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Campylobacter jejuni ferric-enterobactin receptor CfrA is TonB3 dependent and mediates iron acquisition from structurally different catechol siderophores.
- Source :
-
Metallomics : integrated biometal science [Metallomics] 2013 Aug; Vol. 5 (8), pp. 988-96. - Publication Year :
- 2013
-
Abstract
- Campylobacter jejuni NCTC11168 does not produce any endogenous siderophores of its own yet requires the CfrA enterobactin transporter for in vivo colonization. In addition, the genome of C. jejuni NCTC11168 contains three distinct TonB energy transduction systems, named TonB1, TonB2, and TonB3, that have not been tested for their role in siderophore uptake or their functional redundancy. We demonstrate that C. jejuni NCTC11168 transports ferric-enterobactin in an energy dependent manner that requires TonB3 for full activity with TonB1 showing partial functional redundancy. Moreover C. jejuni NCTC11168 can utilize a wide variety of structurally different catechol siderophores as sole iron sources during growth. This growth is solely dependent on the CfrA enterobactin transporter and highlights the wide range of substrates that this transporter can recognize. TonB3 is also required for growth on most catechol siderophores. Furthermore, either TonB1 or TonB3 is sufficient for growth on hemin or hemoglobin as a sole iron source demonstrating functional redundancy between TonB1 and TonB3. In vivo colonization assays with isogenic deletion mutants revealed that both TonB1 and TonB3 are required for chick colonization with TonB2 dispensable in this model. These results further highlight the importance of iron transport for efficient C. jejuni colonization.
- Subjects :
- Animals
Cattle
Chickens
Enterobactin chemistry
Gene Deletion
Genetic Complementation Test
Genome, Bacterial
Genotype
Humans
Ligands
Mutation
Phenotype
Siderophores chemistry
Time Factors
Bacterial Outer Membrane Proteins chemistry
Bacterial Proteins chemistry
Campylobacter jejuni metabolism
Carrier Proteins chemistry
Catechols chemistry
Iron chemistry
Membrane Proteins chemistry
Receptors, Cell Surface chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1756-591X
- Volume :
- 5
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Metallomics : integrated biometal science
- Publication Type :
- Academic Journal
- Accession number :
- 23702883
- Full Text :
- https://doi.org/10.1039/c3mt20254b