Abstract

Iron is a key transition metal required by most microorganisms and is prominently utilised in the transfer of electrons during metabolic reactions. The acquisition of iron is essential and becomes a crucial pathogenic event for opportunistic fungi. Iron is not readily available in the natural environment as it exists in its insoluble ferric form, i.e., in oxides and hydroxides. During infection, the host iron is bound to proteins such as transferrin, ferritin, and haemoglobin. As such, access to iron is one of the major hurdles that fungal pathogens must overcome in an immunocompromised host. Thus, these opportunistic fungi utilise three major iron acquisition systems to overcome this limiting factor for growth and proliferation. To date, numerous iron acquisition pathways have been fully characterised, with key components of these systems having major roles in virulence. Most recently, proteins involved in these pathways have been linked to the development of antifungal resistance. Here, we provide a detailed review of our current knowledge of iron acquisition in opportunistic fungi, and the role iron may have on the development of resistance to antifungals with emphasis on species of the fungal basal lineage order Mucorales, the causative agents of mucormycosis.

Highlights

  • In biology, iron is an essential micronutrient for almost all eukaryotes and most prokaryotes [1].Iron is the fourth most abundant trace element in the environment, but the bioavailability (Fe2+ ) is limited due to oxidation into the insoluble ferric hydroxides (Fe3+ ) by atmospheric oxygen [2]

  • We provide a detailed review of our current knowledge of iron acquisition in opportunistic fungi, and the role iron may have on the development of resistance to antifungals with emphasis on species of the fungal basal lineage order Mucorales, the causative agents of mucormycosis

  • Growth is seen when higher concentrations of haemin are used as the only iron source. These results strongly indicate that the Pga7 protein is an essential member of the CFEM haemophore cascade and it is required for the uptake/utilisation of albumin-bound haemin [91]

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Summary

Introduction

Iron is an essential micronutrient for almost all eukaryotes and most prokaryotes [1].Iron is the fourth most abundant trace element in the environment, but the bioavailability (Fe2+ ) is limited due to oxidation into the insoluble ferric hydroxides (Fe3+ ) by atmospheric oxygen [2]. The involvement of iron in numerous important metabolic processes and as enzyme cofactors is due to its capacity for electron exchange [4] This transition metal is required in DNA, RNA and amino acid synthesis, oxygen transport, cellular respiration (iron-sulphur cluster (Fe-S) containing ferredoxins, haem-containing cytochromes), enzymatic reactions such as Fe-S proteins, e.g., fumarase and aconitase of the tricarboxylic acid cycle (TCA cycle) [5,6,7]. It is a key trace element, iron presents a danger to biological systems

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