Influence of rearing temperature on muscle growth and adipose tissue in Nile tilapia (Oreochromis niloticus) strains/Influencia da temperatura de cultivo no crescimento muscular e do tecido adiposo em linhagens de tilapia do Nilo (Oreochromis niloticus).
Tilapias are among the most important species of freshwater fish in tropical climate used for the production (Charo-Karisa et al., 2006). The intensification of production systems has resulted in a rapid expansion in the cultivation of tilapia and new strains have been introduced in Brazil and worldwide.
GIFT (Genetically Improved Farmed Tilapia) strain arrived in Brazil in 2005, from the World Fish Center, Malaysia. It is the largest fish breeding program conducted in the Philippines tilapia (Bentsen et al., 1998). Genomar Supreme Tilapia[TM] strain is the continuation of the GIFT program after a 10-year period, ending in 1998 (Gjoen, 2004), and has since become commercialized in Brazil. Several strains / hybrids of red tilapia have been developed commercially generating great acceptability by the market (Majumdar, Nasaruddin, & Ravinder, 1997; El-Sayed, 2006; Ng & Hanin, 2007; Ramirez-Salomao et al.
Paredes, Garduno-Lugo, & Munoz-Cordova, 2011), however these strains have low production in response to its slower growth, when compared to the common ones (Macaranas et al., 1997; Moreira, Moreira, & Hilsdorf, 2005; Ng & Hanin, 2007; Ramirez-Paredes et al., 2011).
Tilapia strains have different growth rates and this can change the dynamics of muscle growth or fat tissues, affecting carcass quality and meat. In most species of fish, skeletal muscle can represent up to 60% of the animal body weight (Sanger & Stoiber, 2001). This significant percentage of muscle mass is not only a mechanical adaptation, specific to aquatic life, but also serves as an important source of proteins to be used in human food (Weatherley & Gill, 1985).
Many fish show seasonal changes in growth rate, and one of the main factors involved in these changes is the water temperature. Temperature can cause changes in skeletal muscle cellularity (number and size of muscle fibers), by altering the rate of proliferation and differentiation of myogenic cells, although the exact effect of cultivation temperature may vary between species and the seasonal period studied (Vieira & Johnston, 1992; Usher, Stickland, & Thorpe 1994; Johnston, 1999;).
In general, the development and growth rate of fish increases when the water temperature is raised to a temperature near the optimum temperature for growing species. Furthermore, since different species of fish have been introduced in various geographic regions of the world, the adaptation of the animals to the water temperature in their new habitats have received special attention (El-Sayed, 2006).
The development of adipose tissue in fish is considered fundamental the same as occurred in mammals. However the postembryonic development of adipose tissue is influenced by environmental and metabolic factors (Imrie & Sadler, 2010). Nevertheless, fish stock lipid in adipose tissue located around the digestive tract, under the skin, the meat between the myomeres and in the myomeres (Fauconneau, Corraze, Lebail, & Vernier, 1991). The most common measurements of growth of domestic animals are based on measuring the changes in weight. However, during growth, the animals not only increase in weight but also change the proportions in which tissues are deposited. The objective of this study was to evaluate the effect of temperature on the growth of Red, GIFT and Supreme tilapia strains and under morphological aspects of muscle and adipose tissue.
Material and methods
The experiment was conducted in the Sao Paulo Agency for Agribusiness Technology (APTA), headquarter in Presidente Prudente, Sao Paulo State, Brazil.
It was used fingerlings of tilapia (Oreochromis niloticus) of Red, GIFT and Supreme strains. The fish, from a population of sexually reversed males, were kept in three recirculation systems, each system containing six water tanks of 0.5 [m.sup.3]. Each tank received 70 fingerlings weighing approximately 1.4 g, in a density of 140 fish [m.sup.-3]. The temperature of the water in recirculation systems was kept at 22, 28 and 30 [degrees]C. The dissolved oxygen and water temperature were monitored daily, the limnological parameters of the water as pH, alkalinity, hardness, ammonia, nitrite and nitrate were monitored weekly. The experiment was conducted for 60 days.
All tilapias were fed the same commercial feed, specific for each growth phase, with the amount being supplied at 10% of the biomass of the tank and also according to the water temperature.
At the end of the experimental period, samples of 10 fish were collected after 24 hours fasting period. They were anesthetized by heat shock (ice and water) and euthanized. The sampled fish were weighed (g), measured for standard length (cm) and tissue samples were removed for morphometric analysis.
Samples of white muscle were removed in the middle portion of the body below the dorsal fin for subsequent analysis of white fibers (section that only contain a portion of white muscle). The red muscle samples were taken near the caudal fin, the tail areas mostly contain red muscles fibers. Samples of adipose tissue were removed in the visceral and ventral region, as illustrated in Figure 1.
The tissue samples were fixed in buffered formalin (10%), preserved in 70% alcohol and submitted for inclusion in hystoresin (LEICA Historesin). Transverse sections of 4 [micro]m thick were obtained in microtome and stained with hematoxylin and eosin (HE) to evaluate the tissues morphology. Using an image analysis system (Leica Qwin, Germany), it was calculated an area of 200 muscle fibers per animal, and the diameter of each fiber was determined using the following formula: D = 2A0, 5[[pi].sup.0.5] (Valente et al., 1999).
Data were analyzed as a completely randomized design with treatments in a 3 x 3 factorial (temperature x strain), with 10 repetitions each, with each fish as the experimental unit. Variance analysis was made by GLM procedure using SAS for Windows version 9.2. The mean values were compared by Tukey test at 5% significance.
Results and discussion
The means of limnological parameters during the experimental period are presented in Table 1. All parameters were considered appropriate for the culture of tilapia (El-Sayed, 2006).
Variance analysis showed a significant effect of temperature on the length and weight of fish after 60 days of culture (Table 2). Higher weights were found for fish reared at 30[degrees]C compared to those grown at 28 or 22[degrees]C. The difference of 2[degrees]C in temperature cultivation increased the weight of the fish at 33.5%. It can be observed less weight of fish cultured at 22[degrees]C and low survival rate.
Sifa, Chenhong, Dey, Gagalac and Dunham (2002) observed that two wild strains of tilapia, found in China, had better cold tolerance than the GIFT strain, and the authors attributed this to the following factors: the recent introduction of the GIFT strain in China did not allow the selection of this strain to low temperatures, African strains introduced in China for several years, were exposed to low water temperatures and thus allowed a kind of natural selection. Another possibility for this low cold tolerance may be due to possible contamination with Oreochromis mossambicus (which has low cold tolerance) while selecting the GIFT strain.
Images of cross sections of the lateral muscles collected below the dorsal fin (MND), in the region of the anal fin (MNA), subcutaneous ventral adipose tissue (AS) and visceral fat (AV) are shown in Figure 2.
ANOVA also showed a significant effect of temperature on the length of the fish. Similar to the weight of fish, standard length was higher in fish reared at 30[degrees]C, compared to 28 or 22[degrees]C. There was no difference in length between tilapia strains (Table 3). A thorough analysis of the diameters of approximately 200 white muscle fibers showed that fish reared in cold temperature (22[degrees]C) have larger diameter when compared to culture at 28 and 30[degrees]C. The strain x temperature interaction was significant for the diameter of the red fibers. In the GIFT strain, the temperature heated to 30[degrees]C provided greater diameter (33.34 [micro]m) of these fibers when compared to 28 or 22[degrees]C, but this was not observed in the Red and Supreme strains. The Red strain showed smaller diameter in the red fibers at the three growth temperatures, although at 22 and 28[degrees]C it was not different to GIFT strain.
The analysis of cells from subcutaneous adipose tissue of each fish was performed and showed significant interaction of strain x temperature at 60 days (Table 2). The lowest diameter adipocyte was found in Red strain in the three temperatures, although at 22[degrees]C this strain was similar to GIFT. The temperature influenced the diameter of visceral adipocytes at 60 days of cultivation and this effect was similar between tilapia strains. Fish cultivated at 22[degrees]C showed larger diameter (92.74 [micro]m) when compared to the ones cultured at 30[degrees]C (77.28 [micro]m). Among the strains, the Red one had a smaller diameter (73.71 [micro]m) compared with GIFT (91.99 [micro]m) and Supreme (88.13 [micro]m) ones.
With few exceptions, most species of fish tend to have indeterminate growth. In these animals, muscle growth occurs through two processes: hypertrophy and hyperplasia, which contribute throughout the growth period of post-embryonic skeletal muscle. The growth 'hyperplastic' refers to muscle increase in the number of muscle fibers due to the formation of new fibers. The production of new myotubes and muscle fibers continues until the fish reach about 40% of the maximum length of the body (Johnston, 2004).
In hyperplasia, the fusion between satellite cell activated results in the formation of new myotubes on the surface of existing fibers, with subsequent differentiation into muscle fibers (Stellabotte & Devoto, 2007).
During the hypertrophic growth, satellite cells activated fuse with existing muscle fibers by increasing the number of myonuclei and synthesis of myofibrils, leading to an increase in the diameter or area of muscle fibers (Johnston, 1999). Muscle fibers grow by hypertrophy throughout the period of post-larval growth, until they reach a maximum functional diameter which is around 100 micron (white fibers). The rate of hypertrophic growth varies with the rate of somatic growth and in different stages of life of the animal.
The white muscle is approximately 70% of the total volume of muscle tissue (Sanger & Stoiber, 2001). This ratio varies along the length of the fish with a higher proportion in the anterior region of the animal and a large decline towards the caudal region. When compared with the red fibers, these have larger diameters (between 50 and 100 micron) and lower supply of blood capillaries, also have lower concentration of myoglobin and fewer mitochondria (Sanger & Stoiber, 2001). This type of muscle is recruited in sudden movements of swimming, how to capture food and escaping from predators (Altringham & Johnston, 1981).
The red musculature normally corresponds to 5 to 15% relative to the entire myotomal muscle of the fish (Altringham & Johnston, 1981). This muscle is found in the surface region below the dermis, in a higher proportion in the tail region and close to the lateral line. This compartment is composed of red muscle fibers, slow twitch and oxidative metabolism, have small diameter (between 25 and 45 [micro]m), excellent blood supply, high concentration of myoglobin, many mitochondria in the subsarcolemmal region and between the myofibrils, and many droplets lipids (Altringham & Johnston, 1981, Johnston, 1981, Sanger & Stoiber, 2001). The red fibers are recruited when performing slow movements and support, such as migration (Bone, 1978).
The lipids compartments are the most predominant source of energy for fish (Leaver, Bautista, Bjornsson, & Jonsson, 2008). The development of adipose tissue in fish is considered essential the same as occurred in mammals, appears as a result of recruitment of new adipocytes and increasing the size of adipocytes due to the deposition of lipids. According Serlachius & Anderson (2004), fats mature cells are terminally differentiated and do not proliferate, while areas of adipose tissue harboring perivascular and stromal precursor cells such as fibroblasts, pre-adipocytes with mitotic capacity and committed to differentiation into adipocytes.
Figure 3 shows the frequency distribution in diameter classes of ventral subcutaneous adipocytes of tilapia cultured at 22[degrees]C. It was observed that the Red strain showed higher frequency adipocytes in the < 50 [micro]m and 50-100 [micro]m classes, whereas the Supreme strain showed a higher frequency of adipocytes in major classes of diameters, 100-150 [micro]m and > 150 [micro]m. The GIFT strain was in middle position. Similar results occurred with fish reared at 28 and 30[degrees]C.
Fauconneau et al. (1997) analyzed four distinct regions of fat deposition, perivisceral, subcutaneous ventral, dorsal subcutaneous and red muscle of different strains of rainbow trout. At each of these sites, fat cells were found with a variety of size 5-200 microns. The relative proportions of large and medium-sized cells were dependent on the location of the adipose tissue. In the ventral adipose tissue, the population of large cells and their average sizes were larger than in the dorsal adipose tissue. No difference was found in mean size of muscle fibers and fat cells between strains. However, strains with high growth rates were also characterized by a high rate of fat deposition. This may explain the larger diameter and the higher frequency in large adipocytes in GIFT and Supreme strains when compared with Red one.
Red, GIFT and Supreme tilapia strains show differences in growth of muscle and adipose tissues in response to growth temperature. The cold temperature (22[degrees]C) may have caused hypertrophy of white muscle fibers and visceral adipocytes in fingerlings.
These strains present differentiated morphological aspect in red fibers and subcutaneous ventral adipocytes diameters. Furthermore, heating to 30[degrees]C may have contributed to the hypertrophy of red fibers in the GIFT strain.
The authors acknowledge the financial support given by Fapesp, Sao Paulo State, Brazil.
DOI: 10.4025/actascianimsci.v40i1.35686 AQUICULTURE
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Received on March 1, 2017.
Accepted on June 19, 2017.
Rondinelle Artur Simoes Salomao (1) *, Vander Bruno dos Santos (2) and Edson Assuncao Mareco (3)
(1) Centro de Aquicultura, Universidade Estadual Paulista 'Julio Mesquita Filho', Via de Acesso Prof. Paulo Donato Castellane, s/n, 14884-900, Jaboticabal, Sao Paulo, Brazil. (2) Agencia Paulista de Tecnologia do Agronegocio, Presidente Prudente, Sao Paulo, Brazil. (3) Universidade do Oeste Paulista, Presidente Prudente, Sao Paulo, Brazil. * Author for correspondence. E-mail: email@example.com
Caption: Figure 1. Location of tissue samples in Nile tilapia on the left longitudinal view highlighting regions of collecting samples of muscle and adipose tissue in the middle portion of the body below the dorsal fin (MND) and the region immediately posterior to the anal fin (MNA) on the right, cross section of the body, highlighting again the sample of muscle tissue taken at the middle region of the body just below the dorsal fin (MND); visceral adipose tissue samples (AV) and subcutaneous adipose ventral (AS).
Caption: Figure 2. Photomicrographs of cross-sectional images of tissue samples from GIFT tilapia strain of 60 days of cultivation A) White muscle in the dorsal region B) Red muscle in the caudal tail C) Subcutaneous ventral adipose tissue D) Visceral adipose tissue. Abbreviations: (AS) subcutaneous adipose (AV) visceral adipose (FB) white fibers (FM) muscle fibers (FI) intermediate fibers (FV) red fibers (m) myofibrils (ms) myosepta (n) nucleus (P) skin. Coloration HE and toluidine blue Increase 40 x and 10x image D.
Caption: Figure 3. Frequency distribution of subcutaneous ventral adipocytes of tilapia strains cultured at 22[degrees]C.
Table 1. Mean of limnological parameters of water recirculation systems of tilapia cultivation at different temperatures. Parameter Temperature 22[degrees]C 28[degrees]C 30[degrees]C Oxygen (mg [L.sup.-1]) 5.24 5.15 4.71 pH 7.05 7.16 7.08 Alkalinity 114.56 100.24 110.98 (mg [L.sup.-1]) Hardness (mg [L.sup.-1]) 229.12 273.87 297.14 Ammonia (mg [L.sup.-1]) 0.03 0.03 0.05 Nitrite (mg [L.sup.-1]) 1.3 3.3 2.75 Nitrate (mg [L.sup.-1]) 50 70 68.5 Table 2. Initial and final weight (after 60 days of culture), coefficient of variation and survival rate of Nile tilapia strains grown at different temperatures. Temperature Lineage weight (g) Survival rate Initial CV Final CV (%) (%) (%) 22[degrees]C Red 1.47 a 36.05 8.38 35.22 90.88 GIFT 1.48 a 32.43 10.63 42.08 92.05 Supreme 1.43 a 21.68 12.57 22.52 96.93 Mean 10.52 c 28[degrees]C Red 1.57 a 18.47 34.49 17.79 97.69 GIFT 1.88 a 43.34 50.19 34.32 97.69 Supreme 1.67 a 13.17 41.68 13.43 100.00 Mean 42.12 b 30[degrees]C Red 1.80 a 27.22 45.92 26.25 98.46 GIFT 1.76 a 36.93 66.93 18.65 98.30 Supreme 1.73 a 22.54 55.82 15.53 100.00 Mean 56.23 a Values followed by the same letter in the column are not significantly different by Tukey test (p < 0.05). Table 3. Mean and standard deviation of standard length (SL), diameter of white muscle fibers (WFD) and red muscle fibers (RFD), subcutaneous (SA) and visceral adipocytes (VA) in tilapia strains grown at different temperatures for 60 days. Strain 22[degrees]C 28[degrees]C Red 5.60 (0.51) 9.36 (0.43) SL (cm) GIFT 6.24 (0.85) 10.62 (1.37) Supreme 6.81 (0.63) 10.28 (0.57) Means 6.22 C * 10.08 B WFD (pm) Red 59.53 (5.04) 55.93 (5.58) GIFT 71.66 (4.80) 67.65 (9.12) Supreme 68.77 (8.91) 65.05 (6.70) Means 67.10 A * 62.71 B RFD (pm) Red 22.49 (2.88)Ab * 25.33 (3.41)Ab GIFT 26.53 (2.48)Bab 27.06 (2.84)Bab Supreme 31.37 (4.15)Aa 30.59 (2.74)Aa SA (pm) Red 81.36 (12.52)Ab * 66.64 (8.12)Ab GIFT 89.42 (12.29)Aab 99.28 (15.91)Aa Supreme 105.8 (7.27)Aa 109.6 (14.21)Aa VA (pm) Red 82.10 (1.77) 73.34 (8.62) GIFT 101.6 (12.90) 88.09 (10.61) Supreme 88.67 (13.37) 96.57 (12.09) Means 92.74 A * 84.63 AB 30[degrees]C 10.26 (0.98) SL (cm) 11.92 (0.80) 11.26 (0.63) 11.14 A WFD (pm) 51.13 (5.96) 66.10 (8.12) 64.76 (5.13) 60.32 B RFD (pm) 24.27 (1.97)Ab 33.34 (3.46)Aa 31.28 (3.88)Aab SA (pm) 72.58 (6.47)Ab 91.97 (11.25)Aa 100.6 (16.21)Aa VA (pm) 70.27 (9.71) 85.01 (19.87) 80.62 (11.64) 77.28 B * Means followed by the same capital letters in the row and small letters in the column are not different by Tukey test at 5%.
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|Author:||Salomao, Rondinelle Artur Simoes; Santos, Vander Bruno dos; Mareco, Edson Assuncao|
|Publication:||Acta Scientiarum. Animal Sciences (UEM)|
|Date:||Jan 1, 2018|
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