The problem of marine noise pollution has a long history. Strong noise (>120 dB re 1 µPa) will affects the growth, development, physiological responses, and behaviors of fish, and also can induce the stress response, posing a mortal threat. Although many studies have reported that underwater noise may affect the survival of fish by disturbing their nervous system and endocrine system, the underlying causes of death due to noise stimulation remain unknown. Therefore, in this study, we used the underwater noise stress models to conduct underwater strong noise (50–125 dB re 1 µPa, 10–22,000 Hz) stress experiments on small yellow croaker for 10 min (short-term noise stress) and 6 days (long-term noise stress). A total of 150 fishes (body weight: 40–60 g; body length: 12–14 cm) were used in this study. Omics (metabolomics and transcriptomics) studies and quantitative analyses of important genes (HPA (hypothalamic–pituitary–adrenal)-axis functional genes) were performed to reveal genetic and metabolic changes in the important tissues associated with the HPA axis (brain, heart, and adrenal gland). Finally, we found that the strong noise pollution can significantly interfere with the expression of HPA-axis functional genes (including corticotropin releasing hormone (CRH), corticotropin releasing hormone receptor 2 (CRHR2), and arginine vasotocin (AVT)), and long-term stimulation can further induce metabolic disorders of the functional tissues (brain, heart, and adrenal gland), posing a lethal threat. Meanwhile, we also found that there were two kinds of death processes, direct death and chronic death, and both were closely related to the duration of stimulation and the regulation of the HPA axis.

Underwater noise pollution has become a potential threat to aquatic animals in the natural environment. The main causes of such pollution are frequent human activities creating underwater environmental noise, including commercial shipping, offshore energy platforms, scientific exploration activities, etc. However, in aquaculture environments, underwater noise pollution has also become an unavoidable problem due to background noise created by aquaculture equipment. Some research has shown that certain fish show adaptability to noise over a period of time. This could be due to fish’s special auditory organ, i.e., their “inner ear”; meanwhile, otoliths and sensory hair cells are the important components of the inner ear and are also essential for the function of the auditory system. Recently, research in respect of underwater noise pollution has mainly focused on adult fish, and there is a lack of the research on the effects of underwater noise pollution on the development process of the auditory system in the embryonic development period. Thus, in this study, we collected embryo–larval samples of the small yellow croaker (Larimichthys polyactis) in four important stages of otic vesicle development through artificial breeding. Then, we used metabonomics and transcriptomics analyses to reveal the development process of the auditory system in the embryonic development period under background noise (indoor and underwater environment sound). Finally, we identified 4026 differentially expressed genes (DEGs) and 672 differential metabolites (DMs), including 37 DEGs associated with the auditory system, and many differences mainly existed in the neurula stage (20 h of post-fertilization/20 HPF). We also inferred the regulatory mode and process of some important DEGs (Dnmt1, CPS1, and endothelin-1) in the early development of the auditory system. In conclusion, we suggest that the auditory system development of L. polyactis begins at least in the neurula stage or earlier; the other three stages (tail bud stage, caudal fin fold stage, and heart pulsation stage, 28–35 HPF) mark the rapid development period. We speculate that the effect of underwater noise pollution on the embryo–larval stage probably begins even earlier.

Thyroid dysfunction may affect the intestinal microbiota through short-chain fatty acids (SCFAs) in marine fish. This study investigated the effects of triiodothyronine (T3, 20 ng/g) and thyroxine (T4, 20 ng/g), and propylthiouracil (PTU, 5000 ng/g) on growth performance, intestinal SCFA profiles, and microbiota composition in little yellow croakers Larimichthys polyactis. The results showed that dietary thyroid-active agent supplementation significantly decreased weight gain, and specific growth ratio. Moreover, dietary T3, T4, and PTU induced the states of hyperthyroidism, hyperthyroidism, and hypothyroidism, respectively, leading to differential alterations in intestinal SCFA profiles. Specifically, only dietary T4 supplementation significantly increased the diversity of intestinal microbiota. Our findings suggest that the genera Vibrio and Sediminibacterium play key roles in multiple metabolic pathways within the host intestine. Correlation analyses further indicated that intestinal acetic acid and isobutyric acid were characteristic metabolites involved in the alteration of the genus Vibrio abundance. These results provide a foundation for further investigation into the effects of thyroid-disrupting activities on growth, intestinal SCFA profiles, and microbiota composition in marine fish.

This study is to explore the alleviating effects of glutamate on intestinal damage in cultured little yellow croaker. A total of 900 juvenile fish at a weight of 30.68 ± 0.12 g were randomly separated into six groups with three replicates each, and were fed a basic diet (protein at 44.42% and lipid at 12.48%) with additional glutamate at 0.00%, 0.40%, 0.80%, 1.2%, 1.60%, and 2.00%. Each replica group consisted of 50 fish in a breeding barrel (radius 1.0 m, height 1.5 m), and the experiment lasted for 54 days. The results showed that supplementation with 0.4–1.2% glutamate significantly improved the survival rate, which increased from 75.56% to 91.11%, reduced the feed conversion rate from 1.75 to 1.57, and increased the protein efficiency ratio from 1.55 to 1.85 (p < 0.05). In the intestines, the addition of 0.40–1.2% glutamate increased muscle thickness and villus height (p < 0.05), as well as the activities of pepsin, trypsin, α-amylase, and lipase (p < 0.05). Enzyme activity analysis indicated that the addition of 0.4–1.2% glutamate in the feed significantly enhanced the activities of serum Total Superoxide Dismutase (T-SOD), catalase (CAT), and glutathione peroxidase (GPx) antioxidant enzymes (p < 0.05). Transcriptome analysis of the 1.2% and 0% groups revealed that differentially expressed genes were enriched in glutathione synthesis, nutrient absorption and metabolism, and viral protein interaction with cytokine and cytokine receptor pathways. qPCR experiments verified that the addition of 1.2% glutamate significantly up-regulated the expression of antioxidant-related genes, including glutathione synthetase and Nrf2. In conclusion, the addition of glutamate can enhance growth performance, increase intestinal digestive capacity, activate intestinal glutathione synthesis to alleviate intestinal damage, and maintain intestinal health.

Over the past few years, China has become a hotspot for the domestication of the commercially valuable largemouth bass (Micropterus salmoides). Although the food preference of this fish has been studied, little is known about the genes regulating its growth. Population breeding was performed using two indigenous strains (QT1 and QT2), with the results showing that the organ/body ratio, abdominal fat rate and the body weight gain of QT1 and QT2 were higher than for the offspring YL1 and Y3 which are extensively cultured in China. Subsequent RNA sequencing (RNA-Seq) allowed for the identification of potential genes and pathways involved in growth performance. Overall, the transcriptome analysis generated 89,056 transcripts and 42,529 Unigenes. A PCA revealed significant differences between QT1 and the other three strains, while the other three strains did not show much difference. A KEGG enrichment analysis of differentially expressed genes showed that steroid biosynthesis was the most enriched pathway among the four strains. These pathways could be related to the growth of largemouth bass. In addition, a co-expression network analysis suggested a strong interaction between liver steroid biosynthesis and the genes for photosynthesis, secondary metabolism and stress response. Taken together, the above results can provide new insights into the liver metabolism of different strains of largemouth bass during culture and provide references for the subsequent domestication and breeding programs of largemouth bass.

Commercial feeds formulated for Larimichthys crocea are commonly used in intensive farming of Larimichthys polyactis; however, their nutritional composition is suboptimal for the latter. The study evaluated the effects of dietary chenodeoxycholic acid (CDCA) and ursodeoxycholic acid (UDCA) supplementation on mitigating nutritional mismatch-induced growth retardation and hepatopancreatic–intestinal metabolic disorders in L. polyactis. Fish were fed seven feeds: a commercial feed (control) and feeds supplemented with 300, 600, and 1200 mg/kg of CDCA or UDCA. Results showed that both bile acids (BAs) supplementation improved growth, altered thyroid hormone metabolism, with significant changes in hepatopancreatic–intestinal types of deiodination. Both BAs increased hepatopancreatic energy metabolism and cholic acid synthesis, while inducing hepatopancreatic oxidative damage. Notably, 300 mg/kg CDCA and 600 mg/kg UDCA significantly reduced hepatopancreatic vacuolation and lipid accumulation, which was associated with enhanced protease and lipase activities (p < 0.05). Dietary both BAs supplementation enhanced intestinal antioxidant capacity, but contributed to the inflammation, with 300 mg/kg UDCA improving intestinal mucosal morphology (p < 0.05). These findings suggest that supplementation with dietary 300 mg/kg CDCA, 300 and 600 mg/kg UDCA could alleviate growth restriction and liver–intestinal structural damage caused by nutritional mismatch, reduce hepatic fat accumulation, and enhance intestinal antioxidant capacity of L. polyactis.