Plasma Metabolites and Liver Composition of Broilers in Response to Dietary Ulva lactuca with Ulvan Lyase or a Commercial Enzyme Mixture

The effect of a high incorporation level of Ulva lactuca, individually and supplemented with a Carbohydrate-Active enZyme (CAZyme) on broilers’ plasma parameters and liver composition is assessed here. Twenty one-day-old Ross 308 male broilers were randomly assigned to one of four treatments (n = 10): corn/soybean meal based-diet (Control); based-diet with 15% U. lactuca (UL); UL diet with 0.005% of commercial carbohydrase mixture; and UL diet with 0.01% of recombinant ulvan lyase. Supplementing U. lactuca with the recombinant CAZyme slightly compromised broilers’ growth by negatively affecting final body weight and average daily gain. The combination of U. lactuca with ulvan lyase also increased systemic lipemia through an increase in total lipids, triacylglycerols and VLDL-cholesterol (p < 0.001). Moreover, U. lactuca, regardless of the CAZyme supplementation, enhanced hepatic n-3 PUFA (mostly 20:5n-3) with positive decrease in n-6/n-3 ratio. However, broilers fed with U. lactuca with ulvan lyase reduced hepatic α- and γ-tocopherol concentrations relative to the control. Conversely, the high amount of pigments in macroalga diets led to an increase in hepatic β-carotene, chlorophylls and total carotenoids. Furthermore, U. lactuca, alone or combined with CAZymes, enhanced hepatic total microminerals, including iron and manganese. Overall, plasma metabolites and liver composition changed favorably in broilers that were fed 15% of U. lactuca, regardless of enzyme supplementation.


Introduction
Poultry meat is expected to represent 41% of all the protein meat sources by 2030 [1]. Macroalgae, due to their high growth rates and richness in nutritive and bioactive compounds, have emerged as sustainable alternative resources to conventional feedstuffs (i.e., corn and soybean) that could hinder the existing food-feed competition for grains or legumes [2]. Green macroalgae species, mostly Ulva sp., are rich in carbohydrates (up to 65% of dry matter, DM) [3], antioxidant chlorophylls and carotenoids [4] They are also rich in minerals including calcium, magnesium and iron, and have a balanced sodium and potassium proportion [5].
The protein content of Ulva sp. is variable (4.8-41.8% DM) [2], but with a good nutritional quality [5]. However, lipids are present in low amounts in alga biomass (<6.6% DM), although they contain health-promoting polyunsaturated fatty acids (PUFA) [6]. Moreover, ulvan is a sulphated soluble heteropolysaccharide, which is the major compound of the Ulva sp. cell wall (up to 30% DM) [7], followed by insoluble cellulose. This polymer has various bioactive functions as it can act as an anti-tumor, anti-coagulant, antihyperlipidemic, hepato-protective and immuno-stimulating agent [7].
The inclusion of Ulva sp. in poultry diets can influence animal growth performance and plasma biochemical parameters [8][9][10][11], with some studies showing a positive effect on the latter, such as the decrease of serum cholesterol [8]. However, the level of macroalga used in these reports was only up to 3-3.5% [8,10,11] and 6% [9] in the feed. In fact, although there are sustainable seaweed production methods (i.e., Integrated Multitrophic Aquaculture, ITMA), macroalga cultivation technology is still in development in order to reduce its production costs and environmental impact [2]. In addition, some studies suggested that the maximum level of Ulva sp. incorporated in a chicken diet should not surpass 10% in the feed, due to the presence of cell wall polysaccharides that are indigestible for monogastric diets with consequent impairment of nutrient digestibility [12,13].
The objective of the present study was to test if U. lactuca, when replacing 15% of corn and soybean meal, combined or not with a commercial carbohydrase mixture or recombinant ulvan lyase (PL25), would enhance a broiler's metabolic state and relate that with results of growth performance previously discussed in a companion report [18]. Thus, the effects of U. lactuca, supplemented or not with CAZymes, on a broiler's diet on plasma biochemical parameters and liver composition, including lipids, antioxidant pigments and mineral profile, were assessed. Table 1 shows the effect of the experimental diets on the zootechnical parameters of broilers. Supplementing U. lactuca with the recombinant ulvan lyase decreased the final body weight (p = 0.016) relative to the control. Similarly, body weight gain decreased by 15.6 g/d in broilers that were fed macroalga supplemented with ulvan lyase (p = 0.018) in relation to the control. However, dietary treatments had no significant influence on the feed intake and the feed conversion ratio (p > 0.05).

Plasma Biochemical Profile
Plasma metabolites, key electrolytes such as chloride, sodium and potassium, and hepatic markers of broilers that were fed U. lactuca, supplemented or not with CAZymes, are presented in Table 2. Total lipids (p < 0.001), triacylglycerols (TAG) (p < 0.001) and VLDL-cholesterol (p < 0.001) were increased in broilers fed with U. lactuca supplemented with ulvan lyase compared to the other diets. Conversely, total cholesterol (p < 0.001) and LDL-cholesterol (p < 0.001) were reduced in broilers that were fed diets with U. lactuca alone or supplemented with commercial Rovabio ® . Among all dietary treatments, HDLcholesterol (p < 0.001) reached the highest values in broilers that were fed the control diet. Glucose (p = 0.013) and total protein (p < 0.001) were increased in broilers that were fed U. lactuca with the recombinant ulvan lyase diet relative to the other treatments. Urea (p = 0.102) was unaffected by dietary treatments, and residual creatinine concentrations (<0.001 mg/dL) were found for all treatments. The lowest value of the C-reactive protein (p < 0.001) was observed in broilers fed with U. lactuca alone. Regarding the ionogram, chloride (p < 0.001) and potassium (p < 0.001) concentrations were consistently higher in broilers that were fed U. lactuca with the recombinant CAZyme, when compared to the other groups. However, no differences were found between broilers fed with only U. lactuca or supplemented with commercial CAZyme (p > 0.05). In contrast, U. lactuca, with or without enzymes, increased sodium levels (p < 0.001) relative to the control. For the hepatic markers, macroalga containing diets, with or without CAZyme supplementation, reduced alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels (p < 0.001). In addition, broilers fed with U. lactuca alone or supplemented with commercial Rovabio ® had reduced alkaline phosphatase (ALP) levels (p < 0.001) in relation to the control, whereas gamma-glutamyltransferase (GGT) was highest (p < 0.001) in broilers that were fed U. lactuca supplemented with the recombinant CAZyme.

Hepatic Vitamin E, Pigments and Mineral Profile
Hepatic vitamin E homologues, pigments and mineral composition of broilers that were fed U. lactuca, with or without CAZyme supplementation, are presented in Table 4. α-Tocopherol (p = 0.013) and γ-tocopherol (p = 0.009) contents were reduced in broilers fed with U. lactuca supplemented with the recombinant ulvan lyase compared to the control diet. In contrast, liver β-carotene (p < 0.001), chlorophyll-a (p < 0.001), chlorophyll-b (p < 0.001) and total carotenoids (p < 0.001) increased with U. lactuca, supplemented or not with CAZymes, relative to the control. Although macrominerals in the liver did not change across diets (p > 0.05), the most predominant were potassium and phosphorous with average values of 425 and 351 mg/100 g, respectively. In contrast, some trace elements, including iron and manganese, were affected by dietary treatments (p < 0.05). Iron (p = 0.001) was significantly higher in broilers that were only fed U. lactuca, intermediate in broilers that were fed U. lactuca combined with Rovabio ® , and lower in those that were fed U. lactuca supplemented with ulvan lyase or the control diet, influencing in the same manner the total of microminerals (p = 0.001). Manganese levels (p = 0.001) were higher in broilers that were fed macroalga diets in comparison to the control.

Principal Component Analysis (PCA)
The variability of plasma parameters into two dimensions is shown in Figure 1. The first two factors ( Figure 1A) account for 66% of the total variation (36.4% for factor 1 and 29.2% for factor 2). The control group was gathered in quadrant (a) while macroalga supplemented with the recombinant ulvan lyase was more dispersed in quadrants (b) and (d), but plainly discriminated from the other two groups. Data from U. lactuca alone or supplemented with the commercial Rovabio ® (UL and ULR) were located in quadrants (d) and (c) with no possible discrimination between them. These groups appear to overlap suggesting that the plasma biochemical profiles of these dietary treatments were partially similar. The loadings for the first two factors are presented in Figure 1B and Table 5

Discussion
The majority of the studies carried out so far reported the dietary effect of low levels of U. lactuca (up to 3.5% feed) on broilers' growth and plasma biochemical parameters [8,19]. Previously, we reported that the dietary incorporation of high levels (15%) of U. lactuca, especially when supplemented with ulvan lyase, slightly impaired broilers' performance but improved meat composition through an accumulation of antioxidant carotenoids, n-3 PUFA and total minerals [18]. The negative effect of macroalga in animal performance was probably due to the presence of algal indigestible polysaccharides and high mineral content, which might have compromised the digestibility of feed compounds [24]. Although not significant, the tendency for a decrease in feed intake in broilers fed with U. lactucacontaining diets probably contributed to a reduction of average daily gain and final body weight, especially in those animals fed the diet supplemented with ulvan lyase. A numerical decrease in feed intake was also reported by Ventura et al. [12] when feeding increasing levels of Ulva sp. and, thus, it is possible that some algal compounds could have decreased feed palatability. Herein, we hypothesized that the addition of 15% U. lactuca, alone or in combination with both exogenous enzymes, might improve the plasma biochemical profile and change lipid metabolism in broilers. Most of the plasma metabolites were largely affected by the experimental diets; however, the values are within the reference values reported for broilers [25,26]. Total lipids, TAG and VLDL-cholesterol were consistently increased in broilers that were fed U. lactuca with the recombinant ulvan lyase, followed by reduced HDL-cholesterol levels, pointing towards a negative impact on the lipemia profile. In turn, U. lactuca was responsible for a reduction in total and LDL-cholesterol, which agrees with the findings of some works using 1 to 3% [27] and 2 to 6% [9] of U. lactuca, respectively, in broilers' diet. It was reported higher total cholesterolemia levels (183.8 mg/dL) [25] than the ones found in our study, probably, due to the use of chicken layers instead of broilers. Total cholesterol, TAG, HDL-cholesterol and LDL-cholesterol have been used as key indicators of lipid metabolism balance [28,29]. The reverse cholesterol transport is the mechanism by which the organism removes excess of cholesterol from peripheral tissues and delivers it to the liver, where it will be redistributed to other tissues or removed from the organism, being HDL-cholesterol the main lipoprotein responsible for this process, whereas LDL-cholesterol has the opposite function [30]. Moreover, the majority of fatty acids is synthesized in the liver and transported via LDL for storage as triacylglycerols in the adipose tissue.
Broilers fed U. lactuca with or without the recombinant ulvan lyase displayed an increased glycemic response. Even if the levels were higher than the ones reported elsewhere [25], this small increment is thought to be devoid of clinical physiological relevance. The same rational applies for total protein. Unaffected renal function was proven by the non-variations of urea and creatinine across the experimental groups. The acute phase C-reactive protein (CRP) is produced by the liver and secreted into the blood in response to inflammation [31]. Herein, we found that CRP was lower in broilers fed U. lactuca, intermediate if supplemented with Rovabio ® Excel AP and recombinant ulvan lyase, and higher in the control group, pointing towards a beneficial anti-inflammatory effect of this macroalga. Notwithstanding, the highest value of CRP obtained for animals fed the control diet (0.026 mg/dL) was still below the normal averaged value found in the plasma of 35-dold broilers (14 mg/dL) [32]. Sodium, potassium and chloride are electrolytes positively affected by dietary U. lactuca. While chloride and potassium presented a similar variation, with the highest levels in broilers fed U. lactuca with recombinant ulvan lyase, sodium was increased by U. lactuca, with or without enzymes. Potassium and sodium help the body maintaining fluid and blood volume so it can function normally [33]. Sodium is responsible for the regulation of the membrane potential of cells and, along with potassium, is exchanged across cell membranes as part of active transport. Chloride is an anion occurring predominantly in the extracellular fluid whose serologic levels are mostly regulated by the kidney [33]. AST, ALT and ALP were reduced by U. lactuca, regardless of the CAZyme supplementation. These changes on aminotransferases activity are within the reference values reported for birds using both micro-and macroalga species, Arthrospira platensis [14] and L. digitata [17], respectively. GGT levels were higher in broilers fed U. lactuca alone and supplemented with the recombinant ulvan lyase than the control diet, in resemblance to the variations observed previously by some authors [14,17], yet not implying any kind of liver injury or dysfunction.
Liver is the anatomical site for cholesterol synthesis and fatty acid oxidation in broilers. De novo lipogenesis, a highly regulated metabolic pathway, occurs in the liver but also in the adipose tissue [34]. Hepatic total lipids did not change by dietary incorporation of 15% U. lactuca, supplemented or not with exogenous feed enzymes, conversely to the plasma lipid profile. However, the addition of macroalga at this level in broilers' diet promoted an increase of total cholesterol concentration in the liver, contrasting with our own results obtained with the dietary incorporation of 15% L. digitata [17]. Also, the dietary inclusion of the microalga Chlorella vulgaris at 10% level, alone or supplemented with CAZymes, had no effect on total cholesterol content in the liver of finishing pigs [35]. This discrepancy observed in different trials in response to total cholesterol in liver could be partly attributed to the dose and origin of the alga. Moreover, an effect of algal carotenoids, particularly xanthophylls, on increasing blood cholesterol levels might have occurred. This phenomenon was previously described in rodents [36,37], and then suggested when feeding the animals with extracted lipids from the brown seaweed, Undaria pinnatifida [38]. However, this mechanism of action is still unclear, and its occurrence in broilers lacks evidence.
Major variations were observed in hepatic n-3 fatty acids of broilers fed U. lactuca, supplemented or not with CAZymes. These functional fatty acids are of particular interest in animal feeds due to their anti-microbial and antioxidant properties [39]. The enhancement of n-3 PUFA and their antioxidant properties in the liver have been associated with the downregulation of PUFA oxidation-related genes expression and mitigation of lipid peroxidation [40]. The percentage of α-linolenic acid (18:3n-3), EPA and DHA increased in the liver about 2-fold, 4.5-fold and 3-fold, respectively, in broilers fed U. lactuca, with or without CAZyme supplementation, relative to the control. Also, U. lactuca alone or in combination with the commercial Rovabio ® increased the amounts of 18:4n-3. The raise in 18:3n-3 and 18:4n-3 is in line with the composition of the diets, but EPA was only 1.3-fold higher in macroalgae-containing diets than in the control and DHA was not even present in the diets (Table S1. Therefore, the increase of the sum n-3 PUFA, and particularly of n-3 long-chain PUFA, in the liver of broilers fed U. lactuca, alone or supplemented with exogenous CAZymes, could be explained by de novo lipogenesis through the intake of the precursor 18:3n-3 in the biosynthetic pathway of n-3 long-chain PUFA [41]. These findings corroborate those of Costa et al. [17], who also documented an increase in hepatic n-3 fatty acids, as well as a decrease of n-6/n-3 ratio, with the incorporation of 15% L. digitata, with or without feed enzymes, to broiler diets. Similarly, Costa et al. [18] reported an increase in meat n-3 PUFA, including EPA, DPA and DHA, with the addition of U. lactuca combined with ulvan lyase. In contrast, the combination of U. lactuca and the recombinant CAZyme decreased cis-MUFA, particularly 18:1c9, which is not in agreement with the in vitro release of MUFA from U. lactuca biomass [23]. The impact of 15% U. lactuca incorporation in broilers' diet, with or without feed CAZymes, on hepatic levels of tocopherols and pigments was also explored. α-Tocopherol is the major vitamin E compound with the highest antioxidant activity [42]. The combination of U. lactuca and ulvan lyase reduced both αand γ-tocopherol contents compared to the control. Recently, a decrease of hepatic α-tocopherol was reported with 15% of dietary L. digitata and the commercial carbohydrase Rovabio ® [17]. Similarly, a reduction of α-tocopherol was observed in the meat of broilers fed 15% of U. lactuca [18]. Explaining the present results remains a challenge, since literature documenting the effect of macroalgae incorporation in broiler diets on hepatic vitamin E is scarce [17]. There is a high variability of vitamin E levels between and within macroalgae species [2], which, therefore, compromises the amount of vitamin deposited in the liver. The chemical composition of macroalgae biomass varies not only between species, but also with location and season of cultivation and maturity of the algae [43]. However, the concentration of α-tocopherol found in U. lactuca biomass was 0.793 mg/kg DM, which is below the value previously reported for Ulva intestinalis (8.8 mg/kg DM) [44]. In contrast, a consistent increase of the sum of carotenoids, including β-carotene, and chlorophylls-a and -b was observed in the liver with macroalgae treatments relative to the control, which is supported by the 72 and 23-fold higher total chlorophylls and carotenoids, respectively, in U. lactuca-containing diets. In general, Ulva sp. are rich in carotenoids, such as βand α-carotenes and xanthophylls, and chlorophylls [4]. Carotenoids are natural lipophilic compounds that have been used in animal feed due to their potential to modify meat and yolk color and health benefits including antioxidant, antimicrobial, anti-inflammatory and anticarcinogenic activities [45,46]. The antioxidant potential of chlorophylls is less studied, although there is evidence of their ability to scavenge peroxyl radicals with a synergistic effect with vitamin E [46].
Regarding trace elements, the incorporation of 15% U. lactuca in broiler diets was not enough to promote major modifications on hepatic mineral concentrations, despite their high amounts in this microalga. Only iron and manganese, as well as total microminerals, were influenced by dietary inclusion of macroalga. These trace metals play an important role in metabolic processes by acting as cofactors of antioxidant enzymes [47]. Unfortunately, iodine and bromine were not determined in the present study, in spite of a high bioaccumulation of these elements by U. lactuca reaching up to 45.1 mg/kg DM of iodine and 694 mg/kg DM of bromine. However, other studies reported an increase of these minerals in the meat of broilers fed 15% of L. digitata {16] or U. lactuca [18], although within safe levels for human health. A similar result occurred in piglets fed 10% L. digitata [48]. In further studies, these minerals should be analyzed due to the well-known benefits of iodine in the general metabolism [49] and the toxicity of bromine [50].

Experimental Design, Diets and Samples Collection
The procedures agreed with the Ethics Commission of CIISA/FMV and ORBEA/ISA (protocol code number 1/ORBEA-ISA/2020, date of approval 7 July 2020), were accepted by the Animal Care Committee of National Veterinary Authority (Direção Geral de Alimentação e Veterinária, Lisboa, Portugal) and followed ARRIVE Guidelines for in vivo trials. One hundred and twenty 1-d-old male Ross 308 broiler chicks with an average body weight of 39.8 ± 0.20 g, vaccinated against Marek disease and infectious bronchitis, were individually tagged, and 3 broilers were housed per pen in a total of 40 wired-floor cages, with 10 replicate pens per treatment, for 35 d. The animals were maintained in an environmentally controlled room under standard brooding practices, with constant light. Room temperature and ventilation (relative humidity) were monitored continuously, following the guidelines for the Ross 308 broiler strain. The number of animals used in the experiment was chosen to follow the 3R s principle [14,15]. After an adaptation period of 21 d with a corn and soybean meal-based diet, broilers received one of the 4 experimental diets for 14 d until the standard slaughter age of 35 d, as follows: (1) a corn-soybean meal based diet (Control); (2) a diet with 15% of U. lactuca powder (Algolesko; Plobannalec-Lesconil, Brittany, France) (UL); (3) the UL diet supplemented with 0.005% of a commercial CAZyme mixture (Rovabio ® Excel AP; Adisseo, Antony, France), containing endo-1,3(4)-βglucanase and endo-1,4-β-xylanase activities (ULR); and (4) the UL diet supplemented with 0.01% of ulvan lyase, which is a recombinant enzyme from the family 25 of polysaccharide lyases (ULL) that is able to cleave the glyosidic bond between 3-sulfated rhamnose and D-glucuronic acid or L-iduronic acid residues in ulvan [23]. All diets were formulated to be isocaloric and isonitrogenous. The details about dietary ingredients are provided in Table 6. The chemical composition of U. lactuca and diets is shown in Table S1. Feed was provided daily, and broilers were weighed weekly. Feed intake, weight gain, and the feed conversion ratio were determined weekly. At the end of the experiment, one broiler per pen was slaughtered using electrical stunning and exsanguination. Blood and liver samples were collected from each of the 10 animals per experimental group, vacuum packed and stored at −20 • C.

Recombinant Ulvan Lyase Production
The recombinant gene was expressed in Escherichia coli (BL21) cells using the NZY autoinduction LB medium (Nzytech, Lisbon, Portugal) after overnight incubation at 140 rpm and 19 • C [23]. Ultrasonication was applied to disrupt cells followed by centrifugation. The protein extract was freeze-dried and incorporated at 0.01% in the ULL diet.

Chemical Analysis of U. lactuca and Diets
The proximate composition and gross energy of the green macroalga and diets were analysed using standard methods [51], whereas fatty acid methyl esters (FAME), diterpenes (tocopherols and tocotrienols) and pigments (β-carotene, chlorophyll-a, chlorophyll-b and total carotenoids) and minerals were determined as previously reported [16,18].

Assessment of Hepatic Diterpenes, Pigments and Mineral Profile
Diterpenes pigments and total cholesterol in the liver were determined by High-Performance Liquid Chromatography [HPLC] after the direct saponification of samples. For HPLC procedure, a normal-phase silica column (Zorbax RX-Sil, 250 mm × 4.6 mm i.d., 5 µm particle size, Agilent Technologies Inc., Palo Alto, CA, USA) was used allowing fluorescence detection of tocopherols and tocotrienols, and UV-visible photodiode array detection of cholesterol and β-carotene [52]. The analysis of pigments was carried out following the procedure of Teimouri et al. [53] and quantified as suggested by Hynstova et al. [54].
The mineral profile of the liver was evaluated as previously reported [16,18], and expressed as mg/kg dry matter. Succinctly, all minerals, except for iodine and bromine, were determined using Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES, iCAP 7200 duo Thermo Scientific, Waltham, MA, USA), after digestion of samples with concentrated nitric and hydrochloric acids reacting with hydrogen peroxide followed by dilution and filtration through 90 mm diameter-filter papers. The digestion conditions were as follows: 1 h until 95 • C and 1 h at 95 • C. Calibration curves were created with multi-element standards (SCP Science, Quebec, Canada, PlasmaQual S22) for quantification of the elements. The iodine and bromine were determined in the macroalga and diets using an inductively coupled plasma mass spectrometer (ICP-MS) (Thermo X series II, Thermo Fisher Scientific, Waltham, MA, USA) preceded by alkaline extraction with Tetramethylammonium hydroxide (TMAH) solution at 25% v/v. Afterwards, samples were spiked with chemical standards in a Heating Graphite Block System for 3 h at 90 • C, and centrifuged and filtered with 0.45 µm filters.

Assessment of Hepatic Total Lipid Content and Fatty Acid Profile
Total lipids, in duplicate, were extracted from lyophilised (−60 • C and 2.0 hPa, lyophilizator Edwards Modulyo, Crawley, UK) liver samples [55]. Afterwards, fatty acids were converted into FAME by combined alkaline and acidic transesterification reaction (Sukhija and Palmquist, 1988). The analysis of FAME was carried out through gas-chromatography (GC-FID HP7890A Hewlett-Packard, Avondale, PA, USA), using nonadecanoic acid (19:0) methyl ester as internal standard [15]. Fatty acids were identified by comparison with the reference standard (FAME mix 37 compounds, Supelco Inc., Bellefonte, PA, USA) and expressed as percentage of total fatty acids.

Analysis of Plasma Biochemical Parameters
Total cholesterol, HDL-cholesterol, LDL-cholesterol, TAG, phospholipids, total protein, urea, creatinine and glucose concentrations, AST, ALT, ALP and GGT, as well as the electrolytes chloride, sodium and potassium were analysed using an automated Modular Hitachi Analytical System (Roche Diagnostics, Mannheim, Germany), through diagnostic kits (Roche Diagnostics). The determination of VLDL-cholesterol and total lipids were calculated using the formulas reported in the literature [56,57].

Statistical Analysis
The Statistical Analysis System (SAS) program (SAS Institute Inc., Cary, NC, USA) was used to analyze data by ANOVA from Generalized Linear Model (GLM) adjusted to the Tukey-Kramer method (PDIFF option) for multiple comparisons of least squares means at p < 0.05. The statistical model considered either the cage (for feed intake and feed conversion ratio) or the broiler (for body weight, body weight gain, plasma metabolites and hepatic parameters), as the experimental units. Additionally, plasma parameters and hepatic lipid composition were subjected to principal component analysis (PCA) using the SPSS Statistics for Windows (IBM Corp. released 2020, version 27.0, Armonk, NY, USA) for data exploratory purposes and a comprehension of underlying trends in the data structure.

Conclusions
Overall, a high-level (15%) incorporation of U. lactuca in broiler diets induced beneficial changes in plasma lipids, particularly a hypocholesterolaemic effect. However, when combined with the recombinant CAZyme, it increased systemic lipemia with no effect on plasma cholesterol. The macroalga was also responsible for an enhancement of liver antioxidant capacity and metabolism through an increase of antioxidant pigments, n-3 fatty acids and total microminerals including iron and manganese. Although these results indicate possible the health benefits of U. lactuca for animals, caution must be taken towards the slight growth impairment in broilers fed macroalgae and the fact that recombinant ulvan lyase did not ameliorate the effects of such a high level of alga in the diet. Further investigations are required to evaluate the incorporation of U. lactuca at lower levels in poultry diets.
Supplementary Materials: The following supporting information can be downloaded at: https://www. mdpi.com/article/10.3390/molecules27217425/s1, Figure S1: Loading plot of the first and second principal factors of the pooled data (A) and component score vectors (B) using hepatic metabolites from broilers fed with different diets: Control, corn-soybean based-diet; UL, based-diet plus 15% U. lactuca; ULR, UL diet with 0.005% commercial CAZyme (Rovabio ® Excel AP); ULL, UL diet with 0.01% recombinant ulvan lyase. Table S1: Chemical composition of seaweed Ulva lactuca and experimental diets (n = 3), used in this work and taken from [18].

Institutional Review Board Statement:
The study was approved by the Animal Care Committee of National Veterinary Authority (Direção Geral de Alimentação e Veterinária, Portugal) and the Ethics Commission of CIISA/FMV, ORBEA/ISA (protocol code number 1/ORBEA-ISA/2020, date of approval 7 July 2020).

Informed Consent Statement: Not applicable.
Data Availability Statement: Not applicable.