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Evidence for a link between iron metabolism and Nramp1 gene function in innate resistance against Mycobacterium avium
Author(s) -
Maria Salomé Gomes,
Rui Appelberg
Publication year - 1998
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.1998.00630.x
Subject(s) - biology , gene , microbiology and biotechnology , allele , mycobacterium , congenic , phagosome , in vivo , function (biology) , transmembrane protein , phagocytosis , genetics , bacteria , receptor
In the mouse, the progression of the Mycobacterium avium infection is highly dependent on the Nramp1 gene. Strains of mice that express the Nramp1 D169 allele are highly susceptible to M. avium infections, while Nramp1 G169 strains of mice can control them. Recently, the Nramp1 gene has been cloned and characterized as coding a transmembrane protein, probably involved in divalent cation transport. One possible function of this protein could be the transport of iron out of the parasite‐harbouring phagosome. Previous work in our lab has shown both in vitro (in macrophage cultures) and in vivo , that the growth rate of M. avium is highly dependent on the amount of iron available in the system. To try to correlate this with the Nramp1 gene function, BALB/c (susceptible) and C.D2 (resistant) congenic mice were treated for 20 days with different doses of iron‐dextran, so as to induce different degrees of iron overload, and infected with M. avium 2447. Iron administration increased M. avium growth in infected organs in a dose‐dependent manner at the same time as it decreased the difference in mycobacterial growth between the two mouse strains. These results indicate that an excess of iron hampers Nramp1 ‐encoded function, strongly suggesting a direct involvement of the Nramp1 ‐encoded protein in the transport of this cation.