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      Poly (I:C)-Potentiated Vaccination Enhances T Cell Response in Olive Flounder ( Paralichthys olivaceus) Providing Protection against Viral Hemorrhagic Septicemia Virus (VHSV)

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          Abstract

          Viral hemorrhagic septicemia (VHS), caused by viral hemorrhagic septicemia virus (VHSV), is a viral disease affecting teleosts, and is the major cause of virus-related deaths in olive flounder ( Paralichthys olivaceus). Research has focused on ways to control VHS, and recently, the use of polyinosinic-polycytidylic acid poly (I:C)-potentiated vaccination has been investigated, whereby fish are injected with poly (I:C) and then with live pathogenic virus, resulting in a significant decrease in VHSV-related mortality. T cell responses were investigated in the present study after vaccinating olive flounder with poly (I:C)-potentiated vaccination to understand the ability of poly (I:C) to induce T cell immunity. Stimulation of T cell responses with the poly (I:C)-potentiated vaccination was confirmed by examining levels of CD3 + T cells, CD4-1 + T cells and CD4-2 + T cells. Higher levels of CD4-2 + T cells were found in vaccinated fish than CD4-1 + T cells, believed to result from a synergistic effect between poly (I:C) administration and pathogenic VHSV immunization. More importantly, the role of CD4-2 + T cells in the antiviral response was clearly evident. The results of this study suggest that the outstanding protection obtained with the poly (I:C)-potentiated vaccination is due to the robust immune response initiated by the CD4-2 + T cells.

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          On the Dependency of Cellular Protein Levels on mRNA Abundance.

          The question of how genomic information is expressed to determine phenotypes is of central importance for basic and translational life science research and has been studied by transcriptomic and proteomic profiling. Here, we review the relationship between protein and mRNA levels under various scenarios, such as steady state, long-term state changes, and short-term adaptation, demonstrating the complexity of gene expression regulation, especially during dynamic transitions. The spatial and temporal variations of mRNAs, as well as the local availability of resources for protein biosynthesis, strongly influence the relationship between protein levels and their coding transcripts. We further discuss the buffering of mRNA fluctuations at the level of protein concentrations. We conclude that transcript levels by themselves are not sufficient to predict protein levels in many scenarios and to thus explain genotype-phenotype relationships and that high-quality data quantifying different levels of gene expression are indispensable for the complete understanding of biological processes.
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            The generation of antibody-secreting plasma cells.

            The regulation of antibody production is linked to the generation and maintenance of plasmablasts and plasma cells from their B cell precursors. Plasmablasts are the rapidly produced and short-lived effector cells of the early antibody response, whereas plasma cells are the long-lived mediators of lasting humoral immunity. An extraordinary number of control mechanisms, at both the cellular and molecular levels, underlie the regulation of this essential arm of the immune response. Despite this complexity, the terminal differentiation of B cells can be described as a simple probabilistic process that is governed by a central gene-regulatory network and modified by environmental stimuli.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Interleukin-12 and the regulation of innate resistance and adaptive immunity.

              Interleukin-12 (IL-12) is a heterodimeric pro-inflammatory cytokine that induces the production of interferon-gamma (IFN-gamma), favours the differentiation of T helper 1 (T(H)1) cells and forms a link between innate resistance and adaptive immunity. Dendritic cells (DCs) and phagocytes produce IL-12 in response to pathogens during infection. Production of IL-12 is dependent on differential mechanisms of regulation of expression of the genes encoding IL-12, patterns of Toll-like receptor (TLR) expression and cross-regulation between the different DC subsets, involving cytokines such as IL-10 and type I IFN. Recent data, however, argue against an absolute requirement for IL-12 for T(H)1 responses. Our understanding of the relative roles of IL-12 and other factors in T(H)1-type maturation of both CD4+ and CD8+ T cells is discussed here, including the participation in this process of IL-23 and IL-27, two recently discovered members of the new family of heterodimeric cytokines.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Vaccines (Basel)
                Vaccines (Basel)
                vaccines
                Vaccines
                MDPI
                2076-393X
                10 May 2021
                May 2021
                : 9
                : 5
                : 482
                Affiliations
                [1 ]Laboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, 501-201, 501, Jinju-daero, Jinju-si 52828, Korea; hilanamang@ 123456naver.com (J.H.C.); wjdwodnr0605@ 123456gmail.com (J.W.J.); yl0808@ 123456nate.com (Y.R.K.); jassylazarte@ 123456yahoo.com (J.M.S.L.); ksw0017@ 123456hanmail.net (S.W.K.); afteru70@ 123456gmail.com (J.K.)
                [2 ]Moredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Midlothian EH26 0PZ, UK; Kim.Thompson@ 123456moredun.ac.uk
                [3 ]Pathology Research Division, OIE Reference Laboratory for Viral Haemorrhagic Septicaemia (VHS), National Institute of Fisheries Science, 216, Gijanghaean-ro, Gijang-eup, Busan 46083, Korea; hjkim1882@ 123456korea.kr
                [4 ]Centre for Marine Bioproducts Development, Flinders University, Bedford Park, SA 5042, Australia
                Author notes
                [* ]Correspondence: jungts@ 123456gnu.ac.kr
                Author information
                https://orcid.org/0000-0003-3550-4842
                Article
                vaccines-09-00482
                10.3390/vaccines9050482
                8151365
                9e881916-ffc3-48da-9d27-bf6333b1c9de
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 25 March 2021
                : 28 April 2021
                Categories
                Article

                viral haemorrhagic septicaemia (vhs),poly (i:c),vaccination,t cell responses,flow cytometry,olive flounder (paralichthys olivaceus)

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