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Iron acquisition and siderophore production in the fish pathogen Renibacterium salmoninarum
Author(s) -
Bethke J,
PobleteMorales M,
Irgang R,
Yáñez A,
AvendañoHerrera R
Publication year - 2016
Publication title -
journal of fish diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.819
H-Index - 85
eISSN - 1365-2761
pISSN - 0140-7775
DOI - 10.1111/jfd.12456
Subject(s) - biology , siderophore , pathogen , microbiology and biotechnology , fish <actinopterygii> , fish farming , aquaculture , fishery , bacteria , genetics
Abstract Renibacterium salmoninarum is the causative agent of bacterial kidney disease, which significantly affects salmonid farming worldwide. Despite this impact, there is scarce data on its iron uptake ability, a factor of pathogenesis. This study investigated the iron acquisition mechanisms of R. salmoninarum and its capacity to uptake iron from different sources. Thirty‐two Chilean isolates and the DSM 20767 T type strain grew in the presence of 2,2′‐Dipyridyl at varying concentrations (250–330 μ m ), and all isolates positively reacted on chrome azurol S agar. Subsequently, inocula of four Chilean isolates and the type strain were prepared with or without 200 μ m of 2,2′‐Dipyridyl for uptake assays. Assay results revealed differences between the isolates in terms of iron acquisition. While a prior iron‐limited environment was, for most isolates, not required to activate the uptake of iron ( II ) sulphate, ammonium iron ( III ) citrate or iron ( III ) chloride at higher concentrations (100 μ m ), it did facilitate growth at lower iron concentrations (10 μ m and 1 μ m ). An exception was the H‐2 isolate, which only grew with 100 μ m of iron sulphide. In turn, 100 μ m of haemin was toxic when isolates were grown in normal KDM ‐2. In silico R. salmoninarum ATCC 33209 T genome analysis detected various genes coding iron uptake‐related proteins. This is the first study indicating two iron acquisition systems in R. salmoninarum : one involving siderophores and another involving haem group utilization. These data represent a first step towards fully elucidating this virulence factor in the pathogenic R. salmoninarum .

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