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Impact of high dietary plant protein with or without marine ingredients in gut mucosa proteome of gilthead seabream (Sparus aurata, L.)

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Impact of high dietary plant protein with or without marine ingredients in gut mucosa proteome of gilthead seabream (Sparus aurata, L.)

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Estruch, G.; Martínez-Llorens, S.; Tomas-Vidal, A.; Monge-Ortiz, R.; Jover Cerda, M.; Brown, PB.; Peñaranda, D. (2020). Impact of high dietary plant protein with or without marine ingredients in gut mucosa proteome of gilthead seabream (Sparus aurata, L.). Journal of Proteomics. 216:1-13. https://doi.org/10.1016/j.jprot.2020.103672

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Title: Impact of high dietary plant protein with or without marine ingredients in gut mucosa proteome of gilthead seabream (Sparus aurata, L.)
Author: Estruch, Guillem Martínez-Llorens, Silvia Tomas-Vidal, A. Monge-Ortiz, Raquel Jover Cerda, Miguel Brown, Paul B. Peñaranda, D.S.
UPV Unit: Universitat Politècnica de València. Departamento de Ciencia Animal - Departament de Ciència Animal
Issued date:
Abstract:
[EN] The digestive tract, particularly the intestine, represents one of the main sites of interactions with the environment, playing the gut mucosa a crucial role in the digestion and absorption of nutrients, and in the ...[+]
Subjects: Gilthead seabream , Plant sources , Gut mucosa , Alternative marine ingredients , Proteome , Label-free LC-MS/MS assay
Copyrigths: Reconocimiento - No comercial - Sin obra derivada (by-nc-nd)
Source:
Journal of Proteomics. (issn: 1874-3919 )
DOI: 10.1016/j.jprot.2020.103672
Publisher:
Elsevier
Publisher version: https://doi.org/10.1016/j.jprot.2020.103672
Project ID:
info:eu-repo/grantAgreement/MECD//FPU13%2F01278/ES/FPU13%2F01278/
Thanks:
The first author was supported by a contract-grant (Contrato Pre doctoral para la Formacion de Profesorado Universitario) from Subprogramas de Formacion y Movilidad within the Programa Estatal de Promocion del Talento y ...[+]
Type: Artículo

References

Martínez-Llorens, S., Moñino, A. V., Tomás Vidal, A., Salvador, V. J. M., Pla Torres, M., & Jover Cerdá, M. (2007). Soybean meal as a protein source in gilthead sea bream (Sparus aurata L.) diets: effects on growth and nutrient utilization. Aquaculture Research, 38(1), 82-90. doi:10.1111/j.1365-2109.2006.01637.x

Moutinho, S., Martínez-Llorens, S., Tomás-Vidal, A., Jover-Cerdá, M., Oliva-Teles, A., & Peres, H. (2017). Meat and bone meal as partial replacement for fish meal in diets for gilthead seabream ( Sparus aurata ) juveniles: Growth, feed efficiency, amino acid utilization, and economic efficiency. Aquaculture, 468, 271-277. doi:10.1016/j.aquaculture.2016.10.024

Piccolo, G., Iaconisi, V., Marono, S., Gasco, L., Loponte, R., Nizza, S., … Parisi, G. (2017). Effect of Tenebrio molitor larvae meal on growth performance, in vivo nutrients digestibility, somatic and marketable indexes of gilthead sea bream (Sparus aurata). Animal Feed Science and Technology, 226, 12-20. doi:10.1016/j.anifeedsci.2017.02.007 [+]
Martínez-Llorens, S., Moñino, A. V., Tomás Vidal, A., Salvador, V. J. M., Pla Torres, M., & Jover Cerdá, M. (2007). Soybean meal as a protein source in gilthead sea bream (Sparus aurata L.) diets: effects on growth and nutrient utilization. Aquaculture Research, 38(1), 82-90. doi:10.1111/j.1365-2109.2006.01637.x

Moutinho, S., Martínez-Llorens, S., Tomás-Vidal, A., Jover-Cerdá, M., Oliva-Teles, A., & Peres, H. (2017). Meat and bone meal as partial replacement for fish meal in diets for gilthead seabream ( Sparus aurata ) juveniles: Growth, feed efficiency, amino acid utilization, and economic efficiency. Aquaculture, 468, 271-277. doi:10.1016/j.aquaculture.2016.10.024

Piccolo, G., Iaconisi, V., Marono, S., Gasco, L., Loponte, R., Nizza, S., … Parisi, G. (2017). Effect of Tenebrio molitor larvae meal on growth performance, in vivo nutrients digestibility, somatic and marketable indexes of gilthead sea bream (Sparus aurata). Animal Feed Science and Technology, 226, 12-20. doi:10.1016/j.anifeedsci.2017.02.007

Nengas, I., Alexis, M. N., & Davies, S. J. (1999). High inclusion levels of poultry meals and related byproducts in diets for gilthead seabream Sparus aurata L. Aquaculture, 179(1-4), 13-23. doi:10.1016/s0044-8486(99)00148-9

Monge-Ortiz, R., Martínez-Llorens, S., Márquez, L., Moyano, F. J., Jover-Cerdá, M., & Tomás-Vidal, A. (2016). Potential use of high levels of vegetal proteins in diets for market-sized gilthead sea bream (Sparus aurata). Archives of Animal Nutrition, 70(2), 155-172. doi:10.1080/1745039x.2016.1141743

Sitjà-Bobadilla, A., Peña-Llopis, S., Gómez-Requeni, P., Médale, F., Kaushik, S., & Pérez-Sánchez, J. (2005). Effect of fish meal replacement by plant protein sources on non-specific defence mechanisms and oxidative stress in gilthead sea bream (Sparus aurata). Aquaculture, 249(1-4), 387-400. doi:10.1016/j.aquaculture.2005.03.031

Santigosa, E., Sánchez, J., Médale, F., Kaushik, S., Pérez-Sánchez, J., & Gallardo, M. A. (2008). Modifications of digestive enzymes in trout (Oncorhynchus mykiss) and sea bream (Sparus aurata) in response to dietary fish meal replacement by plant protein sources. Aquaculture, 282(1-4), 68-74. doi:10.1016/j.aquaculture.2008.06.007

Kiron, V. (2012). Fish immune system and its nutritional modulation for preventive health care. Animal Feed Science and Technology, 173(1-2), 111-133. doi:10.1016/j.anifeedsci.2011.12.015

Minghetti, M., Drieschner, C., Bramaz, N., Schug, H., & Schirmer, K. (2017). A fish intestinal epithelial barrier model established from the rainbow trout (Oncorhynchus mykiss) cell line, RTgutGC. Cell Biology and Toxicology, 33(6), 539-555. doi:10.1007/s10565-017-9385-x

Gómez, G. D., & Balcázar, J. L. (2008). A review on the interactions between gut microbiota and innate immunity of fish: Table 1. FEMS Immunology & Medical Microbiology, 52(2), 145-154. doi:10.1111/j.1574-695x.2007.00343.x

Yu, Y., Sitaraman, S., & Gewirtz, A. T. (2004). Intestinal Epithelial Cell Regulation of Mucosal Inflammation. Immunologic Research, 29(1-3), 055-068. doi:10.1385/ir:29:1-3:055

Ivanov, A. I., Parkos, C. A., & Nusrat, A. (2010). Cytoskeletal Regulation of Epithelial Barrier Function During Inflammation. The American Journal of Pathology, 177(2), 512-524. doi:10.2353/ajpath.2010.100168

Lokman, P., & Symonds, J. (2014). Molecular and biochemical tricks of the research trade: -omics approaches in finfish aquaculture. New Zealand Journal of Marine and Freshwater Research, 48(3), 492-505. doi:10.1080/00288330.2014.928333

Forné, I., Abián, J., & Cerdà, J. (2009). Fish proteome analysis: Model organisms and non-sequenced species. PROTEOMICS, 10(4), 858-872. doi:10.1002/pmic.200900609

Rodrigues, P. M., Silva, T. S., Dias, J., & Jessen, F. (2012). PROTEOMICS in aquaculture: Applications and trends. Journal of Proteomics, 75(14), 4325-4345. doi:10.1016/j.jprot.2012.03.042

Pandey, A., & Mann, M. (2000). Proteomics to study genes and genomes. Nature, 405(6788), 837-846. doi:10.1038/35015709

Karpievitch, Y. V., Polpitiya, A. D., Anderson, G. A., Smith, R. D., & Dabney, A. R. (2010). Liquid chromatography mass spectrometry-based proteomics: Biological and technological aspects. The Annals of Applied Statistics, 4(4). doi:10.1214/10-aoas341

Ahmed, F., Kumar, G., Soliman, F. M., Adly, M. A., Soliman, H. A. M., El-Matbouli, M., & Saleh, M. (2019). Proteomics for understanding pathogenesis, immune modulation and host pathogen interactions in aquaculture. Comparative Biochemistry and Physiology Part D: Genomics and Proteomics, 32, 100625. doi:10.1016/j.cbd.2019.100625

Sissener, N. H., Martin, S. A. M., Cash, P., Hevrøy, E. M., Sanden, M., & Hemre, G.-I. (2009). Proteomic Profiling of Liver from Atlantic Salmon (Salmo salar) Fed Genetically Modified Soy Compared to the Near-Isogenic non-GM Line. Marine Biotechnology, 12(3), 273-281. doi:10.1007/s10126-009-9214-1

Morais, S., Silva, T., Cordeiro, O., Rodrigues, P., Guy, D. R., Bron, J. E., … Tocher, D. R. (2012). Effects of genotype and dietary fish oil replacement with vegetable oil on the intestinal transcriptome and proteome of Atlantic salmon (Salmo salar). BMC Genomics, 13(1), 448. doi:10.1186/1471-2164-13-448

Martin, S. A. M., Cash, P., Blaney, S., & Houlihan, D. F. (2001). Fish Physiology and Biochemistry, 24(3), 259-270. doi:10.1023/a:1014015530045

Martin, S. A. M., Vilhelmsson, O., Médale, F., Watt, P., Kaushik, S., & Houlihan, D. F. (2003). Proteomic sensitivity to dietary manipulations in rainbow trout. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics, 1651(1-2), 17-29. doi:10.1016/s1570-9639(03)00231-0

Vilhelmsson, O. T., Martin, S. A. M., Médale, F., Kaushik, S. J., & Houlihan, D. F. (2004). Dietary plant-protein substitution affects hepatic metabolism in rainbow trout (Oncorhynchus mykiss). British Journal of Nutrition, 92(1), 71-80. doi:10.1079/bjn20041176

Kumar, G., Hummel, K., Razzazi-Fazeli, E., & El-Matbouli, M. (2019). Modulation of posterior intestinal mucosal proteome in rainbow trout (Oncorhynchus mykiss) after Yersinia ruckeri infection. Veterinary Research, 50(1). doi:10.1186/s13567-019-0673-8

Rajan, B., Lokesh, J., Kiron, V., & Brinchmann, M. F. (2013). Differentially expressed proteins in the skin mucus of Atlantic cod (Gadus morhua) upon natural infection with Vibrio anguillarum. BMC Veterinary Research, 9(1). doi:10.1186/1746-6148-9-103

Saleh, M., Kumar, G., Abdel-Baki, A.-A., Dkhil, M. A., El-Matbouli, M., & Al-Quraishy, S. (2018). Quantitative shotgun proteomics distinguishes wound-healing biomarker signatures in common carp skin mucus in response to Ichthyophthirius multifiliis. Veterinary Research, 49(1). doi:10.1186/s13567-018-0535-9

Saleh, M., Kumar, G., Abdel-Baki, A.-A. S., Dkhil, M. A., El-Matbouli, M., & Al-Quraishy, S. (2019). Quantitative proteomic profiling of immune responses to Ichthyophthirius multifiliis in common carp skin mucus. Fish & Shellfish Immunology, 84, 834-842. doi:10.1016/j.fsi.2018.10.078

ENYU, Y.-L., & SHU-CHIEN, A. C. (2011). Proteomics analysis of mitochondrial extract from liver of female zebrafish undergoing starvation and refeeding. Aquaculture Nutrition, 17(2), e413-e423. doi:10.1111/j.1365-2095.2010.00776.x

Boonanuntanasarn, S., Nakharuthai, C., Schrama, D., Duangkaew, R., & Rodrigues, P. M. (2019). Effects of dietary lipid sources on hepatic nutritive contents, fatty acid composition and proteome of Nile tilapia (Oreochromis niloticus). Journal of Proteomics, 192, 208-222. doi:10.1016/j.jprot.2018.09.003

Ghisaura, S., Anedda, R., Pagnozzi, D., Biosa, G., Spada, S., Bonaglini, E., … Addis, M. F. (2014). Impact of three commercial feed formulations on farmed gilthead sea bream (Sparus aurata, L.) metabolism as inferred from liver and blood serum proteomics. Proteome Science, 12(1). doi:10.1186/s12953-014-0044-3

Sabbagh, M., Schiavone, R., Brizzi, G., Sicuro, B., Zilli, L., & Vilella, S. (2019). Poultry by-product meal as an alternative to fish meal in the juvenile gilthead seabream (Sparus aurata) diet. Aquaculture, 511, 734220. doi:10.1016/j.aquaculture.2019.734220

Piazzon, M. C., Calduch-Giner, J. A., Fouz, B., Estensoro, I., Simó-Mirabet, P., Puyalto, M., … Pérez-Sánchez, J. (2017). Under control: how a dietary additive can restore the gut microbiome and proteomic profile, and improve disease resilience in a marine teleostean fish fed vegetable diets. Microbiome, 5(1). doi:10.1186/s40168-017-0390-3

Wulff, T., Petersen, J., Nørrelykke, M. R., Jessen, F., & Nielsen, H. H. (2012). Proteome Analysis of Pyloric Ceca: A Methodology for Fish Feed Development? Journal of Agricultural and Food Chemistry, 60(34), 8457-8464. doi:10.1021/jf3016943

Pérez-Sánchez, J., Estensoro, I., Redondo, M. J., Calduch-Giner, J. A., Kaushik, S., & Sitjà-Bobadilla, A. (2013). Mucins as Diagnostic and Prognostic Biomarkers in a Fish-Parasite Model: Transcriptional and Functional Analysis. PLoS ONE, 8(6), e65457. doi:10.1371/journal.pone.0065457

Mirghaed, A. T., Yarahmadi, P., Soltani, M., Paknejad, H., & Hoseini, S. M. (2019). Dietary sodium butyrate (Butirex® C4) supplementation modulates intestinal transcriptomic responses and augments disease resistance of rainbow trout (Oncorhynchus mykiss). Fish & Shellfish Immunology, 92, 621-628. doi:10.1016/j.fsi.2019.06.046

Estruch, G., Tomás-Vidal, A., El Nokrashy, A. M., Monge-Ortiz, R., Godoy-Olmos, S., Jover Cerdá, M., & Martínez-Llorens, S. (2018). Inclusion of alternative marine by-products in aquafeeds with different levels of plant-based sources for on-growing gilthead sea bream (Sparus aurata, L.): effects on digestibility, amino acid retention, ammonia excretion and enzyme activity. Archives of Animal Nutrition, 72(4), 321-339. doi:10.1080/1745039x.2018.1472408

Peres, H., & Oliva-Teles, A. (2009). The optimum dietary essential amino acid profile for gilthead seabream (Sparus aurata) juveniles. Aquaculture, 296(1-2), 81-86. doi:10.1016/j.aquaculture.2009.04.046

Cox, J., Hein, M. Y., Luber, C. A., Paron, I., Nagaraj, N., & Mann, M. (2014). Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ. Molecular & Cellular Proteomics, 13(9), 2513-2526. doi:10.1074/mcp.m113.031591

Metsalu, T., & Vilo, J. (2015). ClustVis: a web tool for visualizing clustering of multivariate data using Principal Component Analysis and heatmap. Nucleic Acids Research, 43(W1), W566-W570. doi:10.1093/nar/gkv468

Conesa, A., Gotz, S., Garcia-Gomez, J. M., Terol, J., Talon, M., & Robles, M. (2005). Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics, 21(18), 3674-3676. doi:10.1093/bioinformatics/bti610

Huang, D. W., Sherman, B. T., & Lempicki, R. A. (2008). Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nature Protocols, 4(1), 44-57. doi:10.1038/nprot.2008.211

Huang, D. W., Sherman, B. T., & Lempicki, R. A. (2008). Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Research, 37(1), 1-13. doi:10.1093/nar/gkn923

Kader, M. A., Bulbul, M., Koshio, S., Ishikawa, M., Yokoyama, S., Nguyen, B. T., & Komilus, C. F. (2012). Effect of complete replacement of fishmeal by dehulled soybean meal with crude attractants supplementation in diets for red sea bream, Pagrus major. Aquaculture, 350-353, 109-116. doi:10.1016/j.aquaculture.2012.04.009

HERBINGER, C. M., & FRIARS, G. W. (1991). Correlation between condition factor and total lipid content in Atlantic salmon, Salmo salar L., parr. Aquaculture Research, 22(4), 527-529. doi:10.1111/j.1365-2109.1991.tb00766.x

Johansson, L., Kiessling, A., Kiessling, K.-H., & Berglund, L. (2000). Effects of altered ration levels on sensory characteristics, lipid content and fatty acid composition of rainbow trout (Oncorhynchus mykiss). Food Quality and Preference, 11(3), 247-254. doi:10.1016/s0950-3293(99)00073-7

De Francesco, M., Parisi, G., Médale, F., Lupi, P., Kaushik, S. J., & Poli, B. M. (2004). Effect of long-term feeding with a plant protein mixture based diet on growth and body/fillet quality traits of large rainbow trout (Oncorhynchus mykiss). Aquaculture, 236(1-4), 413-429. doi:10.1016/j.aquaculture.2004.01.006

Berg, O. K., Thronæs, E., & Bremset, G. (1998). Energetics and survival of virgin and repeat spawning brown trout (Salmo trutta). Canadian Journal of Fisheries and Aquatic Sciences, 55(1), 47-53. doi:10.1139/f97-208

Saera-Vila, A., Calduch-Giner, J. A., Gómez-Requeni, P., Médale, F., Kaushik, S., & Pérez-Sánchez, J. (2005). Molecular characterization of gilthead sea bream (Sparus aurata) lipoprotein lipase. Transcriptional regulation by season and nutritional condition in skeletal muscle and fat storage tissues. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 142(2), 224-232. doi:10.1016/j.cbpb.2005.07.009

Panserat, S., & Kaushik, S. J. (2010). Regulation of gene expression by nutritional factors in fish. Aquaculture Research, 41(5), 751-762. doi:10.1111/j.1365-2109.2009.02173.x

Khurana, S., & George, S. P. (2008). Regulation of cell structure and function by actin-binding proteins: Villin’s perspective. FEBS Letters, 582(14), 2128-2139. doi:10.1016/j.febslet.2008.02.040

Bedford, L., Paine, S., Sheppard, P. W., Mayer, R. J., & Roelofs, J. (2010). Assembly, structure, and function of the 26S proteasome. Trends in Cell Biology, 20(7), 391-401. doi:10.1016/j.tcb.2010.03.007

Wu, Y.-X., Yang, J.-H., & Saitsu, H. (2016). Bortezomib-resistance is associated with increased levels of proteasome subunits and apoptosis-avoidance. Oncotarget, 7(47), 77622-77634. doi:10.18632/oncotarget.12731

Fararjeh, Chen, Ho, Cheng, Liu, Chang, … Tu. (2019). Proteasome 26S Subunit, non-ATPase 3 (PSMD3) Regulates Breast Cancer by Stabilizing HER2 from Degradation. Cancers, 11(4), 527. doi:10.3390/cancers11040527

Pastorelli, L., De Salvo, C., Mercado, J. R., Vecchi, M., & Pizarro, T. T. (2013). Central Role of the Gut Epithelial Barrier in the Pathogenesis of Chronic Intestinal Inflammation: Lessons Learned from Animal Models and Human Genetics. Frontiers in Immunology, 4. doi:10.3389/fimmu.2013.00280

Babbin, B. A., Laukoetter, M. G., Nava, P., Koch, S., Lee, W. Y., Capaldo, C. T., … Nusrat, A. (2008). Annexin A1 Regulates Intestinal Mucosal Injury, Inflammation, and Repair. The Journal of Immunology, 181(7), 5035-5044. doi:10.4049/jimmunol.181.7.5035

Leoni, G., Neumann, P.-A., Sumagin, R., Denning, T. L., & Nusrat, A. (2015). Wound repair: role of immune–epithelial interactions. Mucosal Immunology, 8(5), 959-968. doi:10.1038/mi.2015.63

Bakke-McKellep, A. M., Penn, M. H., Salas, P. M., Refstie, S., Sperstad, S., Landsverk, T., … Krogdahl, Å. (2007). Effects of dietary soyabean meal, inulin and oxytetracycline on intestinal microbiota and epithelial cell stress, apoptosis and proliferation in the teleost Atlantic salmon (Salmo salar L.). British Journal of Nutrition, 97(4), 699-713. doi:10.1017/s0007114507381397

Wolf, H. K., & Dittrich, K. L. (1992). Detection of proliferating cell nuclear antigen in diagnostic histopathology. Journal of Histochemistry & Cytochemistry, 40(9), 1269-1273. doi:10.1177/40.9.1354677

Ducker, G. S., & Rabinowitz, J. D. (2017). One-Carbon Metabolism in Health and Disease. Cell Metabolism, 25(1), 27-42. doi:10.1016/j.cmet.2016.08.009

Cunningham, K. E., & Turner, J. R. (2012). Myosin light chain kinase: pulling the strings of epithelial tight junction function. Annals of the New York Academy of Sciences, 1258(1), 34-42. doi:10.1111/j.1749-6632.2012.06526.x

Fanning, A. S., & Anderson, J. M. (1999). PDZ domains: fundamental building blocks in the organization of protein complexes at the plasma membrane. Journal of Clinical Investigation, 103(6), 767-772. doi:10.1172/jci6509

Werner, T., & Haller, D. (2007). Intestinal epithelial cell signalling and chronic inflammation: From the proteome to specific molecular mechanisms. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 622(1-2), 42-57. doi:10.1016/j.mrfmmm.2007.05.010

Lee, S. H. (2015). Intestinal Permeability Regulation by Tight Junction: Implication on Inflammatory Bowel Diseases. Intestinal Research, 13(1), 11. doi:10.5217/ir.2015.13.1.11

Turner, J. R. (2009). Intestinal mucosal barrier function in health and disease. Nature Reviews Immunology, 9(11), 799-809. doi:10.1038/nri2653

Ulluwishewa, D., Anderson, R. C., McNabb, W. C., Moughan, P. J., Wells, J. M., & Roy, N. C. (2011). Regulation of Tight Junction Permeability by Intestinal Bacteria and Dietary Components. The Journal of Nutrition, 141(5), 769-776. doi:10.3945/jn.110.135657

Knudsen, D., Jutfelt, F., Sundh, H., Sundell, K., Koppe, W., & Frøkiær, H. (2008). Dietary soya saponins increase gut permeability and play a key role in the onset of soyabean-induced enteritis in Atlantic salmon (Salmo salar L.). British Journal of Nutrition, 100(1), 120-129. doi:10.1017/s0007114507886338

Hu, H., Kortner, T. M., Gajardo, K., Chikwati, E., Tinsley, J., & Krogdahl, Å. (2016). Intestinal Fluid Permeability in Atlantic Salmon (Salmo salar L.) Is Affected by Dietary Protein Source. PLOS ONE, 11(12), e0167515. doi:10.1371/journal.pone.0167515

Strober, W., Fuss, I. J., & Blumberg, R. S. (2002). The Immunology of Mucosal Models of Inflammation. Annual Review of Immunology, 20(1), 495-549. doi:10.1146/annurev.immunol.20.100301.064816

Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004). Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis. Cell, 118(2), 229-241. doi:10.1016/j.cell.2004.07.002

Neal, M. D., Leaphart, C., Levy, R., Prince, J., Billiar, T. R., Watkins, S., … Hackam, D. J. (2006). Enterocyte TLR4 Mediates Phagocytosis and Translocation of Bacteria Across the Intestinal Barrier. The Journal of Immunology, 176(5), 3070-3079. doi:10.4049/jimmunol.176.5.3070

Fink, M. P., & Delude, R. L. (2005). Epithelial Barrier Dysfunction: A Unifying Theme to Explain the Pathogenesis of Multiple Organ Dysfunction at the Cellular Level. Critical Care Clinics, 21(2), 177-196. doi:10.1016/j.ccc.2005.01.005

Estruch, G., Collado, M. C., Peñaranda, D. S., Tomás Vidal, A., Jover Cerdá, M., Pérez Martínez, G., & Martinez-Llorens, S. (2015). Impact of Fishmeal Replacement in Diets for Gilthead Sea Bream (Sparus aurata) on the Gastrointestinal Microbiota Determined by Pyrosequencing the 16S rRNA Gene. PLOS ONE, 10(8), e0136389. doi:10.1371/journal.pone.0136389

Snelgrove, R. J. (2011). Leukotriene A4 hydrolase: an anti-inflammatory role for a proinflammatory enzyme. Thorax, 66(6), 550-551. doi:10.1136/thoraxjnl-2011-200234

Banerjee, S., Oneda, B., Yap, L. M., Jewell, D. P., Matters, G. L., Fitzpatrick, L. R., … Bond, J. S. (2009). MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel disease. Mucosal Immunology, 2(3), 220-231. doi:10.1038/mi.2009.3

Hashimoto, T., Perlot, T., Rehman, A., Trichereau, J., Ishiguro, H., Paolino, M., … Penninger, J. M. (2012). ACE2 links amino acid malnutrition to microbial ecology and intestinal inflammation. Nature, 487(7408), 477-481. doi:10.1038/nature11228

Kokou, F., Sarropoulou, E., Cotou, E., Kentouri, M., Alexis, M., & Rigos, G. (2017). Effects of graded dietary levels of soy protein concentrate supplemented with methionine and phosphate on the immune and antioxidant responses of gilthead sea bream ( Sparus aurata L.). Fish & Shellfish Immunology, 64, 111-121. doi:10.1016/j.fsi.2017.03.017

Kokou, F., Sarropoulou, E., Cotou, E., Rigos, G., Henry, M., Alexis, M., & Kentouri, M. (2015). Effects of Fish Meal Replacement by a Soybean Protein on Growth, Histology, Selected Immune and Oxidative Status Markers of Gilthead Sea Bream, Sparus aurata. Journal of the World Aquaculture Society, 46(2), 115-128. doi:10.1111/jwas.12181

Tort, L. (2011). Stress and immune modulation in fish. Developmental & Comparative Immunology, 35(12), 1366-1375. doi:10.1016/j.dci.2011.07.002

Burrells, C., Williams, P. D., Southgate, P. J., & Crampton, V. O. (1999). Immunological, physiological and pathological responses of rainbow trout (Oncorhynchus mykiss) to increasing dietary concentrations of soybean proteins. Veterinary Immunology and Immunopathology, 72(3-4), 277-288. doi:10.1016/s0165-2427(99)00143-9

Estruch, G., Collado, M. C., Monge-Ortiz, R., Tomás-Vidal, A., Jover-Cerdá, M., Peñaranda, D. S., … Martínez-Llorens, S. (2018). Long-term feeding with high plant protein based diets in gilthead seabream (Sparus aurata, L.) leads to changes in the inflammatory and immune related gene expression at intestinal level. BMC Veterinary Research, 14(1). doi:10.1186/s12917-018-1626-6

Estensoro, I., Ballester-Lozano, G., Benedito-Palos, L., Grammes, F., Martos-Sitcha, J. A., Mydland, L.-T., … Pérez-Sánchez, J. (2016). Dietary Butyrate Helps to Restore the Intestinal Status of a Marine Teleost (Sparus aurata) Fed Extreme Diets Low in Fish Meal and Fish Oil. PLOS ONE, 11(11), e0166564. doi:10.1371/journal.pone.0166564

Baeza-Ariño, R., Martínez-Llorens, S., Nogales-Mérida, S., Jover-Cerda, M., & Tomás-Vidal, A. (2014). Study of liver and gut alterations in sea bream,Sparus aurataL., fed a mixture of vegetable protein concentrates. Aquaculture Research, 47(2), 460-471. doi:10.1111/are.12507

Bakke-McKellep, A. M., Nordrum, S., Krogdahl, Å., & Buddington, R. K. (2000). Fish Physiology and Biochemistry, 22(1), 33-44. doi:10.1023/a:1007872929847

Ambardekar, A. A., Reigh, R. C., & Williams, M. B. (2009). Absorption of amino acids from intact dietary proteins and purified amino acid supplements follows different time-courses in channel catfish (Ictalurus punctatus). Aquaculture, 291(3-4), 179-187. doi:10.1016/j.aquaculture.2009.02.044

Santigosa, E., García-Meilán, I., Valentin, J. M., Pérez-Sánchez, J., Médale, F., Kaushik, S., & Gallardo, M. A. (2011). Modifications of intestinal nutrient absorption in response to dietary fish meal replacement by plant protein sources in sea bream (Sparus aurata) and rainbow trout (Onchorynchus mykiss). Aquaculture, 317(1-4), 146-154. doi:10.1016/j.aquaculture.2011.04.026

Dhabhar, F. S. (2009). Enhancing versus Suppressive Effects of Stress on Immune Function: Implications for Immunoprotection and Immunopathology. Neuroimmunomodulation, 16(5), 300-317. doi:10.1159/000216188

Gong, H., Lawrence, A. L., Jiang, D.-H., Castille, F. L., & Gatlin, D. M. (2000). Lipid nutrition of juvenile Litopenaeus vannamei. Aquaculture, 190(3-4), 305-324. doi:10.1016/s0044-8486(00)00414-2

Schrama, D., Richard, N., Silva, T. S., Figueiredo, F. A., Conceição, L. E. C., Burchmore, R., … Rodrigues, P. M. L. (2016). Enhanced dietary formulation to mitigate winter thermal stress in gilthead sea bream (Sparus aurata): a 2D-DIGE plasma proteome study. Fish Physiology and Biochemistry, 43(2), 603-617. doi:10.1007/s10695-016-0315-2

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