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Molecular cloning of IL-6, IL-10, IL-11, IFN-ɤ and modulation of pro- and anti-inflammatory cytokines in cobia (Rachycentron canadum) after Photobacterium damselae subsp. piscicida infection.

Authors :
Tran, Hung B.
Chen, Shih-Chu
Chaung, Hso-Chi
Cheng, Ta-Chih
Source :
Comparative Biochemistry & Physiology - Part B: Biochemistry & Molecular Biology. Apr2019, Vol. 230, p10-18. 9p.
Publication Year :
2019

Abstract

Abstract Photobacterium damselae subsp. piscicida (P. damselae subsp. piscicida) is the agent of Photobacteriosis, a serious fish disease that produces an acute infection and high mortality in farmed cobia. It has been proved that regulation of pro- and anti-inflammatory cytokines play a central role in initiation of proper inflammatory responses against bacterial infection. Here we have analyzed the expression of pro-inflammatory cytokines (IL-1β, TNF-α, IL-6, IL-8 and IFN-ɤ) and anti-inflammatory cytokines (IL-10 and IL-11) in spleen and head kidney during acute P. damselae subsp. piscicida infection of cobia. Our data revealed that cytokines tested showed distinct patterns of expression. While TNF-α and IL-8 showed a decay pattern of expression, IL-1β response was quite late. Moreover, P. damselae subsp. piscicida infection induced the simultaneous expressions of pro-inflammatory (IL-6, IFN-ɤ) and anti-inflammatory (IL-10, IL-11) cytokines. Together these results indicate the innate immunity of cobia is actively suppressed by P. damselae subsp. piscicida. Highlights • IL-6, IL-10, IL-11 and IFN-ɤ have been identified in cobia. • The expression pattern of cytokines was characterized by a depression of TNF-α and IL-8, a delayed response of IL-1β and simultaneous up-regulations of IL-6, IL-10, IL-11 and IFN-ɤ. • The cytokine disparity may explain the suppression of innate immunity by P. damselae subsp. piscicida in cobia. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10964959
Volume :
230
Database :
Academic Search Index
Journal :
Comparative Biochemistry & Physiology - Part B: Biochemistry & Molecular Biology
Publication Type :
Academic Journal
Accession number :
134689018
Full Text :
https://doi.org/10.1016/j.cbpb.2019.01.004