to levels more closely
approximating those in man) by pretreatment with iron-binding proteins
or endotoxin inhibits the lethality of some virulent bacteria. Those
bacteria whose virulence was reduced include the Shigella, Vibrio
cholerae and strains of Neisseria gonorrhoeae, all of which are
nondisseminating pathogens in the normal human host. Pathogens which
produce septicemic and disseminating infections such as Neisseria
meningitidis, Haemophilus influenzae type B, Escherichia coli
possessing K-1 antigen, Pseudomonas aeruginosa and Salmonella
typhimurium and disseminating strains of N. gonorrhoeae were, in
general, unaffected by reduced serum iron saturation. These
disseminating bacteria appeared to produce greater quantities of
compounds (siderophores) which stimulated microbial growth in low-iron
media than did the nondisseminating pathogens. Thus, the gram-negative
bacteria tested can be divided into four major classes according to
their responses to modifications in iron levels in the chick embryo
model and these results correlate with the nature of the infections
which they typically produce in man.
MeSH Terms:
* Animal
* Bacteria/drug effects
* Bacteria/metabolism
* Bacteria/pathogenicity
* Bacterial Infections/immunology
* Bacterial Infections/metabolism
* Chick Embryo
* Conalbumin/pharmacology
* Iron/metabolism
* Iron/pharmacology
* Iron Chelates/metabolism
* Support, U.S. Gov't, P.H.S.
_________________________________________________________________
(HOME)