Iron is known to catalyze a wide range of biochemical reactions essential for most living organisms, including Campylobacter jejuni. Paradoxically, this iron reactivity is also responsible for the generation of hydroxyl radicals (·OH), which are particularly biotoxic. In order to avoid iron toxicity, microorganisms must achieve an effective iron homeostasis by tightly regulating the expression of genes encoding the proteins involved in iron acquisition, metabolism and oxidative stress defences in response to iron availability. Interestingly, in addition to the classical ferric uptake regulator Fur, C. jejuni carries another member of the Fur family of metalloregulators, PerR. PerR is a peroxide-sensing regulator and typically regulates peroxide stress response in Gram-positive bacteria. Recent work indicates that the regulatory functions of Fur and PerR extend beyond their classically ascribed roles. These diverse functions include energy metabolism, protein glycosylation and flagella biogenesis. Moreover, the Fur and PerR regulons appear to overlap and co-regulate key genes at specific junctions.

Further reading: Iron Uptake and Homeostasis in Microorganisms

Labels: Campylobacter, Iron acquisition mechanisms, Iron transporters, Iron uptake in Campylobacter, Iron uptake systems, Iron-homeostasis, Iron-metabolism, Iron-uptake

Bacteroides spp. have an essential requirement for heme and non-heme iron. They cannot synthesize the tetrapyrrole macrocycle ring due to a lack of genes for the heme biosynthetic pathway. It is remarkable that heme-dependent organisms outnumber heme-independent organisms in the lower intestinal tract suggesting that heme biosynthesis is not essential for colonization of the colonic environment. However, this colonization advantage may be due to the fact that under anaerobic conditions in the presence of heme, B. fragilis can generate nearly the double amount of ATP than Escherichia coli per mol of glucose. This high energy yield is linked to a rudimentary heme-induced fumarate reductase and cytochrome b-dependent electron transport energy metabolism pathway which uses fumarate as the terminal electron acceptor. Moreover, Bacteroides spp. can incorporate iron-deuteroporphyrin and iron-mesoporphyrin into a functional type-b cytochrome. Heme can be demetalated without cleaving the tetrapyrrole ring releasing free iron and free protoporphirin IX. The ability of the opportunistic human pathogen B. fragilis to cause infections seems to be due in part to its ability to scavenge heme and iron from host proteins. The in-frame translated intergenic region of the fused FeoAB proteins are exclusively present in gastro-intestinal colonizers belonging to the Bacteroidetes, Firmicutes and Actinobacteria phyla. Several members of the Bacteroides group have three orthologs of the mammalian-type bacterial ferritin gene, ftnA. FtnA may play an important role in protection against iron-induced oxidative stress in this group of highly aerotolerant anaerobes.

Further reading: Iron Uptake and Homeostasis in Microorganisms

Labels: Bacteroides, Iron acquisition mechanisms, Iron transporters, Iron uptake in Bacteroides, Iron uptake systems, Iron-homeostasis, Iron-metabolism, Iron-uptake

Francisella tularensis is unusual among Gram-negative bacteria in that its genome does not encode orthologs for TonB, ExbB and ExbD that typically energize the uptake of iron across the outer membrane. This organism secretes however a siderophore similar in structure to rhizoferrin. The fsl operon of six genes encodes functions for biosynthesis and uptake of the siderophore. Two of these genes encode a siderophore synthetase belonging to the nonribosomal peptide synthetase (NRPS)-independent synthetase (NIS)-family and a protein belonging to the pyridoxyl phosphate-dependent decarboxylase family, and both are required for siderophore production. Siderophore utilization involves the product of the fslE gene, a protein unique to Francisella species that could function as a siderophore receptor. Additionally, genes related in sequence to fslE also play a role in siderophore acquisition. The mechanism for TonB-independent iron uptake in this microorganism remains to be elucidated.

Further reading: Iron Uptake and Homeostasis in Microorganisms

Labels: Francisella, Iron acquisition mechanisms, Iron transporters, Iron uptake in Francisella, Iron uptake systems, Iron-homeostasis, Iron-metabolism, Iron-uptake

The critical role of iron in host-pathogen relationships has been elucidated in infectious diseases of mammals, where the importance of siderophores in microbial pathogenesis has been demonstrated. Our group has established the role of iron and its ligands in the virulence of the plant pathogenic bacteria Dickeya dadantii (Erwinia chrysanthemi) and Erwinia amylovora. The genomes of the two pectinolytic enterobacterial species Pectobacterium atrosepticum SCRI1043 and D. dadantii 3937 have been sequenced and annotated. This review focuses on the functions involved in iron acquisition in both species. Besides the production and utilization of siderophores, P. atrosepticum and D. datantii have the capacity to use other iron sources. Indeed, both species are able to use haem iron, whereas only P. atrosepticum can transport the ferric citrate complex and only D. dadantii can acquire ferrous iron. These different modes of iron capture indicate that these species have to cope with various environmental and ecological conditions during their pathogenic life cycle.

Further reading: Iron Uptake and Homeostasis in Microorganisms

Labels: Erwinia, Iron capture, Iron transport systems, Iron uptake in Erwinia, Iron uptake systems, Iron-homeostasis, Iron-metabolism, Iron-uptake

Shigella spp. and pathogenic E. coli are characterized by a variety and abundance of iron transport systems. Although members of this group of bacteria are closely related genetically, they differ widely in the iron transport systems they use. This may reflect the different niches occupied by different strains and the nature of the source of iron available in a specific environment. Only the ferrous iron transporter Feo is common to all the commensals and pathogens. All members of this group produce one or more siderophore, but no single siderophore is produced by all. Other iron transport systems include heme transporters and the ferrous iron transporters Sit and Efe. With the exception of the genes for enterobactin and the Feo system, the iron transport genes in the enterics are found within pathogenicity islands or on plasmids and their presence often increases pathogenicity or colonization of niches within the host.

Further reading: Iron Uptake and Homeostasis in Microorganisms

Labels: E. coli, Iron transport systems, Iron-homeostasis, Iron-metabolism, Iron-uptake, Shigella

The rhizobia live as free-living soil bacteria or in symbiosis with leguminous plants. The success of these organisms in each milieu involves the ability to sense the environment to assess the availability of nutrients, and to optimize cellular systems for their acquisition. Iron in the rhizosphere is mostly inaccessible due to low solubility, and microorganisms must compete for this limited nutrient. Rhizobia belong to the alpha-Proteobacteria, a diverse taxonomic group that includes numerous species that form close or intracellular associations with eukaryotic hosts in a symbiotic or pathogenic context.

Thus, in addition to their agricultural and economic importance, rhizobia are model organisms that have given new insights into related, but less tractable animal pathogens. In particular, genetic control of iron homeostasis in the rhizobia and other alpha-Proteobacteria has moved away from the Fur paradigm to an iron sensing mechanism responding to the metal indirectly. Moreover, utilization of heme as an iron source is not unique to animal pathogens, but is an acquisition strategy employed by the rhizobia with some interesting novel features.

Further reading: Iron Uptake and Homeostasis in Microorganisms

Labels: Iron transporters, Iron uptake in Rhizobia, Iron uptake systems, Iron-homeostasis, Iron-metabolism, Iron-uptake, Proteobacteria, Rhizobia, Rhizobium

Iron is essential for almost all living organisms as it is involved in a wide variety of important metabolic processes. However, iron is not readily available and microorganisms therefore employ various iron uptake systems to secure sufficient supplies from their surroundings. There is considerable variation in the range of iron transporters and iron sources utilised by different microbial species. Pathogens, in particular, require efficient iron acquisition mechanisms to enable them to compete successfully for iron in the highly iron-restricted environment of the host's tissues and body fluids.

Further reading: Iron Uptake and Homeostasis in Microorganisms

Labels: Iron acquisition mechanisms, Iron transporters, Iron uptake systems, Iron-homeostasis, Iron-metabolism, Iron-uptake