This study aimed to investigate effects of bovine serum albumin immune‐stimulating complexes (BSA ISCOMs) on immune‐related genes expression, serum nonspecific immunity and disease resistance of large yellow croaker (Pseudosciaena crocea). Fish were fed diets containing 3.5 ml of BSA ISCOMs per kg feed (experimental group) or 3.5 ml of phosphate‐buffered saline per kg feed (control group) for 1 week. The liver, spleen, head‐kidney tissues were sampled for determining gene expression of myxovirus‐resistant protein (Mx), major histocompatibility complex class II alpha chain (MHC II α), tumour necrosis factor‐alpha (TNF‐α) and interleukin‐10 (IL‐10) 30 and 90 days after feeding. Also, blood samples were collected for determining activities of serum superoxide dismutase (SOD), interferon alpha (IFN‐α), TNF‐α and alkaline phosphatase (ALP). TNF‐α and MHCⅡα gene expression in the liver, spleen, head‐kidney, as well as IFN‐α, TNF‐α and ALP activities in the serum, of experimental fish were significantly higher 30 days after feeding; while only TNF‐α and MHC II gene expression in the head‐kidney remained upregulated 90 days after feeding. The cumulative mortality of the experimental fish was significantly lower than control. This study indicated that BSA ISCOMs improved the immune response and induced protective immunity in large yellow croaker. 相似文献
Two experiments were conducted to investigate the active components of soybean lecithin for juvenile Litopenaeus vannamei. The first experiment was conducted to determine the dietary phosphatidylcholine (PC) requirement of juvenile L. vannamei, and to investigate whether other phospholipids (PL), mainly phosphatidylethanolamine (PE) and phosphatidylinositol (PI) were the active fractions of soybean lecithin. Seven levels of PC (0%, 0.35%, 0.7%, 1.4%, 2.1%, 2.8%, 4.2%) extracted from soybean lecithin (PC purity 93%) were used to determine the PC requirement; also, PE and PI (in a 25:22 proportion) were tested at 0.84% and 1.68% levels with PC levels controlled at 0.35% and 0.52% of diet to investigate the combined PE and PI effects. Results showed that no dietary PC requirement was evident based on shrimp growth and survival. Increasing purified PC in the diet decreased total lipid, free fatty acid and other PL levels in shrimp hepatopancreas (mid-gut gland) and increased PC level in shrimp muscle. However, other PL, mainly PE and PI, showed significant enhancing effects on shrimp growth when PC was provided at 0.35% or 0.52% of diet.
Another 4×2 factorial experiment was concluded to reevaluate the requirement of shrimp for PC by including purified PC at 0%, 0.7%, 1.4 % and 2.8% of diet with or without 0.1% cholesterol in the diet. A diet containing 1.4% PC provided by deoiled lecithin also was tested for comparison. Results showed no interaction between PC and cholesterol on shrimp growth, survival and feed conversion ratio (FCR). Compared with the apparent growth-enhancing effect of dietary cholesterol, the effect of purified PC was negligible. With PC at 1.4% of diet, the presence of other PL from lecithin or 0.1% cholesterol significantly enhanced shrimp growth and FCR.
In summary, purified soybean PC showed different effects from deoiled lecithin on shrimp growth, lipid composition, and relationship with dietary cholesterol. Beneficial effects of soybean lecithin on growth of L. vannamei could be attributed to the presence of PL other than PC in the diet under the experimental conditions of this study. 相似文献
Infection of a Myxobolus species, previously identified as Myxobolus rotundus, was detected in 182 of 7892 (2.31%) allogynogenetic gibel carp, Carassius auratus gibelio, in a closed pond culture system in China. Morphological and molecular data showed that this myxosporean is a different species from M. rotundus parasitizing Abramis brama in Europe and is thus designated as a new species, Myxobolus turpisrotundus. M. rotundus (s.l.) ex C. auratusauratus is a synonym of M. turpisrotundus. Plasmodia of M. turpisrotundus develop in the subepidermal tissues of the body surface resulting in an unaesthetic appearance and causing severe economic losses. Prevalence of infection with the myxosporean plasmodia varied seasonally, increasing in winter and decreasing in spring. Prevalence was positively correlated to host size, but no host sex‐specificity was found. No infection was observed in other fish species (grass carp, bighead carp and yellow catfish) reared in the same pond, suggesting that the parasite has a relatively strict host specificity. Plasmodia grew gradually as the parasite developed, and reached up to a maximum 5.6 mm in diameter. Plasmodia ruptured naturally to release the mature spores and host fish completely recovered with no mortality. Release of spores and regeneration of lesions were not correlated with water temperature. Histology showed that plasmodia developed sub‐epidermally, and that the wall of the plasmodia was composed of a multiple complex structure, including layers of fibroblasts, a collagenous membrane, melanophores and a layer of cup‐like cells of unknown derivation and function. The cup‐like cells are in direct contact with pre‐sporogonic stages located in the peripheral parts of the large plasmodia. No severe host inflammatory response was seen. 相似文献