Cargando…

Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.)

The Gram-negative bacterium Vibrio salmonicida is the causative agent of cold-water vibriosis (CV), a hemorrhagic septicemia that primarily affects farmed Atlantic salmon (Salmo salar L.). The mechanisms of disease development, host specificity and adaptation, as well as the immunogenic properties o...

Descripción completa

Detalles Bibliográficos
Autores principales: Bjelland, Ane M., Fauske, Aud K., Nguyen, Anh, Orlien, Ingvild E., Østgaard, Ingrid M., Sørum, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868895/
https://www.ncbi.nlm.nih.gov/pubmed/24391635
http://dx.doi.org/10.3389/fmicb.2013.00401
_version_ 1782296512064126976
author Bjelland, Ane M.
Fauske, Aud K.
Nguyen, Anh
Orlien, Ingvild E.
Østgaard, Ingrid M.
Sørum, Henning
author_facet Bjelland, Ane M.
Fauske, Aud K.
Nguyen, Anh
Orlien, Ingvild E.
Østgaard, Ingrid M.
Sørum, Henning
author_sort Bjelland, Ane M.
collection PubMed
description The Gram-negative bacterium Vibrio salmonicida is the causative agent of cold-water vibriosis (CV), a hemorrhagic septicemia that primarily affects farmed Atlantic salmon (Salmo salar L.). The mechanisms of disease development, host specificity and adaptation, as well as the immunogenic properties of V. salmonicida are largely unknown. Therefore, to gain more knowledge on the pathogenesis of CV, 90 Atlantic salmon parr were injected intraperitoneally with 6 × 10(6) CFU of V. salmonicida LFI1238. Samples from blood and spleen tissue were taken at different time points throughout the challenge for gene expression analysis by two-step reverse transcription (RT) quantitative real-time polymerase chain reaction. Out of a panel of six housekeeping genes, accD, gapA, and 16S rDNA were found to be the most suitable references for expression analysis in Vibrio salmonicida. The bacterial proliferation during challenge was monitored based on the expression of the 16S rRNA encoding gene. Before day 4, the concentrations of V. salmonicida in blood and spleen tissue demonstrated a lag phase. From day 4, the bacterial proliferation was exponential. The expression profiles of eight genes encoding potential virulence factors of V. salmonicida were studied. Surprisingly, all tested virulence genes were generally highest expressed in broth cultures compared to the in vivo samples. We hypothesize that this general muting of gene expression in vivo may be a strategy for V. salmonicida to hide from the host immune system. To further investigate this hypothesis, the expression profiles of eight genes encoding innate immune factors were analyzed. The results demonstrated a strong and rapid, but short-lasting innate immune response against V. salmonicida. These results suggest that the bacterium possesses mechanisms that inhibit and/or resist the salmon innate immune system until the host becomes exhausted of fighting the on-going and eventually overwhelming infection.
format Online
Article
Text
id pubmed-3868895
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-38688952014-01-03 Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.) Bjelland, Ane M. Fauske, Aud K. Nguyen, Anh Orlien, Ingvild E. Østgaard, Ingrid M. Sørum, Henning Front Microbiol Microbiology The Gram-negative bacterium Vibrio salmonicida is the causative agent of cold-water vibriosis (CV), a hemorrhagic septicemia that primarily affects farmed Atlantic salmon (Salmo salar L.). The mechanisms of disease development, host specificity and adaptation, as well as the immunogenic properties of V. salmonicida are largely unknown. Therefore, to gain more knowledge on the pathogenesis of CV, 90 Atlantic salmon parr were injected intraperitoneally with 6 × 10(6) CFU of V. salmonicida LFI1238. Samples from blood and spleen tissue were taken at different time points throughout the challenge for gene expression analysis by two-step reverse transcription (RT) quantitative real-time polymerase chain reaction. Out of a panel of six housekeeping genes, accD, gapA, and 16S rDNA were found to be the most suitable references for expression analysis in Vibrio salmonicida. The bacterial proliferation during challenge was monitored based on the expression of the 16S rRNA encoding gene. Before day 4, the concentrations of V. salmonicida in blood and spleen tissue demonstrated a lag phase. From day 4, the bacterial proliferation was exponential. The expression profiles of eight genes encoding potential virulence factors of V. salmonicida were studied. Surprisingly, all tested virulence genes were generally highest expressed in broth cultures compared to the in vivo samples. We hypothesize that this general muting of gene expression in vivo may be a strategy for V. salmonicida to hide from the host immune system. To further investigate this hypothesis, the expression profiles of eight genes encoding innate immune factors were analyzed. The results demonstrated a strong and rapid, but short-lasting innate immune response against V. salmonicida. These results suggest that the bacterium possesses mechanisms that inhibit and/or resist the salmon innate immune system until the host becomes exhausted of fighting the on-going and eventually overwhelming infection. Frontiers Media S.A. 2013-12-20 /pmc/articles/PMC3868895/ /pubmed/24391635 http://dx.doi.org/10.3389/fmicb.2013.00401 Text en Copyright © 2013 Bjelland, Fauske, Nguyen, Orlien, Østgaard and Sørum. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Bjelland, Ane M.
Fauske, Aud K.
Nguyen, Anh
Orlien, Ingvild E.
Østgaard, Ingrid M.
Sørum, Henning
Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.)
title Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.)
title_full Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.)
title_fullStr Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.)
title_full_unstemmed Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.)
title_short Expression of Vibrio salmonicida virulence genes and immune response parameters in experimentally challenged Atlantic salmon (Salmo salar L.)
title_sort expression of vibrio salmonicida virulence genes and immune response parameters in experimentally challenged atlantic salmon (salmo salar l.)
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868895/
https://www.ncbi.nlm.nih.gov/pubmed/24391635
http://dx.doi.org/10.3389/fmicb.2013.00401
work_keys_str_mv AT bjellandanem expressionofvibriosalmonicidavirulencegenesandimmuneresponseparametersinexperimentallychallengedatlanticsalmonsalmosalarl
AT fauskeaudk expressionofvibriosalmonicidavirulencegenesandimmuneresponseparametersinexperimentallychallengedatlanticsalmonsalmosalarl
AT nguyenanh expressionofvibriosalmonicidavirulencegenesandimmuneresponseparametersinexperimentallychallengedatlanticsalmonsalmosalarl
AT orlieningvilde expressionofvibriosalmonicidavirulencegenesandimmuneresponseparametersinexperimentallychallengedatlanticsalmonsalmosalarl
AT østgaardingridm expressionofvibriosalmonicidavirulencegenesandimmuneresponseparametersinexperimentallychallengedatlanticsalmonsalmosalarl
AT sørumhenning expressionofvibriosalmonicidavirulencegenesandimmuneresponseparametersinexperimentallychallengedatlanticsalmonsalmosalarl