Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).

Short-term feed deprivation (or fasting) is a common occurrence in aquacultured fish species whether due to season, production strategies, or disease. In channel catfish (Ictalurus punctatus) fasting impacts susceptibility to several bacterial pathogens including Flavobacterium columnare, the causat...

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Main Authors: Lisa Liu, Chao Li, Baofeng Su, Benjamin H Beck, Eric Peatman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24023952/?tool=EBI
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spelling doaj-7e16721228524b6599a5a1dc21bd3a972021-03-03T20:20:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7458110.1371/journal.pone.0074581Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).Lisa LiuChao LiBaofeng SuBenjamin H BeckEric PeatmanShort-term feed deprivation (or fasting) is a common occurrence in aquacultured fish species whether due to season, production strategies, or disease. In channel catfish (Ictalurus punctatus) fasting impacts susceptibility to several bacterial pathogens including Flavobacterium columnare, the causative agent of columnaris disease. As columnaris gains entry through the gills and skin of fish, we examined here changes in transcriptional regulation induced in these surface mucosal tissues due to short-term (7 day) fasting. RNA-seq expression analysis revealed a total of 1,545 genes perturbed by fasting. Fasting significantly altered expression of critical innate immune factors in a manner consistent with lower immune fitness as well as dysregulating key genes involved in energy metabolism and cell cycling/proliferation. Downregulation of innate immune actors such as iNOS2b, Lysozyme C, and peptidoglycan recognition protein 6 is predicted to impact the delicate recognition/tolerance balance for commensal and pathogenic bacteria on the skin and gill. The highlighted expression profiles reveal potential mechanistic similarities between gut and surface mucosa and underscore the complex interrelationships between nutrition, mucosal integrity, and immunity in teleost fish.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24023952/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Lisa Liu
Chao Li
Baofeng Su
Benjamin H Beck
Eric Peatman
spellingShingle Lisa Liu
Chao Li
Baofeng Su
Benjamin H Beck
Eric Peatman
Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).
PLoS ONE
author_facet Lisa Liu
Chao Li
Baofeng Su
Benjamin H Beck
Eric Peatman
author_sort Lisa Liu
title Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).
title_short Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).
title_full Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).
title_fullStr Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).
title_full_unstemmed Short-term feed deprivation alters immune status of surface mucosa in channel catfish (Ictalurus punctatus).
title_sort short-term feed deprivation alters immune status of surface mucosa in channel catfish (ictalurus punctatus).
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Short-term feed deprivation (or fasting) is a common occurrence in aquacultured fish species whether due to season, production strategies, or disease. In channel catfish (Ictalurus punctatus) fasting impacts susceptibility to several bacterial pathogens including Flavobacterium columnare, the causative agent of columnaris disease. As columnaris gains entry through the gills and skin of fish, we examined here changes in transcriptional regulation induced in these surface mucosal tissues due to short-term (7 day) fasting. RNA-seq expression analysis revealed a total of 1,545 genes perturbed by fasting. Fasting significantly altered expression of critical innate immune factors in a manner consistent with lower immune fitness as well as dysregulating key genes involved in energy metabolism and cell cycling/proliferation. Downregulation of innate immune actors such as iNOS2b, Lysozyme C, and peptidoglycan recognition protein 6 is predicted to impact the delicate recognition/tolerance balance for commensal and pathogenic bacteria on the skin and gill. The highlighted expression profiles reveal potential mechanistic similarities between gut and surface mucosa and underscore the complex interrelationships between nutrition, mucosal integrity, and immunity in teleost fish.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24023952/?tool=EBI
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