The Yfe system of Yersinia pestis transports iron and manganese and is required for full virulence of plague

Iron acquisition in Yersinia pestis is fundamental to the success of plague pathogenesis, We have previously identified an approximate to 5.6kb region (yfe) of Y. pestis genomic DNA, capable of restoring iron-deficient growth but not siderophore production to an Escherichia coli mutant (SAB11) incap able of synthesizing the siderophore, enterobactin. The yfe locus of Y. pes tis, found in both pigmented (Pgm(+)) and nonpigmented (Pgm(-)) strains, co mprises five genes arranged in two distinct operons (yfeA-D and yfeE), The larger of these, yfeABCD, encodes an ABC transport system, whose expression is iron and Fur regulated and is repressed in cells grown in the presence of manganese. Cells from a Pgm(-), Yfe(-) (Delta yfeAB) mutant strain of Y. pestis exhibited reduced transport of both Fe-55 and Mn-54. Furthermore, c ells containing an intact yfe locus showed reduced Fe-55 uptake when compet ing amounts of MnCl2 or ZnCl2 were present, whereas Mn-54 uptake was inhibi ted by FeCl3 but not by ZnCl2. Similarly, yfe mutants of Y. pestis exhibite d growth defects on media supplemented with the iron chelators 2,2'-dipyrid yl or conalbumin. These growth defects were not relieved by supplementation with MnCl2. A ybt(-), Delta yfeAB mutant of Y. pestis was completely aviru lent in mice infected intravenously (LD50 > 1.7 x 10(7) cfu) compared with its parental ybt(-), yfe(+) strain, which had an LD50 of < 12, In addition, compared with its ybt(+), yfe(+) parent, a ybt(+), Delta yfeAB mutant of Y . pestis had an approximate to 100-fold increase in the LD50 from a subcuta neous route of infection. These data suggest that the Yfe and Ybt systems m ay function effectively to accumulate iron during different stages of the i nfectious process of bubonic plague.