2023
DOI: 10.1016/j.aquaculture.2022.739222
|View full text |Cite
|
Sign up to set email alerts
|

Micro- and macroalgae blend modulates the mucosal and systemic immune responses of European seabass (Dicentrarchus labrax) upon infection with Tenacibaculum maritimum

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

2
5
1

Year Published

2023
2023
2024
2024

Publication Types

Select...
5

Relationship

1
4

Authors

Journals

citations
Cited by 5 publications
(11 citation statements)
references
References 65 publications
2
5
1
Order By: Relevance
“…Since this challenge model was also able to successfully induce tenacibaculosis clinical signs and mortality in the bacteria exposed fish, it is suggested that immersion challenge (with a 2 h period of bacterial exposure) is an effective method to experimentally reproduce this disease in European sea bass. Similar mortality traits were also observed in previous studies following the same immersion challenge procedure ( 56 , 57 ).…”
Section: Discussionsupporting
confidence: 88%
See 1 more Smart Citation
“…Since this challenge model was also able to successfully induce tenacibaculosis clinical signs and mortality in the bacteria exposed fish, it is suggested that immersion challenge (with a 2 h period of bacterial exposure) is an effective method to experimentally reproduce this disease in European sea bass. Similar mortality traits were also observed in previous studies following the same immersion challenge procedure ( 56 , 57 ).…”
Section: Discussionsupporting
confidence: 88%
“…In this same study, the ACC13.1 T. maritimum strain (the same used in the present study) (9.6 × 10 5 cells mL −1 ) lead to cumulative mortalities of approximately 50% in Senegalese sole. In the last years, immersion challenge has been frequently used as a reliable method to experimentally reproduce tenacibaculosis in fish ( 52 57 ). In the present study, a mortality rate of 32.1% was obtained for the bath-challenged fish, while displaying tenacibaculosis clinical signs (e.g.…”
Section: Discussionmentioning
confidence: 99%
“…Total RNA was extracted from the different intestinal sections (~ 30 mg; n = 16 per treatment), using TRIzol reagent (Invitrogen, USA) and NZY Total RNA Isolation kit (NZYTech, Portugal), according to the method described by Ferreira et al 31 . The quantity and purity of the extracted RNA were spectrophotometrically evaluated, while RNA integrity was assessed using an agarose electrophoresis gel as previously described 17 . Using 1 μg of RNA, first strand cDNA was synthesized, and real-time (RT) PCR assays were performed on a CFX384 Touch Real-Time PCR Detection System (Bio-Rad Laboratories, USA) with SsoAdvanced Universal SYBR Green Supermix (Bio-Rad Laboratories, USA).…”
Section: Methodsmentioning
confidence: 99%
“…Using 1 μg of RNA, first strand cDNA was synthesized, and real-time (RT) PCR assays were performed on a CFX384 Touch Real-Time PCR Detection System (Bio-Rad Laboratories, USA) with SsoAdvanced Universal SYBR Green Supermix (Bio-Rad Laboratories, USA). Following the protocol described by Ferreira et al 17 , reactions were performed in duplicate. The employed thermal cycling conditions were: 95 °C for 30 s, followed by 35 cycles of two steps of 95 °C for 5 s and 60 °C for 30 s. The specificity of the RT-PCR reaction was ensured by a post-amplification dissociation curve, while PCR efficiency for each gene was determined using a fivefold serial dilution of cDNA from all the samples used in the experiment.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation