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Digestible Threonine to Lysine Ratios for Meat-Type Quails

ABSTRACT

Three experiments were conducted to estimate the optimal digestible threonine to lysine ratios (Thr:Lys) of meat-type quails during the pre-starter (1 to 7 days), starter (8 to 14 days) and grower I (15 to 21 days) phases. In each experiment, 600 birds were distributed according to a completely randomized experimental design into five treatments, consisting of five dietary Thr:Lys ratios (0.66, 0.71, 0.76, 0.81 and 0.86%), with eight replicates of 15 quails each. Performance parameters and intestinal morphology were evaluated. During the pre-starter phase, feed intake, threonine intake, weight gain, and ileal villus height linearly increased (p<0.01) as dietary digestible Thr:Lys increased. During the starter phase, increasing digestible Thr:Lys ratios had a linear effect (p<0.01) on threonine intake and livability, and linear and quadratic effects (p<0.01) on feed intake. During the grower I phase, increasing digestible Thr:Lys ratios promoted linear increase in threonine intake and feed conversion ratio (p<0.05), and a linear decrease in weight gain. The estimated digestible Thr:Lys ratios recommended for meat-type quails are 0.85, 0.73 and 0.66%, for the pre-starter, starter and grower I phases, respectively.

Keywords:
Amino acids, Coturnix coturnix; ideal protein, performance

INTRODUCTION

Although threonine is the third limiting amino acid, after methionine and lysine, in poultry feeds based on corn and soybean meal, it is currently considered a key amino acid in least-cost formulations as it may allow reducing dietary crude protein level (Fernandez et al., 1994Fernandez SR, Aoyagi S, Han Y, Parsons CM, Baker DH. Limiting order to amino acids in corn and soybean meal for growth of the chick. Poultry Science 1994;(73)12:1887-1889.; Umigi et al., 2007Umigi RT, Barreto SLT, Donzele JL, Reis RS, Sousa MF, Leite CDS. Níveis de treonina digestível em dietas para codornas japonesa em postura. Revista Brasileira de Zootecnia 2007;36:1868-1874.). Threonine is directly involved in the immune response as it is essential for the maintenance of immune cells (immunoglobulins) and for the gastrointestinal production of mucin (Mao et al., 2011Mao X, Zeng X, Qiao S, Wu G, Li D. Specific roles of threonine in intestinal integrity and barrier function. Frontier in Bioscience 2011;E3:1192-1200.), contributing for the maintenance and development of intestinal mucosa integrity. In addition, threonine is essential for feather growth, enzyme synthesis, and lean meat accretion (Kidd, 2000Kidd MT. Nutritional considerations concerning threonine in broilers. World's Poultry Science Journal 2000;56:139-151; Wang et al., 2009Wang WW, Qiao SY, Li DF. Amino acids and gut function. Amino Acids 2009;37:105-110.).

A significant fraction of dietary threonine is absorbed in the small intestine, especially in the ileum, which is the main site of amino acid uptake due to the presence large numbers of carriers (Le Bellego et al., 2002Le Bellego L, Relandeau C, Van Cauwenberghe S. Threonine: a key nutrient for the gut. Ajinomoto Animal Nutrition. Eurolysine Information 2002;26:14-17.). The development of the lumen surface area and villus height determine the efficiency of nutrient digestion and absorption, and are essential for optimal animal performance (Cera et al., 1988Cera KR, Mahan DC, Cross RF, Reinhart GA, Whitmoyer RE. Effect of age, weaning and post-weaning diet on small intestinal growth and jejunal morphology in young swine. Journal Animal Science 1988;66:574-584.; Wang et al., 2007Wang X, Qiao S, Yin Y, Yue L, Wang Z, Wu G. A deficiency or excess of dietary threonine reduces protein synthesis in jejunum and skeletal muscle of young pigs. Journal of Nutrition 2007;137:1442-1446.). There is limited information on the threonine: lysine ratio (Thr:Lys) requirements for meat-type quails compared with other poultry. Therefore, the objective of this study was to estimate optimal digestible threonine: lysine ratios of meat-type quails for the pre-starter (1 to 7 days), starter (8 to 14 days) and grower I (15 to 21 days) phases.

MATERIAL AND METHODS

Animal care

The experimental procedures applied in the present study were approved by the Ethics Committee on Animal Use of the Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), state of Minas Gerais, Brazil (protocol n. 032/2012).

Birds, housing and experimental design

Three experiments were conducted at the Laboratory for Research on Non-Ruminant Animals of the Department of Animal Science of UFVJM between January and June 2013.

In each experiment, 600 non-sexed meat-type quails (Coturnix coturnix) were evaluated during the pre-starter (1 to 7 days of age; Experiment 1), starter (8 to 14 days of age; Experiment 2) and grower I (15 to 21 days of age; Experiment 3). Initial average body weights were determined as 9.41 ± 0.1 g; 36.5 ± 0.1 g; 86.2 ± 0.5 g, respectively.

Quails were housed in galvanized-wire cages (60 cm long x 60 cm wide x 35 cm-high) in three 4-tiered batteries. Each cage was equipped with a trough drinker and a trough feeder placed in the front of the cage. Cages were heated with incandescent 100, 60, and 40 watt lamps. Room temperature was monitored twice a day (08:00 and 15:00 h) by a digital thermometer placed each battery. Bird behavior was daily observed to evaluate their thermal comfort. The bulbs were changed as the birds grew to prevent overheating.

In all three experiments, birds were distributed in a completely randomized design, consisting of five treatments (dietary dig. Thr:Lys ratios), with eight replicates of 15 birds each.

Experimental diets

The experimental standard diet was based on corn and soybean meal, and formulated to contain 0.82% digestible threonine in order to obtain a Thr:Lys ratio of 0.66. The digestible Thr:Lys ratios of 0.66, 0.71, 0.76, 0.81 and 0.86% of the five experimental diets were obtained by the supplementation of five L-threonine (99%) levels (Tables 1, 2, and 3). L-threonine was included in replacement of glutamic acid in protein equivalents, and of starch in energy equivalents, in order to obtain equal protein and energy levels in all experimental diets.

Table 1
Ingredients and calculated composition of the pre-starter experimental diets (1 to 7 days of age).
Table 2
Ingredients and calculated composition of the starter experimental diets (8 to 14 days of age).
Table 3
Ingredients and calculated composition of the starter experimental diets (15 to 21 days of age).

The experimental diets were balanced for digestible amino acid contents, according the nutritional requirements established by Rostagno et al. (2011Rostagno HS, Albino LFT, Donzele JL, Gomez PC, Oliveira RF, Lopes DC, et al. Tabelas brasileiras para aves e suínos: composição de alimentos e exigências nutricionais. 3.ed. Viçosa: UFV; 2011.), and the nutritional recommendations of Silva & Costa (2009Silva JHV, Costa FGP. Tabelas para codornas japonesas e européias. 3.ed. Jaboticabal: Funep; 2009. p.79 - 82.), except for digestible lysine, which level was 8.5% lower than the recommendations. Dietary digestible methionine+cystine ratios were estimated according to Castro (2014Castro MR. Relações metionina + cistina: lisina digestíveis para codornas de corte [dissertation]. Diamantina (MG): Universidade Federal dos Vales do Jequitinhonha e Mucuri; 2014.). The amino acid to lysine ratios proposed by Silva & Costa (2009) were applied, except for digestible threonine (Tables 1, 2 and 3). All amino acids, except for digestible lysine and threonine, were included at 3% higher levels than those recommended in order to ensure the supply of their requirements.

Performance parameters and intestinal morphometry

The performance parameters evaluated were feed intake (g/bird), threonine intake (mg/bird), weight gain (g/bird), feed conversion ratio (g/g) and livability (%).

Small intestine morphological parameters were evaluated in 8-d-old birds. Eight birds per treatment were selected according to the average weight of each replicate and sacrificed. The duodenum, jejunum and ileum were opened in the mesenteric region and fragments of approximately 2.0 cm in length were stretched by the serous tunic and fixed in commercial formaldehyde at 4%. Samples were dehydrated in graded ethanol series, cleared in xylol, embedded in paraffin and cut into 5-µm sections (Prophet et al., 1992Prophet EB, Millis B, Arrington JB, Sobin LH. Laboratory methods in histotechnology. Washington: America Registry of Pathology; 1992. p.275.). Three slides were prepared using three semi-serial sections of each intestinal fragment (duodenum, jejunum, ileum). Two slides were stained with hematoxylin-eosin, while the third was stained with Alcian blue and hematoxylin-eosin. Images (5x magnitude) were obtained using an optical microscope and a Leica Qwin camera. Straight-line lengths of 30 villi of each intestinal segment were randomly measured using the software ImageJ, and are expressed in µm.

Statistical analysis

The obtained data were tested for normality and homoscedasticity, and then subjected to analysis of variance, and then to polynomial linear, quadratic and linear response plateau regression models. The software package Sistemas de Análises Estatísticas e Genéticas (SAEG, 2007Sá LM, Gomes PC, Cecon PR, Rostagno HS, D'agostini P. Exigência nutricional de treonina digestível para galinhas poedeiras no período de 34 a 50 semanas de idade. Revista Brasileira de Zootecnia 2007;36(6):1848-4853.) was used for statistical analyses.

RESULTS AND DISCUSSION

Average environmental temperatures recorded during the experimental periods were 35º C±1.26 (minimum) and 38º C±0.88 (maximum) during the pre-starter phase (1 to 7 days age); 34º C±1.39 (minimum) and 37 ºC±0.95 (maximum) during the starter phase (8 to 14 days age); and 31º C±1.30 (minimum) and 34º C±1.15 (maximum) during grower I phase (15 to 21 days age). According to Sousa (2013Sousa, MS. Determinação das faixas de conforto térmico para codornas de corte de diferentes idades [dissertation]. Viçosa (MG): Universidade Federal de Viçosa; 2013.), the thermal comfort range for meat-type quails is 36-39ºC during the first week, 27-30ºC during the second week, and 24ºC during the third week of age. Consequently, during the pre-starter phase, temperature values were close to the quails’ thermal comfort range, whereas during the starter and grower I phases, birds experienced heat stress, which may have reduced their feed intake and productivity.

In Experiment 1, evaluating the pre-starter phase (1 to 7 days old), increasing digestible Thr:Lys ratios resulted in a linear (p<0.01) increase in feed intake (FI), Thr intake (TI) and weight gain (WG), as estimated by the equations: FI = 25.366 + 13.416X, R² = 0.88; TI = -10.025 + 57.567X, R² = 0.99; and WG = 16.943 + 12.013X, R² = 0.94 (Table 4). Using the LRP model, an optimal ratio Thr:Lys of 0.85% was estimated for maximum FI (36.83 g), according to the equation: FI = 36.8314 - 14.052 (0.848 - X), R² = 0.99. The digestible Thr:Lys ratios recommended by Silva & Costa (2009Silva JHV, Costa FGP. Tabelas para codornas japonesas e européias. 3.ed. Jaboticabal: Funep; 2009. p.79 - 82.) for meat-type quails during the starter phase (1 to 21 days old) and by Rostagno et al. (2017Rostagno HS, Albino LFT, Hannas MI, Donzele J, Sakomura NK, Perazzo FG, et al. Tabelas brasileiras para aves e suínos. composição de alimentos e exigências nutricionais. 4.ed. Viçosa: UFV; 2017.) for Japanese quails during the starter phase (1 to 14 days old) are 76% and 67%, respectively. Amino acids requirement estimates to achieve optimal performance are influenced by age, growth phase, lean meat accretion rate, dietary protein levels, and the statistical methods applied (Rangel-Lugo et al., 1994Rangel-Lugo M, Su CL, Austic RE. Threonine requirement and threonine imbalance in broiler chickens. Poultry Science 1994;73:670-681.; Smith et al., 1998Smith, ER, Pesti GM, Bakalli RI, Ware GO, Menten JFM. Further studies on the influence of genotype and dietary protein on the performance of broilers. Poultry Science 1998;77:1678-1687.; Kidd, 2000Kidd MT. Nutritional considerations concerning threonine in broilers. World's Poultry Science Journal 2000;56:139-151, Rosa et al., 2001Rosa AP, Pesti GM, Edwards HMJR, Bakalli RI. Threonine requirements of different broiler genotypes. Poultry Science 2001; 80:1710-1717.; Dozier et al., 2015Dozier WA, Meloche KJ, Tillman PB, Jiang Z. Growth performance of male broilers fed diets varying in digestible threonine to lysine ratio from 1 to 14 days of age. Poultry Science 2015;4:457-462.). Furthermore, Silva et al. (2012) compared the genotypes of European and Japanese quails and reported that, although the protein and energy requirements of European quails are similar to those of Japanese quails, European quails require higher amino acids levels, possibly due to their higher growth rate and a heavier body weight.

Table 4
Growth performance of meat-type quails fed increasing digestible Thr:Lys ratios from 1 to 7 days of age (pre-starter phase).

In Experiment 2, evaluating the starter phase (8 to 14 days old), no effects of digestible Thr:Lys ratios were detected (p>0.05) on weight gain and feed conversion ratio. However, linear and quadratic effects (p<0.01) were observed on feed intake, given by the equations: FI = 84.400 + 9.252X, R2= 0.38; and FI= 190.01 - 271.69X + 185.24X2, R2=0.90, respectively. The quadratic model estimated 0.73% digestible Thr:Lys ratio at the lowest feed intake (90.38%), after which feed intake gradually increased. Threonine intake (TI = -8.249 + 124.754X; R² = 0.98) linearly increased as dietary digestible Thr:Lys ratio increased (p<0.01) (Table 5). Adequate threonine intake is important particularly during more advanced growth stages in quails with high potential for lean meat accretion, because threonine requirements for maintenance is proportionally high relative to the other amino acids due to its high content in endogenous intestinal secretions (Fernandez et al., 1994Fernandez SR, Aoyagi S, Han Y, Parsons CM, Baker DH. Limiting order to amino acids in corn and soybean meal for growth of the chick. Poultry Science 1994;(73)12:1887-1889.; Kidd 2001Kidd MT. Lysine and threonine needs of commercial broilers. Proceedings of Ajinomoto Hearthand Poultry Symposium; 2001; Nashville, Tennessee. USA, 2001, p.128.; Sigolo et al., 2017Sigolo S, Zohrabi Z, Gallo A, Seidavi A, Prandini A. Effect of a low crude protein diet supplemented with different levels of threonine on growth performance, carcass traits, blood parameters, and immune responses of growing broilers. Poultry Science 2017; 96(10):3517-3804.). Ton et al. (2013Ton APS, Furlan AC, Martins EL, Batista E, Pasquetti TJ, Scherer C, et al. Nutritional requirements of digestible threonine for growing meat-type quails. Revista Brasileira de Zootecnia 2013;42:504-510.) evaluated the digestible threonine requirements for 1- to 14-d-old meat-type quails, and reported a quadratic effect on feed intake and weight gain, estimating a requirement of 12.60 g digestible threonine/kg of diet, which is equivalent to a 67% Thr:Lys ratio. Dozier et al. (2015Dozier WA, Meloche KJ, Tillman PB, Jiang Z. Growth performance of male broilers fed diets varying in digestible threonine to lysine ratio from 1 to 14 days of age. Poultry Science 2015;4:457-462.) reported an average minimum digestible Thr:Lys ratio of 0.67% for 1- to 14-d-old male broilers for weight gain and feed conversion ratio. In the present study, increasing dietary digestible Thr:Lys ratios reduced quail livability, as estimated by the linear (LIV = 114.65 - 20.556X, R2=0.50) and quadratic (LIV= -52.789 + 423.257X - 291.588X2, R2= 0.85) equations (Table 6).

Table 5
Growth performance of meat-type quails fed digestible Thr:Lys ratios from 8 to 14 days of age (starter phase).

The effects of dietary digestible Thr:Lys ratios on the performance of quails during grower phase I (15 to 21 days old; Experiment 3) are shown in Table 6. Threonine intake (TI = -3.819 + 172.516X; R² = 0.99) linearly increased as dietary digestible Thr:Lys ratios increased (p<0.01) as a result of Thr supplementation in the diets. However, body weight linearly decreased, as determined by the equation: WG = 79.651 - 22.673X (R2= 0.76. Harper et al (1970Harper AE, Benevenga NJ, Wohlheter, RM. Effects of ingestion of disproportionate amounts of amino acids. Phisiological Reviews 1970; (50):428-558.) reported that amino acids in excess did not cause signs of toxicity, differ substantially from those considered to be toxic in their ability to depress feed intake, and threonine is one of the least toxic amino acids. Thus, the evaluated increasing Thr:Lys ratios did not influence feed intake due to the limited effect of an excess of threonine on feed intake depression. However, quail weight gain was negatively influenced possibly due to excessive dietary nitrogen, which demands rapid removal, catabolism and excretion of the amount ingested in excess of the requirements, resulting in excess of uric acid in the excreta. Therefore, energy will be utilized to eliminate that nitrogen excess rather than being used for protein synthesis.

Table 6
Growth performance of meat-type quails fed digestible Thr:Lys ratios from 15 to 21 days of age (grower I phase).

Increasing dietary Thr:Lys ratios also linearly increased feed conversion (FCR = 1.500 + 0.871X, R2=0.75). The best Thr:Lys ratio to achieve the highest weight gain (64.75 g) and the best feed conversion ratio (2.072) was estimated as 0.66%. Although Rostagno et al. (2017Rostagno HS, Albino LFT, Hannas MI, Donzele J, Sakomura NK, Perazzo FG, et al. Tabelas brasileiras para aves e suínos. composição de alimentos e exigências nutricionais. 4.ed. Viçosa: UFV; 2017.) recommended a digestible Thr:Lys ratio of 0.734% for 15- to 35-d-old Japanese quails, the results of the present study indicate that Thr:Lys ratios higher than 0.66% have a negative effect on performance parameters. These results are in agreement with the findings of Edmonds & Baker (1987Edmonds MS, Baker DH. Comparative effects of individual amino acid excesses when added to corn-soybean meal diet: effects on growth and dietary choice in the chick. Journal Animal Science 1987;65:699-705.), Carew et al. (1998Carew LB, Evarts KG, Alster FA. Growth, feed intake, and plasma thyroid hormone levels in chicks fed dietary excesses of essential amino acids. Poultry Science 1998;77:295-298.), and Sigolo et al. (2017Sigolo S, Zohrabi Z, Gallo A, Seidavi A, Prandini A. Effect of a low crude protein diet supplemented with different levels of threonine on growth performance, carcass traits, blood parameters, and immune responses of growing broilers. Poultry Science 2017; 96(10):3517-3804.), who reported that excessive Thr supply reduces broiler feed intake and growth rate. Wang et al. (2007Wang X, Qiao S, Yin Y, Yue L, Wang Z, Wu G. A deficiency or excess of dietary threonine reduces protein synthesis in jejunum and skeletal muscle of young pigs. Journal of Nutrition 2007;137:1442-1446.) observed that excessive dietary threonine reduced the synthesis of intestinal mucus proteins, mucin and muscle protein in weaned piglets, and impaired their performance. According to those authors, a possible explanation would be a reduction in the absorption of neutral amino acids (including branched-chain amino acids) because they share common transport system with threonine, consequently limiting protein synthesis. Rossoni et al. (2008Rossoni MC, Donzele JL, Oliveira RFM, Silva FCO, Abreu MLT, Kill JL, et al. Níveis de treonina digestível para suínos machos castrados, de alto potencial genético para deposição de carne, na fase de terminação. Arquivo Brasileiro de Medicina Veterinária e Zootecnia 2008;60:884-889.) also reported a negative effect of excessive dietary threonine on pig feed intake and fat deposition. Ospina-Roja et al. (2014Ospina-Roja IC, Murakami AE, Eyng C, Picoli K P, Scapinello C, Duarte CRA. Threonine-lysine ratio on the requirements of digestible lysine in diets for broilers. Acta Scientiarum Animal Science 2014;36:157-162.) attributed the worse performance observed in 22- to 42-d-old broilers fed digestible Thr:Lys ratios higher than 57% to impaired protein synthesis caused by dietary amino-acid imbalance. According to those authors, the deamination of threonine excess relative the other amino acid into uric acid requires energy, which consequently impair animal performance.

The evaluated digestible Thr:Lys ratios did not influence (p>0.05) duodenal or jejunal villus height. However, ileal villus height linearly increased as Thr:Lys increased (VHi = 77.07 + 284.00X; R2=0.89), as shown in Table 7. It is important to highlight that the quails evaluated in this study were reared under controlled conditions (environment and disease control), which may explain this effect. Ospina-Roja et al. (2013Ospina-Roja IC, Murakami AE, Oliveira C AL, Guerra AFQG. Supplemental glycine and threonine effects on performance, intestinal mucosa development, and nutrient utilization of growing broiler chickens. Poultry Science 2013;92:2724-2731.) reported that healthy broilers fed diets that supplied their threonine requirements and containing amino acid levels in excess of their requirements did not present any small intestine morphological changes. Moreover, proteins involved in physiological functions have high threonine content, which requirements increase under health challenges due to the strong stimulation of the body’s defense systems, increasing mucus secretion and antibody synthesis (Ajinomoto, 2003). Reis et al. (2016Reis JS, Dionello NJL, Nunes AP, Lopes DCN, Gotuzzo AG, Tyska DU, Rutz F. Morfometria intestinal em codornas de corte alimentadas com treonina digestível. Arquivo Brasileiro de Medicina Veterinaria e Zootecnia 2016; 68:983-990.), evaluating dietary digestible threonine levels (0.98, 1.04, 1.10 and 1.16%) for starter: meat-type quails (1 to 21 days old), estimated a requirement of 1.1% for optimal villus height in the duodenum, jejunum and ileum.

Table 7
Effects of different dietary digestible Thr:Lys ratios on the intestinal morphological parameters of meat-type quails during the pre-starter phase (1 to 7 days of age).

The observed increase in villus height indicates that efficiency of nutrient (amino acids) digestion and absorption. According to Rutz (2002Rutz F. Proteínas: digestão e absorção. In: Macari M, Furlan RL, Gonzales E. Fisiologia aviária aplicada a frangos de corte. 2.ed. Jaboticabal: Funep; 2002. p.135-141.), large membrane carriers are located in the ileum, suggesting that this is the main site of threonine absorption. Similarly, Macari & Maiorka (2000) reported that the development of the intestine mucosa is characterized by an increase in villus height and density, corresponding to an increase in the number of epithelial cells and consequent better nutrient digestion and absorption. On the other hand, Ospina-Roja et al. (2013Ospina-Roja IC, Murakami AE, Oliveira C AL, Guerra AFQG. Supplemental glycine and threonine effects on performance, intestinal mucosa development, and nutrient utilization of growing broiler chickens. Poultry Science 2013;92:2724-2731.), evaluating the effects of glycine and threonine supplementation on the performance and intestinal mucosa development of growing broilers (21-35 days old), reported that increasing dietary glycine+serine and threonine levels enhanced mucin secretion, but had no effect on villus height. Significant amounts of threonine are required by growing poultry, particularly for maintenance, due to their high body protein turnover rate (Sá et al., 2007). According to Myerie et al. (2001) and Berres et al. (2007Berres J, Vieira SL, Coneglian JLB, Olmos AR, Freitas DM, Bortolini TCK, et al. Respostas de frangos de corte a aumentos graduais na relação entre treonina e lisina. Ciência Rural 2007;37:510-517.), approximately 60% of dietary threonine is retained in the intestine for mucin synthesis. However, because mucin is resistant to digestion, it is fermented by intestinal microorganisms or excreted in feces, and therefore, is not utilized for body protein synthesis.

CONCLUSION

The estimated digestible Thr:Lys ratios recommended for meat-type quails are 0.85, 0.73 and 0.66%, for the pre-starter, starter and grower I phases, respectively.

ACKNOWLEDGMENTS

The authors wish to thank Fundação de Apoio a Pesquisa do Estate of Minas Gerais (FAPEMIG) for the financial support provided and to Ajinomoto Brazil® for the donation of the amino acids.

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Publication Dates

  • Publication in this collection
    05 June 2020
  • Date of issue
    2020

History

  • Received
    10 Oct 2019
  • Accepted
    10 Feb 2020
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