1. Introduction
Phosphorus (P) is an indispensable nutrient for birds and has important impacts on various physiological functions, especially in the formation of eggshells and skeletal development [
1] and in working together with calcium to maintain bone mineralization [
2]. Phosphorus deficiency may result in abnormal growth and development, bone diseases, digestive tract problems, impaired immune systems, and reduced eggshell quality in birds [
3]. Most P in poultry diets is in the form of phytate P, and P availability in birds is less than 40% [
4,
5]. This necessitates dietary supplementation with inorganic P and exogenous phytase to meet the P requirements for optimal animal growth and production. However, several studies have shown increased P retention and utilization and reduced P excretion into the environment as a result of adding phytase to poultry diets [
6,
7]. However, the efficiency of exogenous phytases remains a challenge because it is affected by various physical, chemical, and biological factors [
8]. Excess P is discharged in feces and retained in the soil, resulting in a decline in soil quality [
9]. Therefore, to avoid excessive inorganic P in bird diets for maximal growth and bone development, the minimum P requirements of birds should be fully investigated.
Non-phytate P (NPP) recommendations for birds are mainly based on the National Research Council’s (NRC) guidelines [
10]. The NPP requirements of laying hens vary significantly at different stages of growth and development due to their differing physiological characteristics [
11,
12,
13]. In addition, most of the existing experiments were conducted with broilers, and it is known that the sex and breed of birds are two factors that influence their nutritional requirements [
14,
15]. Although layer chicks grow slower than broilers during the brooding period (1–42 d), this period is equally crucial for layer chicken farming. Adequate early nutrition is essential for the growth and health of layer chicks and their health and production performance in later stages [
16,
17,
18].
Jing Tint 6 layer chicks are a breed based on Rhode Island Red and White Leghorn with high egg yield, low mortality, excellent egg quality, and modest body weight; as such, they make up more than 1/4 of the market for laying hens in China [
19,
20,
21]. The amino acid requirements of Jing Tint 6 layer chicks aged 1–42 d of age have been well assessed [
20]; however, micronutrient requirements, such as phosphorus, still need to be evaluated. Therefore, this study aimed to investigate the optimal dietary P levels in Jing Tint 6 layer chicks from hatching to d 42. Non-linear models based on the criteria of tibia length, growth performance, and serum parameters, combined with the factorial method, were used to obtain the most accurate estimates possible for the NPP requirements of Jing Ting 6 layer chicks.
2. Materials and Methods
This study was conducted following the guidelines of the National Act on the Use of Experimental Animals (People’s Republic of China). All animal procedures were approved by the Animal Welfare Committee of the Institute of Subtropical Agriculture, Chinese Academy of Sciences (IACUC # 201302).
2.1. Experimental Diets
Corn–soybean meal-based diets were formulated to meet the nutrient requirements according to the NRC (1994) [
10] (
Table 1). The NPP levels were 0.36, 0.41, 0.46, 0.51, and 0.56%, respectively. Samples of each diet were analyzed for calcium, crude protein, and total P following AOAC International (2016) [
22]. Metabolizable energy (ME) and other dietary nutrient values were calculated according to the China Feed Database [
23].
2.2. Birds and Housing
A total of 720 chicks procured from a commercial supplier (Beijing Huadu Yukou Poultry Industry Co., Ltd., Beijing, China) were weighed and randomly allocated to 5 treatments with 6 replicates of 24 birds per cage (90 cm deep × 600 cm wide × 40 cm high) at 1 d of age. Each cage was considered an experimental replicate, and each dietary treatment was fed to six replicates. The photoperiod was gradually reduced by 2 h per week from 24 to 12 h. The temperature was slowly decreased from 35 to 34 °C for 1–7 d, from 34 to 30 °C for 8–14 d, and from 30 to 24 °C for 15–42 d. The relative humidity was maintained at 65% with a 12 h/12 h light/dark cycle. During the experimental period, all birds had free access to feed and water, and the body weights and feed intake were recorded weekly.
2.3. Growth Performance
Experiments on NPP requirements were divided into two phases: phase 1, 1–14 d of age, and phase 2, 15–42 d of age. Feed consumption and the body weight of each cage were measured weekly, and the feed conversion ratio (FCR) was calculated.
2.4. Serum Biochemical Analysis
On d 14 and 42, 3 mL of blood samples were taken from a wing vein with a syringe from 2 birds close to the average weight randomly chosen from each cage, and serum was obtained via centrifugation at 3000 rpm at 4 °C for 10 min for biochemical analysis using an automated analyzer (Cobas c311, Basel, Switzerland) and commercial reagent kits (Lidman Biotech, Beijing, China). The serum biochemical indices included serum Ca, serum P, alkaline phosphatase (ALP), total protein (TP), and albumin (ALB).
2.5. Bone Characteristics
The same birds used for blood sampling were sacrificed, and their left tibias were collected and frozen at −20 °C until analyses were performed. The length and strength of the tibia were measured using an electronic universal testing machine (WDS-2000, Wenzhou, China).
2.6. Phosphorus Utilization
Titanium dioxide was incorporated into the diets (3 g/kg, as-fed) to calculate nutrient utilization using the index method. On d 10 and 38, excreta collection trays were introduced, and total excreta samples were collected during the last 3 d. Feathers and debris in the excreta were removed; it was sprayed with 10% hydrochloric acid and mixed well, and then stored at −20 °C. The collected excreta samples were thawed and mixed, dried to a constant weight at 56 °C, and ground to pass through a 0.5 mm screen before analysis. The collected excreta were analyzed for total P and Ti, which were then used to determine the apparent total tract digestibility coefficients (ATTDC) and endogenous P loss using Ti marker ratios in the diet and excreta [
15,
24].
2.7. Whole-Body Phosphorus Contents of Chickens (Carcass and Feathers)
On d 14 and 42, 2 chickens close to the average body weight were randomly selected from each cage. After weighing, the animals were euthanized using a non-bleeding asphyxiation method. The chickens were immediately scalded in hot water at 60–70 °C and then plucked. All feathers were collected in pre-weighed cotton bags, dried at 25 °C for 24 h, and then crushed to make feather samples for sealed storage. The gastrointestinal contents were discarded. The carcass was then ground using a meat grinder and mixed thoroughly before sufficient initial samples were collected and further homogenized at high speed. All samples (approximately 200 g) were collected and stored at −20 °C for further analysis. The P contents of the carcasses and feathers were analyzed to estimate the weight gain requirements using the factorial method.
2.8. Chemical Analysis
To determine the Ti concentration of the feed and fecal samples, inductively coupled plasma mass spectrometry (iCAPRQ, Schaumburg, IL, USA) was used according to the method described by AOAC International (2016) [
22]. The P of the feed and fecal samples were determined using an inductively coupled plasma optical emission spectrometer (ICP-OES Optima 8000, Waltham, MA, USA), according to the method described by AOAC International (2016) [
22]. The diets were analyzed for calcium and crude protein [
22].
2.9. Calculations for Factorial Method
Calculation of P maintenance requirement:
where P
M represents the P maintenance requirement, EP represents the endogenous P loss estimate on a DMI basis, DFI represents daily feed intake and DM represents dry matter percentage of feed.
Calculation of the P requirement for weight gain:
where P
W represents P requirement for weight gain, BWG represents daily weight gain, and Pc represents carcass and feather P concentration.
Calculation of total net P requirement:
where P
T represents the total net P requirement.
2.10. Statistical Analyses
All data were subjected to a one-way ANOVA using IBM SPSS Statistics 22 (Palo Alto, CA, USA), with the NPP level as the factor and the cage serving as the experimental unit for all statistical analyses. Regression analyses of non-linear models were performed in Origin 2023 (Northampton, MA, USA), and the best-fit models between the response criteria and dietary NPP levels were used to determine the dietary NPP requirements of the birds [
25]. The level of statistical significance was set at
p ≤ 0.05.
4. Discussion
Phosphorus participates in many metabolic pathways [
26,
27,
28] and plays an essential role in skeletal integrity [
29,
30]. In recent years, studies on phosphorus requirements have received considerable attention, and nutritionists have used various methods, including the dose–response method, factorial method, and non-linear mode, to obtain accurate requirements for different breeds and feeding stages [
13]. However, the results regarding P requirements invariably differ across studies [
11], which is partially attributed to the different breeds, diets, and methods used. In this study, non-linear models (tibia length, growth performance, and serum parameters) were combined with the factorial method to study the NPP requirements of birds and obtain the P requirements as accurately as possible.
A sufficient supply of P is critical for the growth and development of animals. In previous studies, growth performance was usually used as the target when studying the P requirements of birds [
13,
31]. However, the P availability differs when P levels vary among feeds. In low-P diets, birds improve their absorption and utilization efficiency of P while reducing the excretion of redundant P nutrients to adapt to the P levels [
32]. In addition, the P levels available differ across diets, although the total P was consistent. Thus, the NPP levels in the diets were used in the current study, and the results showed that an increase in the dietary NPP level from 0.41% or 0.46% to 0.56% had a negative impact on the growth rate at the 1–14 d and 15–42 d stages. A possible reason for the negative effect of a high-NPP diet on pullet BWG may be that the relatively high NPP reduced Ca availability [
33,
34]. However, the phosphorus requirements in other studies vary. One study reported that birds achieved their greatest weight gain with 0.38% dietary NPP for 0–14 d broilers [
35]. However, another study reported that a reduction in dietary NPP did not affect the growth performance of broilers at 0–28 d [
36]. In the current study, the optimal dietary NPP was 0.41% for 1–14 d, and 0.46% for 15–42 d, indicating the most favorable growth performance.
P is an important component of bone and is essential for bone growth and density, as it can improve the mechanical strength of bones and reduce the occurrence of fractures. Studies have shown that providing an appropriate level of P improves the bone quality and sustainability of poultry production [
1,
13]. Tibial characteristics, such as breaking strength and length, have been traditionally used in birds to evaluate bone mineralization [
13]. Compared with the concentrations of Ca or P, the ratio of Ca to NPP has been suggested to be more critical for the skeletal health of birds [
37,
38]. One study reported significant interactions between dietary Ca and NPP with the breaking strength and bone density of the tibia, which were improved when birds received 0.90% Ca and 0.40% NPP, or 1.00% Ca and 0.45% NPP [
36]. In the current study, the NPP requirement of the 1–14 d birds was 0.41% based on tibia length.
Ca and P levels in serum are considered better parameters to reflect the nutritional status of NPP in birds [
39,
40]. The changes in Ca and P homeostasis are always indicated by the levels of serum Ca and P, which are essential for bone mineralization and normal physiology [
37,
41]. The current study observed that when the NPP level in the diet increased, serum P and Ca levels tended to increase in a quadratic manner. This indicates that an NPP level of 0.41% is sufficient to meet the pullet’s requirements, which is close to the results reported by Wang [
36]. Ca or P deficiency interferes with both Ca and P homeostasis and impairs bone mineralization and growth rates [
39,
42]. Low serum P levels activate osteoclasts and decrease bone P levels to maintain P homeostasis. Additionally, serum ALB levels are a potential indicator of nutritional metabolism and health status. High dietary Ca and P levels result in a significant decrease in serum ALB [
43]. Our results suggest that when the NPP level increased, the serum ALB level tended to increase in a quadratic manner, and the calculated NPP requirement for 15–42 d birds was 0.46% based on serum ALB.
Furthermore, the apparent P digestibility is used as a parameter to track the nutritional status of birds [
44,
45]. According to the studies by Liu et al. [
15] and Xue et al. [
46], increasing dietary P and Ca may decrease their apparent digestion rates. A similar decrease was observed in the current study. An increase in dietary NPP level from 0.41 or 0.46 to 0.56% had a negative impact on the apparent P digestibility of birds from 1–14 or 15–42 d. One study reported that the output of endogenous P was 0.73–0.81 g/kg DMI in broiler chickens aged 0–15 d by setting different Ca/P ratios [
15]. These results are slightly lower than those of this study, and they may be related to the chicken breed, age in days, performance, P source, diet type, and other factors. Currently, few reports exist on the application of phosphate-free diets in China and abroad, and the exact measured value of the endogenous P output was not provided.
The methods used for nutritional requirement studies include the dose–response method (non-linear model), factorial method, and slaughter test method. Hurwitz et al. and Sun et al. have conducted numerous studies on the amino acid requirements of poultry using factorial methods [
20,
47]. The factorial analysis is a typical method for establishing dynamic models of nutrient requirements and can be used to dissect the components of nutrient requirements and nutrient utilization rates. As the tested parameters can be comprehensively applied, they are widely used to study nutritional requirements. In the current study, the individual body composition and growth performance of birds aged 1–42 d were analyzed using the factorial method, with results showing that the NPP requirements of 0–14 d and 15–42 d birds were 0.367% and 0.439%, respectively.