Aquaculture 500 (2019) 99–106

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Aquaculture
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Sardine (Sardinella spp.) protein hydrolysate as growth promoter in South T

American catfish (Rhamdia quelen) feeding: Productive performance,
digestive enzymes activity, morphometry and intestinal microbiology
Natalia Haa, Gabriel Fernandes Alves Jesusb, André Fernando Nascimento Gonçalvesa,
Nandara Soares de Oliveiraa, Juliet Kiyoko Sugaib, Marcos Luiz Pessattic,
⁎
José Luiz Pedreira Mouriñob, Thiago El Hadi Perez Fabregata,
a
Universidade do Estado de Santa Catarina, UDESC, Av. Luiz de Camões, 2090, Lages, SC 88520-000, Brazil
b
Universidade Federal de Santa Catarina, UFSC, Rod. Admar Gonzaga, 1346 - Itacorubi, Florianópolis, SC 88034-000, Brazil
c
Universidade do Vale do Itajaí, UNIVALI, R. Uruguai, 458 - Centro, Itajaí, SC 88302-202, Brazil

A R T I C LE I N FO A B S T R A C T

Keywords: This study evaluated the effects of dietary inclusion of sardine (Sardinella spp.) protein hydrolysate (SPH) on
Prebiotic effect productive performance, digestive enzymatic activity, morphology and intestinal microbiology of South
Digestive enzymes American catfish (Rhamdia quelen) juveniles. SPH was produced from sardine processing wastes using Protamex®
Enzymatic hydrolysis protease complex from Novozymes A/S. Four levels of inclusion were evaluated (0, 2, 5 and 10%). A total of 480
Biologically-active peptides
South American catfish juveniles (average weight 11.3 ± 2.46 g) were distributed in 24 polyethylene con-
Growth promoter
Fish by-products
tainers, in a completely randomized design with four treatments and six replications. The fish were fed twice
daily until apparent satiation with isoproteic (39%) and isoenergetic (4376 kcal.kg−1) diets for 56 days.
Regardless of the SPH inclusion levels in the diets, average weight gains (36.28 g), specific growth rate (2.56%
day−1), apparent feed intake (40.51 g) and apparent feed conversion rate (1.12) were improved when compared
to the control treatment (average of 24.95 g; 2.11% day−1; 31.00 g and 1.28, respectively). Total alkaline
protease activity of the gastrointestinal tract of the South American catfish juveniles was higher in the treatment
that received 5% SPH (0.61 ± 0.23 U. mg−1 of protein) than in the control (0.26 ± 0.08 U.mg−1 of protein).
The amylase activity was higher in the treatments with 2% SPH (1.58 ± 0.19 U. mg−1 of protein) and 5% SPH
(1.43 ± 0.44 U. mg−1 of protein) when compared to the control (0.40 ± 0.18 U. mg−1 of protein). In the 5%
SPH treatment, higher amounts of lactic acid bacteria and Vibrionaceae were detected than in the other treat-
ments. No difference was found for total heterotrophic bacteria. There was no difference in the intestinal
morphometry of the South American catfish for any one of the analyzed parameters. Inclusion levels of up to
10% SPH in the diets of South American catfish showed improvement in the productive performance and nu-
tritional efficiency, acting as a growth promoter. The inclusion level of 5% SPH caused an increase in the
digestive enzymatic activity and populations of intestinal lactic acid bacteria. Thus, a prebiotic effect on the
fishes was observed and the inclusion level may determine the effects of SPH.

1. Introduction development of by-products increases profit and sustainability for the

catch production of fish. The by-products of fish processing can provide
The total global catch production of ocean fishes reached 81.5 high quality nutrients to meet the animal protein requirements in fish
million tons in 2014, with Sardinella spp. as one of the most caught feeds. Fish protein hydrolysate (FPH) results from the enzymatic hy-
species (FAO, 2016). Residues generated from fish processing are ap- drolysis of processed fish wastes and is rich in free amino acids and in
proximately 50% of the total catch (Bechtel, 2003). As a result, re- low molecular weight peptides (Liaset et al., 2000).
cycling such wastes has become of interest for alternative uses. The The benefits of incorporating fish hydrolysates in diets are due to

⁎
Corresponding authors at: UDESC, Universidade do Estado de Santa Catarina, Avenida Luiz de Camões, 2090, Lages, SC 88520-000, Brazil.
E-mail addresses: [email protected] (N. Ha), [email protected] (G.F.A. Jesus), [email protected] (A.F.N. Gonçalves),
[email protected] (N.S. de Oliveira), [email protected] (J.K. Sugai), [email protected] (M.L. Pessatti), [email protected] (J.L.P. Mouriño),
[email protected] (T. El Hadi Perez Fabregat).

https://doi.org/10.1016/j.aquaculture.2018.10.004
Received 4 October 2017; Received in revised form 27 July 2018; Accepted 3 October 2018
Available online 04 October 2018
0044-8486/ © 2018 Elsevier B.V. All rights reserved.
N. Ha et al. Aquaculture 500 (2019) 99–106

the enzymatic treatment, which facilitates the absorption of the mole- Table 1
cules by the intestinal epithelial cells (Bakke et al., 2010). Di- and tri- Composition of the sardine (Sardinella spp.) protein hydrolysate.
peptides may also improve palatability (Aguila et al., 2007; Oliva-Teles GE (kcal/kg) GP⁎ (%) EE⁎ (%) MM⁎ (%) DH (%)
et al., 1999), disease resistance in fish and survival (Kotzamanis et al.,
2007). They also enhance the nutritional properties to stimulate the Sardine protein 5285.60 72.2 9.20 7.50 47.5
hydrolysate
feed consumption, increase intake of nutrients and enhance growth, as
observed with the Atlantic salmon Salmo salar (Berge and Storebakken, ⁎
Values based on dry matter; GE = Gross energy; GP = Gross protein;
1996), cobia Rachycentron canadum (Costa-Bomfim et al., 2016), large EE = Ethereal extract; MM = Mineral matter; DH = Degree of hydrolysis.
yellow croaker Pseudosciaena crocea (Tang et al., 2008), olive flounder
Paralichthys olivaceus (Khosravi et al., 2014), red seabream Pagrus major the total protein in the feedstock. The tests were conducted in trans-
(Bui et al., 2014) and rainbow trout Oncorhynchus mykiss (Aksnes et al., parent bottom microplates by adding 40 μl of the sample and 260 μl of
2006). the OPA reagent. Absorbance readings were performed at 340 nm in a
Previous studies that sought to develop novel feeds have suggested Genius (Tecan®) microplate reader and the results were expressed as
that FPH holds several benefits for fish through the formation of bio- DH (%) by the equation:
logically-active peptides resulted from enzymatic hydrolysis (Bøgwald DH (%) = [(Serine-NH2 - β)/α meqv/g of protein]/htot * 100.
et al., 1996; Kotzamanis et al., 2007), which includes antioxidant The α, β and htot values were previously determined for fishes as
(García-Moreno et al., 2014; Jemil et al., 2014; Sabeena-Farvin et al., 1.00, 0.40 and 8.6, respectively (Adler-Nissen, 1986).
2014) and antimicrobial (Safari et al., 2012; Wald et al., 2016) prop-
erties, increased digestive enzymatic activity (Kotzamanis et al., 2007;
Srichanun et al., 2014) and improved immune responses in fish (Bui 2.1.1. Hydrolysate electrophoresis
et al., 2014;. Khosravi et al., 2015; Tang et al., 2008). Protein hydro- For the determination of the molecular weight distribution of the
lysates may also have a prebiotic effect in the digestive tract (Arihara, peptides of the hydrolysates, electrophoretic runs were performed in
2006), which was affirmed by the proliferation of the bacteria Lacto- Tricine-SDS-PAGE (Schägger, 2006), in a mini-Protean electrophoresis
bacillus sp. in in vitro experiments (Safari et al., 2012). Preliminary re- system (BioRad). BioRad® polypeptide standards (cat.161–0326), be-
sults have shown the positive effects of sardine protein hydrolysate on tween 26,625 and 1423 Da were used as a control marker. The gel was
the intestinal morphometry of South American catfish (Rhamdia quelen) stained with 0.025% Coomassie Blue. Gels were also stained with silver
(Wosniak et al., 2016), but further in vivo studies are necessary to de- nitrate after Coomassie discoloration according to Schagger (2006),
scribe the effects on the intestinal microbiology. using the Silver Stain Plus kit (BioRad®). To visualize the molecular
The bioactive amino acids and peptides composition of the FPH weight peptides that were less detected by Coomassie Blue, the gels
depends on the raw material source, the enzyme and the hydrolysis were treated with imidazole-SDS, followed by a zinc stain, according to
conditions (Klompong et al., 2009; Kotzamanis et al., 2007). To obtain Fernandez-Patron et al. (1995). The density of the protein bands was
positive responses in fish production, sufficient inclusion levels of FPH measured using the freeware Gel Analyzer, developed by Istvan Lazar
should be established (Espe et al., 1992). The South American catfish (Table 2).
(Rhamdia quelen) is an omnivorous species found from Argentina to
Mexico (Fishbase, 2017). This species is targeted for commercial fish-
eries due to its resistance to cold weather, high growth rate and carcass 2.2. Experimental diets
yields (Salhi et al., 2004). It is also a good model organism for nutrition
studies because the morphology of the gastrointestinal tract is homo- The SPH was evaluated at four levels of inclusion (0, 2, 5 and 10%).
logous to that of the Channel catfish (Ictalurus punctatus). This study Diets were isoproteic (39% of crude protein) and isoenergetic (about
evaluated the inclusion levels of sardine muscle protein hydrolysate 4376 kcal of gross energy kg−1), formulated as required for South
(SPH) in diets of South American catfish (Rhamdia quelen) juveniles. American catfish (Meyer and Fracalossi, 2004) (Table 3). In addition to
Effects of SPH on the growth and health were evaluated through the the hydrolysate, diets were formulated using fish meal and soybean
productive performance, morphometry, microbiology and enzymatic meal as protein sources, and fish oil and corn meal as energy sources.
activity of the gastrointestinal tract. The marine fishmeal was purchased from Agroforte® (Laguna, Santa
Catarina, Brazil) and the other ingredients were acquired from local
2. Materials and methods suppliers. All ingredients were ground in a knife mill with a 2-mm mesh
screen, mixed, pelletized with the addition of water (30%) and placed
2.1. Production and characterization of sardine protein hydrolysate in an oven at 45 °C for 48 h. The diets were stored in plastic containers
and placed in refrigerators (4 °C) until the time of use. All ingredients
Sardine protein hydrolysates (SPH) were produced from muscle and commercial diets were analyzed according to the methods de-
(free of head, tail and viscera) of sardines (Sardinella spp.), obtained scribed in AOAC (2000).
from a fish processing facility in Itajaí, in the state of Santa Catarina,
Brazil. The samples were homogenized in water at a ratio of 1:0.85 (v:v)
and incubated with Protamex® Novozymes A/S (1:100 enzyme:fish) at Table 2
55 °C for 90 min, followed by enzyme inactivation at 85 °C for 15 min. Distribution of peptides in sardine (Sardinella spp.) protein hydrolysate.
The resulting material was placed in a forced-air oven at 55–60 °C to Apparent molecular weight profile of Amount (%) Amount (%) Including
reduce moisture to 35% and was kept at −20 °C until the time of use. peptides of SPH Zinc Bands revealed
Chemical analyses were carried out following methods described in
> 100,000 Da 6.3 6.0
AOAC (2000). Moisture content was determined by infrared radiation,
50,100–100,000 Da 4.3 4.1
and the content of lipids by the Soxhlet method. Protein content was 30,100–50,000 Da 20.5 19.3
determined according to the Kjeldahl method, and mineral content by 20,100–30,000 Da 15.5 14.7
incineration in a muffle furnace at 550–600 °C. The degree of hydrolysis 10,100–20,000 Da 0.3 0.3
(DH%) was determined by using a method modified from Nielsen et al. 5100–10,000 Da 39.2 37.0
2100–5000 Da 10.6 10.0
(2001) (Table 1). The analysis consists of quantifying the proportion of
1100–2000 Da 0.4 0.4
free amino groups in the soluble fraction of the protein hydrolysate via < 1000 Da 2.64 8.07
the reaction of these groups with o-phthalaldehyde (OPA), in relation to

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N. Ha et al. Aquaculture 500 (2019) 99–106

Table 3 2.5. Enzymatic analyses

Composition of the experimental diets.
Experimental diets Enzymatic analyses of the total alkaline protease and amylase ac-
tivities of the gastrointestinal tract were carried out with one fish from
0% 2% 5% 10% each container (n = 6 fish per treatment). The digestive tract was ex-
tracted by making an incision from the stomach to the anus. The tract
Soybean meal 25.0 25.0 25.0 25.0
Wheat meal 10.0 10.0 10.0 10.0 was weighted (w) and homogenized in chilled distilled water (v) (1:6,
Corn meal 10.5 12.0 13.5 16.0 w/v) using a van Potter homogenizer for 2.5 min (five times for 30 s in
Fish meal 46.5 43.5 39.5 33.0 ice bath) and centrifuged at 27,167 ×g (Eppendorf centrifugal, model
Sardine hydrolysate – 2.0 5.0 10.0 5804 R) for 15 min at 4 °C, and the supernatants were used to determine
Fish oil 2.0 1.5 1.0 –
the activity of the digestive enzymes. The amylase activity in the
Soybean oil 5.0 5.0 5.0 5.0
Premix1 1.0 1.0 1.0 1.0 samples was quantified by starch hydrolysis (E. Merck, Darmstadt,
Analyzed composition Germany), using methodology developed by Rick and Stegbauer (1974)
Dry matter (%) 91.21 91.15 91.10 91.01 and described by Aguilar-Quaresma and Sugai (2005). The reaction was
Crude protein (%) 39.44 39.39 39.52 39.83
stopped with dinitrosalicylic acid reagent and the hydrolysis product
Gross energy (%) 4316.05 4382.67 4395.80 4407.75
Crude lipid (%) 11.64 11.16 10.70 9.79
was quantified by the reducing sugar method of dinitrosalicylic acid
Crude fiber (%) 3.09 3.13 3.16 3.21 (Sigma-Aldrich, St. Louis, MO, USA) according to Miller (1959), using
Ash (%) 14.62 13.99 13.16 11.83 maltose (E. Merck, Darmstadt, Germany) as a standard and read at
540 nm. The total alkaline protease activity was determined by azoca-
1
Folic acid – 2400 mg, nicotinic acid – 48 g, pantothenic acid – 24 g, biotin – sein hydrolysis (Sigma, St. Louis, Mo, USA), using the method described
96 mg, vit. A – 2400,000 IU, vit. D3–400,000 IU, vit. E – 24,000 IU, vit.
by Garcia–Carreño et al. (1997). The amylase activity was expressed as
B1–9600 mg, vit. B2–9600 mg, vit. B6–9600 mg, vit. B12–9600 mg, vit
specific activity μmol reducing sugars. min−1 mL−1 mg−1 of protein in
K3–4800 mg, vit. C – 96 g, iron – 100 g, manganese – 40 g, zinc – 6000 mg,
cobalt – 20 mg, iodine – 200 mg, selenium – 200 mg, antioxidant – 19.6 g. the extract (U mg−1 of protein). The specific activity of the alkaline
protease was expressed as the difference in absorbance at 366 nm be-
2.3. Animals and facilities tween the sample and the control min−1 mL−1 mg−1 of protein in the
extract (U mg−1 of protein). Soluble protein concentration of super-
This experiment was approved by the Ethics Committee of the Santa natant was determined by the Bradford method (Bradford, 1976) with
Catarina State University (protocol number CEUA 7119220216). A total bovine serum albumin (Sigma-Aldrich, St. Louis, MO) as the standard.
of 480 South American catfish juveniles (average weight 11.3 ± 2.5 g) All the assays were analyzed in triplicate.
were acquired from a commercial fishery and were acclimated to the
experimental conditions for 30 days. At the end of the acclimation
period, the fish were distributed into 24 polyethylene containers with a 2.6. Microbiological assessments
net volume of 70 l, connected to a water recirculation system equipped
with a mechanical and biological filter and a UV light. The photoperiod The digestive tract was sampled from one fish of each tank (n = 6
was 12 h of light. Constant temperature was maintained with heaters fish per treatment) to evaluate the intestinal microbiota. The intestines
with thermostats, and the water was oxygenated using an air com- were removed, weighted, crushed and homogenized in 0.65% sterile
pressor coupled to silicone hoses and porous stones. The water quality saline solution. Then, the intestines were serially diluted (1:10) in test
was monitored daily using portable instruments (YSI PROPLUS, Yellow tubes containing sterile saline solution and transplanted on Petri plates
Springs Instruments, Yellow Springs, OH, USA) to determine the fol- with TCBS (thiosulfate citrate bile sucrose) agar, MRS (Man Rogosa
lowing: dissolved oxygen (6.77 ± 0.42 mg dl−1), temperature Sharpe) agar and TSA (tryptone soy agar) to quantify the Vibrionaceae,
(28.82 ± 0.9 °C), pH (7.24 ± 0.35) and total ammonia (LabconTest, lactic acid and total heterotrophic bacteria, respectively. The intestinal
Alcon Pet, Brazil) (0.19 ± 0.1 mg NH3 l−1). All parameters were homogenates transplanted on Petri plates were incubated in an oven at
within the limits considered adequate for fish farming (Boyd, 1998). 35 °C. Total colony-forming units (CFU) were counted 24 h after in-
The fish were fed twice daily (9 a.m. and 4 p.m.) with the experimental cubation in the TCBS and TSA media. In the MRS medium, counting
diets until apparent satiation for 56 days. There was no leftover feed in was performed 48 h after incubation.
the tanks after feeding. The organic matter deposited on the bottom of
the containers was removed by siphoning with a rubber hose.
2.7. Intestinal morphometry

2.4. Productive performance The histological analysis of the intestines was performed with one
fish from each tank (n = 6 fish per treatment). Portions of nearly 3 cm
At the beginning of the study and at 56 days, all fish received no in length were collected from the mid intestine, and each sample was
feed for 24 h and were anesthetized in eugenol solution (1 g 10 l−1 of fixed in a 10% buffered formalin solution for 24 h, dehydrated in an
water), and weighed and measured individually. The productive per- ascending series of alcohols, diaphanized in xylene, paraffin-embedded
formance was analyzed as described in Tacon (1990): weight gain (WG, and cut in 5-μm sections for preparation of the slides. This sample was
g = final mean weight – initial mean weight), apparent feed intake (FI, then stained according to the Harris-Eosin (HE) staining method. The
g = food consumed during the experimental period/number of fish per slides were observed under an optical microscope (OptiCam, 10×) and
container); apparent feed conversion rate (FCR = feed intake/total photographed using a digital camera (Moticam 2300, 3 MP, resolution
weight gain) and specific growth rate (SGR, % day−1 = [(ln final 3264 × 2448). Total villi height, villi height, width and thickness were
weight – ln initial weight)/experimental period]*100). measured by analyzing 15 villi per fish using the ToupTek ToupView -
At 56 days, the animals were anesthetized and then euthanized by x64 image analyzer software, versions 2270/07/03. The height and
medullar sectioning to collect the biological materials for the analyses total height of the villi corresponded to the distance from the apex of
described below. the villi to the beginning of the muscular layer and the apex of the villi
until the end of the serosa (Mello et al., 2013). The width is of the villi
and the thickness is relative to the villi epithelium.

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N. Ha et al. Aquaculture 500 (2019) 99–106

Table 4
Productive performance of South American catfish juveniles fed diets with in-
clusion levels of 0, 2, 5 and 10% of sardine protein hydrolysate for 56 days.
0% 2% 5% 10%

WG (g) 24.9 ± 8.8b 37.1 ± 4.1a 33.9 ± 4.3a 37.8 ± 6.3a

SGR (% day−1) 2.1 ± 0.2b 2.5 ± 2.0a 2.4 ± 0.2a 2.7 ± 0.1a
FI (g) 31.0 ± 7.2b 39.8 ± 5.7a 39.9 ± 5.8a 41.8 ± 7.4a
FCR 1.28 ± 0.13b 1.08 ± 0.13a 1.17 ± 0.07a 1.11 ± 0.07a

Values are expressed as means ± standard deviation. Different letters in rows

represent statistical difference according to the Tukey test (P < .05). Weight
gain (WG), Specific Growth Rate (SGR), Apparent Feed Intake (FI), Apparent
Feed Conversion Rate (FCR).
Fig. 1. Concentration of Vibrionacea, total heterotrophic bacteria and total
2.8. Design and statistical analysis lactic microorganisms (CFU.g-¹ intestine) of South American catfish fed diets
supplemented with 0, 2, 5 and 10% of sardine protein hydrolysate for 56 days.
The experiment was carried out in a completely randomized design The intestines were incubated in TCBS for Vibrionaceae, in TSA for total het-
with four treatments and six replications, and the treatments corre- erotrophic bacteria and in MRS for total lactic microorganisms. Values are
sponded to the addition of 0, 2, 5 and 10% of SPH to the diets. Data expressed as means ± standard error of mean. Means with different letters
were subjected to the Cramer-von Mises test for normality and the differed from each other according to the Tukey test (P < 0.05).
Levene test to assess homoscedasticity of variances. Percentage values
were submitted to arcsine transformation. The results were subjected to and feed efficiency when compared to the control treatment. The im-
the analysis of variance (ANOVA), and the means were compared by the proved feed conversion can be explained by the greater bioavailability
Tukey test using the SAS statistical program, version 9.0. of protein in the hydrolysates due to their composition, which has
greater amounts of low molecular weight peptides and free amino acids
3. Results (Berge and Storebakken, 1996). The hydrolysis process has been used to
enhance the chemical and functional properties of the feed without
At 56 days of the experiment, weight gain, specific growth rate and diminishing its nutritional value (Ziegler et al., 1990). Free amino
apparent feed intake were higher (P < .05) in the treatments that re- acids, di- and tri-peptides are easily absorbed by enterocytes and can
ceived the SPH diet when compared to the control treatment (Table 4), enter the body at higher rates than intact proteins (Ganapathy et al.,
regardless of the concentrations. The apparent feed conversion rate was 1994).
lower (P < .05) in the treatments with SPH when compared to the The inclusion of up to 10% SPH had positive effects on the fish
control. No fish mortality was observed during the experiment. productive performance. Previous studies found similar results for other
Total alkaline protease of the gastrointestinal tract of South fish species (Espe et al., 1999; Hevrøy et al., 2005; Tang et al., 2008).
American catfish juveniles was higher (P < .05) in the treatment that Tang et al. (2008) found a better performance (total weight gain, re-
received 5% of SPH than in the control (Table 5). Amylase levels were lative weight gain, and specific growth rate) with the addition of 10%
greater (P < .05) in the treatments with 2% and 5% of SPH than in the of pollock (Theragra chalcogramma) protein hydrolysate for large yellow
control treatment and the treatment with 10% of the hydrolysate. croaker. On the other hand, according to Costa-Bomfim et al. (2016),
In the microbiological analysis of the South American catfish in- the addition of 12 and 18% of shrimp protein hydrolysate to the feed of
testines (Fig. 1), the amounts of lactic acid bacteria were greater cobia juveniles resulted in lower performance when compared to the
(P < .05) in the treatment supplemented with 5% of SPH than in the fish that received diets with inclusion levels below 6%. High quantities
other treatments. The amount of Vibrionaceae bacteria was smaller of low molecular weight compounds can lead to saturation of the in-
(P < .05) in the control treatment when compared to the other treat- testine transport mechanisms (Tonheim et al., 2005). This results in an
ments. There was no difference for total heterotrophic bacteria unbalanced absorption of amino acids, which in turn leads to an in-
(P > .05). crease of amino acid oxidation and reduced retention of dietary protein
No alterations were shown in the histological organization of the (Aragão et al., 2004).
catfish intestine when fed with the diets containing FPH (Fig. 2). No The high degree of hydrolysis of fish protein hydrolysate (FPH) fa-
difference (P > .05) was shown between the treatments for any of the vors its detection by the fish gustative system, which is sensitive to
intestinal morphometry parameters (Table 6). dissolved water-soluble substances and consequently increases feed
consumption (Halver and Hardy, 2002; Hevroy et al., 2005; Marui and
4. Discussion Caprio, 1992). Certain free amino acids are known for being chemo-
attractants and are used for fish baits (Jones, 1989). Therefore, the
In the present study, inclusion of SPH in South American catfish increased feed consumption by the animals that received diets with SPH
diets resulted in improved productive performance, feed consumption indicates that the hydrolysate was more attractive for the fishes when

Table 5
Specific activity of total alkaline protease and amylase in the gastrointestinal tract of South American catfish juveniles fed diets supplemented with 0, 2, 5 and 10% of
sardine protein hydrolysate for 56 days.
0% 2% 5% 10%

⁎
Total alkaline protease activity 0.26 ± 0.04 b 0.49 ± 0.07 ab 0.61 ± 0.15 a 0.37 ± 0.04 ab
Amylase activity⁎ 0.40 ± 0.07 b 1.58 ± 0.09 a 1.43 ± 0.29 a 0.76 ± 0.18b

Values are expressed as means ± standard error of mean. Different letters in rows represent statistical difference according to the Tukey test (P < .05).
⁎
The amylase activity was expressed in U.mg−1 of protein, 1 Unit is 1 μmol of maltose produced by unit of time and unit of incubation system (μmol min−1 mL−1),
and the total alkaline protease activity as the difference in the absorbance at 366 nm between sample and blank per minute, per mL, and per mg protein in the extract,
specific activity.

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N. Ha et al. Aquaculture 500 (2019) 99–106

Fig. 2. Histological organization of the intestine of South American catfish juveniles fed with different diets after 56 days. A: diet without hydrolysate. B: diet
supplemented with 2% of sardine protein hydrolysate (SPH). C: diet supplemented with 5% of SPH. D: diet supplemented with 10% of SPH.

Table 6 as growth and health promoters (Aksnes et al., 2006; Bui et al., 2014;
Morphometry of the gastrointestinal tract of South American catfish juveniles Khosravi et al., 2015; Robert et al., 2015). The growth promotion effect
fed diets supplemented with 0, 2, 5 and 10% of sardine protein hydrolysate for can explain the higher productive performance (Aksnes et al., 2006;
56 days. Martínez-Alvarez et al., 2015), which was observed with the lowest
0% 2% 5% 10% concentrations of SPH as well. Most of the studies that evaluated pro-
tein hydrolysates as growth promoters suggested no association of the
Total height 716.4 ± 74.5 758.1 ± 55.6 747.3 ± 80.3 784.1 ± 43.3 degree of hydrolysis and the peptide profile with the inclusion level
(μm)
Height (μm) 591.1 ± 74.7 604.4 ± 47.1 620.5 ± 66.7 638.7 ± 31.7
(Bui et al., 2014; Khosravi et al., 2015; Zheng et al., 2013). Further
Width (μm) 83.5 ± 7.7 101.9 ± 3.8 87.5 ± 5.0 101.5 ± 11.6 studies about the relationship between these parameters are necessary.
Thickness (μm) 38.5 ± 2.7 42.4 ± 1.9 37.4 ± 1.7 41.5 ± 3.8 Fish fed with diets containing 5% of hydrolysate showed higher
activity of alkaline protease when compared to the control diet. The low
Values are expressed as means ± standard error of mean. Means did not differ molecular weight peptides may have reached the intestine faster with
from each other according to the Tukey test (P > .05).
diets containing SPH (Ganapathy et al., 1994), with a consequent
higher stimulation of alkaline protease (Lundstedt et al., 2004). In the
compared to the control diet (Hevroy et al., 2005; Zheng et al., 2013). control treatment, in which animals fed on fish meal, peptides reached
Thus, the amount of SPH and the degree of hydrolysis used in this study the intestine slower than with the hydrolysate due to the longer time
were assumed to be adequate and with no bitter taste from the hy- needed for the acid proteases to break the fish meal proteins. According
drolysate, which has been previously observed (Tang et al., 2008). The to Lundstedt et al. (2004), this increase in enzyme secretion in the di-
bitter taste is associated with the release of hydrophobic clusters found gestive tract occurs to a certain extent because excess protein in the
in protein molecules, which become exposed during enzymatic hydro- intestines may cause an opposite effect, as observed with the 10% SPH
lysis (Kristinsson, 2006). treatment. The small number of samples (n = 6) may have affected this
The degree of hydrolysis is the parameter used to compare protein result, requiring more studies for a stronger conclusion.
hydrolysates (Mahmoud, 1994) and can be expressed as the percentage Amylase activity was higher in the treatments with 2% and 5% of
of broken peptide bonds (Adler-Nissen, 1986; Lahl and Braun, 1994; SPH when compared to the other treatments. However, this outcome
Mahmoud et al., 1992). The SPH exhibited a considerably high DH may not be directly associated with the addition of SPH. In the diets
(47.5%), which indicates the presence of a considerable level of com- containing the hydrolysate, the percentage of corn meal was slightly
pounds of low molecular weight. The higher DH correlates to the higher higher (up to 16%) than in the control treatment (10.5%). The amount
proportion of bioactive peptides that act as growth promoters (Halver of starch in the digestive tract may have stimulated amylase activity
and Hardy, 2002; Marui and Caprio, 1992). The molecular weight due to the ability of the fish to modulate the digestive and absorptive
profile of the SPH showed that 52.8% of the peptides were smaller than physiology according to the diet composition (Buddington et al., 1997;
10 kDa. This fraction includes the biologically active peptides that act Corrêa et al., 2007; Lundstedt et al., 2004; Moro et al., 2010). However,

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as suggested with excessive protein, excessive starch in the intestines 5. Conclusion

may cause an opposite effect, diminishing the amylase secretion as
observed with the 10% hydrolysate treatment. The SPH functioned as a growth promoter in South American catfish
The change in the microbiota observed in the different treatments with inclusion levels up to 10%, with improved productive performance
may have interfered with the amylase and protease results (Hoseinifar and nutritional efficiency. An enhanced activity of digestive enzymes
et al., 2017; Verschuere et al., 2000; Yanbo and Zirong, 2006). In- and lactic acid bacteria in the intestines was observed with the addition
creased digestive enzymatic activity in fish fed with prebiotics and of 5% SPH. Thus, a prebiotic effect on fish is evident and the inclusion
probiotics has been reported in several studies (Ghosh et al., 2008; levels may determine the effects of SPH.
Suzer et al., 2008; Wang, 2011; Wang and Xu, 2006). Kuz'mina (2011)
reported that proteolytic and amylolytic enzymes derived from micro- Acknowledgements
organisms contribute to the fish digestion process. The production of
amylase by the intestinal microbiota was detected in ayu (Plecoglossus This study was financed in part by the Coordenação de
altivelis), common carp (Cyprinus carpio), channel catfish, Japanese eel Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) -
(Anguilla japonica) and tilapia (Oreochromis niloticus) (Sugita et al., Finance Code 001.
1997).
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