Identification of a novel CCR7 gene in rainbow trout with differential expression in the context of mucosal or systemic infection
► A CCR7 orthologue has been identified in rainbow trout (Oncorhynchus mykiss). ► CCR7 is strongly transcribed in thymus and spleen T cells. ► CCR7 transcription is down-regulated in head kidney and spleen of VHSV-infected fish. ► VHSV bath infection induces significant changes in CCR7 transcription...
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Published in | Developmental and comparative immunology Vol. 38; no. 2; pp. 302 - 311 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Ltd
01.10.2012
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Abstract | ► A CCR7 orthologue has been identified in rainbow trout (Oncorhynchus mykiss). ► CCR7 is strongly transcribed in thymus and spleen T cells. ► CCR7 transcription is down-regulated in head kidney and spleen of VHSV-infected fish. ► VHSV bath infection induces significant changes in CCR7 transcription in the gills. ► CCR7 is up-regulated in B cells recruited to the gut in response to Ceratomyxa shasta.
In mammals, CCR7 is the chemokine receptor for the CCL19 and CCL21 chemokines, molecules with a major role in the recruitment of lymphocytes to lymph nodes and Peyer’s patches in the intestinal mucosa, especially naïve T lymphocytes. In the current work, we have identified a CCR7 orthologue in rainbow trout (Oncorhynchus mykiss) that shares many of the conserved features of mammalian CCR7. The receptor is constitutively transcribed in the gills, hindgut, spleen, thymus and gonad. When leukocyte populations were isolated, IgM+ cells, T cells and myeloid cells from head kidney transcribed the CCR7 gene. In blood, both IgM+ and IgT+ B cells and myeloid cells but not T lymphocytes were transcribing CCR7, whereas in the spleen, CCR7 mRNA expression was strongly detected in T lymphocytes. In response to infection with viral hemorrhagic septicemia virus (VHSV), CCR7 transcription was down-regulated in spleen and head kidney upon intraperitoneal infection, whereas upon bath infection, CCR7 was up-regulated in gills but remained undetected in the fin bases, the main site of virus entry. Concerning its regulation in the intestinal mucosa, the ex vivo stimulation of hindgut segments with Poly I:C or inactivated bacteria significantly increased CCR7 transcription, while in the context of an infection with Ceratomyxa shasta, the levels of transcription of CCR7 in both IgM+ and IgT+ cells from the gut were dramatically increased. All these data suggest that CCR7 plays an important role in lymphocyte trafficking during rainbow trout infections, in which CCR7 appears to be implicated in the recruitment of B lymphocytes into the gut. |
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AbstractList | ► A CCR7 orthologue has been identified in rainbow trout (Oncorhynchus mykiss). ► CCR7 is strongly transcribed in thymus and spleen T cells. ► CCR7 transcription is down-regulated in head kidney and spleen of VHSV-infected fish. ► VHSV bath infection induces significant changes in CCR7 transcription in the gills. ► CCR7 is up-regulated in B cells recruited to the gut in response to Ceratomyxa shasta.
In mammals, CCR7 is the chemokine receptor for the CCL19 and CCL21 chemokines, molecules with a major role in the recruitment of lymphocytes to lymph nodes and Peyer’s patches in the intestinal mucosa, especially naïve T lymphocytes. In the current work, we have identified a CCR7 orthologue in rainbow trout (Oncorhynchus mykiss) that shares many of the conserved features of mammalian CCR7. The receptor is constitutively transcribed in the gills, hindgut, spleen, thymus and gonad. When leukocyte populations were isolated, IgM+ cells, T cells and myeloid cells from head kidney transcribed the CCR7 gene. In blood, both IgM+ and IgT+ B cells and myeloid cells but not T lymphocytes were transcribing CCR7, whereas in the spleen, CCR7 mRNA expression was strongly detected in T lymphocytes. In response to infection with viral hemorrhagic septicemia virus (VHSV), CCR7 transcription was down-regulated in spleen and head kidney upon intraperitoneal infection, whereas upon bath infection, CCR7 was up-regulated in gills but remained undetected in the fin bases, the main site of virus entry. Concerning its regulation in the intestinal mucosa, the ex vivo stimulation of hindgut segments with Poly I:C or inactivated bacteria significantly increased CCR7 transcription, while in the context of an infection with Ceratomyxa shasta, the levels of transcription of CCR7 in both IgM+ and IgT+ cells from the gut were dramatically increased. All these data suggest that CCR7 plays an important role in lymphocyte trafficking during rainbow trout infections, in which CCR7 appears to be implicated in the recruitment of B lymphocytes into the gut. In mammals, CCR7 is the chemokine receptor for the CCL19 and CCL21 chemokines, molecules with a major role in the recruitment of lymphocytes to lymph nodes and Peyer’s patches in the intestinal mucosa, especially naïve T lymphocytes. In the current work, we have identified a CCR7 orthologue in rainbow trout (Oncorhynchus mykiss) that shares many of the conserved features of mammalian CCR7. The receptor is constitutively transcribed in the gills, hindgut, spleen, thymus and gonad. When leukocyte populations were isolated, IgM⁺ cells, T cells and myeloid cells from head kidney transcribed the CCR7 gene. In blood, both IgM⁺ and IgT⁺ B cells and myeloid cells but not T lymphocytes were transcribing CCR7, whereas in the spleen, CCR7 mRNA expression was strongly detected in T lymphocytes. In response to infection with viral hemorrhagic septicemia virus (VHSV), CCR7 transcription was down-regulated in spleen and head kidney upon intraperitoneal infection, whereas upon bath infection, CCR7 was up-regulated in gills but remained undetected in the fin bases, the main site of virus entry. Concerning its regulation in the intestinal mucosa, the ex vivo stimulation of hindgut segments with Poly I:C or inactivated bacteria significantly increased CCR7 transcription, while in the context of an infection with Ceratomyxa shasta, the levels of transcription of CCR7 in both IgM⁺ and IgT⁺ cells from the gut were dramatically increased. All these data suggest that CCR7 plays an important role in lymphocyte trafficking during rainbow trout infections, in which CCR7 appears to be implicated in the recruitment of B lymphocytes into the gut. In mammals, CCR7 is the chemokine receptor for the CCL19 and CCL21 chemokines, molecules with a major role in the recruitment of lymphocytes to lymph nodes and Peyer's patches in the intestinal mucosa, especially naïve T lymphocytes. In the current work, we have identified a CCR7 orthologue in rainbow trout ( Oncorhynchus mykiss ) that shares many of the conserved features of mammalian CCR7. The receptor is constitutively transcribed in the gills, hindgut, spleen, thymus and gonad. When leukocyte populations were isolated, IgM + cells, T cells and myeloid cells from head kidney transcribed the CCR7 gene. In blood, both IgM + and IgT + B cells and myeloid cells but not T lymphocytes were transcribing CCR7, whereas in the spleen, CCR7 mRNA expression was strongly detected in T lymphocytes. In response to infection with viral hemorrhagic septicemia virus (VHSV), CCR7 transcription was down-regulated in spleen and head kidney upon intraperitoneal infection, whereas upon bath infection, CCR7 was up-regulated in gills but remained undetected in the fin bases, the main site of virus entry. Concerning its regulation in the intestinal mucosa, the ex vivo stimulation of hindgut segments with Poly I:C or inactivated bacteria significantly increased CCR7 transcription, while in the context of an infection with Ceratomyxa shasta , the levels of transcription of CCR7 in both IgM + and IgT + cells from the gut were dramatically increased. All these data suggest that CCR7 plays an important role in lymphocyte trafficking during rainbow trout infections, in which CCR7 appears to be implicated in the recruitment of B lymphocytes into the gut. In mammals, CCR7 is the chemokine receptor for the CCL19 and CCL21 chemokines, molecules with a major role in the recruitment of lymphocytes to lymph nodes and Peyer's patches in the intestinal mucosa, especially naïve T lymphocytes. In the current work, we have identified a CCR7 orthologue in rainbow trout (Oncorhynchus mykiss) that shares many of the conserved features of mammalian CCR7. The receptor is constitutively transcribed in the gills, hindgut, spleen, thymus and gonad. When leukocyte populations were isolated, IgM(+) cells, T cells and myeloid cells from head kidney transcribed the CCR7 gene. In blood, both IgM(+) and IgT(+) B cells and myeloid cells but not T lymphocytes were transcribing CCR7, whereas in the spleen, CCR7 mRNA expression was strongly detected in T lymphocytes. In response to infection with viral hemorrhagic septicemia virus (VHSV), CCR7 transcription was down-regulated in spleen and head kidney upon intraperitoneal infection, whereas upon bath infection, CCR7 was up-regulated in gills but remained undetected in the fin bases, the main site of virus entry. Concerning its regulation in the intestinal mucosa, the ex vivo stimulation of hindgut segments with Poly I:C or inactivated bacteria significantly increased CCR7 transcription, while in the context of an infection with Ceratomyxa shasta, the levels of transcription of CCR7 in both IgM(+) and IgT(+) cells from the gut were dramatically increased. All these data suggest that CCR7 plays an important role in lymphocyte trafficking during rainbow trout infections, in which CCR7 appears to be implicated in the recruitment of B lymphocytes into the gut. In mammals, CCR7 is the chemokine receptor for the CCL19 and CCL21 chemokines, molecules with a major role in the recruitment of lymphocytes to lymph nodes and Peyer's patches in the intestinal mucosa, especially naieve T lymphocytes. In the current work, we have identified a CCR7 orthologue in rainbow trout (Oncorhynchus mykiss) that shares many of the conserved features of mammalian CCR7. The receptor is constitutively transcribed in the gills, hindgut, spleen, thymus and gonad. When leukocyte populations were isolated, IgM+ cells, T cells and myeloid cells from head kidney transcribed the CCR7 gene. In blood, both IgM+ and IgT+ B cells and myeloid cells but not T lymphocytes were transcribing CCR7, whereas in the spleen, CCR7 mRNA expression was strongly detected in T lymphocytes. In response to infection with viral hemorrhagic septicemia virus (VHSV), CCR7 transcription was down-regulated in spleen and head kidney upon intraperitoneal infection, whereas upon bath infection, CCR7 was up-regulated in gills but remained undetected in the fin bases, the main site of virus entry. Concerning its regulation in the intestinal mucosa, the ex vivo stimulation of hindgut segments with Poly I: C or inactivated bacteria significantly increased CCR7 transcription, while in the context of an infection with Ceratomyxa shasta, the levels of transcription of CCR7 in both IgM+ and IgT+ cells from the gut were dramatically increased. All these data suggest that CCR7 plays an important role in lymphocyte trafficking during rainbow trout infections, in which CCR7 appears to be implicated in the recruitment of B lymphocytes into the gut. |
Author | Sunyer, J. Oriol Ordás, M. Camino Köllner, Bernd Cuesta, Alberto Castro, Rosario Bartholomew, Jerri Dixon, Brian Korytar, Tomas Bjork, Sarah Tafalla, Carolina |
AuthorAffiliation | a Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain d Friedrich-Loeffler-Institute, Federal Research Institute for Animal Health, Institute of Infectology, 17493 Greifswald-Insel Riems, Germany e Department of Microbiology, Oregon State University, Corvallis, OR 97331, USA c Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA b Department of Biology, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 |
AuthorAffiliation_xml | – name: e Department of Microbiology, Oregon State University, Corvallis, OR 97331, USA – name: c Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA – name: a Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain – name: b Department of Biology, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 – name: d Friedrich-Loeffler-Institute, Federal Research Institute for Animal Health, Institute of Infectology, 17493 Greifswald-Insel Riems, Germany |
Author_xml | – sequence: 1 givenname: M. Camino surname: Ordás fullname: Ordás, M. Camino organization: Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain – sequence: 2 givenname: Rosario surname: Castro fullname: Castro, Rosario organization: Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain – sequence: 3 givenname: Brian surname: Dixon fullname: Dixon, Brian organization: Department of Biology, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 – sequence: 4 givenname: J. Oriol surname: Sunyer fullname: Sunyer, J. Oriol organization: Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA – sequence: 5 givenname: Sarah surname: Bjork fullname: Bjork, Sarah organization: Department of Microbiology, Oregon State University, Corvallis, OR 97331, USA – sequence: 6 givenname: Jerri surname: Bartholomew fullname: Bartholomew, Jerri organization: Department of Microbiology, Oregon State University, Corvallis, OR 97331, USA – sequence: 7 givenname: Tomas surname: Korytar fullname: Korytar, Tomas organization: Friedrich-Loeffler-Institute, Federal Research Institute for Animal Health, Institute of Infectology, 17493 Greifswald-Insel Riems, Germany – sequence: 8 givenname: Bernd surname: Köllner fullname: Köllner, Bernd organization: Friedrich-Loeffler-Institute, Federal Research Institute for Animal Health, Institute of Infectology, 17493 Greifswald-Insel Riems, Germany – sequence: 9 givenname: Alberto surname: Cuesta fullname: Cuesta, Alberto organization: Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain – sequence: 10 givenname: Carolina surname: Tafalla fullname: Tafalla, Carolina email: tafalla@inia.es organization: Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22858409$$D View this record in MEDLINE/PubMed |
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Keywords | CCR7 Mucosal immunity Lymphocytes Chemokines Chemokine receptors Rainbow trout |
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Snippet | ► A CCR7 orthologue has been identified in rainbow trout (Oncorhynchus mykiss). ► CCR7 is strongly transcribed in thymus and spleen T cells. ► CCR7... In mammals, CCR7 is the chemokine receptor for the CCL19 and CCL21 chemokines, molecules with a major role in the recruitment of lymphocytes to lymph nodes and... |
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SubjectTerms | Animals B-lymphocytes bacteria CCR7 CCR7 receptor Ceratomyxa Ceratomyxa shasta chemokine CCL19 chemokine CCL21 Chemokine receptors Chemokines Fish Diseases - immunology Fish Proteins - genetics Fish Proteins - immunology Gastrointestinal Tract - immunology gene expression gene expression regulation genes gills hindgut intestinal mucosa kidneys Leukocytes - immunology lymph nodes Lymphocytes mammals messenger RNA Mucosal immunity Mucous Membrane - immunology Myxozoa Novirhabdovirus Oncorhynchus mykiss Oncorhynchus mykiss - genetics Oncorhynchus mykiss - immunology Organ Specificity Parasitic Diseases, Animal - immunology Phylogeny population Rainbow trout Receptors, CCR7 - genetics Receptors, CCR7 - immunology Rhabdoviridae Infections - immunology Rhabdoviridae Infections - veterinary spleen T-lymphocytes thymus gland Transcriptome Viral hemorrhagic septicemia virus viruses |
Title | Identification of a novel CCR7 gene in rainbow trout with differential expression in the context of mucosal or systemic infection |
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