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Bacterial iron transporter (None standardized; individual systems may use abbreviations (e.g., FeoB, SitABCD, Yfe, Ftr1p, ABC transporters))

Target
None standardized; individual systems may use abbreviations (e.g., FeoB, SitABCD, Yfe, Ftr1p, ABC transporters)
Molecular classification
Transporter, ABC transporter (ATP-binding cassette), Major facilitator superfamily transporter, Siderophore receptor, Iron/lead transporter family (ILT)
01

Overview

Bacterial iron transporters are membrane proteins and complexes responsible for the uptake of iron, an essential nutrient for bacterial metabolism and growth. Since iron is tightly sequestered in hosts, bacteria have evolved multiple specialized transporters to acquire iron from the environment or host during infection. These include ABC transporters, major facilitator superfamily transporters, and a variety of siderophore receptors—proteins that bind iron-chelating agents (siderophores) secreted by bacteria to scavenge iron. Prominent systems include FeoB (ferrous iron transporter), FepA/FhuA (siderophore receptors for ferric iron), and SitABCD and YfeABCD families. Their activity supports bacterial virulence and persistence, thus these transporters are attractive targets for new antimicrobial agents, including drugs that exploit them to enter bacterial cells (“Trojan horse” antibiotics like cefiderocol) or that block iron uptake directly. Redundant and overlapping pathways exist within and between bacterial species, presenting unique challenges for therapeutic targeting[1][2][3][4][5][7].

Other names
Iron transporterFe transporter (e.g., FeoB, FepA, SitABCD, YfeABCD)Siderophore receptor (e.g., FepA, FhuA)Ferrous iron transporter (e.g., FeoB, SitABCD)Ferric iron transporterSiderophore-mediated iron transporters
02

Mechanism of action

Inhibition of iron transport: drugs may block the transporter, preventing iron uptake and starving bacteria of a necessary nutrient; Trojan horse strategy: drugs (e.g., antibiotics) linked to siderophores are transported into bacteria via iron transporters, increasing drug uptake and potency

03

Biological functions

Iron uptake and homeostasisMetabolic supportBacterial proliferationPathogenesis and virulence
04

Disease associations

Infection: essential for bacterial growth during host infection and a key virulence determinantOther: indirectly involved in inflammation due to infectious processes
05

Safety considerations

Bacterial iron acquisition systems are diverse and redundant; inhibition of one transporter may not be sufficient due to compensatory mechanismsSpecificity to bacterial vs. host iron transporters must be ensured to minimize host toxicityRisk of off-target effects in host tissues if drug/siderophore mimicry leads to altered iron metabolism
06

Interacting drugs

Siderophore–antibiotic conjugates (e.g., cefiderocol, a siderophore-cephalosporin)

2 more in the full profile.

07

Biomarkers

Bacterial growth in iron-limited environmentsExpression of iron transport genes (e.g., feoB, sitABCD, yfe)Secreted siderophore detection in patient samples

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