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A 10‐week feeding trial of using housefly (Musca domestica) maggot meal (MM) in practical feeds for Nile tilapia (Oreochromis niloticus) was conducted to assess the growth performance, ingredient utilization, flesh quality, innate immunity and its influence on water environment. Fish were fed five isonitrogenous and isoenergetic diets, where fishmeal (FM) was substituted by MM at the level of 0, 90, 180, 270 and 360 g kg‐1 diet (remaining FM content: 360, 270, 180, 90 and 0 g kg‐1). There was no significant difference in feed intake and apparent digestibility coefficient between the treatments. Replacing up to 270 g kg‐1 FM did not have an impact on the growth performance and ingredient utilization, whereas the complete replacement of FM caused significantly lower survival rate, weight gain, specific growth rate and higher feed conversion rate. Dietary MM was also proved positively influential in flesh quality, whereas replacing 180 g kg‐1 or more FM suppressed the innate immunity of tilapia. When compared by the effects on the water environment, the increasing substitute levels were accompanied with the declining concentrations of nitrite nitrogen and total phosphorus in the water. Our study verified the feasibility of using MM as a partial substitute of FM in aquatic feed. When replacing 180 g kg‐1 FM (corresponding to half of the FM content in control diet) in the diet of Nile tilapia, it can serve as a renewable and environmentally superior alternative without compromising the performance criteria.

While microcystins (MCs) have been reported to exert reproductive toxicity on fish with a sexdependent effect, the underlying mechanism has been rarely investigated. In the present study, zebrafish were exposed to 1, 5 and 20 μg/L MC-LR for 30 d. The gonad-somatic index declined in all treated males. 17β-estradiol (E 2 ), testosterone (T), 11-keto testosterone (11-KT) and follicle-stimulating hormone (FSH) levels increased in serum from all treated females, while T, FSH and luteinizing hormone (LH) levels changed in all treated males. Histomorphological observation showed that MC-LR exposure evidently retarded oogenesis and spermatogenesis. Transcriptional changes of 22 genes of the hypothalamic-pituitary-gonad (HPG) axis exhibited sex-specific responses, and the relationship between gene transcriptions and gametogenesis was evaluated by principle component analysis (PCA). Major contributors to PC1 (gnrh2, gnrhr3, ar, lhr, hmgra, hmgrb and cyp19a) were positively correlated with the number of post-vitellogenic oocytes, while PC1 (gnrh2, lhβ, erβ, fshr, cyp11a and 17βhsd) were positively correlated with the number of spermatozoa. The protein levels of 17βHSD and CYP19a were affected in both females and males. In conclusion, this study first investigated the sex-dependent effects of microcystins on fish reproduction and revealed some important molecular biomarkers related to gametogenesis in zebrafish suffered from MC-LR.Cyanobacteria are photosynthetic, oxygen producing, gram-negative microorganisms found ubiquitously in nature even at extreme climatic conditions 1,2 . Increasing global temperature, nutrient and pollutant enrichment via anthropogenic runoff, drought and flooding lead to eutrophication and outbreak of cyanobacterial blooms 3,4 . The toxic cyanobacterial blooms can produce and release cyanotoxins, the secondary metabolites of cyanobacteria, into water 5 . Among all the cyanobacterial toxins, microcystins (MCs) represent a family of potent hepatotoxins and are considered as the most resistant of cyanotoxins to degradation because of their stable cyclic peptide structure 6 . To date, over 100 variants of MCs have been isolated, and microcystin-LR (MC-LR), a hydrophobic variant, is considered to be the most commonly occurring and lethal toxin 7 . In fish, MCs accumulate mainly in liver and therefore liver is considered as the first target organ of MCs 8,9 . A provisional safety guideline of 1.0 μg/L MC-LR in drinking water was recommended by the World Health Organization (WHO) 10 . MCs are released from the cyanobacterial cells into the water bodies where fish spends their whole life stage, including growth, reproduction and embryonic development 11 . Gonad has been recognized as the second important target organ of MCs 12 and MCs exert negative effects on the reproductive system of fish [13][14][15] . Lysis of the gonadosomatic tissue in ovary and disruption of spermatogenesis in testis were observed in medaka fish exposed to MC-LR 13. Hou et al. also suggested MC-LR had adverse effects on histologic...

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The Paneth cells are highly specialized cells in the epithelium of the small intestine of many vertebrate species. These cells reside at the base of crypts of the Lieberkühn and contain abundant secretory granules. Previous studies suggesting the existence of Paneth cells in the chicken (Gallus gallus) remained controversial. Here we seek to identify the Paneth cells in the chicken small intestine through morphological examination and specific gene expression. Histological staining and transmission electron microscope confirmed the presence of granulated secretory cells at the base of the crypts in the chicken small intestine. Western blotting experiment also manifested the expression of lysozyme protein, which is specifically secreted by the Paneth cells in the small intestine. Moreover, lysozyme c and lysozyme g mRNAs were expressed in the small intestine of chickens at different ages. Lysozyme c mRNA, in particular, was located at the base of the small intestinal crypts as displayed by in situ hybridization. Collectively, we provide evidences that the Paneth cells indeed exist in the small intestine of the chicken.