2013
DOI: 10.1016/j.aquaculture.2012.11.016
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Comparison of the effects of the dietary addition of two lactic acid bacteria on the development and conformation of sea bass larvae, Dicentrarchus labrax, and the influence on associated microbiota

Abstract: Comparison of the effects of the dietary addition of two lactic acid bacteria on the development and conformation of sea bass larvae, Dicentrarchus labrax, and the influence on associated microbiota

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Cited by 48 publications
(44 citation statements)
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“…Newly-hatched sea bass larvae were provided by Aquastream (Ploemeur, France), allotted at 2 dph (day post hatch) in 15 tanks of 35 L, and then reared in the general conditions described elsewhere [40]. The 15 tanks were divided in three groups of five tanks, which were fed the compound diets from 7 dph onwards (Fig.…”
Section: Methodsmentioning
confidence: 99%
“…Newly-hatched sea bass larvae were provided by Aquastream (Ploemeur, France), allotted at 2 dph (day post hatch) in 15 tanks of 35 L, and then reared in the general conditions described elsewhere [40]. The 15 tanks were divided in three groups of five tanks, which were fed the compound diets from 7 dph onwards (Fig.…”
Section: Methodsmentioning
confidence: 99%
“…Importantly, the ecological relations among gastrointestinal bacteria are responsible for benefits to the immune system [13,14,15,16,17,18,19,20], nutrient metabolism [21], growth [22], stress tolerance [23,24], vertebral column deformities, bone calcification and density [25,26,27,28], development [29,30] and reproduction [31,32,33,34], all deriving from their administration.…”
Section: Introductionmentioning
confidence: 99%
“…The method allowed us to discriminate the bacterial phylotypes after their partial sequences of 16S and 26S rRNA for bacteria and fungi, respectively. The sequences could not be systematically read, but some bands were extracted from the DGGE gels for bacterial sequencing, when feasible (Lamari et al, 2013). …”
mentioning
confidence: 99%
“…The intestinal sections from the juveniles were also placed in sterile Petri dishes on ice after thawing, to squeeze out the gut mucosae and the associated microbiota with a metallic spatula. The samples were immediately collected with sterile tweezers, and immersed in Extract-All ® (Eurobio) for RNA extraction and subsequent RT-PCR-DGGE, as described for bacterial profiling by Lamari et al (Lamari et al, 2013). Fungi were analysed using the primers NL1GC and LS2 (Verdugo Valdez et al, 2011) with the same PCR conditions as for bacteria.…”
mentioning
confidence: 99%