Potential ameliorative role of Spirulina platensis in powdered or extract forms against cyclic heat stress in broiler chickens.

Global warming has become intensified and widespread, threatening the world with causing acute heatwaves that adversely affect poultry production and producers' profitability. Spirulina platensis is a precious and promising mitigating strategy to combat the detrimental impacts of heat stress due to its high contents of nutrients and bioactive components. The current study was designed to compare the incorporation impact of S. platensis powder or aqueous extract on the growth and physiological responses of heat-stressed broiler chicks. Six hundred 1-day-old Ross 308 male broiler chicks were allocated into five experimental groups with six replicates of 20 chicks each. The control group fed the basal diet without additives, SPP1 and SPP2 groups fed the basal diet with 1 g/kg and 2 g/kg S. platensis powder, respectively, while SPE1 and SPE2 groups received 1 ml/L and 2 ml/L S. platensis aqueous extract in the drinking water, respectively. All birds were exposed to cyclic heat stress (34 ± 2 °C for 12 h) for three successive days a week from day 10 to day 35. In vitro analysis showed that total phenols, flavonoids, and antioxidant activity of S. platensis were remarkably decreased (P < 0.001) in the aqueous extract compared to the powder form. Body weight, weight gain, and feed conversion ratio were improved (P < 0.001) in all treated groups, while carcass yield and dressing percentage were increased only in SPP1 and SPP2. Feed and water intake and blood biochemical parameters were not affected. Both forms of S. platensis enhanced the lipid profile, redox status, and humoral immune response of heat-stressed chicks superior to the powder form. Conclusively, the powder form of S. platensis was more effective in enhancing the productivity of broilers and alleviating the negative impacts of heat stress than the aqueous extract form.

Introduction

Climate change and global warming have become rapid, widespread, and intensified, threatening the world with causing longer warm seasons and more heatwaves. These conditions adversely affect poultry production globally, in particular, in subtropical and tropical countries. Because of the lack of sweat glands, chickens are vulnerable to the elevation in ambient temperature, which causes many physiological disturbances such as suppressed immunocompetence, endocrine disorders, acid-based imbalance, muscle tremors, weakness, and oxidative stress (Bogin et al. 1996; Tao and Xin, 2003). These physiological disorders lead to reduced weight gain and feed consumption, increased water consumption and mortality, and impairment of birds’ overall welfare and productivity (Abdel-Moneim et al. 2021b; Abo Ghanima et al. 2020b; Sakamoto et al. 2020). In addition, the heat stress-induced excessive amount of reactive oxygen species (ROS) contributes to severe tissue injuries and deteriorates the maintenance of homeostasis (Khan et al. 2012; Surai 2007). To combat these detrimental impacts of heat stress, implementing environmental and nutritional mitigation strategies has become mandatory. Lowering stocking densities, increasing the ventilation rate, using different flooring systems, establishing intermittent light schedules, and implementing wet feeding or early feed restriction are among the environmental strategies (Abo Ghanima et al. 2020a; Sahin et al. 2009; Saleh et al. 2021). However, the nutritional strategies are including the use of probiotics (Abd El‐Hack et al. 2020b; Abdel-Latif et al. 2018; Abdel-Moneim et al. 2020b; Abdel-Moneim et al. 2020c; Abou-Kassem et al. 2021), prebiotics (Abd El-Hack et al. 2021; Houshmand et al. 2012), organic acids (Ding et al. 2020; Elbaz et al. 2021), minerals and vitamins (Abd El-Hack et al. 2018; Abdel-Moneim et al. 2021c; Harsini et al. 2012; Khan et al. 2012; Mohamed et al. 2020; Saleh et al. 2020), and herbal extracts and derivatives (Abd El-Hack et al. 2019; Abd El-Hack et al. 2020a, b; Abd El-Moneim and Sabic, 2019; Abd El-Moneim et al. 2019; Sugiharto 2020). Furthermore, phytochemicals, such as polyphenols, have been characterized for their antioxidant capabilities and presented as potential mitigators of heat stress in poultry (Abdel-Latif et al. 2021; Abdel-Moneim et al. 2020d; Hu et al. 2019; Saeed et al. 2018; Saeed et al. 2020).

Spirulina platensis (the blue-green algae) is a unicellular microalga that can be grown in fresh and salt aquatic systems and is known as a good source of minerals, proteins, phytopigments, and vitamins (Farag et al. 2016). The high contents of various nutrients in S. platensis made it a promising alternative feed additive in poultry diets. Furthermore, S. platensis contains numerous bioactive components in high amounts, such as phycocyanins, steroid, saponin, chlorophyll, β-carotene, flavonoid, triterpenoid, and phenolic acids (Agustini et al. 2015). These bioactive compounds have numerous biological activities such as antioxidant, antiviral, anti-inflammatory, hepatoprotective, immunostimulatory, and antimicrobial (Abdel-Daim et al. 2019; Abdel-Moneim et al. 2021a; Abedin and Taha, 2008; Aladaileh et al. 2020). A growing body of literature has attributed these medicinal properties of S. platensis to their ability to modulate cytokines and antibodies production, inhibit lipid peroxidation, enhance disease resistance, and scavenge free radicals effectively, thereby improving the productivity and profitability of the poultry industry (Abdel-Daim et al. 2019, 2020; Abdelkhalek et al. 2015; Aladaileh et al. 2020; Evans et al. 2015; Farag et al. 2016). Taken together, these different mechanisms qualify S. platensis to be used to mitigate the deleterious impacts of heat stress in poultry (Abdel-Moneim et al. 2021c).

To our knowledge, however, no previous studies have compared the efficacy of S. platensis in powder and aqueous extract forms in alleviating the deleterious impacts of heat stress in broiler chicks. Therefore, the current study was designed to compare the incorporation effect of S. platensis in its powder and aqueous extract forms on growth, blood biochemical constituents, redox status, and humoral immune response of heat-stressed broiler chickens.

Materials and methods

Preparation Spirulina platensis aqueous extract

The dried powder of Spirulina platensis was supplied by the project entitled “Utilization of marine algae for salt fodders, milk, meat, and fish production under saline conditions,” Desert Research Center of Egypt. The aqueous extract of S. platensis was prepared as described by Quoc andDubacq (1997). Briefly, equal amounts of the dried powder of Spirulina platensis and distilled water were mixed and shaken well. In an autoclave, S. platensis was extracted with water at 120 °C for 1 h. To adjust the pH to 4.0, the citric acid was added to the hot aqueous extract. The hot blend was then centrifuged at 2500 × g for 15 min to discard the insoluble fractions and obtain the water-soluble extract. During the experiment, the aqueous extract was prepared as needed to be used fresh.

Chemical evaluation and antioxidant assays of Spirulina platensis

Total phenolic content

The total phenolic contents of dried powder and water extract forms of S. platensis were quantified following the Folin-Ciocalteu assay (Kalagatur et al. 2018). A reaction mixture of 150 µl Na2CO3 (7.5%, w/v) and 150 µl of S. platensis aqueous extract or its dried powder suspension was prepared, mixed well, added to 75 µl Folin-Ciocalteu reagent, and diluted ten times with water (1:10, v/v). After a 30-min incubation time, a microtiter plate reader (BioTek Elx808, USA) was used to analyze the mixtures at 750 nm. The results were expressed as Gallic acid equivalent (mg GAE/100 g).

Total flavonoid content

The spectrophotometric method was used to quantify the total flavonoid concentration as described by Zhishen et al. (1999). A 2 ml of S. platensis aqueous extract or its dried powder suspension and 8 ml distilled deionized water were mixed, and 0.6 ml NaNO2 (1:20) was added to the mixture. The solution was vortexed for 5 min, then 1.2 ml AlCl3 (1:10) was added. A 4 ml NaOH (1 mol/L) and 4 ml distilled deionized water were added 6 min later. The absorbance was measured at 510 nm after 5 min centrifugation (3300 × g) at room temperature, and the results were expressed as Quercetin equivalent (mg QE/100 g).

DPPH assay

The antioxidant activity of S. platensis aqueous extract or dried powder was estimated by the scavenging 1,1-diphenyl-2-picrylhydrazyl (DPPH˙) radical (Herald et al. 2012). A 1 ml of S. platensis sample was mixed with 2 ml ethanolic DPPH. The absorbance was assayed at 517 nm after 30 min of dark incubation. DPPH˙ scavenging activity (%) was estimated as follows:

where A0 is the blank absorbance while A1 is the sample absorbance.

Total antioxidant capacity

The total antioxidant capacity of S. platensis powder or aqueous extract was estimated as described by Prieto et al. (1999). A 1 ml of the sample was added to a 10 ml reagent mixture (28 mM sodium phosphate, 0.6 M sulfuric acid, and 4 mM ammonium molybdate), mixed well, and incubated. After an incubation period of 90 min at 95 °C, samples were kept to cool near room temperature. The sample absorbance was measured against a blank at 695 nm, and the results were expressed as equivalents of ascorbic acid (mg AA/100 g).

Birds and experimental design

Six hundred 1-day-old Ross 308 male broiler chicks with similar body weight (40.2 ± 0.5 g) were obtained from a commercial hatchery and equally distributed into five experimental groups. Each group contained six replications of 20 chicks each. Birds were housed in a litter floor system with free access to feed and water via manual drinkers and feeders. Chicks were fed a corn-soybean meal-based grower and finisher (1–21 days and 22–35 days) diets (Table 1), which were formulated to meet the nutrients requirements of Aviagen (2014). The experimental groups were divided: The first group (control) fed the basal diet without additives (C). The second and third groups fed the basal diet with 1 g/kg and 2 g/kg S. platensis powder (SPP1 and SPP2), while the fourth and fifth groups received treatments of 1 ml/L and 2 ml/L S. platensis aqueous extract (SPE1 and SPE2) in the drinking water. All birds were located in the same conditions. Chicks were kept at standard rearing conditions until day 10, and then the ambient temperature was increased from 29 °C to 34 ± 2 °C for 12 h (from 9:00 am to 9:00 pm) for three consecutive days a week until 35 days of age (Abo Ghanima et al. 2020b). Relative humidity ranged from 50 to 60% throughout the experimental period. Broilers were vaccinated orally against Newcastle disease (NDV, Nobilis® ND Clone 30) at 7 and 19 days and Gumboro disease (IBD, Bursine® Plus) at 14 days, and subcutaneously injections against avian influenza and Newcastle disease (H9N1, CEVAC® NEW FLU H9 K) at 7 days. These vaccines were manufactured by MSD animal health Co., Egypt, Zoetis, US, and Ceva Animal Health, Egypt, respectively.

Table 1

Feed ingredients and nutrient content of the basal diets

Ingredients	Starter (1–21 days)	Grower (22–35 days)
Maize	55.00	59.00
Soybean meal	38.7	33.4
Soybean oil	2.38	3.90
Limestone	1.17	1.06
Di-calcium phosphate	2.00	1.82
Premix1	0.30	0.30
Sodium chloride	0.25	0.25
L-lysine HCl	0.04	0.10
DL-Methionine	0.16	0.17
Calculated composition
ME (kcal/kg)	2913	3060
CP (%)	22.06	20.15
Calcium (%)	1.04	0.94
Ava. Phosphorus (%)	0.52	0.48
Methionine (%)	0.52	0.50
Lysine (%)	1.30	1.29
TSAA (%)	0.87	0.82

1Premix provides per kg of diet: vitamin A, 14,000 IU; vitamin K, 0.004 g; vitamin E, 0.05 g; vitamin D3, 3000 IU; pyridoxine, 0.003 g; cobalamin, 0.006 g; niacin, 0.06 g; pantothenic acid, 0.02 g; choline, 0.15 g; folic acid, 0.0002 g; Ca, 0.048 g; P, 0.00032 g; Mn, 0.1 g; Fe, 0.05 g; Zn, 0.08 g; Cu, 0.01 g; Co, 0.000025 g; iodine, 0.000015 g

Growth performance and carcass traits

Body weight (BW), weight gain (BWG), and daily feed intake (FI) per replicate were monitored on day 21 and day 35 to estimate the feed conversion ratio (FCR) as (g feed/ g gain). Daily water intake (WI) was also recorded at the same time interval. On day 35, six birds/group (one per replicate) were randomly selected for evaluating carcass traits and collecting blood samples. Dressing (%), carcass yield (%), and relative weight of abdominal fat were calculated. The indices of the immune organs bursa of Fabricius, spleen, and thymus were also calculated as described by Abo Ghanima et al. (2020a).

Blood biochemical indices

During slaughtering, blood samples were gathered in non-heparinized tubes, kept to clot, and centrifuged at 3000 × g for 15 min. Sera samples were separated and stored at -25 °C till the biochemical analyses. Serum concentrations of aspartate and alanine aminotransferases (AST and ALT), alkaline phosphates (ALP), glucose, total proteins (TP), albumin (ALB), creatinine (CR), uric acid (UA), triglycerides (TG), high-density lipoprotein (HDL-cholesterol), low-density lipoprotein (LDL-cholesterol), total cholesterol (TC), and very-low-density lipoprotein (VLDL-cholesterol) were determined spectrophotometrically (Spectronic 1,201, Milton Roy, Ivyland, PA, USA) following the manufacturer’s instructions of the commercial kits (Bio-Diagnostic Co., Egypt). Triiodothyronine hormone (T3) was assayed using radioimmunoassay (RIA) kits (Ibrahim et al. 2020).

Antioxidant activity

Levels of glutathione peroxidase (GPx), malondialdehyde (MDA), and superoxide dismutase (SOD) in sera samples were measured using the ELISA kit of QuantiChrom (BioAssay Systems, USA and Cayman Chemical Company, USA), following the recommended protocol.

Humoral immunity

Levels of circulating immunoglobulin IgG, IgA, and IgM were evaluated using chicken-specific immunoglobulin ELISA quantitation kits (Bethyl Laboratories Inc., Montgomery, TX, USA). The humoral immune responses against NDV, H9N1, and IBD were estimated using the hemagglutination inhibition test ELISA assay (Indical Bioscience-GmbH, Leipzig, Germany), as described by (Abdel-Moneim et al. 2020a; Elbaz et al. 2021).

Statistical analysis

All in vitro measurements were performed in triplicate, and data of total antioxidant capacity, total phenols and flavonoids contents, and DPPH assay of dried powder and aqueous extract of S. platensis were recorded and analyzed using the independent sample t-test of SPSS package (v 19, SPSS Inc., Chicago, IL, USA). The rest of the measurements were analyzed using the two-way ANOVA as a completely randomized design of the SPSS software procedure. Tukey’s multiple comparison test was used to assess the statistical differences among means at P < 0.05.

Results

Total phenolic and flavonoid contents and antioxidant activity of S. platensis

The total phenols and flavonoids of S. platensis in the powder and aqueous extract forms and their antioxidant activity are shown in Table 2. The aqueous extraction of S. platensis reduced (P < 0.01) the abovementioned indices compared to the powdered form. Total phenols and flavonoids contents of S. platensis powder were 4.9 and 5.2 times higher than that of the aqueous extract, respectively. The DPPH˙ scavenging activity and total antioxidant capacity of S. platensis were significantly (P < 0.01) declined in the form of the aqueous extract compared to the powdered form (89.11 vs. 57.64, and 4663 vs. 980.4), respectively.

Table 2

Total phenolic and flavonoids contents, DPPH assay, and total antioxidant capacity of Spirulina platensis in powdered and aqueous extract forms

Items	Powder	Aqueous extract	P values
Total phenols (mg GAE/100 g)	1580a ± 63.2	321.3b ± 18.4	< 0.001
Total flavonoids (mg QE/100 g)	176.3a ± 7.65	34.12b ± 5.03	< 0.001
DPPH˙ scavenging activity, %	89.11a ± 5.11	57.64b ± 2.72	< 0.001
Total antioxidant capacity (mg AA/100 g)	4663a ± 117.1	980.4b ± 44.9	< 0.001

AA ascorbic acid equivalent, QE quercetin equivalent, DPPH 1,1-diphenyl-2-picrylhydrazyl, GAE gallic acid equivalent

Growth performance and carcass characteristics

The effects of incorporation levels and forms of S. platensis on the growth and carcass traits of Ross 308 male broiler chicks exposed to cyclic heat stress are shown in Table 3. The dietary incorporation of S. platensis improved (P < 0.01) BW at 21 days, while its inclusion via the drinking water route did not affect the same parameter. At 35 days, final BW was increased (P < 0.01) in all treated birds compared with the unsupplemented ones. The highest BW was recorded in SPP2 followed by SPP1. FI and WI did not differ among experimental groups. During the starter (1–21 days) phase, BWG and FCR were improved only in SPP1 and SPP2 groups; however, during the grower (22–35 days) and overall (1–35 days) periods, they were improved in all treated groups compared to the control. The best BWG and FCR were observed in groups fed dietary levels of S. platensis followed by those treated via the drinking water route. Dressing percentage and carcass yield were elevated (P < 0.01) only in SPP1 and SPP2 compared to the control, while abdominal fat (%) was not affected. The relative weights of the immune organs (bursa of Fabricius, spleen, and thymus) were not significantly affected by dietary and water treatments (Table 6).

Table 3

Effect of Spirulina platensis in powdered or aqueous extract forms on growth performance of broiler chickens exposed to cyclic heat stress

Indices	Dietary treatments1					SEM2	Significance levels
	C	SPP1	SPP2	SPE1	SPE2		Leveleffect(L)	Fromeffect(F)	L × Finteraction
Body weight, g
Initial	40.59	40.18	40.68	40.78	40.74	0.033	0.530	0.535	0.830
21 days	863.7c	879.5b	891.8a	862.4c	864.7c	1.405	< 0.001	< 0.001	< 0.001
35 days	1945.2d	1993.5b	2020.6a	1960.6c	1970.1c	3.656	< 0.001	< 0.001	< 0.001
Body weight gain, g.bird.day−1
1–21 days	39.20c	39.94b	40.53a	39.13c	39.23c	0.067	< 0.001	< 0.001	< 0.001
22–35 days	77.25d	79.57b	80.63a	78.44c	78.96bc	0.170	< 0.001	< 0.001	0.002
1–35 days	54.42d	55.79b	56.57a	54.85c	55.12c	0.104	< 0.001	< 0.001	< 0.001
Water intake, ml.bird.day−1
1–21 days	85.02	84.06	85.52	87.38	85.78	2.074	0.109	0.121	0.091
22–35 days	357.4	353.1	350.2	366.1	361.8	7.163	0.616	0.150	0.176
1–35 days	194.0	191.7	191.4	198.9	196.3	7.097	0.561	0.085	0.073
Feed intake, g.bird.day−1
1–21 days	47.31	46.72	47.03	46.79	47.30	0.087	0.057	0.508	0.799
22–35 days	161.8	160.1	159.6	160.6	160.2	0.602	0.072	0.631	0.940
1–35 days	93.11	92.10	92.07	92.31	92.46	0.315	0.081	0.518	0.908
Feed conversion ratio, g feed.g gain−1
1–21 days	1.21a	1.17b	1.16b	1.20a	1.21a	0.005	< 0.001	< 0.001	< 0.001
22–35 days	2.09a	2.01c	1.98d	2.05b	2.03bc	0.008	< 0.001	< 0.001	0.006
1–35 days	1.71a	1.65c	1.63d	1.68b	1.68b	0.007	< 0.001	< 0.001	< 0.001
Carcass characteristics, %
Dressing	70.52b	72.11a	71.94a	70.56b	69.96b	0.189	< 0.001	< 0.001	< 0.001
Carcass yield	75.70b	77.30a	77.22a	75.88b	74.99b	0.203	< 0.001	< 0.001	< 0.001
Abdominal fat	0.625	0.589	0.569	0.579	0.602	0.008	0.002	0.292	0.092

1Treatment groups: C corn-soybean meal-based diet, SPP11 g Spirulina platensis powder/kg, SPP2 2 g S. platensis powder/kg, SPE1 1 ml S. platensis aqueous extract/L, SPE2 2 ml S. platensis aqueous extract/L; a–dmeans with different superscripts are significantly different; 2SEM standard error of means

Table 6

Effect of Spirulina platensis in powdered or aqueous extract forms on humoral immunity and immune organs relative weights of broiler chickens exposed to cyclic heat stress

Indices	Dietary treatments1					SEM2	Significance levels
	C	SPP1	SPP2	SPE1	SPE2		Leveleffect(L)	Fromeffect(F)	L × Finteraction
Immunoglobulin (Ig), mg.dl−1
IgM	88.00c	200.6b	243.5a	179.0b	177.5b	10.44	< 0.001	0.002	0.012
IgG	547.0c	818.3a	770.5ab	687.5abc	610.0bc	28.99	0.006	0.059	0.383
IgA	263.3	240.7	253.3	241.5	267.0	5.719	0.262	0.682	0.867
Antibody titers against
NDV	6.50b	8.00a	8.17a	7.17ab	7.33ab	0.181	0.005	0.084	0.458
H9N1	4.67	5.33	5.50	4.83	4.86	0.164	0.435	0.254	0.701
IBD	305.8	335.5	330.2	319.0	316.8	3.489	0.022	0.127	0.536
Relative weights of immune organs, %
Bursa of Fabricius	0.283	0.271	0.279	0.277	0.270	0.006	0.626	0.890	0.775
Spleen	0.253	0.278	0.311	0.269	0.275	0.008	0.001	0.245	0.600
Thymus	0.261	0.303	0.274	0.265	0.270	0.009	0.325	0.264	0.369

1Treatment groups: C corn-soybean meal-based diet, SPP1 1 g Spirulina platensis powder/kg, SPP2 2 g S. platensis powder/kg, SPE1 1 ml S. platensis aqueous extract/L, SPE2 2 ml S. platensis aqueous extract/L; IBD infectious bursal disease, H9N1 avian influenza, NDV Newcastle disease virus; a–cmeans with different superscripts are significantly different; 2SEM standard error of means

Serum biochemical indices

The effect of S. platensis in the powder or aqueous extract forms on blood biochemical indices of broiler chicks exposed to cyclic heat stress are presented in Table 4. Hepatic and renal functions biomarkers (AST, TP, UA, ALB, ALT, and CR) were not affected by the dietary or water treatments except ALP, which was increased in SPE1 compared to the control. Serum glucose and T3 concentrations were also non-significantly altered.

Table 4

Effect of Spirulina platensis in powdered or aqueous extract forms on blood biochemical indices of broiler chickens exposed to cyclic heat stress

Indices	Dietary treatments1					SEM2	Significance levels
	C	SPP1	SPP2	SPE1	SPE2		Leveleffect(L)	Fromeffect(F)	L × Finteraction
Protein fractions, g.dl−1
total protein	3.40	3.33	3.26	3.48	3.32	0.025	0.120	0.168	0.456
Albumin	1.53	1.56	1.58	1.61	1.46	0.018	0.277	0.460	0.133
Liver enzymes activity, U.L−1
AST	68.08	72.14	71.33	62.62	69.75	1.907	0.793	0.358	0.581
ALT	23.74	24.04	22.53	22.69	22.22	0.534	0.597	0.627	0.876
ALP	175.6bc	165.1c	194.2ab	208.0a	174.7bc	3.504	0.254	0.230	< 0.001
Renal function biomarkers, mg.dl−1
uric acid	7.08	6.64	6.59	6.82	6.65	0.099	0.157	0.689	0.931
creatinine	0.608	0.591	0.608	0.592	0.617	0.013	0.821	0.916	0.992
Thyroid activity, ng.ml−1
T3	1.548	1.693	1.429	1.77	1.63	0.037	0.038	0.191	0.505
Glucose, mg.dl−1	248.3	244.8	250.0	230.9	239.4	3.087	0.388	0.198	0.638

1Treatment groups: C corn-soybean meal-based diet, SPP11 g Spirulina platensis powder/kg, SPP2 2 g S. platensis powder/kg, SPE1 1 ml S. platensis aqueous extract/L, SPE2 2 ml S. platensis aqueous extract/L, AST aspartate aminotransferase, ALP alkaline phosphatase, ALT alanine aminotransferase, T3 triiodothyronine; a–cmeans with different superscripts are significantly different; 2SEM standard error of means

Serum lipid profile

The serum lipid profile of heat-stressed broiler chickens was greatly influenced (P < 0.05) by the treatment of S. platensis in its powder or aqueous extract forms (Table 5). Serum levels of TG, TC, LDL, and VLDL-cholesterol were decreased in all treated groups except for TC and LDL-cholesterol, which were not altered in SPE2 compared to the control. Blood HDL-cholesterol concentration was elevated (P < 0.01) in SPP2 and decreased (P < 0.01) in SPE2 compared to the untreated group. Dietary incorporation of S. platensis was more effective than its water administration in enhancing the lipid profile of heat-stressed birds.

Table 5

Effect of Spirulina platensis in powdered or aqueous extract forms on serum lipid profile and antioxidative status of broiler chickens exposed to cyclic heat stress

Indices	Dietary treatments1					SEM2	Significance levels
	C	SPP1	SPP2	SPE1	SPE2		Leveleffect(L)	Fromeffect(F)	L × Finteraction
Lipid profile, mg.dl−1
triglycerides	253.5a	223.1c	226.2bc	235.4b	227.8bc	2.404	< 0.001	0.073	0.015
total cholesterol	219.4a	187.9bc	194.0bc	180.6c	206.4ab	3.670	< 0.001	0.770	0.381
HDL-cholesterol	46.25b	46.46b	50.81a	45.96b	41.84c	0.521	0.988	< 0.001	< 0.001
LDL-cholesterol	129.9a	97.88b	99.22b	87.57b	119.0a	3.410	< 0.001	0.508	0.033
VLDL-cholesterol	50.69a	44.62b	45.25bc	47.07b	45.56bc	0.481	< 0.001	0.073	0.015
Antioxidative biomarkers
MDA, nmol.ml−1	1.053a	0.759b	0.810b	0.875ab	1.025a	0.030	0.007	0.057	0.034
SOD, U.ml−1	128.8c	144.8a	145.3a	136.8b	134.9b	1.532	0.001	0.538	0.043
GPx, U.ml−1	24.88c	37.81a	34.31a	30.50b	30.75b	0.492	< 0.001	0.104	0.019

1Treatment groups: C corn-soybean meal-based diet, SPP1 1 g Spirulina platensis powder/kg, SPP2 2 g S. platensis powder/kg, SPE1 1 ml S. platensis aqueous extract/L, SPE2 2 ml S. platensis aqueous extract/L; HDL high-density lipoprotein, VLDL very-low-density lipoprotein, LDL low-density lipoprotein, SOD superoxide dismutase, MDA malondialdehyde, GPx glutathione peroxidase; a–cmeans with different superscripts are significantly different; 2SEM standard error of means

Serum redox status

The redox status of heat-stressed broiler chickens affected by dietary or water administration of S. platensis is presented in Table 5. The incorporation of S. platensis in the powder form was superior to the aqueous extract form in enhancing the blood antioxidative biomarkers of birds subjected to cyclic heat stress. Serum MDA concentration was reduced (P < 0.05) in SPP1 and SPP2 but did not differ in SPE1 and SPE2. Serum levels of SOD and GPx were elevated in all treated groups compared to the control with the superior to SPP1 and SPP2 groups.

Humoral immune response

The humoral immune response of broiler chickens treated with S. platensis in powdered or aqueous extract forms and exposed to cyclic heat stress is shown in Table 6. Serum level of IgM was increased (P < 0.01) in all treated groups, while IgG level and antibody titer against NDV were elevated (P < 0.01) only in SPP1 and SPP2 compared to the control. S. platensis level, form and their interaction did not affect the circulating IgA level and antibody titers of H9N1 and IBD.

Discussion

Spirulina platensis, as an alga, was approved on 16 June 2011 by the commission regulation (EU) No. 575/2011 to be used in animal feeds in its raw, processed, dried, oil, or extract forms. To our knowledge, no earlier studies compared the incorporation impacts of S. Platensis in poultry nutrition in the dried or the extract forms, particularly under heat stress conditions. Considering the increase in water consumption and the decrease in voluntary feed consumption of birds in hot climates, the extract form of algae may be more suitable for alleviating the detrimental impact of heat stress on birds. Nevertheless, the extraction techniques differ in efficiency, costs, solvents (water, hexane, or ethanol), and composition and yield of the extract (Michalak et al. 2017). In the present study, we decided to use the hot water extract because most antioxidant constituents and bioactive substances are extracted in water after a pre-treatment of thermal, enzymatic, chemical, or physical cell disruption (Mesalam et al. 2021; Michalak &Chojnacka 2014). Additionally, a mechanical cell disruption was performed to increase the extraction yield and improve the results obtained (Michalak et al. 2017). Deterioration of cell wall structure is required to elaborate its bioactive ingredients such as polysaccharides, polyphenols, cellulose, lignin, minerals, and pigments (Saeid and Chojnacka, 2015). After all the pre-treatments performed in this study, however, the antioxidant activity and total flavonoid and phenolic contents of the aqueous extract of S. Platensis were 4 to 5 times lower than that of the dried powder form, which affects its biological activities and impacts on broilers’ productivity and physiological responses.

This study demonstrated that treating heat-stressed birds with S. platensis, dried powder improved their growth and feed efficiency better than its aqueous extract. The promoting activity of S. platensis of the broilers’ performance and feed efficiency exposed to heat stress has been well-documented (Abdel-Moneim et al. 2021c; Mirzaie et al. 2018). The favorable effect of S. platensis could be justified by enhancing the nutrient uptake and balancing the microbial enumeration in the gut due to its content of antibacterial substances such as laminarin and fucoidan (Alwaleed et al. 2021; Khan et al. 2020b; Park et al. 2018). Additionally, the high contents of highly digestible nutrients in S. platensis such as carotenoids, proteins (e.g., lectins), essential unsaturated fatty acids, pigments, essential amino acids, and polyphenols exhibit strong antioxidative potential and contribute to improving the health and growth of birds subjected to high ambient temperature (Abdel-Moneim et al. 2021b; Abdel-Moneim et al. 2020d; Shehata et al. 2020; Tavernari et al. 2018). The low potential of S. platensis water extract to improve birds’ growth compared to the dried powder form may be due to its low contents of phenols and flavonoids, as we mentioned before. During the extraction, thermal pre-treatment of S. platensis may be another cause as it may generate detrimental molecules not appropriate for poultry feeding or induce thermal degradation of some compounds of interest (Starmans and Nijhuis, 1996). Furthermore, the extraction method requires eliminating the insoluble parts of Spirulina, which may contain high protein content and active substances that have not been fully extracted.

Carcass traits were positively influenced in broilers received diets with S. platensis powder as carcass yield, and dressing (%) was improved. At the same time, these parameters were not affected by the water administration of S. platensis extract. Abdominal fat (%) was not altered in all treated groups. These results agree with Moustafa et al. (2021) and Hajati andZaghari (2019), who reported that dietary inclusion of S. platensis powder at 0.25, 0.5, and 1% improved carcass traits of broilers reared under hot and thermoneutral conditions. Moreover, Khan et al. (2020a) documented that 0.2% of dietary S. platensis increased dressing percentage but did not affect abdominal fat (%). The improvement in carcass traits can be justified by the potential of S. platensis powder to provide ample metabolizable energy and nutrients, leading to improved muscle growth and conversion of nutrients to lean meat (Tavernari et al. 2018).

In the present study, both forms of Spirulina did not affect renal or hepatic functions of birds exposed to cyclic heat burden. Previous studies reported conflicting results concerning Spirulina’s impact on hepatic and renal function of experimental animals. Roy-Lachapelle et al. (2017) and Iwasa et al. (2002) reported that Spirulina might contain cyanotoxins and microcystin (hepatotoxin), which may disrupt hepatic function. However, Sugiharto et al. (2018) showed no detrimental effect of Spirulina on hepatic or renal function biomarkers. In contrast, Moustafa et al. (2021) showed that dietary inclusion of Spirulina enhanced liver enzymes activity and renal biomarkers of heat-stressed broilers.

Hypolipidemic activity of S. platensis has been documented (Hamza et al. 2020; Mirzaie et al. 2018) and might be attributed to its potential to inhibit cholesterol synthesis and absorption in the gut. Furthermore, the polyphenols content of S. platensis may inhibit the pancreatic lipase activity and thereby decrease blood lipid concentration (Abdel-Moneim et al. 2020d; Deng and Chow, 2010). In the current study, treatment of both forms of S. platensis reduced the serum concentrations of TG, TC, LDL-cholesterol, and VLDL-cholesterol; however, only SPP2 group was able to elevate blood HDL-cholesterol concentration. Dietary incorporation of S. platensis powder was superior in enhancing the lipid profile of heat-stressed birds than administrating the aqueous extract. The findings of Mirzaie et al. (2018), in line with ours revealed a remarkable decrease in TC, TG, and total lipids of broilers fed diets with 2% S. platensis. Abdel-Moneim et al. (2021c) also reported an enhancement in the lipid profile of heat-stressed broilers treated with 0.5 and 1% S. platensis powder.

Oxidative stress is the major negative impact of heat stress which impairs numerous metabolic dysfunctions and growth performance of broilers (Abo Ghanima et al. 2020a; Liu et al. 2020). GPx and SOD represent the first defense line of the cellular antioxidant mechanism (Ighodaro and Akinloye, 2018), and MDA level indicates the degree of lipid peroxidation in the living cell (Mesalam et al. 2021). The role of dietary supplementation of S. platensis to enhance these antioxidative biomarkers of heat-stressed birds has been reported (Abdel-Moneim et al. 2021c; Khan et al. 2020b; Mirzaie et al. 2018; Moustafa et al. 2021). The enhancement in the antioxidant capacity of heat-stressed chicks treated with S. platensis might be attributed to its content of antioxidant substances (e.g., phycocyanin, polyphenols, polyunsaturated fatty acids, and β-Carotene) (Pestana et al. 2020). S. platensis also has other carotenoids, such as lutein and lycopene, and polysaccharides that characterized for their antioxidant properties (Assunção et al. 2021; Wu et al. 2017). In our study, incorporation of S. platensis in the powder form was superior to the aqueous extract form in enhancing the blood antioxidative biomarkers of birds reared under cyclic heat stress. This difference in the antioxidant activity between the powder and aqueous extract forms of S. platensis is matched with our in vitro results that revealed a reduction in the total antioxidant capacity, total phenols and flavonoids contents, and DPPH˙ scavenging activity of the aqueous extract of S. platensis.

It is well-documented that heat stress impairs humoral immunity and antibody production, particularly after immunization by viral antigens (Hirakawa et al. 2020) and induces inflammatory and oxidative stress (Hirakawa et al. 2020; Song et al. 2018) in heat-stressed broilers. Abdel-Moneim et al. (2020c) and Song et al. (2018) reported a reduction of blood concentrations of immunoglobulin subclasses in heat-stressed birds. Repealing antigen-presenting cells ability to activate T cells might cause the suppression of acquired immunity and antibody production (Preynat-Seauve et al. 2003; Quinteiro-Filho et al. 2010). In the present study, both forms of S. platensis increased the serum level of IgM. In contrast, only the powder form elevated serum IgG level and antibody titer against NDV. These findings agree with earlier literature (Khan et al. 2020b; Velten et al. 2018) and confirmed the functional and biological activity of S. platensis.

Conclusion

The present results revealed that incorporating S. platensis dried powder or aqueous extract improved the growth and carcass characteristics of broilers reared under cyclic heat stress. The serum lipid profile, redox status, and humoral immune response of these birds were also improved. The powder form of S. platensis was superior to the aqueous extract form in improving the studied parameters under cyclic heat stress conditions. Further investigations are required to examine new and more environmentally friendly extraction methods of S. Platensis, such as supercritical fluid extraction and microwave-assisted extraction.