Renibacterium salmoninarum iron-acquisition mechanisms and ASK cell line infection : Virulence and immune response
© 2019 John Wiley & Sons Ltd.
Veröffentlicht in: | Journal of fish diseases. - 1998. - 42(2019), 9 vom: 01. Sept., Seite 1283-1291 |
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1. Verfasser: | |
Weitere Verfasser: | , , |
Format: | Online-Aufsatz |
Sprache: | English |
Veröffentlicht: |
2019
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Zugriff auf das übergeordnete Werk: | Journal of fish diseases |
Schlagworte: | Journal Article R. salmoninarum ASK BKD immune response iron siderophore Iron E1UOL152H7 |
Zusammenfassung: | © 2019 John Wiley & Sons Ltd. Renibacterium salmoninarum is the aetiological agent of bacterial kidney disease (BKD) in salmonid farms. This pathogen possesses at least three iron-acquisition mechanisms, but the link between these mechanisms and virulence is unclear. Therefore, this study used RT-qPCR to assess the effects of normal and iron-limited conditions on iron-uptake genes controlled by IdeR and related to iron acquisition in Chilean R. salmoninarum strain H-2 and the type strain DSM20767T . Further evaluated was the in vitro immune-related response of the Atlantic Salmon Kidney (ASK) cell line, derived from the primary organ affected by BKD. R. salmoninarum grown under iron-limited conditions overexpressed genes involved in haemin uptake and siderophore transport, with overexpression significantly higher in H-2 than DSM20767T . These overexpressed genes resulted in higher cytotoxicity and an increased immune response (i.e., TNF-α, IL-1β, TLR1 and INF-γ) in the ASK cell line. This response was significantly higher against bacteria grown under iron-limited conditions, especially H-2. These observations indicate that iron-acquisition mechanisms are possibly highly related to the virulence and pathogenic capacity of R. salmoninarum. In conclusion, treatments that block iron-uptake mechanisms or siderophore synthesis are attractive therapeutic approaches for treating R. salmoninarum, which causes significant aquaculture losses |
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Beschreibung: | Date Completed 28.01.2020 Date Revised 09.12.2020 published: Print-Electronic GENBANK: NC_010168.1 Citation Status MEDLINE |
ISSN: | 1365-2761 |
DOI: | 10.1111/jfd.13051 |