Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius

9 páginas, 5 figuras The effect of a pathogenic Vibrio pelagius, isolated during a mass mortality of turbot larvae, on the non-specific immune response of turbot, Scophthalmus maximus (L.), macrophages was studied both in vitro and in vivo. The in vitro treatment of head kidney (HK) macrophages with...

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Published in:Journal of Fish Diseases
Main Authors: Villamil, L., Figueras Huerta, Antonio, Aranguren, Raquel, Novoa, Beatriz
Format: Article in Journal/Newspaper
Language:English
Published: Wiley-Blackwell 2003
Subjects:
Online Access:http://hdl.handle.net/10261/56331
https://doi.org/10.1046/j.1365-2761.2003.00464.x
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author Villamil, L.
Figueras Huerta, Antonio
Aranguren, Raquel
Novoa, Beatriz
author_facet Villamil, L.
Figueras Huerta, Antonio
Aranguren, Raquel
Novoa, Beatriz
author_sort Villamil, L.
collection Digital.CSIC (Spanish National Research Council)
container_issue 6
container_start_page 321
container_title Journal of Fish Diseases
container_volume 26
description 9 páginas, 5 figuras The effect of a pathogenic Vibrio pelagius, isolated during a mass mortality of turbot larvae, on the non-specific immune response of turbot, Scophthalmus maximus (L.), macrophages was studied both in vitro and in vivo. The in vitro treatment of head kidney (HK) macrophages with viable V. pelagius caused a significant inhibition of the chemiluminescence (CL) response in comparison with untreated macrophages, while incubation with heat-killed bacteria did not affect this response. In vivo, the intraperitoneal injection of V. pelagius resulted in a significant inhibition of the CL response in infected fish at days 1 and 4 post-infection compared with the control fish response. The HK macrophage nitric oxide (NO) production was enhanced by in vitro incubation with intermediate doses of viable V. pelagius (5 × 103 and 5 × 104 bacteria mL−1) and higher doses of the heat-killed bacteria (5 × 104–5 × 106 bacteria mL−1). In both cases, the NO inhibitorN-ω -nitro-L-arginine was capable of down-regulating the specific NO induction caused by incubation with the bacterial treatments. In contrast, incubation with ECPs at higher doses caused a reduction in NO production. In vivo, a significant enhancement in NO production was also observed in macrophage supernatants at day 10 post-infection. Lysozyme concentration in the serum was also significantly increased in the experimentally infected fish at days 4 and 10 post-injection. In addition, viable V. pelagius and its ECPs significantly reduced HK macrophage viability in vitro, whereas no significant differences in viability were observed during the incubation with heat-killed bacteria. As NO production was enhanced in the experimentally infected fish, the inhibitory effect of the NO donor, S-nitroso-acetyl-penicillamine (SNAP), was tested in vitro in a cell-free assay. The results showed that growth of V. pelagius was significantly inhibited using SNAP at a high concentration (1 mm). This work was partially supported by project 1FD97-0044-C03-03 from ...
format Article in Journal/Newspaper
genre Scophthalmus maximus
Turbot
genre_facet Scophthalmus maximus
Turbot
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op_doi https://doi.org/10.1046/j.1365-2761.2003.00464.x
op_relation http://dx.doi.org/10.1046/j.1365-2761.2003.00464.x
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spelling ftcsic:oai:digital.csic.es:10261/56331 2025-02-09T14:39:03+00:00 Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius Villamil, L. Figueras Huerta, Antonio Aranguren, Raquel Novoa, Beatriz 2003 http://hdl.handle.net/10261/56331 https://doi.org/10.1046/j.1365-2761.2003.00464.x en eng Wiley-Blackwell http://dx.doi.org/10.1046/j.1365-2761.2003.00464.x http://hdl.handle.net/10261/56331 none Chemiluminescence Innate immunity Lysozyme Nitirc oxide Scophthalmus maximus Vibrio pelagius artículo http://purl.org/coar/resource_type/c_6501 2003 ftcsic https://doi.org/10.1046/j.1365-2761.2003.00464.x 2025-01-14T18:47:49Z 9 páginas, 5 figuras The effect of a pathogenic Vibrio pelagius, isolated during a mass mortality of turbot larvae, on the non-specific immune response of turbot, Scophthalmus maximus (L.), macrophages was studied both in vitro and in vivo. The in vitro treatment of head kidney (HK) macrophages with viable V. pelagius caused a significant inhibition of the chemiluminescence (CL) response in comparison with untreated macrophages, while incubation with heat-killed bacteria did not affect this response. In vivo, the intraperitoneal injection of V. pelagius resulted in a significant inhibition of the CL response in infected fish at days 1 and 4 post-infection compared with the control fish response. The HK macrophage nitric oxide (NO) production was enhanced by in vitro incubation with intermediate doses of viable V. pelagius (5 × 103 and 5 × 104 bacteria mL−1) and higher doses of the heat-killed bacteria (5 × 104–5 × 106 bacteria mL−1). In both cases, the NO inhibitorN-ω -nitro-L-arginine was capable of down-regulating the specific NO induction caused by incubation with the bacterial treatments. In contrast, incubation with ECPs at higher doses caused a reduction in NO production. In vivo, a significant enhancement in NO production was also observed in macrophage supernatants at day 10 post-infection. Lysozyme concentration in the serum was also significantly increased in the experimentally infected fish at days 4 and 10 post-injection. In addition, viable V. pelagius and its ECPs significantly reduced HK macrophage viability in vitro, whereas no significant differences in viability were observed during the incubation with heat-killed bacteria. As NO production was enhanced in the experimentally infected fish, the inhibitory effect of the NO donor, S-nitroso-acetyl-penicillamine (SNAP), was tested in vitro in a cell-free assay. The results showed that growth of V. pelagius was significantly inhibited using SNAP at a high concentration (1 mm). This work was partially supported by project 1FD97-0044-C03-03 from ... Article in Journal/Newspaper Scophthalmus maximus Turbot Digital.CSIC (Spanish National Research Council) Journal of Fish Diseases 26 6 321 329
spellingShingle Chemiluminescence
Innate immunity
Lysozyme
Nitirc oxide
Scophthalmus maximus
Vibrio pelagius
Villamil, L.
Figueras Huerta, Antonio
Aranguren, Raquel
Novoa, Beatriz
Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius
title Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius
title_full Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius
title_fullStr Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius
title_full_unstemmed Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius
title_short Non-specific immune response of turbot, Scophthalmus maximus (L.), experimentally infected with a pathogenic Vibrio pelagius
title_sort non-specific immune response of turbot, scophthalmus maximus (l.), experimentally infected with a pathogenic vibrio pelagius
topic Chemiluminescence
Innate immunity
Lysozyme
Nitirc oxide
Scophthalmus maximus
Vibrio pelagius
topic_facet Chemiluminescence
Innate immunity
Lysozyme
Nitirc oxide
Scophthalmus maximus
Vibrio pelagius
url http://hdl.handle.net/10261/56331
https://doi.org/10.1046/j.1365-2761.2003.00464.x