2022
DOI: 10.3390/antiox11061143
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Growth, Health, and Gut Microbiota of Female Pacific White Shrimp, Litopenaeus vannamei Broodstock Fed Different Phospholipid Sources

Abstract: Phospholipids have an important antioxidant effect on animals. The effects of different dietary phospholipid sources on the growth, antioxidant activity, immunity, and gut microbiota of female broodstock of Pacific white shrimp Litopenaeus vannamei were investigated. Four isoproteic and isolipid semi-purified diets containing 4% soybean lecithin (SL), egg yolk lecithin (EL), or krill oil (KO) and a control diet without phospholipid supplementation were fed to female broodstock of L. vannamei (34.7 ± 4.2 g) for… Show more

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Cited by 12 publications
(10 citation statements)
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“…Previous studies have reported the interaction between dietary lipids, intestinal microbiota, and the growth performance of the host. 66,67 In this study, dietary OPL-rich oil could promote juvenile growth and regulate intestinal microbiota. Pearson's analysis revealed a positive association of juvenile growth with Streptomyces_mutabilis , Aurantimicrobium_minutum , and Nocardiopsis_kunsanensis , as well as a negative association with Staphylococcus_nepalensis , Bacillus_sp013155385 , and Romboutsia_ilealis .…”
Section: Resultsmentioning
confidence: 84%
See 1 more Smart Citation
“…Previous studies have reported the interaction between dietary lipids, intestinal microbiota, and the growth performance of the host. 66,67 In this study, dietary OPL-rich oil could promote juvenile growth and regulate intestinal microbiota. Pearson's analysis revealed a positive association of juvenile growth with Streptomyces_mutabilis , Aurantimicrobium_minutum , and Nocardiopsis_kunsanensis , as well as a negative association with Staphylococcus_nepalensis , Bacillus_sp013155385 , and Romboutsia_ilealis .…”
Section: Resultsmentioning
confidence: 84%
“…Overall, our results demonstrated that the correlation between juvenile growth and the intestinal microbiota of the host, and the cor- Previous studies have reported the interaction between dietary lipids, intestinal microbiota, and the growth performance of the host. 66,67 In this study, dietary OPL-rich oil could promote juvenile growth and regulate intestinal microbiota. Pearson's analysis revealed a positive association of juvenile…”
Section: Papermentioning
confidence: 87%
“…It is more apparent that SBL enhanced the growth performance of striped catfish. Based on the obtained results, the improved FCR, digestive enzyme activity, and intestinal histological features are the main reasons for the enhanced growth performance of striped catfish [ 51 , 52 ]. The role of phospholipids on the activation of flux rate through the cell membrane enterocytes, thereby facilitating the permeability of digested macromolecules [ 18 , 53 ].…”
Section: Discussionmentioning
confidence: 99%
“…Taxonomically, these papers cover freshwater fish ( Carassius auratus [ 4 ], Monopterus albus [ 5 ], Ictalurus punctatus [ 6 ], Megalobrama amblycephala [ 7 ], Micropterus salmoides [ 8 ], Lateolabrax maculatus [ 9 , 10 , 11 , 12 ], Carassius gibelio [ 13 , 14 ], Aplodinotus grunniens [ 15 ], Pangasianodon hypophthalmus [ 16 ], Danio rerio [ 17 ], and hybrid grouper [ 18 ]), marine fish ( Scophthalus maximus [ 19 ]), crustaceans ( Macrobrachium rosenbergii [ 20 , 21 , 22 ], Litopenaeus vannamei [ 23 , 24 , 25 ], Penaeus monodon [ 26 ], Scylla paramamosain [ 27 ], and Eriocheir sinensis [ 28 ]), and molluscs ( Crassostrea hongkongensis [ 29 ], Trachinotus ovatus [ 30 ], and Pacific abalone [ 31 ]). Meanwhile, these papers reveal several endogenous and exogenous factors that induce oxidative stress, such as environmental factors (water hardness [ 4 ], chronic hyperthermia [ 6 ], acute hypoxic stress [ 10 ], acute ammonia nitrogen [ 12 ], hypothermia [ 15 ], low salinity [ 23 ], and ammonia-N-stress [ 26 ]), nutritional factors (high carbohydrate levels [ 5 ], oxidized lipids [ 7 ], high-fat diet [ 12 , 20 ], and lipopolysaccharide [ 29 ...…”
mentioning
confidence: 99%
“…Meanwhile, these papers reveal several endogenous and exogenous factors that induce oxidative stress, such as environmental factors (water hardness [ 4 ], chronic hyperthermia [ 6 ], acute hypoxic stress [ 10 ], acute ammonia nitrogen [ 12 ], hypothermia [ 15 ], low salinity [ 23 ], and ammonia-N-stress [ 26 ]), nutritional factors (high carbohydrate levels [ 5 ], oxidized lipids [ 7 ], high-fat diet [ 12 , 20 ], and lipopolysaccharide [ 29 , 31 ]), essential or heavy metals (Zn [ 4 ], cadmium [ 13 , 27 ], Cu 2+ [ 28 ], and polyinosinic–polycytidylic acid sodium salt [ 31 ]), pathogenic bacteria or virus (aflatoxin B1 and cyprinid herpesvirus 2 [ 14 ], water bubble disease (WBD) [ 21 ], Vibrio harveyi [ 29 , 31 ], and Streptococcus agalactiae [ 30 ]), and feeding practices (stocking density [ 8 ], transport stress [ 11 ]). Therapeutically, some papers have also explored some medicines or immunostimulants to resist oxidative stress, such as herbal medicine (mulberry leaf flavonoids [ 5 ], emodin [ 7 ], berberine [ 17 ], Sophora flavescens root extract [ 19 ], and tea tree oil [ 22 ]), nutritional stimulants ( Atractylodes macrocephala polysaccharide [ 9 ], taurine alleviates [ 13 ], histamine [ 16 , 18 ], vitamin E [ 20 ], β-Glucan [ 23 ], krill oil [ 24 ], and zinc [ 25 ]), antibiotics (florfenicol and ofloxacin [ 21 ]), and feeding admin...…”
mentioning
confidence: 99%