Dietary Sodium Butyrate Changed Intestinal Histology and Microbiota of Rainbow Trout (Oncorhynchus mykiss), but Did Not Promote Growth and Nutrient Utilization

The study investigated the effects of dietary sodium butyrate (SB) on the growth performance, nutrient utilization, intestinal histology, and microbiota of rainbow trout (Oncorhynchus mykiss). A high fishmeal diet and a low fishmeal diet were formulated to contain 200 g/kg or 100 g/kg fishmeal, respectively. Coated SB (50%) was supplemented to each of the diets at levels of 0, 1.0, and 2.0 g/kg to create 6 diets. The diets were fed to rainbow trout with initial body weight of 29.9 ± 0.2 g for 8 weeks. Compared to the high fishmeal group, the low fishmeal group showed significantly lower weight gain (WG), intestine muscle thickness, and significantly higher feed conversion ratio (FCR) and amylase activity (P < 0.05). The supplementation of SB in high or low fishmeal diet did not significantly affect the WG, FCR, protein retention, and the digestibility of dry matter and crude protein (P > 0.05). The supplementation of 2.0 g/kg SB in low fishmeal diet significantly increased the villus height, villus width, and muscular thickness, while the supplementation of 2.0 g/kg SB in high fishmeal diet also significantly increased the intestinal villus height (P < 0.05). In intestinal microbiota, the supplementation of 2.0 g/kg SB significantly increased the abundance of Proteobacteria and Aeromonas, and decreased the abundance of Firmicutes and Mycoplasma (P < 0.05), but the flora at genus and phylum level were not affected by SB supplementation in low fishmeal diet (P > 0.05). In conclusion, the addition of SB in diets containing 100 or 200 g/kg fishmeal did not enhance the growth performance and nutrient utilization of rainbow trout, but improved intestinal morphology and changed intestinal microbial flora.


Introduction
Rainbow trout (Oncorhynchus mykiss) is an important cold water aquaculture fish in the world. In China, the aquaculture production of rainbow trout reached 37,841 tons in 2020 [1]. Rainbow trout is a carnivorous fish, and the commercial diets usually contain high amount of fishmeal. Due to the scarcity of resource and rising price of fishmeal, reducing the inclusion level of fishmeal in aquafeeds, especially in carnivorous fish diets, has become a hot spot in aquafeed industry [2]. Generally, the high replacement of fishmeal with plant protein sources leads to the decrease of growth performance, feed intake, and digestibility [3] in aquaculture fishes due to the presence of antinutritional factors and deficiencies in some essential amino acids, as well as the damage to physical barrier of the intestine and inflammatory reactions [4]. Therefore, the application of functional nutrients may be an effective way to improve the utilization efficiency of nonfishmeal protein sources.
Sodium butyrate is the sodium salt of butyric acid, and the active ingredient is butyric acid. Previous studies have shown that butyric acid is the direct source of energy for intestinal epithelial cells [5], which can promote intestinal cell proliferation, improve intestinal morphology, increase the digestion and absorption of nutrients, and improve animal growth [6,7]. With its hydrophilic and lipophilic properties, butyric acid can inhibit harmful bacteria and promote the reproduction of beneficial bacteria after entering bacterial cells, thus maintaining intestinal health. The dietary addition of 0.3% sodium butyrate product (70% effective content) increased the specific growth rate of sea bream (Sparus aurata) by 5% and decreased feed conversion ratio by 8% [8]. [9]) found that golden pompano (Trachinotus ovatus) juvenile presented the highest weight gain and specific growth rate when the fish was fed a diet containing 2.0 g/kg sodium butyrate. In black bream (Acanthopagrus schlegelii) juvenile, the dietary addition of 0.2% microencapsulated sodium butyrate increased weight gain and feed efficiency [10]. Abd El-Naby et al. [11] and Dawood et al. [12] reported that the addition of sodium butyrate improved the growth performance and immunity of tilapia (Oreochromis mossambicus). Meanwhile, sodium butyrate supplementation was reported to maintain the intestinal health of tilapia [13]. In addition, dietary sodium butyrate also promoted the growth and improved intestinal function of grass carp (Ctenopharyngodon idella) juveniles [14][15][16], turbot (Scophthalmus maximus) [17], giant bony tongues (Arapaima gigas) [18], and yellow drum (Nibea albiflora) [19].
The previous studies have shown the beneficial effects of sodium butyrate in some fishes, but few studies have been conducted in salmonids, with only a few reports using sodium butyrate as part of a mixture of organic salts. Gao et al. [20] found that the dietary addition of 10 g/kg of a mixture of sodium formate and sodium butyrate did not significantly affect the growth and feed utilization of rainbow trout. In Atlantic salmon (Salmo salar), dietary supplementation of short-chain fatty acid (salt) mixtures (0.5% and 2.0%) (acetic acid: propionic acid: sodium butyrate = 5 : 5 : 2) also showed no significant effects on growth performance, apparent nutrient digestibility, total lipid, and fatty acid composition of fish and intestinal tissues [21]. From the above studies, it is still unclear if salmonids can effectively utilize sodium butyrate or not. Therefore, the present study aimed to investigate the effects of different levels of sodium butyrate supplementation in diets on growth performance, nutrient utilization, intestinal histology, and microbiota of rainbow trout. The results will guide the application of sodium butyrate in aquafeeds.

Materials and Methods
2.1. Ethical Statement. The procedures have been authorized by the Animal Ethics Committee for Experiments on Animals of Shanghai Ocean University and implemented in accordance with the experiment animal welfare regulation formulated by the Chinese Association for Laboratory Animal Science.

Experimental Diets and Design.
A two-factor trial was designed with two levels of fishmeal and three levels of sodium butyrate supplementation. Firstly, a high fishmeal diet was formulated to contain 200 g/kg of fishmeal, and then, 100 g/kg of fishmeal was replaced by soybean meal and other proteins to form a low fishmeal diet with 100 g/kg of fishmeal inclusion. Based on the above two diets, 0, 0.1, and 0.2 g/kg of coated sodium butyrate (effective content 50%, provided by Zhumadian Huazhong Chia Tai Co., Ltd.) were added to form six isonitrogenous and isoenergetic diets. The protein ingredients were crushed and sieved through 60 mesh (diameter of 0.25 mm), and then, all the ingredients including 0.5 g/kg yttrium oxide were mixed and extruded to form sinking pellets of 3.0 mm diameter by single screw extruder (LX-75 Extruder, Longxiang Food Machinery Factory, Longyao, China). The extruding temperature was (85 ± 5)°C, and drying temperature was 50°C. After cooling, all diets were sealed and stored at 4°C until use. Powdered sodium butyrate mixed with other ingredients was added to the diets. Yttrium oxide was added in all diets as an inert marker to determine the apparent digestibility of nutrients. The formulation and proximate composition of experimental diets are shown in Table 1. 2.3. Fish and Feeding Management. Rainbow trout were purchased from Ruominghao Aquaculture Co., Ltd. (Kunming, China). After 2 weeks of adaptation period, all fish were fasted for 24 hours, and then, 396 fish with average body weight of 29:90 ± 0:20 g were randomly divided to 18 tanks with 6 treatments, 3 replicates per treatment, and 22 fish per replicate. The feeding trial was conducted in 18 circular tanks with a diameter of 1.0 m and a depth of 0.8 m (water volume of 650 L). During the feeding period, the fish were fed twice a day (8 : 30 and 15 : 30) with feeding rate of 3%-5% of body weight, which was adjusted appropriately according to the feeding behavior and weather conditions to ensure no diet residue in 2 min after feeding. The feed intake of each tank was kept with the similar amount. The feces at the bottom of the tank were siphoned out in 2 hours after feeding. The water was renewed about 1/3 every three days to ensure the water quality. During the feeding period, the water temperature (12-16°C), dissolved oxygen (6-7 mg/L), pH (7.2-7.6), ammonia nitrogen (≤0.2 mg/L), and nitrite (≤0.1 mg/L) were measured daily. The feeding trial was performed in the indoor aquaculture system at Binhai Aquaculture Station of Shanghai Ocean University for 8 weeks.
2.4. Sample Collection. Before the feeding trial, ten fish were collected and stored at -20°C for the initial whole body composition analysis. At the end of the feeding trial, all fish were fasted for 24 hours, and the fish in each tank were counted and weighed. Nine fish were randomly selected and anesthetized from each tank. Among these fish, three fish were stored at -20°C for the proximate composition analysis of the whole body. Another three fish were measured for body length and body weight, and then, blood was drawn from caudal vein and centrifuged for 10 min at 4000 r/min and 4°C. The serum was collected and stored at -80°C for the determination of biochemical indexes. After blooding, the visceral mass and liver were isolated and weighed, and then, the intestine was isolated, and a part of foregut (1-2 cm) was sampled and preserved in Bouin's solution after removing mesenteric adipose tissue. For the remaining three fish, the hindgut was collected under aseptic conditions after peeling off mesenteric adipose tissue and removing chyme and then stored in liquid nitrogen for intestinal microbiological analysis. Starting from the 5th week of the feeding trial, the intact 2 Aquaculture Nutrition feces was collected daily by siphoning and stored at -20°C for the digestibility measurements.

Measurement Indicators and Methods
2.5.1. Growth Performance and Body Indices. Weight gain (WG), feed conversion ratio (FCR), survival rate (SR), viscerosomatic index (VSI), hepatosomatic index (HSI), and condition factor (K) were calculated as follows: where FBW is the final body weight (g); IBW is the initial body weight (g); W f is the feed intake (g); N t is the final number of fish; N 0 is the initial number of fish; W l is the liver weight (g); W v is the viscera weight (g); W is the body weight (g); and L is the body length (cm).

Proximate Composition of Diets and Whole
Body. Proximate composition of diets and whole body was analyzed according to the Association of Official Analytical Chemists (AOAC) method. Moisture was determined by oven-drying at 105°C to constant weight. Crude ash was measured by burn-ing at 550°C for 6 h in a muffle furnace (SXL-1008 muffle furnace, Shanghai Jinghong Experimental Equipment Company). Crude protein was measured by the Kjeldahl method (2300 Auto analyzer, FOSS Tecator, AB, Hoganas, Sweden), and crude lipid was determined by chloroformmethanol extraction method.

Intestinal Histology.
The intestine tissue was dehydrated in a series of alcohol solutions and embedded in paraffin. Then, sections (5-6 μm) were cut by semi-automatic slicer (LEICA RM2145), patched, baked, dewaxed, rehydrated, stained with hematoxylin-eosin (H.E), and finally sealed with neutral gum. Sections were observed and photographed with an imaging microscope (Nikon 55I, Tokyo, Japan), and the intestinal villus height, width, and muscle thickness were measured.

Intestinal Digestive Enzyme Activity.
Intestinal sample was homogenized with nine times volume of saline (8.6 g/L NaCl) for 1 min and then centrifuged at 3000 r/min (4°C) for 10 min. The supernatant was collected to analyze enzyme activity. The kits used for the measurement of lipase activity and amylase activity were provided by Nanjing Jiancheng Bioengineering Institute (Nanjing, China).   3 Aquaculture Nutrition kit provided by Shanghai Haling Biotechnology Co., Ltd. Superoxide dismutase (SOD) activity was measured by the xanthine oxidase method. The activities of alkaline phosphatase (AKP), acid phosphatase (ACP), diamine oxidase (DAO), and lysozyme (LZM) were assayed by p-nitrophenyl phosphate method, visible spectrophotometric method, spectrophotometric method, and turbidimetric method, respec-tively. The corresponding kits were provided by Nanjing Jiancheng Bioengineering Institute (Nanjing, China).

Nutrient Apparent Digestibility and Retention Coefficient.
The yttrium contents in diet and feces were analyzed by inductivity-coupled plasma optical emission spectroscopy (ICP-OES; Vista MPX; VARIAN). The apparent digestibility     Aquaculture Nutrition coefficient of dry matter (ADCD) and crude protein (ADCP), protein retention (PR), and lipid retention (LR) were calculated according to the following formulas: PRð%Þ = 100 × ½ðfinal body weight × crude protein of final fish − initial body weight × crude protein of initial fishÞ /protein intake, LRð%Þ = 100 × ½ðfinal body weight × crude lipid of final fish − initial body weight × crude lipid of initial fish Þ/lipid intake.

Statistical
Analysis. The data were expressed as mean ± standard deviation (mean ± SD) and statistically analyzed by SPSS 26.0 software using two-way ANOVA, and multiple comparisons were performed by Tukey method. P < 0:05 was the criterion for significant differences. Table 2, dietary fishmeal level significantly affects the FBW, WG, and K value of rainbow trout (P < 0:05), while sodium butyrate level and their interaction did not (P > 0:05). Low fishmeal group showed significantly lower WG and higher FCR than the high fishmeal group (P < 0:05). The addition of sodium butyrate to high or low fishmeal diets had no significant effects on WG and FCR of rainbow trout (P > 0:05). There was no significant difference in VSI, HSI, and K value among the groups (P > 0:05). Table 3, no significant differences are found in moisture, ash, crude fat, and crude protein contents among all the groups (P > 0:05). There were no significant effects of dietary fishmeal level, sodium butyrate level, and their interaction on whole body composition (P > 0:05). Table 4, dietary fishmeal level and sodium butyrate level had no significant effects on the ADCD, ADCP, PR, and LR of rainbow trout, and no significant difference is observed among all the groups (P > 0:05).

Digestive Enzyme Activity.
The digestive enzyme activities in intestine are shown in Table 5. Dietary fishmeal level did not significantly affect lipase activity (P > 0:05), while sodium butyrate level and their interaction did (P < 0:05). Dietary fishmeal level, sodium butyrate level, and their interaction significantly affected intestinal amylase (P < 0:05). The activities of amylase and lipase were significantly higher in the low fishmeal group than in the high fishmeal group (P < 0:05). The addition of 1.0 g/kg and 2.0 g/kg sodium Table 6: Effect of dietary sodium butyrate on serum biochemical indices of rainbow trout.

Items
NaB supplementation in high fishmeal diet NaB supplementation in low fishmeal diet Two-way ANOVA 0.0 butyrate to the low fishmeal diet significantly decreased the activities of lipase and amylase (P < 0:05), but in high fishmeal diet, lipase activity was decreased by 1.0 g/kg sodium butyrate addition, and amylase activity was decreased by 2.0 g/kg sodium butyrate addition (P < 0:05).

Serum Biochemical Indices.
Dietary fishmeal level and sodium butyrate level significantly affected D-LA level (P < 0:05). D-LA was significantly lower in the low fishmeal group than in the high fishmeal group (P < 0:05). The addition of sodium butyrate to the high fishmeal diet had no significant effect on the D-LA level (P > 0:05), while the addition of 2.0 g/kg sodium butyrate to the low fishmeal diet significantly increased the D-LA level (P < 0:05). The addition of 1.0 g/kg sodium butyrate to the low fishmeal diet significantly decreased the activity of DAO and tended to increase the activity of LZM. No significant differences were found in serum SOD, AKP, and ACP activities among all the groups (P > 0:05) ( Table 6). Table 7 and Figure 1. Dietary sodium butyrate and the interaction of fishmeal and sodium butyrate significantly affected intestinal villus height (P < 0:05). The addi-tion of 1.0 and 2.0 g/kg sodium butyrate to high fishmeal diets and 2.0 g/kg sodium butyrate to low fishmeal diet significantly increased intestinal villus height (P < 0:05). Dietary fishmeal, sodium butyrate, and their interaction significantly affected intestinal villus width (P < 0:05). The low fishmeal group showed significantly lower muscle thickness than the high fishmeal group (P < 0:05), and the addition of 1.0 g/kg sodium butyrate to the low fishmeal diet significantly increased the muscle thickness (P < 0:05).

Intestinal Microbial
Community. The addition of 1.0 or 2.0 g/kg sodium butyrate to diet did not promote the growth performance; it may be due to the low addition of sodium butyrate. Therefore, intestinal microbial analysis was performed on the 2.0 g/kg sodium butyrate-treated group. As shown in Table 8, the coverage index of each group is close to 1, which indicated that the bacterial community had been fully sampled and the data could represent the bacterial population. The addition of 2.0 g/kg sodium butyrate to the high and low fishmeal diets increased the Sobs and Chao index, indicating that the species richness of intestinal microbiota was significantly increased.
The composition and diversity of intestinal microbiota at the phylum and genus levels are shown in Figures 2 and 3. At the phylum level, the major intestinal microbiota was Firmicutes, Proteobacteria, Actinobacteria, and Cyanobacteria.
In the high fishmeal group, the dominant phylum was Firmicutes accounting for 93.64%, which was changed to Proteobacteria (89.83%) when 2.0 g/kg sodium butyrate was added. In the low fishmeal group, the dominant phylum was also Firmicutes (90.95%), and the addition of 2.0 g/kg sodium butyrate decreased the abundance of Firmicutes to 80.98% and increased the abundance of Proteobacteria from 5.14 to 13.02%. At the genus level, intestine microbial mainly included Mycoplasma and Aeromonas. In the high fishmeal group, Mycoplasma accounted for 92.51%, followed by Aeromonas with 3.86%. When 2.0 g/kg sodium butyrate was added in high fishmeal diet, the dominant genus was changed to Aeromonas (89.20%). In low fishmeal diet, the abundance of Mycoplasma was decreased from 83.83 to 73.28%, and Aeromonas was increased from 3.30 to 5.46% by the addition of 2.0 g/kg sodium butyrate.

Effect of Dietary Fishmeal and Sodium Butyrate on Growth
Performance of Rainbow Trout. Soybean meal is one of the best plant protein sources to replace fishmeal, but higher levels of fishmeal replacement always imposed a negative influence on fish [22]. In this study, the replacement of 100 g/kg fishmeal with soybean meal (low fish meal diet) significantly decreased the growth performance and decreased feed conversion ratio of rainbow trout, which was consistent with the results in large yellow croaker (Larimichtys crocea) [23] and Japanese flounder (Paralichthy solivaceus) [24]. The presence of antinutritional factors in soybean meal may be associated with such results. Saponins and lectins can damage the intestinal morphology of fish, while protease inhibitors, β-conglycinin, and the imbalanced amino acids in soybean meal also adversely affect the nutrients digestion and absorption [25]. In addition, reduced fishmeal inclusion also leads to the decrease of active components as taurine and unknown growth factors [26].  As the active component in sodium butyrate, butyric acid can promote the absorption of protein and minerals and provide energy to the intestinal epithelial cells for proliferation and differentiation. The dietary supplementation of 1.5 g/kg sodium butyrate nanoparticles significantly improved the growth and feed consumption of tilapia [27]. Silva et al. [28] reported that the feed efficiency and survival of Pacific white shrimp (Litopenaeus vannamei) were improved by adding 0.5% and 2.0% sodium butyrate to diets. The supplementation of microencapsulated sodium butyrate in diets with or without oxidized fish oil inclusion significantly increased the weight gain and decreased the feed conversion ratio of juvenile carp (Cyprinus carpio) [29]. However, dietary addition of sodium butyrate (0.2%) did not produce significant effects on the growth performance of European sea bass (Dicentrarchus labrax) [30,31]. The supplementation of 0.5% or 2.0% shortchain fatty acids (salts) mixture (acetate: propionic acid: sodium butyrate = 5 : 5 : 2) [21] and the supplementation of a mixture of 10 g/kg sodium formate and sodium butyrate (2 : 1) [20] also did not improve the growth performance of Atlantic salmon and rainbow trout, respectively. In this study, the addition of sodium butyrate in high or low fishmeal diets showed no significant effects on weight gain, feed conversion ratio, and apparent digestibility of dry matter and crude protein. Maybe the dietary effects of sodium butyrate on fishes are related to the feeding habits. Carnivorous, omnivorous, and herbivorous fish may have different responses to dietary sodium butyrate, or cold water fish are not as sensitive to dietary sodium butyrate as warm fish [7]. The hypothesis needs to be further studied in the future.

Effect of Dietary Fishmeal and Sodium
Butyrate on the Digestive Enzyme Activities of Rainbow Trout. Digestive enzyme activities are associated with digestive and absorptive capacities, which are crucial to the growth of fish [32]. Results of the present study showed that 50% replacement of fishmeal by soybean meal significantly increased the activities of amylase and lipase, which was similar to the result found in goldfish (Carassius auratus) [33]. Nevertheless, high levels of soybean meal substitution for fishmeal in feed caused negative effects on the digestive enzyme activities of fish. For example, 60% and 75% replacement of fishmeal by soybean significantly decreased the digestive enzyme activities of Chinese sucker (Myxocyprinus asiaticus) [34] and tilapia [35], respectively. In this study, the addition of sodium butyrate to the low and high fishmeal diet decreased the activities of lipase and amylase. However, the addition of 2.0 g/kg sodium butyrate to diets increased the digestive enzyme activities of golden pompano [5]. Zhao et al. [36] found that sodium butyrate supplementation (1.0 g/kg) increased intestinal lipase activity of yellow catfish (Pelteobagrus fulvidraco). Furthermore, in rice field eel (Monopterus albus), the digestive enzyme activities were not affected by dietary sodium butyrate [37]. The different results may be associated with the forms and concentrations of sodium butyrate, the structure of digestive organs, and the experimental environment [36].  [38]. In the current study, the replacement of 50% fishmeal by soybean meal resulted in significant reduction of muscular thickness and disrupted the intestinal mucosa morphology integrity. Zhang et al. [39] reported that replacing 50% or 75% of fishmeal with soybean meal resulted in significant reduction of muscular thickness of Japanese sea bass (Lateolabrax japonicus). Similar findings have also been reported in orange-spotted grouper (Epinephelus coioides) [40]. ANFs in high soybean meal diets are one of the main reasons for the negative impacts on intestinal structure [24]. Sodium butyrate is a direct source of energy for intestinal epithelial cells, which can promote intestinal cell proliferation, development, and repair mucosal damage. Butyrate can also stimulate the absorption of water and sodium ions in the colon, induce the synthesis of intracellular mRNA and protein, and accelerate the proliferation of intestinal villus [41]. Dietary sodium butyrate was found to increase the intestinal villus height and density [42]. Wu et al. [19] reported that dietary sodium butyrate (0.15%) increased the intestinal muscle thickness and villus height of yellow drum. In juvenile black sea bream, the highest foregut villi height was observed in fish fed with 0.2% microencapsulated sodium butyrate-supplemented diets [10]. In this study, the intestinal villus height in high fishmeal group and the intestinal muscle thickness in low fishmeal group were significantly increased by the addition of sodium butyrate, but both viscerosomatic and hepatosomatic indexes were not significantly altered, which was similar to the study on gilthead sea bream [43]. Meanwhile, the improvement in intestinal histology did not lead to an increase in dry matter and crude protein digestibility, which deserves further investigation.
D-lactic acid (D-LA) and diamine oxidase (DAO) are the metabolic product of bacteria and the enzymes in intestinal epithelial cells, respectively, but they do not participate in metabolism when entering the body. If intestinal mucosal cells are damaged, intestinal mucosal permeability will increase, and intestinal bacteria and epithelial cells will produce large amounts of D-LA and DAO, respectively, which enter the blood through damaged mucosal cells, leading to the increase of D-LA level and DAO activity in blood. Thus, the serum change of D-LA level and DAO activity can reflect the permeability of intestinal mucosal and the function of intestinal mucosal barrier [39]. In this study, the addition of 1.0 g/kg sodium butyrate to the low fishmeal diet significantly decreased the serum DAO activity, which meant the intestinal mucosal permeability was decreased, indicating that sodium butyrate could repair the mucosal barrier. Meanwhile, no significant change in serum D-LA level was found when sodium butyrate was added to the high fishmeal diet, but the addition of sodium butyrate to the low fishmeal diet tended to increase the D-LA level. The reason is not clear and needs further study.

Effect of Dietary Fishmeal and Butyrate on the Intestinal
Microbial Community of Rainbow Trout. As an important part of the intestinal tract, intestinal microbial community can promote the digestion and absorption of nutrients and induce mucosal immune protection. A stable microbial com-munity is a guarantee to intestinal health of fish. Long-term exposure of intestine to feeds and microbiota, together with the changes in the internal and external environment, can change the intestinal microbial community [44,45]. The present study indicated that the replacement of fishmeal with soybean meal had no effect on the species of the dominant phylum (Firmicutes and Proteobacteria) in the intestine of rainbow trout, but changed the intestinal microbiota composition and increased the abundance of Proteobacteria. Desai et al. [46] also found that plant diets increased the ratio of Firmicutes to Proteobacteria in intestinal microbiota of rainbow trout and enhanced the overall abundance and diversity of intestinal microbiota. At present, few studies have been conducted on the effect of sodium butyrate on intestinal microbiota of fish. Piazzon et al. [47] found that the relative abundance of Firmicutes, Bacteroidetes, and Fusobacteria in the intestinal microbial community increased 139 times, 8.5 times, and 23.2 times, respectively, when 0.4% sodium butyrate preparation (70% effective content) was added to the diet of sea bream. In turbot, the addition of 0.2% sodium butyrate to high soybean meal diet significantly increased the relative abundance of Proteobacteria, Deinococcus-Thermus, and Actinobacteria and decreased the relative abundance of Bacteroidetes and Deferribacteria [17]. In this trial, the addition of 2.0 g/kg sodium butyrate to high and low fishmeal diets decreased the abundance of Firmicutes and increased the abundance of Proteobacteria in intestine. However, the role of Firmicutes and Proteobacteria in the intestine of rainbow trout is still unclear and needs to be further investigated.

Conclusion
Under the present conditions, the addition of sodium butyrate to diet containing 200 or 100 g/kg fishmeal did not promote the growth performance and feed utilization of rainbow trout, but improved the intestinal morphology and changed the intestinal microbial composition.

Data Availability
All data generated or analyzed during this study are included in this article.

Conflicts of Interest
The authors declare that they have no conflicts of interest.