Identification of a system for hydroxamate xenosiderophore-mediated iron transport in Burkholderia cenocepacia

Author:

Hussein Syakira Mohammed1ORCID,Sofoluwe Aderonke21ORCID,Paleja Ameya1,Duhme-Klair Anne3ORCID,Thomas Mark S.1ORCID

Affiliation:

1. Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Medical School, Beech Hill Road, Sheffield S10 2RX, UK

2. Department of Immunobiology, School of Immunology & Microbial Sciences, King’s College London, London WC2R 2LS, UK

3. Department of Chemistry, University of York, Heslington, York YO10 5DD, UK

Abstract

One of the mechanisms employed by the opportunistic pathogen Burkholderia cenocepacia to acquire the essential element iron is the production and release of two ferric iron chelating compounds (siderophores), ornibactin and pyochelin. Here we show that B. cenocepacia is also able to take advantage of a range of siderophores produced by other bacteria and fungi (‘xenosiderophores’) that chelate iron exclusively by means of hydroxamate groups. These include the tris-hydroxamate siderophores ferrioxamine B, ferrichrome, ferricrocin and triacetylfusarinine C, the bis-hydroxamates alcaligin and rhodotorulic acid, and the monohydroxamate siderophore cepabactin. We also show that of the 24 TonB-dependent transporters encoded by the B. cenocepacia genome, two (FhuA and FeuA) are involved in the uptake of hydroxamate xenosiderophores, with FhuA serving as the exclusive transporter of iron-loaded ferrioxamine B, triacetylfusarinine C, alcaligin and rhodotorulic acid, while both FhuA and FeuA are able to translocate ferrichrome-type siderophores across the outer membrane. Finally, we identified FhuB, a putative cytoplasmic membrane-anchored ferric-siderophore reductase, as being obligatory for utilization of all of the tested bis- and tris-hydroxamate xenosiderophores apart from alcaligin.

Funder

Ministry of Higher Education, Malaysia

Publisher

Microbiology Society

Subject

Microbiology

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