1. Introduction
The growing period of a laying hen is the most critical time in a hen’s life and the mistakes made during this period are difficult to rectify [
1]. Many factors, e.g., quantitative or qualitative feed restriction [
2,
3], feed program [
4,
5], and nutritional imbalance [
4,
6], in the starter, grower, and/or developer phases were reported to affect the growth curve, early egg weight, and sexual maturity of pullets and, consequently, egg production. Therefore, the maximum genetic potential can only be achieved when the bird is provided with all its nutritional requirements [
7,
8], especially when the objective is to extend the productive life of laying hens.
During the pullet-rearing period, the focus is mainly on managing pullet body weight and body weight uniformity. However, current pullet feeding programs can lead to pullets of similar body weight but with markedly different body compositions, which may affect life production [
9]. Advances in genetic selection produced pullets quite different to those from only a few years ago. In the literature, there are reports regarding nutritional recommendations for egg-type hens during the rearing and laying period [
10,
11]; however, information is still needed on combined feeding strategies between both periods in modern lines of hens. The effects of dietary balanced protein for hens in the rearing phase and its impact on the long-term laying cycle were not investigated so far.
The ideal supply of digestible amino acids during pullet formation is essential to ensure the growth of organs, muscles, and the skeleton [
12], while in the productive period, this contribution is essential for body maintenance and for egg component development [
13]. Thus, the lack of balance of essential amino acids in the diet can affect pullet formation and its performance in the laying phase [
14,
15]. In this context, we hypothesize that balanced protein levels affect pullet formation, leading to a shift in the long-term laying cycle, and the repletion in dietary balanced protein may recover the responses of laying hens; therefore, the aim of the present research is to evaluate the impact of depletion and repletion in dietary balanced protein on body composition, performance, and egg quality in laying hens submitted to low and high dietary protein during the rearing period.
2. Materials and Methods
2.1. Ethics Approval
All procedures described were approved by the Ethical Committee on the Use of Animals of the School of Agrarian and Veterinary Sciences, São Paulo State University (UNESP), Jaboticabal, São Paulo, Brazil (Process 012598/2018); approved on 14 February 2019.
2.2. Birds, Husbandry, and Experimental Design
Four hundred Lohmann LITE LSL-NA were obtained from a local commercial facility (Planalto Postura LTDA) at one day old and raised in conventional cages according to genetic guideline recommendations prior to the beginning of the trial. At eight weeks of age, pullets were moved to wire-rearing cages (375 cm2 per pullet) and moved again at 19 weeks of age to wire-laying cages (563 cm2 per hen). Each cage was equipped with a feeder and nipple drinker. Temperature, humidity, and lighting were maintained according to the recommendation of the Lohmann LSL-NA Management Manual (Lohmann Tierzucht GmbH, Cuxhaven, Germany).
At the start of the trial (eight weeks of age), 400 pullets were individually weighed (0.592 ± 0.012 kg) and moved to 20 cages to which two treatments (low and high dietary balanced protein) were randomly assigned, performing 10 replicates of 20 pullets each. At 19 weeks of age, each treatment was separated in two (1-low, 2-high, 3-repletion, and 4-depletion in dietary balanced protein), giving a total of four treatments randomly distributed in five replicates each. During each experimental period, water and feed were provided ad libitum. The lighting program was set at 24 h light at the first week, reduced gradually to 12 h light and 12 h dark up to 10 weeks of age, and maintained until the pullets achieved 5% of egg production (20 weeks of age). After the onset of egg production, the lighting program was gradually increased from 12 to 16 h of light and kept constant up to 102 weeks of age.
A three-phase feeding program was used in the rearing period: grower (8–11 w-old), developer (12–15 w-old), and pre-layer (16–18 w-old); while a five-phase feeding program was used for the laying period: Layer 1 (19 to 26 w-old), Layer 2 (27 to 46 w-old), Layer 3 (47 to 66 w-old), Layer 4 (67 to 82 w-old), and Layer 5 (83 to 102 w-old).
2.3. Experimental Feeds
Experimental feeds consisted of two levels of dietary balanced protein, herein named low (L) and high (H). Dietary balanced protein was defined as a constant ratio of essential amino acids with lysine [
16], and the ratio was the same proposed by the breeding company (Lohmann Tierzucht GmbH, Cuxhaven, Germany). Standardized ileal digestible lysine (SID-Lys) was used as a reference to produce the two levels of dietary balanced protein. The remaining nutrients and energy in the feed were as recommended by the guideline [
10].
The grower, developer, and pre-layer feeds contained, respectively, 0.65, 0.56, and 0.59% of SID-Lys for L feeds and 0.96, 0.84, and 0.89% of SID-Lys for H feeds (
Table 1).
In the laying period (from 19 to 102 weeks of age), half replications continued receiving the L or H dietary balanced protein feeds (LL and HH), and the other half was submitted to repletion (LH) or depletion (HL), where subsequent letters indicate the feed supplied on rearing and laying phases, respectively. In the layer period, each one of the five feeds contained, respectively, 0.54, 0.52, 0,50, 0.48, and 0.46% of SID-Lys for L feeds and 0.82, 0.79, 0.75, 0.73, and 0.70% of SID-Lys for H feeds (
Table 2).
2.4. Performance Data
In the rearing period, cumulated feed intake and body weight were determined at 18 weeks of age. Mortality was registered daily and used to correct the feed intake. During the laying phase, egg production and mortality were recorded daily. Once a week, all eggs produced in one day were weighed and the egg mass was calculated. Feed intake was determined fortnightly and corrected for mortality. The age at sexual maturity was determined for each experimental unit and was defined as the age at 50% of egg production. Hen-housed egg production was calculated as the total number of eggs produced per number of housed hens at 19 w-old.
2.5. Body Composition
Laying hens selected at the beginning of the trial were individually scanned using dual-energy X-ray absorptiometry (DXA, Hologic-QDR
® model 13.4.2., Marlborough, MA, USA). In the rearing phase, DXA measurement was performed on the last day of each feeding phase, whereas in the laying phase, measurements were taken every 28 days. The same birds were scanned over time. For that, a total of 16 pullets per treatment were used in the rearing phase and 8 hens per treatment in the laying phase. The same hens were scanned over time. Prior to each scan, hens were fasted for five hours, weighed, anesthetized with isoflurane (2%) diluted in 100% of oxygen, and positioned in dorsal decubitus with the wings and legs flexed [
17]. The fat mass (g), lean mass (water + protein content, g), bone mineral content (g), and bone mineral density (g/cm
2) were registered. Alves et al. [
17] equations were used to estimate the ash, fat, and protein content, as described below:
where
is Euler’s number,
is the natural logarithm,
is the bone mineral content (g),
is the lean mass (g),
is the fat mass (g), and
is the body weight (g), obtained by DXA.
2.6. Egg Traits and Egg Components Measurement
Every four weeks, three eggs per experimental unit were sampled in three sequential days, totaling nine eggs per experimental unit. The eggs were individually weighed and numbered. The egg components, albumen, yolk, and dry eggshell were measured. Before measurement, the eggshell was washed with tap water and dried using a forced oven at 55 °C for 24 h. Additionally, the strength and shell thickness were analyzed using the Nabel Digital Egg Tester 6000® (Kyoto, Japan).
2.7. Statistical Analysis
The feed intake, body weight, and body composition measured during the rearing period were analyzed with one-way ANOVA, using a generalized linear model. In the laying phase, the age at sexual maturity and hen-housed egg production were evaluated with one-way ANOVA, and other responses were evaluated as a two-factor repeated measure to determine the effects of dietary treatments over time, using a mixed model. Fixed factors are represented by the four treatment groups (LL, LH, HH, and HL) and the age of the hens, whereas the experimental unit represents the random factor. The data were analyzed considering 21 cycles of 4 weeks each. Orthogonal contrasts were elaborated to investigate the effects of repletion (LL vs. LH) and depletion (HH vs. HL) in dietary balanced protein. Differences were considered to be significant at a probability of 5%. The Statistical Analysis System (SAS Institute Inc., Cary, NC, USA) was used to perform both a one-way ANOVA and the two-factor repeated measure analysis procedures.
To investigate how the responses differed between treatment groups over time, non-linear regression with groups was used, the groups being the dietary balanced protein [
18]. The average data per replicate were treated as the experimental unit. Two exponential models were applied and those with the lower Akaike information criterion value [
19], were used to describe the response variable in function of age (weeks). The models used were:
where
and
are the y-intercept and slope of the linear segment, respectively,
is the y-intercept of the exponential segment, and
is the exponential base.
where
is the y-intercept, and
is the exponential base.
4. Discussion
The nutrition given to laying hens in the rearing phase may influence the growth and, consequently, their degree of body maturity. However, it is well known that sexual maturity is most influenced by the photoperiod, with body weight having a minor effect [
20], opening an opportunity to change the pullet’s nutrition without affecting the sexual maturity, but the hens’ response over long-term egg production needs to be investigated. The objective herein was to evaluate laying hens regarding the effect of dietary balanced protein given in the rearing phase and how they respond to a repletion or depletion in dietary balanced protein in the laying phase. We hypothesized that offering a low dietary balanced protein feed to pullets from 8 to 18 weeks of age would produce a lighter hen with, perhaps, higher body fat content when compared with a hen consuming a high balanced protein feed. Those differences would have a minimum impact on the age at sexual maturity, but the low dietary balanced protein feed would not be sufficient to sustain a high egg production or egg mass. An even more interesting question to be answered is whether those effects are reversible if the dietary balanced protein is repleted in the laying phase.
In this study, the age at sexual maturity (50% of egg production) was influenced by the feed given in the rearing phase, where pullets in the higher dietary balanced protein feed reached sexual maturity approximately 7 days before, which may have elicited an increase in feed intake prior to the laying hens consuming the L feed, minimizing the difference in cumulated feed intake at the end of the rearing phase (18 weeks of age). In fact, the results published elsewhere by Da Nóbrega et al. [
21] demonstrate an increase in feed intake due to a reduction in dietary balanced protein, which is minimized when pullets approach 15 weeks of age. According to Bendezu et al. [
22], the development of the ovary and oviduct is maximized around 15 to 16 weeks of age, which affects the needs for energy and nutrients and, consequently, feed intake. Body weight, on the other hand, was clearly affected by dietary balanced protein, with no effect on body composition. Those results indicate that pullets from distinct groups were at a different degree of body maturity, which may also influence the age at sexual maturity. Lewis and Morris [
20] found evidence that laying hens maintained in the same photoperiod but with different body weights achieved the onset of lay and the age at sexual maturity on different days, corroborating our observations. However, the aforementioned authors highlighted that the photoperiod has much more influence on the onset of lay than body weight.
The rate of sexual maturation is coordinated by hormones such as the luteinizing hormone (LH) and follicle-stimulating hormone (FSH), produced in the pituitary gland [
23]. The release of LH and FSH is stimulated by the gonadotropin-releasing hormone (GnRH), produced in the hypothalamus [
24], also referred to as the extra-retinal or deep encephalic photoreceptor, since light perceived in this region of the brain will control the secretion of GnRH. A system called the hypothalamo–hypophyseal–gonadal axis allows the GnRH to reach the pituitary gland and initiate the release of LH and FSH [
23]. Another hormone that also controls the LH and FSH release is the gonadotropin inhibitory hormone (GnIH). The GnIH, also produced in the hypothalamus, is antagonistic to GnRH and will prevent the pituitary from releasing the LH and FSH hormones [
25]. Both GnRH and GnIH are peptide hormones, thus, requiring a receptor in the site of action to bring about its function. The GnIH receptors in the pituitary are reported to decrease in Lohmann hens between 17 to 20 weeks of age, while the GnRH receptors increase at the same age [
26]. Those events may increase the release of LH and FSH and contribute to the onset of lay. A possible explanation for the shift in the age at sexual maturity for hens submitted to the same photostimulation but consuming different levels of dietary balanced protein is that a delay in the degree of body maturity observed in hens consuming the L feed may also delay the changes in GnRH and GnIH receptors in the pituitary gland, but this hypothesis needs to be tested.
The objective to produce different laying hens at the end of the rearing phase was achieved, but the body composition was similar between groups. The effect of dietary balanced protein over body fat is well documented in the literature for broilers and breeders [
27,
28]. Those studies report that body fat percentage increases with the reduction in dietary balanced protein. Our results demonstrate that body fat content was similar between treatment groups at the end of the rearing phase, showing a different trend from the ones reported for broilers and breeders. One may expect that reducing dietary balanced protein would reduce the amount of protein available for deposition, and hence, the energy once used for protein deposition would be available for lipid deposition. These events become especially true if the feed intake is constant or increases with the reduction in dietary balanced protein. However, our observations suggest that this is not the case for growing pullets after eight weeks of age. The degree of body maturity may, again, be one possible explanation. The reduction in dietary balanced protein delays the body protein deposition and, perhaps, the development of reproductive organs in laying hens. As the hens approach their sexual maturity, the development ratio of the ovary and oviduct increases rapidly, and lipid deposition in the ovary contributes mostly to such an increase [
22]. Since laying hens in the H group were advanced in body development, their ovary and oviduct development may have started earlier when compared with hens in the L group, increasing the lipid deposition in the body and minimizing the differences from pullets consuming the L feed.
Once in production, it is useful to know if the consequences of giving a low protein feed in the rearing phase can be reversed. For that, a repletion treatment was included in the treatment design. The overall results demonstrate that repleted hens (LH) increased all responses evaluated, with an exception for daily feed intake and eggshell traits. The data presented (
Table 5) demonstrate that repletion in dietary balanced protein could be a strategy to recover a pullet that reaches sexual maturity with low body weight. In addition, there may be an economic benefit to reduce balanced protein in the feed because the feed price would decrease [
27]. Since feed intake was similar between groups, the feeding cost (feed intake x feed price) would also reduce. The egg mass was similar between hens consuming the H feed in the laying phase (LH and HH), suggesting that the revenue obtained from either group of hens would be the same. Nevertheless, an economic investigation is necessary to better understand this issue, which was not the goal of this study. Another issue that is worth investigating is related to the effects of depletion in dietary balanced protein. The change in the price of feed ingredients may trigger nutritionists to reduce the price of a feed formula, sometimes by reducing the dietary balanced protein level. To properly evaluate the laying hens’ response due to a reduction in dietary balanced protein, the current status of the bird needs to be accounted for.
We showed herein that laying hens receiving a high dietary balanced protein feed in the rearing phase were able to increase feed intake at the beginning of egg production when dietary balanced protein was depleted. As a result, this group of birds had the highest lipid content in the body, even though, on average, such a difference was not statistically different from hens in the HH group, possibly because to recover the amount of dietary balanced protein that was removed from the feed, laying hens would need to increase their feed intake approximately 40%, which was, perhaps, beyond the intestinal bulk capacity of these hens. In this study, to reduce dietary balanced protein, it was necessary to include more wheat bran in the feed compared with other treatments. That might have limited the bulk capacity of the gastrointestinal tract, constraining the feed intake. Recently, Nascimento et al. [
29] demonstrated that broiler breeders could increase their feed intake as the feed was diluted to achieve their nutrients and energy needs, but the intake of feed decreased at a higher dilution.
An interesting piece of data produced in this study is the time necessary to change the response of laying hens when a repletion or a depletion feed is offered. According to the repeated measures analysis, it took 11 weeks to detect a difference in egg production between groups, while for egg weight and egg mass, seven weeks after the beginning of the repletion and depletion treatments were necessary to affect those variables. The nonlinear regression also indicates that the ratio of increase for each mentioned variable was different, which is demonstrated in
Figure 2. A decrease in egg production, egg weight, and egg mass was reported in laying hens consuming crescent levels of dietary balanced protein from 26 to 77 weeks of age [
30]. The pattern of body chemical components over time changed consistently after 50 weeks of age, especially for body fat. Laying hens in the LL group demonstrated the lowest body fat content compared to the other treatments. The reduction in body fat content for laying hens consuming a low dietary balanced protein feed was not expected; however, Kumar et al. [
31] found a quadratic response in abdominal fat in function of dietary balanced protein concentration.
In the present study, the results from repletion and depletion groups might require a separate interpretation. When compared with hens from the LL group, the higher value of body fat content observed in repleted hens might be related to the lipid content in the ovarium, since those hens produced eggs with heavier yolk. On the other hand, compared with the HH group, depleted hens increased body fat deposition, possibly due to an increase in feed intake during the first weeks after the depleted feed was offered, increasing energy intake. In either situation, any conclusion over the dynamics of body fat content in laying hens should be carefully evaluated, and more studies are necessary to better elucidate this response.
In this study, the results observed for egg production and egg weight suggest that the feed offered in the rearing phase has little influence on those responses. The hen-housed egg production, however, was influenced only by the feed offered in the rearing phase (LL + LH vs. HH + HL). The observed differences might be a consequence of the viability observed during the trial. The viability of laying hens consuming the L feed during the rearing phase was 87.5%, whereas hens consuming the H feed had a viability of 90%. Grossman et al. [
32] suggest that hens with similar rates of egg production may have different egg production curves, mainly due to persistency. The persistency in egg production is defined as the decline ratio observed over time [
33,
34]. In this study, the parameter C in the equation adjusted for egg production in function of time is related to a declining ratio after the maximum point (peak of egg production). The results indicate that laying hens in the LL group reduced their egg production after the peak faster than the other groups, followed by HH, LH, and HL.