Modulation of splenic immune responses to bacterial lipopolysaccharide in rainbow trout ( Oncorhynchus mykiss) fed lentinan, a beta-glucan from mushroom Lentinula edodes
Immunostimulants (IS) are considered a promising approach for improving resistance to pathogens in fish aquaculture. At present, development of IS are complicated due to limited knowledge on the mechanisms of their action. To assess the use of global gene expression analysis for screening of candida...
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description | Immunostimulants (IS) are considered a promising approach for improving resistance to pathogens in fish aquaculture. At present, development of IS are complicated due to limited knowledge on the mechanisms of their action. To assess the use of global gene expression analysis for screening of candidate IS we applied lentinan, a β-glucan from the mushroom
Lentinula edodes, as a model. After feeding rainbow trout (
Oncorhynchus mykiss) with lentinan-supplemented (L) and control (C) diets for 37 days, fish were injected with bacterial lipopolysaccharide (LPS), a classical inducer of inflammation. Gene expression was analyzed in LPS-challenged compared to saline-injected fish using a salmonid 1.8
k cDNA microarray (SFA2.0 immunochip) and real-time qPCR. Spleen was selected for data analyses due to highest magnitude of responses and its key role in the fish immune system. A group of genes implicated in acute inflammatory responses was higher induced in C versus L, including IFN-related and TNF-dependent genes (galectins and receptors, signal transducers and transcription factors), genes involved in MHC class I antigen presentation and leukocyte recruitment. A similar trend was observed in metabolism of iron and xenobiotics, markers of oxidative and cellular stress. Interestingly, differences between C and L were similar to those observed between salmon with low and high resistance to infectious salmon anemia virus. Genes with equal responses to LPS in L and C were related to cell communication (cytokines, chemokines and receptors), signal transduction, activation of immune cells, apoptosis, cellular maintenance and energy metabolism. In conclusion, lentinan decreased the expression of genes involved in acute inflammatory reactions to the inflammatory agent while major parts of the immune response remained unchanged. Such effects are expected for IS, which should modify immunity by enhancing beneficial and reducing detrimental responses. |
doi_str_mv | 10.1016/j.fsi.2008.10.012 |
format | Article |
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Lentinula edodes, as a model. After feeding rainbow trout (
Oncorhynchus mykiss) with lentinan-supplemented (L) and control (C) diets for 37 days, fish were injected with bacterial lipopolysaccharide (LPS), a classical inducer of inflammation. Gene expression was analyzed in LPS-challenged compared to saline-injected fish using a salmonid 1.8
k cDNA microarray (SFA2.0 immunochip) and real-time qPCR. Spleen was selected for data analyses due to highest magnitude of responses and its key role in the fish immune system. A group of genes implicated in acute inflammatory responses was higher induced in C versus L, including IFN-related and TNF-dependent genes (galectins and receptors, signal transducers and transcription factors), genes involved in MHC class I antigen presentation and leukocyte recruitment. A similar trend was observed in metabolism of iron and xenobiotics, markers of oxidative and cellular stress. Interestingly, differences between C and L were similar to those observed between salmon with low and high resistance to infectious salmon anemia virus. Genes with equal responses to LPS in L and C were related to cell communication (cytokines, chemokines and receptors), signal transduction, activation of immune cells, apoptosis, cellular maintenance and energy metabolism. In conclusion, lentinan decreased the expression of genes involved in acute inflammatory reactions to the inflammatory agent while major parts of the immune response remained unchanged. Such effects are expected for IS, which should modify immunity by enhancing beneficial and reducing detrimental responses.</description><identifier>ISSN: 1050-4648</identifier><identifier>EISSN: 1095-9947</identifier><identifier>DOI: 10.1016/j.fsi.2008.10.012</identifier><identifier>PMID: 19010422</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adjuvants, Immunologic - administration & dosage ; Adjuvants, Immunologic - pharmacology ; Animals ; Bacteria ; Beta-glucan ; Brackish ; Escherichia coli - chemistry ; Freshwater ; Functional genomics ; Gene Expression Regulation - drug effects ; Genes - genetics ; Immune System - drug effects ; Immunostimulant ; Infectious salmon anemia virus ; Lentinan ; Lentinan - administration & dosage ; Lentinan - pharmacology ; Lentinula edodes ; Lipopolysaccharides - pharmacology ; LPS ; Marine ; Microarray ; Oncorhynchus mykiss ; Oncorhynchus mykiss - immunology ; Rainbow trout ; Shiitake Mushrooms - chemistry ; Spleen - drug effects ; Spleen - immunology</subject><ispartof>Fish & shellfish immunology, 2009-02, Vol.26 (2), p.201-209</ispartof><rights>2008 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-3340c880b45446b82c10ecc471369e5b750fcd25869f64ac4ce2fc65a8ce77d93</citedby><cites>FETCH-LOGICAL-c382t-3340c880b45446b82c10ecc471369e5b750fcd25869f64ac4ce2fc65a8ce77d93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1050464808002349$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19010422$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Djordjevic, Brankica</creatorcontrib><creatorcontrib>Škugor, Stanko</creatorcontrib><creatorcontrib>Jørgensen, Sven Martin</creatorcontrib><creatorcontrib>Øverland, Margareth</creatorcontrib><creatorcontrib>Mydland, Liv Torunn</creatorcontrib><creatorcontrib>Krasnov, Aleksei</creatorcontrib><title>Modulation of splenic immune responses to bacterial lipopolysaccharide in rainbow trout ( Oncorhynchus mykiss) fed lentinan, a beta-glucan from mushroom Lentinula edodes</title><title>Fish & shellfish immunology</title><addtitle>Fish Shellfish Immunol</addtitle><description>Immunostimulants (IS) are considered a promising approach for improving resistance to pathogens in fish aquaculture. At present, development of IS are complicated due to limited knowledge on the mechanisms of their action. To assess the use of global gene expression analysis for screening of candidate IS we applied lentinan, a β-glucan from the mushroom
Lentinula edodes, as a model. After feeding rainbow trout (
Oncorhynchus mykiss) with lentinan-supplemented (L) and control (C) diets for 37 days, fish were injected with bacterial lipopolysaccharide (LPS), a classical inducer of inflammation. Gene expression was analyzed in LPS-challenged compared to saline-injected fish using a salmonid 1.8
k cDNA microarray (SFA2.0 immunochip) and real-time qPCR. Spleen was selected for data analyses due to highest magnitude of responses and its key role in the fish immune system. A group of genes implicated in acute inflammatory responses was higher induced in C versus L, including IFN-related and TNF-dependent genes (galectins and receptors, signal transducers and transcription factors), genes involved in MHC class I antigen presentation and leukocyte recruitment. A similar trend was observed in metabolism of iron and xenobiotics, markers of oxidative and cellular stress. Interestingly, differences between C and L were similar to those observed between salmon with low and high resistance to infectious salmon anemia virus. Genes with equal responses to LPS in L and C were related to cell communication (cytokines, chemokines and receptors), signal transduction, activation of immune cells, apoptosis, cellular maintenance and energy metabolism. In conclusion, lentinan decreased the expression of genes involved in acute inflammatory reactions to the inflammatory agent while major parts of the immune response remained unchanged. Such effects are expected for IS, which should modify immunity by enhancing beneficial and reducing detrimental responses.</description><subject>Adjuvants, Immunologic - administration & dosage</subject><subject>Adjuvants, Immunologic - pharmacology</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Beta-glucan</subject><subject>Brackish</subject><subject>Escherichia coli - chemistry</subject><subject>Freshwater</subject><subject>Functional genomics</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Genes - genetics</subject><subject>Immune System - drug effects</subject><subject>Immunostimulant</subject><subject>Infectious salmon anemia virus</subject><subject>Lentinan</subject><subject>Lentinan - administration & dosage</subject><subject>Lentinan - pharmacology</subject><subject>Lentinula edodes</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>LPS</subject><subject>Marine</subject><subject>Microarray</subject><subject>Oncorhynchus mykiss</subject><subject>Oncorhynchus mykiss - immunology</subject><subject>Rainbow trout</subject><subject>Shiitake Mushrooms - chemistry</subject><subject>Spleen - drug effects</subject><subject>Spleen - immunology</subject><issn>1050-4648</issn><issn>1095-9947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcuO1DAQRSMEYh7wAWyQV4iRSONXnESzQiNeUqPZwNpyyhXaTWIH2wH1J_GXuOmW2MHK5dKpa6tOVT1jdMMoU6_3mzG5Dae0K_cNZfxBdclo39R9L9uHx7qhtVSyu6iuUtpTSpVQ9HF1wXrKqOT8svr1Kdh1MtkFT8JI0jKhd0DcPK8eScS0BJ8wkRzIYCBjdGYik1vCEqZDMgA7E51F4jyJxvkh_CQ5hjWTl-TeQ4i7g4fdmsh8-OZSuiEjWlKeyM4b_4oYMmA29ddpBePJGMNM5jXtYijF9g9V_kbQBovpSfVoNFPCp-fzuvry7u3nuw_19v79x7s32xpEx3MthKTQdXSQjZRq6DgwigCyZUL12AxtQ0ewvOlUPyppQALyEVRjOsC2tb24rl6ccpcYvq-Ysp5dApwm4zGsSSvVc8FF-1-QU9H0jegKyE4gxJBSxFEv0c0mHjSj-ihS73URqY8ij60issw8P4evw4z278TZXAFuTwCWXfxwGHUChx7QuoiQtQ3uH_G_AcBssgs</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Djordjevic, Brankica</creator><creator>Škugor, Stanko</creator><creator>Jørgensen, Sven Martin</creator><creator>Øverland, Margareth</creator><creator>Mydland, Liv Torunn</creator><creator>Krasnov, Aleksei</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>7TN</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20090201</creationdate><title>Modulation of splenic immune responses to bacterial lipopolysaccharide in rainbow trout ( Oncorhynchus mykiss) fed lentinan, a beta-glucan from mushroom Lentinula edodes</title><author>Djordjevic, Brankica ; 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At present, development of IS are complicated due to limited knowledge on the mechanisms of their action. To assess the use of global gene expression analysis for screening of candidate IS we applied lentinan, a β-glucan from the mushroom
Lentinula edodes, as a model. After feeding rainbow trout (
Oncorhynchus mykiss) with lentinan-supplemented (L) and control (C) diets for 37 days, fish were injected with bacterial lipopolysaccharide (LPS), a classical inducer of inflammation. Gene expression was analyzed in LPS-challenged compared to saline-injected fish using a salmonid 1.8
k cDNA microarray (SFA2.0 immunochip) and real-time qPCR. Spleen was selected for data analyses due to highest magnitude of responses and its key role in the fish immune system. A group of genes implicated in acute inflammatory responses was higher induced in C versus L, including IFN-related and TNF-dependent genes (galectins and receptors, signal transducers and transcription factors), genes involved in MHC class I antigen presentation and leukocyte recruitment. A similar trend was observed in metabolism of iron and xenobiotics, markers of oxidative and cellular stress. Interestingly, differences between C and L were similar to those observed between salmon with low and high resistance to infectious salmon anemia virus. Genes with equal responses to LPS in L and C were related to cell communication (cytokines, chemokines and receptors), signal transduction, activation of immune cells, apoptosis, cellular maintenance and energy metabolism. In conclusion, lentinan decreased the expression of genes involved in acute inflammatory reactions to the inflammatory agent while major parts of the immune response remained unchanged. Such effects are expected for IS, which should modify immunity by enhancing beneficial and reducing detrimental responses.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>19010422</pmid><doi>10.1016/j.fsi.2008.10.012</doi><tpages>9</tpages></addata></record> |
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subjects | Adjuvants, Immunologic - administration & dosage Adjuvants, Immunologic - pharmacology Animals Bacteria Beta-glucan Brackish Escherichia coli - chemistry Freshwater Functional genomics Gene Expression Regulation - drug effects Genes - genetics Immune System - drug effects Immunostimulant Infectious salmon anemia virus Lentinan Lentinan - administration & dosage Lentinan - pharmacology Lentinula edodes Lipopolysaccharides - pharmacology LPS Marine Microarray Oncorhynchus mykiss Oncorhynchus mykiss - immunology Rainbow trout Shiitake Mushrooms - chemistry Spleen - drug effects Spleen - immunology |
title | Modulation of splenic immune responses to bacterial lipopolysaccharide in rainbow trout ( Oncorhynchus mykiss) fed lentinan, a beta-glucan from mushroom Lentinula edodes |
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