“…In turn, the degradation of ferroportin in macrophages not only limits the availability of iron to bacteria, but also promotes tissue restoration, eventually attenuating lung injury induced by pneumonia. In addition, iron overload is associated with the increased virulence of multiple microbes, including Yersinia enterocolitica , Escherichia coli, and Klebsiella pneumonia [ 24 , 64 , 65 ]. During infection, the body uses some iron-binding proteins to control the iron supply accessible to microbes, such as neutrophil gelatinase–associated lipocalin (NGAL or lipocalin-2), lactoferrin, and natural resistance–associated macrophage protein 1 (NRAMP1).…”