Resistant and susceptible rainbow trout (Oncorhynchus mykiss) lines show distinctive immune response to Lactococcus garvieae.


Journal

Fish & shellfish immunology
ISSN: 1095-9947
Titre abrégé: Fish Shellfish Immunol
Pays: England
ID NLM: 9505220

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 24 03 2020
revised: 16 06 2020
accepted: 18 06 2020
pubmed: 17 7 2020
medline: 23 4 2021
entrez: 17 7 2020
Statut: ppublish

Résumé

Lactococcosis is one of the main bacterial diseases affecting rainbow trout (Oncorhynchus mykiss), with significant economic and sanitary repercussion. Vaccination and antibiotic treatments are commonly used to prevent and control the infection outbreaks; however, these strategies have some drawbacks including limited coverage, handling costs, induction of antibiotic resistance and chemical residues in the environment. Selective breeding programs represent a promising complementary approach for increasing fish disease resistance in commercial farms and some immunological parameters may be tentatively used as indirect indicators for this purpose. The present study investigated for the first time some innate and adaptive immune responses in two groups of rainbow trout derived from selected lines (susceptible and resistant) showing a different "in field" phenotypical resistance to Yersinia ruckeri, Flavobacterium branchiophilum, F. psychrophilum, and Ichthyophthirius multifiliis, after an immersion-dilution based exposure to Lactococcus garvieae carried out in controlled experimental conditions. Twenty-six resistant and twenty-six susceptible female rainbow trout (mean body weight 80 g, 9 months aged, F5 generation) were obtained from an intensive farm considered L. garvieae free and were exposed to the pathogen. Moreover, 10 resistant and 10 susceptible fish were used as uninfected controls. After 5 days, blood and tissue samples were collected for immunological analyses. A significantly higher serum and mucus lysozyme activity was recorded in resistant rainbow trout compared to susceptible fish (P ≤ 0.05), both before and after exposure to L. garvieae. Similarly, respiratory burst activity of head kidney leukocytes resulted more intense in resistant fish (P ≤ 0.05), suggesting that phagocytes could more quickly activate their microbicidal mechanisms to counteract the bacterial spread. Resistant group displayed also an up-regulation of immunoglobulins M (IgM), major histocompatibility complex II (MHC-II) and interleukin 8 (IL-8) gene expression (P ≤ 0.05) and a significantly higher blood lymphocytes count (P ≤ 0.05), highlighting their potential better ability to trigger the recruitment of defensive cells and the initiation of specific immune processes such as antigen presentation to CD4

Identifiants

pubmed: 32673645
pii: S1050-4648(20)30463-0
doi: 10.1016/j.fsi.2020.06.040
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

457-468

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Chiara Bulfon (C)

University of Udine, Department of Agricultural, Food, Environmental and Animal Sciences (DI4A), Section of Animal and Veterinary Sciences, via Sondrio 2/a, 33100, Udine, UD, Italy.

Marino Prearo (M)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

Donatella Volpatti (D)

University of Udine, Department of Agricultural, Food, Environmental and Animal Sciences (DI4A), Section of Animal and Veterinary Sciences, via Sondrio 2/a, 33100, Udine, UD, Italy. Electronic address: donatella.volpatti@uniud.it.

Omkar Byadgi (O)

University of Udine, Department of Agricultural, Food, Environmental and Animal Sciences (DI4A), Section of Animal and Veterinary Sciences, via Sondrio 2/a, 33100, Udine, UD, Italy.

Marzia Righetti (M)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

Maria Grazia Maniaci (MG)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

Valentina Campia (V)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

Paolo Pastorino (P)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

Francesco Pascoli (F)

Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), Viale dell'Università 10, 35020, Legnaro, PD, Italy.

Anna Toffan (A)

Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), Viale dell'Università 10, 35020, Legnaro, PD, Italy.

Cristina Biolatti (C)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

Pier Luigi Acutis (PL)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

Silvia Colussi (S)

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), via Bologna 148, 10154, Torino, TO, Italy.

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Classifications MeSH