Digestibility and nitrogen balance of diets that include marine fish meal, catfish (Pangasius hypophthalmus) by-product meal and silage, and processing waste water in growing pigs.
Pig production is the dominant form of livestock production in Vietnam and accounts for around 80% of the total meat consumption of the country (Livestock Department, 2006). Conventional protein supplements for commercial pigs, such as fish meal and soya bean meal have become relatively expensive. The resulting imbalance between feed and animal production prices has reduced profitability for pig farmers. Catfish production for export has increased rapidly in recent years in the Mekong Delta, and significant amounts of head, bone, scrap meat and skin by-products (710-900 tons/d; Thuy et al., 2007) are produced from fillet processing. By-products account for approximately 65% of the whole catfish (Nortvedt, 2007). Catfish by-product meal (CBM), ensiled by-product (CBE) and processing waste water (WWB) from the CBM processing are potentially valuable alternative protein sources in pig rations to conventional protein supplements such as soya bean meal and fish meal. However, there are no published data on the digestibility of these by-products, especially ileal amino acid digestibility in pigs. The aim of this study was to determine the nitrogen retention and the apparent digestibility of dietary components and amino acids in diets containing catfish by-product meal, ensiled by-product and processing waste water resulting from catfish processing.
MATERIAL AND METHODS
Animals and experimental design
Four crossbred castrated male (Yorkshire x Landrace) pigs with an average live weight of 35.5[+ or -]0.41 kg at the start, and 60.1[+ or -]1.31 kg (mean[+ or -]SD) at the termination of the experiment, were used to determine the coefficient of apparent ileal (CIAD) and total tract digestibility (CTTAD) of the experimental diets. The pigs were treated against intestinal parasites and vaccinated against hog cholera and foot and mouth disease during the initial 7 days, then surgically fitted with post-valve T-cecum cannulas (Van Leeuwen et al., 1991) to allow collection of ileal digesta. The pigs were housed in individual metabolism cages in an environmentally controlled house with an average temperature of 30-33[degrees]C. Urine and feces were collected separately, and water from nipple drinkers was freely available.
Four experimental diets were introduced to the pigs two weeks after surgery according to a 4 x 4 Latin Square design. Experimental periods were 12 days, consisting of 5 days of adaptation to each diet followed by 4 days of collection of feces and urine, one day of ileal digesta collection, one day of rest and finally a second day of ileal digesta collection. Dietary treatments consisted of broken rice, rice bran and maize meal as energy sources with four different test protein sources: A fish meal diet (FMD) as control, and diets including catfish by-product meal (CBMD), ensiled catfish by-product (CBED) and processing waste water (WWBD). All diets were supplemented with a standard mixture of vitamins and minerals, and chromium oxide was added as an indigestible marker at 0.5% of the diet.
Fish meal was bought from factories which specifically process small marine fish. The CBM was bought from catfish by-product meal factories which purchase the CBP from fillet exporting companies, and includes the head, bone, skin and abdominal organs that remain after the two side fillets have been removed. This residue is then ground fresh, boiled and the oil removed, and then dried to produce CBM. The ground boiled CBP was collected from CBM factories, then mixed with molasses at a ratio of 8:2 (wet basis). The mixture was placed in plastic bags and sealed to prevent air contamination and then ensiled for 3-4 weeks. A new batch of the ensiled product was made every week and then mixed daily with the basal ingredients. The WWB was collected each week, preserved with acetic acid and then stored before being mixed daily with the basal ingredients. The FM and CBM were mixed with the basal ingredients initially and stored for the whole period of data collection. The feeding level during the collection period was set slightly below the maximum level consumed during the adaptation period. The pigs were given two meals per day at 7:00 and 17:00 h, and water was available ad libitum.
Digesta, feces and urine collection and calculations
On each day of ileal digesta collection, samples were taken after every 2 h during the 12 h period between the morning and afternoon feedings, with a 1 h adjustment between days to cover every hour during the 12 h period. At each sample collection, digesta were quantitatively collected for 1 h in a plastic bag through a soft plastic tube connected to the ileal cannula. The plastic bags were then removed, new bags installed, and the samples stored in a refrigerator. The 6 samples (bags) per day of collection, in total 12 samples of digesta from each pig from 2 days of ileal digesta collection in each experimental period, were mixed together and kept frozen at -18[degrees]C. During each collection period, feces were also quantitatively collected daily at 8:00 and 16:00 h and representative samples stored in a refrigerator. After 4 days of feces collection, the samples were mixed and representative samples were kept frozen at -20[degrees]C for analysis. Urine was collected in 50 ml of 10% [H.sub.2]S[O.sub.4]. Finally, prior to chemical analysis, individual samples of ileal digesta and feces were thawed and pooled within pigs and periods, and then dried at 60[degrees]C before analysis.
The digestibility of the diets at each sampling site was calculated using the indicator technique according to the following equation:
[CAD.sub.D] = 1 - ([DC.sub.F] x [I.sub.D])/([DC.sub.D] x [I.sub.F])
Where: [CAD.sub.D] is the coefficient of apparent digestibility of dietary components in the assay diet; [DC.sub.F]: Dietary component concentration in ileal digesta or feces (g/kg); [I.sub.D]: Indicator concentration in the assay diet (g/kg); [DC.sub.D]: Dietary component concentration in the assay diet (g/kg); [I.sub.F]: Indicator concentration in ileal digesta or feces (g/kg).
The chemical composition of feed, feces and urine was determined using the following Association of Official Analytical Chemists methods (AOAC, 1990): Dry matter (DM) was measured by drying the fresh samples at 105[degrees]C until dry. Crude protein was determined by the Kjeldahl method. Total ash was the residue after ashing the samples at 550[degrees]C and organic matter (OM) was calculated by difference. The ether extract (EE) was determined by Soxhlet extraction. Neutral detergent fiber (NDF) and acid detergent fiber (ADF) were determined by the methods of Van Soest et al. (1991). Amino acids (AA) were analyzed on an ion-exchange column using an HPLC (Spackman et al., 1958). Chromium was measured by atomic absorption spectrophotometer after ashing and digesting the sample in a mixture containing perchloric and nitric acid (Fenton and Fenton, 1979).
Analysis of variance was performed according to a 4 x 4 Latin Square arrangement, using the General Linear Model of Minitab Statistical Software Version 15. Tukey pair-wise comparisons were used to determine differences between treatment means at p<0.05.
The experiment was carried out without any problems regarding illness or behavior of the animals. All diets offered to the pigs were completely consumed at every meal. The chemical composition of the ingredients is shown in Table 1. The DM, CP and EE contents were different between CBP (43.5%, 37.5% and 19.8%, respectively), CBM (83.7%, 41.9% and 15.6%, respectively) and CBE (52.0%, 29.2% and 14.2%, respectively), and the contents in WWB (24.2%, 32.5% and 19.8%, respectively) and FM (82.3%, 47.7% and 10.3%, respectively) were different. The amino acid composition of the experimental ingredients is shown in Table 2, and of the diets in Table 4. Lysine and total essential amino acids contents were similar in FM (51.1 and 253 g/kg, respectively) and CBM (49.0 and 216 g/kg, respectively), and were also similar in CBE (33.5 and 156 g/kg, respectively) and WWB (36.3 and 155 g/kg, respectively). The concentration of lysine in the FMD was lowest, while CBED had higher lysine, leucine and methionine concentrations than the other diets. The ingredient and chemical composition of the experimental diets is shown in Table 3. All experimental diets had the same level of CP (13.3-13.4%). The DM was lowest in WWBD, but there were no significant differences in OM, CF, ADF, NDF and NFE among FMD, CBMD, CBED and WWBD. The EE content in FMD was lower (4.71%) than in CBMD (5.6%), CBED (6.5%) and WWBD (7.3%). The daily DM and N intake and N-retention and utilization were not different among diets (Table 5).
The coefficient of ileal apparent digestibility (CIAD) of OM in the WWBD was higher than in the other three diets (p<0.05), while the CIAD of EE was lower (p<0.05) in the FMD compared with CBED and WWBD (Table 5). The coefficient of total tract apparent digestibility (CTTAD) of OM was lower (p<0.05) in CBED than in the other diets, while the CTTAD of EE was lower (p<0.05) in FMD compared with WWBD. There was a trend (p<0.1) towards higher CP digestibility at both ileal and total tract level in CBED than in the other diets. The CIAD and CTTAD of amino acids (Table 6) were not different among diets (p>0.05). In all diets, the highest CIAD of essential AA (EAA) was for leucine (74.3%), lysine (75.6%) and methionine (73.8%) in CBED, and the highest CTTAD of EAA was for arginine (78.5%), lysine (80.2%), methionine (78.7%) and valine (79.8%), also in CBED.
The catfish by-product meals bought from the different CBM processing factories had different DM, CP and EE contents. This can be explained by the different proportions between the scrap meat, skin, head and bone added, as well as by differences in the average weights of the fish processed, and also different procedures for oil extraction between factories. Generally, meals that have a high scrap meat proportion are high in CP content (Thuy et al., 2007). The CBP used for ensiling was in fresh form and consisted of head and bone by-product, which explains the low DM and CP contents compared with CBM. The sugarcane molasses was used as carbohydrate silage additive because it is very effective in reducing pH, and the silage rapidly attained a pH of 4.5, with significant increases in lactic acid content. The low DM content in WWB was a result of the water added before cooking and oil extraction, and the high fat content of WWB was probably due to an inefficient oil extraction process. The slightly higher lysine, methionine and leucine concentration in CBED was probably a result of the high proportion of CBE in the diet (23%).The fish meal used in the experiment was produced from very small, whole marine fish, so the CP content was low and ash content high.
The ileal and total tract apparent digestibility of amino acids was similar in all diets, irrespective of protein source. Moreover, nitrogen retention and N utilization were similar among diets. This indicates similarity in amino acid utilization among diets, as there were only minor differences in essential amino acid composition among diets. However, amino acid digestibility in the experimental diets was low in comparison with previous studies by Jergensen et al. (1984) and Knabe et al. (1989) on fish meal. There could be several explanations for this, such as a high ash content in the products, heating during processing and diet CP content. The results from Noblet and Perez (1993) showed that diets with a higher ash content had lower fecal apparent digestibility of amino acids. Moreover, the fact that the fish meal was dried at a temperature of >80[degrees]C and catfish by-product was boiled at a temperature of >100[degrees]C would also have contributed to reduce amino acid digestibility. Opstvedt et al. (2003) showed that fish meal produced at processing temperatures below 70-80[degrees]C had higher CP digestibility than when the meal was processed at temperatures above 100[degrees]C. Ohh et al. (2002) also concluded that the quality of fish meal may show considerable variation depending on the quality of raw material and the processing method used in manufacturing . Similarly, Wang and Parsons (1998) found that high processing temperatures of meat and bone meal generally resulted in lower amino acid digestibility than did low processing temperatures. Finally, Fan et al. (1994) showed that there was a quadratic increase in ileal apparent amino acid digestibility as dietary CP content was increased from 4 to 24%, and reduction of dietary CP content was shown to decrease the ileal apparent digestibility of most amino acids in weaning pigs (Htoo et al., 2007).
As expected, the ileal digestibilities of OM, CP and EE in all diets were lower than the total tract digestibilities, and were of a similar order of magnitude to the values reported by Ngoan and Lindberg (2001). The trend towards increased ileal and total tract CP digestibility in CBED may be due to the impact of microbial activity in the diet prior to feeding. Bacterial lactic acid fermentation of the feed has been shown to enhance digestibility (Hong and Lindberg, 2007). The resulting low pH and high acid content has also been shown to stimulate the pancreatic secretion and can improve the digestion and absorption of nutrients (Scholten et al., 1999). The improved feed efficiency that can be obtained by feeding fermented liquid feed is due to changes in the gastro-intestinal tract environment, reduced pH in the stomach and the lower number of enterobacteria (Moon et al., 2004).
The digestibility of EE was low in all diets. This could be explained by the feed processing, as the total tract digestibility of dietary nutrients in pigs can be influenced by the characteristics of the feed, such as chemical composition and processing treatment (Le Goff and Noblet, 2001). Moreover, the digestibility of EE in FMD was lower than in the other diets, which can be explained by a low fat content in this diet as compared with the other diets. This is in agreement with Noblet and Perez (1993), who showed that the lower EE digestibility obtained when dietary fat content was low was due to the concomitant high proportion of fecal endogenous fat, so the amount of digestible EE was relatively and positively related to the dietary EE content. In addition, catfish oil is very high in unsaturated fatty acids (Thuy et al., 2007), with concentrations of between 67.7% (Sathivel et al., 2003) to 75% (Men et al., 2007) of poly-unsaturated fatty acids, which are more efficiently digested and absorbed than saturated fatty acids. This was also demonstrated by Duran-Montge et al. (2007), who found that individual fatty acid digestibility increases with increasing unsaturation, and that digestibility of fat sources is a function of fatty acid content.
We are very grateful to the Swedish International Development Cooperation Agency, Department for Research Cooperation (Sida-SAREC) through the regional MEKARN project, for the financial support of this study. Also thanks to Associate Professor Le Van Tho of Nong Lam University for carrying out the surgery.
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Nguyen Thi Thuy, Jan Erik Lindberg (1) and Brian Ogle (1) *
College of Agriculture and Applied Biology, CanTho University, CanTho City, Vietnam
* Corresponding Author: Brian Ogle. Tel: +46-18-67-21-02, Fax: +46-18-67-29-95, E-mail: Brian.Ogle@huv.slu.se
(1) Department of Animal Nutrition and Management, Swedish University of Agricultural Sciences, P.O. Box 7024, S-750 07 Uppsala, Sweden.
Received September 23, 2009; Accepted February 2, 2010
Table 1. Dry matter content (%), and crude protein (CP), ether extract (EE), crude fiber (CF), NFE, NDF and ADF (% of DM) contents of diet ingredients Ingredient DM CP EE Ash Rice bran 82.5 9.9 9.2 8.2 Maize meal 85.4 8.5 1.0 4.2 Broken rice 88.0 7.2 0.8 4.1 FM (1) 82.3 47.7 10.3 33.2 CBM (2) (meat, scraps, 83.7 41.9 15.6 31.4 head and bone) CBE (3) 52.0 29.2 14.2 28.5 WWB (4) 24.2 32.5 19.8 29.5 Catfish by-product 43.5 37.5 19.8 33.8 (head and bone) Ingredient CF NFE ADF NDF Rice bran 9.2 63.5 20.2 37.5 Maize meal 3.6 82.6 2.7 8.6 Broken rice 6.8 81.1 1.8 7.1 FM (1) 2.5 6.3 1.8 8.3 CBM (2) (meat, scraps, 3.7 7.4 1.7 8.8 head and bone) CBE (3) 2.1 26.0 5.3 14.5 WWB (4) 2.6 15.6 1.6 6.5 Catfish by-product 2.1 6.7 1.6 3.1 (head and bone) (1) Fish meal. (2) Catfish by-product meal. (3) Catfish by-product ensiled with molasses at a ratio of 8:2. (4) Waste water from catfish by-product meal processing. Table 2. Amino acid composition of the experimental feed ingredients (g/kg DM) Ingredients * FM CBM CBE WWB Essential amino acids (EAA) Arginine 28.8 32.8 16.5 14.0 Isoleucine 20.1 11.1 11.0 11.6 Leucine 30.1 23.2 23.5 21.4 Lysine 51.1 49.0 33.5 36.3 Histidine 13.5 13.5 5.9 6.2 Methionine 18.9 16.8 11.5 10.6 Phenylalnine 17.8 13.1 11.6 12.9 Threonine 18.9 12.9 10.7 12.1 Tyrosine 26.6 24.0 14.7 11.2 Valine 27.7 20.1 16.9 19.0 Total EAA 253 216 156 155 Non-essential amino acids Alanine 40.6 36.1 21.5 30.9 Aspartic acid 1.5 1.6 3.2 4.5 Glutamic acid 61.0 53.0 34.7 24.5 Glycine 46.7 32.8 29.2 31.9 Proline 49.8 36.0 30.9 29.5 Serine 34.0 31.6 17.6 14.5 Sum of amino acids (SAA) 487 408 293 291 * FM = Fish meal; CBM = Catfish by-product meal; CBE = Ensiled catfish by-product; WWB = Processing waste water. Table 3. Ingredient (% of DM) and chemical composition (% of DM) of the experimental diets Diet * FMD CBMD CBED WWBD Ingredients (%) Rice bran 32.0 32.0 30.0 32.0 Maize meal 35.3 33.3 26.3 27.3 Broken rice 20.0 20.0 20.0 20.0 Fish meal 12.0 CBM 14.0 CBE 23.0 WWB 20.0 Vitamin-mineral premix (1) 0.2 0.2 0.2 0.2 [Cr.sub.2][O.sub.3] 0.5 0.5 0.5 0.5 Chemical composition (%) Organic matter 91.1 90.0 89.0 89.5 Crude protein 13.3 13.3 13.4 13.4 Ether extract 4.7 5.6 6.5 7.3 Ash 8.9 10.0 11.0 10.5 Crude fiber 5.9 6.0 5.5 5.8 ADF 8.0 7.9 8.3 7.5 NDF 17.5 17.5 16.4 18.4 NFE 66.4 65.8 62.9 62.2 ME (MJ/kg DM) 13.1 13.2 13.1 13.2 (1) Per kg complete diet: Vitamins: A 48 x [10.sup.5] UI; D 48 x [10.sup.4] IU; E 44 x [10.sup.2]; [K.sub.3] 280 mg; [B.sub.1] 600 mg; [B.sub.2] 200 mg; [B.sub.6] 320 mg; [B.sub.12] 6 x [10.sub.3] mcg; Biotin [10.sub.4] mcg; Folic acid 160 mg; Nicotinic acid 44 x [10.sup.2] mg; Pantothenic acid 24 x [10.sup.2] mg. Minerals: Fe 475 x [10.sup.2] mg; Cu 315 x [10.sup.2] mg; Zn 475 x [10.sup.2]; I 350 mg; Co 47 mg; Mn 195 x [10.sup.2]; Se 39 mg. * FMD = Fish meal diet; CBMD = Catfish by-product meal diet; CBED = Ensiled catfish by-product diet; WWBD = Processing waste water diet. Table 4. Amino acid composition of the experimental diets (g/kg DM) Diet * FMD CBMD CBED WWBD Essential amino acids (EAA) Arginine 10.3 11.3 9.9 9.2 Isoleucine 5.8 4.9 5.6 5.5 Leucine 10.9 10.2 11.7 10.8 Lysine 9.5 10.2 10.7 10.4 Histidine 4.2 4.4 3.6 3.6 Methionine 3.9 3.9 4.0 3.6 Phenylalnine 5.3 4.9 5.3 5.4 Threonine 4.9 4.3 4.7 4.8 Tyrosine 6.0 6.0 5.8 4.8 Valine 7.5 6.9 7.6 7.6 Total EAA 68.2 67.0 68.9 65.6 Non-essential amino acids Alanine 9.7 9.0 8.5 9.9 Aspartic acid 1.0 1.1 1.6 1.8 Glutamic acid 13.0 13.0 13.0 10.2 Glycine 9.0 7.9 9.7 9.5 Proline 10.7 9.6 11.2 10.1 Serine 9.6 8.6 7.9 6.8 Sum of amino acids (SAA) 121 116 121 114 * FMD = Fish meal diet; CBMD = Catfish by-product meal diet; CBED = Ensiled catfish by-product diet; WWBD = Processing waste water diet. Table 5. Ileal and total tract apparent digestibility (%), and nitrogen balance of the experimental diets Diet * FMD CBMD CBED Ileal digestibility (%) OM 78.4 (a) 77.0 (a) 78.4 (a) CP 73.2 73.1 74.9 EE 64.0 (a) 67.0 (ab) 67.8 (b) Total tract digestibility (%) OM 84.2 (a) 84.4 (a) 83.5 (b) CP 77.2 77.8 78.8 EE 70.1 (a) 71.9 (ab) 72.0 (ab) Daily DM intake (g/d) 1,278 1,272 1,267 N intake (g/d) 27.2 27.1 27.6 N in feces (g/d) 6.6 5.8 6.1 N in urine (g/d) 8.2 9.1 7.8 N-balance (g/d) 12.3 12.4 13.7 N utilization (%) 59.9 53.2 63.2 Diet * WWBD SE p Ileal digestibility (%) OM 79.8 (b) 0.28 0.03 CP 72.5 0.56 0.09 EE 68.4 (b) 0.70 0.02 Total tract digestibility (%) OM 84.8 (a) 0.15 0.01 CP 76.8 0.43 0.08 EE 73.2 (b) 0.48 0.02 Daily DM intake (g/d) 1,218 75.8 0.87 N intake (g/d) 26.8 1.67 0.98 N in feces (g/d) 6.5 0.99 0.92 N in urine (g/d) 8.0 1.21 0.88 N-balance (g/d) 12.3 2.51 0.97 N utilization (%) 57.4 6.73 0.31 * FMD = Fish meal diet; CBMD = Catfish by-product meal diet; CBED = Ensiled catfish by-product diet; WWBD = Processing waste water diet. (a,b) Within rows, values with different superscript letters are different (p<0.05). Table 6. Ileal and total tract apparent digestibility (%) of amino acids in pigs fed diets containing fish meal and different catfish by-products * Ileal digestibility FMD CBMD CBED WWBD SE p Essential amino acids Arginine 73.7 73.5 74.2 74.5 1.48 0.96 Isoleucine 72.4 71.2 73.1 72.7 0.84 0.50 Leucine 73.2 74.6 74.3 72.7 0.60 0.20 Lysine 74.5 74.1 75.6 74.8 1.32 0.86 Histidine 72.7 73.0 73.8 71.6 1.13 0.60 Methionine 73.8 72.9 73.8 73.2 1.36 0.94 Phenylalanine 72.5 73.2 73.9 72.2 1.32 0.80 Threonine 70.9 70.3 71.4 69.7 1.08 0.70 Tyrosine 72.7 73.0 71.1 71.3 0.71 0.25 Valine 73.3 73.4 73.2 72.8 0.83 0.95 Non-essential amino acids Alanine 71.4 69.2 69.5 70.8 0.54 0.07 Aspartic acid 70.1 70.5 69.3 69.7 0.84 0.76 Glutamic acid 72.4 72.7 71.3 72.7 0.53 0.31 Glycine 70.4 69.6 70.8 70.6 0.84 0.78 Proline 72.1 72.1 74.3 73.4 0.80 0.24 Serine 72.8 71.2 72.3 71.8 0.85 0.62 Total tract digestibility FMD CBMD CBED WWBD SE p Essential amino acids Arginine 77.5 77.3 78.5 76.3 0.78 0.35 Isoleucine 75.4 74.2 75.4 75.6 1.37 0.89 Leucine 76.7 77.8 77.4 76.9 0.25 0.07 Lysine 78.0 78.9 80.2 77.6 0.90 0.28 Histidine 76.6 76.4 78.4 76.1 1.91 0.82 Methionine 76.1 77.6 78.7 77.0 1.11 0.45 Phenylalanine 77.0 77.7 77.8 75.5 0.93 0.39 Threonine 73.2 72.6 72.2 71.6 1.30 0.83 Tyrosine 77.9 78.6 77.6 76.5 0.45 0.08 Valine 79.1 78.8 79.8 78.8 0.34 0.88 Non-essential amino acids Alanine 76.9 75.5 75.3 75.4 0.37 0.06 Aspartic acid 75.9 77.7 75.1 76.7 0.61 0.09 Glutamic acid 78.4 78.5 78.6 78.8 0.17 0.49 Glycine 74.0 73.2 74.5 74.3 0.49 0.34 Proline 75.0 75.0 75.3 74.2 1.18 0.91 Serine 77.1 78.7 78.8 77.2 0.57 0.14 * FMD = Fish meal diet; CBMD = Catfish by-product meal diet; CBED = Ensiled catfish by-product diet; WWBD = Processing waste water diet.
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|Author:||Thuy, Nguyen Thi; Lindberg, Jan Erik; Ogle, Brian|
|Publication:||Asian - Australasian Journal of Animal Sciences|
|Date:||Jul 1, 2010|
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