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Identification of diverse defense mechanisms in rainbow trout red blood cells in response to halted replication of VHS virus.
Nombela, Ivan; Puente-Marin, Sara; Chico, Veronica; Villena, Alberto J; Carracedo, Begoña; Ciordia, Sergio; Mena, Maria Carmen; Mercado, Luis; Perez, Luis; Coll, Julio; Estepa, Amparo; Ortega-Villaizan, Maria Del Mar.
Afiliação
  • Nombela I; Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Elche, Spain.
  • Puente-Marin S; Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Elche, Spain.
  • Chico V; Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Elche, Spain.
  • Villena AJ; Área de Biología Celular, Departamento de Biología Molecular, Universidad de León, León, Spain.
  • Carracedo B; Área de Biología Celular, Departamento de Biología Molecular, Universidad de León, León, Spain.
  • Ciordia S; Unidad de Proteómica, Centro Nacional de Biotecnología, Madrid, Spain.
  • Mena MC; Unidad de Proteómica, Centro Nacional de Biotecnología, Madrid, Spain.
  • Mercado L; Instituto de Biología, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile.
  • Perez L; Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Elche, Spain.
  • Coll J; INIA-SIGT-Biotecnología, Madrid, Spain.
  • Estepa A; Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Elche, Spain.
  • Ortega-Villaizan MDM; Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Elche, Spain.
F1000Res ; 6: 1958, 2017.
Article em En | MEDLINE | ID: mdl-29527292
ABSTRACT

Background:

It has been described that fish nucleated red blood cells (RBCs) generate a wide variety of immune-related gene transcripts when viruses highly replicate inside them and are their main target cell. The immune response and mechanisms of fish RBCs against viruses targeting other cells or tissues has not yet been explored and is the objective of our study.

Methods:

Trout RBCs were obtained from peripheral blood, ficoll purified and exposed to Viral Haemorrhagic Septicaemia virus (VHSV). Immune response was evaluated by means of RT-qPCR, flow cytometry, immunofluorescence and isobaric tag for relative and absolute quantification (iTRAQ) protein profiling

Results:

VHSV N gene transcripts incremented early postexposure and were drastically decreased after 6 hours postexposure (hpe). The expression of the type I interferon ( ifn1) gene was significantly downregulated at early postexposure (3 hpe), together with a gradual downregulation of interferon-inducible mx and pkr genes until 72 hpe. Type I IFN protein was downregulated and interferon-inducible Mx protein was maintained at basal levels. Co-culture assays of RBCs with TSS (stromal cell line from spleen) revealed the IFN crosstalk between both cell types. On the other hand, anti-microbial peptide ß-defensin 1 and neutrophil chemotactic factor interleukin 8 were slightly upregulated in VHSV-exposed RBCs Isobaric tag for relative and absolute quantification (iTRAQ) revealed that VHSV exposure can induce a global protein downregulation in trout RBCs, mainly related to RNA stability and proteasome pathways. The antioxidant/antiviral response is also suggested to be involved in the response of trout RBCs to VHSV.

Conclusions:

A variety of mechanisms are proposed to be implicated in the antiviral response of trout RBCs against VHSV halted infection. Ongoing research is focused on understanding the mechanisms in detail. To our knowledge, this is the first report that implicates fish RBCs in the antiviral response against viruses not targeting RBCs.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: F1000Res Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: F1000Res Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Espanha