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Potential Effects of Garlic (Allium sativum L.) on the Performance, Immunity, Gut Health, Antioxidant Status, and Blood Parameters of Poultry: An Updated Comprehensive Review

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15 December 2023

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18 December 2023

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Abstract
The use of antibiotics as growth promotors or for the prevention of some poultry diseases has face global concern and serious criticism. Their addition to poultry feed show hazardous effects including development of antimicrobial resistance and the potential harmful effect on humans’ health. To eliminate these threats, there is increasing interest to search for natural alternatives. Plant derivatives such as garlic (Allium sativum L.) and its derivatives are nowadays extensively used in poultry production system. Dietary supplementation of broilers and layers with garlic induced improvement of production parameters, carcass quality, and intestinal integrity. Modulation of the immune response against important viral diseases and increasing the immune organs body weight ratio resulting from supplementation of poultry with garlic. Moreover, garlic showed modulation of gut health through the antibacterial and antiparasitic activities. Treatment with garlic also can mitigate the oxidative stress and reduce the free radicals production. Reduction of cholesterol level, but improvement of some liver and blood parameters were also reported following dietary inoculation of garlic. This review was designed to search on the impact of garlic as feed additives on performance, immunity, gut health, antioxidant status, and blood parameters of poultry.
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Subject: Biology and Life Sciences  -   Animal Science, Veterinary Science and Zoology

1. Introduction

With the ban of the use of antibiotics as growth promoters in most countries, attention has been focused on finding alternatives without resistance or residues [1]. Through the global trend to go back to nature, the World Health Organization encourages using of natural phytogenic substances to replace or reduce the use of antibiotic growth promotors. Phytobiotics or phytogenic are plant derivatives which have been used as feed additives to improve the health and performance of animals [2]. Over the past decade, this safe source of active ingredients is regarded as an attractive research subject and shows promising results [3]. Herbal plants possess multiple therapeutic properties and different effects.
Garlic (Allium sativum) is perennial bulb producing plants that belongs to genus Allium in the family Liliaceae. Since antiquity, garlic has been grown on a large scale on all countries and widely used as feed additives or growth pro moter substance [4]. It has a specific smell and taste, as well as therapeutic activities in alternative medicine [5].
Garlic is estimated to contain almost 33 sulfur compounds (alliin, diallyl sulfides, and allicin), 17 amino acids, essential oils, vitamins (ascorbic acid, ribofavin, niacin, thiamine, and folic acid), minerals (germanium, selenium, phosphates, calcium, and iron), and enzymes [6,7]. The allin and alliinase enzymes collaborate to produce allicin [8]. It enzymatically released from precursor form when the garlic bulbs are crushed or destroyed by digestion. Allicin or daily thiosolphinic acid is active inhibitory principle of garlic [9]. Moreover, allicin ingredients can decompose forming many volatile organosulfur compounds with bioactivities [10].
Garlic contains more than two hundred chemical substances that used for prevention and treatment of cardiovascular diseases [11] as well as antioxidants [12], antimicrobial [13,14], anti-inflammatory [15], anti-atherosclerotic, anti-thrombotic, anti-hypertensive, anti-diabetic, and anti-cancer as well as hypoglycemic properties [14,16,17].
Garlic could be given to poultry in the form of powder, aqueous extract, essential oil, and other commercial products either in the feed or in the drinking water. Dietary feeding of poultry on garlic resulted in enhancement in growth performance, gut health, dressing yield, and production cost [18-20], modulation of immunity and blood parameters [12], prevention of bacterial and parasitic infections [21,22], and mitigation of heat stress [23]. Addition of garlic to the feed of broilers has no negative influence due to it does not leave any residue, and the birds’ manure does not contaminate the environment. Therefore, products from garlic-consuming animals are safe for consumption.
The objectives of this review was to investigate the findings on the impact of garlic as feed additives on performance, immunity, gut health, antioxidant status, and blood parameters of poultry.

2. The different influences of dietary garlic on poultry health

2.1. Production parameters

2.1.1. Performance

The different effects dietary garlic on the production performance parameters of broilers and layers are presented in Tables (1 and 2). Inoculation of garlic in the diets of birds could enhance the production performance parameters including the feed intake (FI), body weight (BW), body weight gain (BWG), and the feed conversion ratio (FCR) [54]. The mechanism by which the garlic powder can improve these parameters could be related to presence of many organosulfur compounds such as allicin, alliin, ajoene, diallylsulfide, dithiin, and S allylcys teine [55]. Similarly, the study of Ross et al. [56] demonstrated that the antibacterial compound, dialkylpolysulphide, in garlic plays axial role in improving the BWG in broilers. A combined diet contains garlic and turmeric (10 g/kg each) reduced the pH of the crop, proventriculus, and ceca, and improved digestible and apparent metabolized energy in ileum of broiler chickens [57]. Besides, garlic might increase the enzymes activity of pancreas, which offer a better environment for the digestion and absorption of nutri ents [12].
The FI of broilers [58] and layers [46] was increased by increasing the level of garlic powder inoculation in the diet is may be owing of rich aromatic oil content of garlic which enhances digestion.
Table 1. The different effects dietary garlic on the production performance parameters of broilers.
Table 1. The different effects dietary garlic on the production performance parameters of broilers.
Dose/route Effects Reference
Garlic paste (3.8%), solvent fractions, or garlic oil equal to this quantity in feed No effect on FI
[24]
Garlic 0, 0.01, 0.1 or 1% in meal No improvement in the performance [25]
Garlic powder 0.2% and 0.4% of feed No effects on BWG, FI, FCR, carcass cuts, and visceral organs [26]
Garlic at 1 kg/ton feed Enhanced carcass yield [27]
Garlic 1, 3, and 5% and 3% garlic powder + 200 IU of α-tocopherol/kg of feed No influence on performance
Increased crude protein
Decreased crude fat contents of carcass, the pH, and thiobarbituric acid reactive substances of meat
[28]
Garlic 0.5%, 1.0%, and 3% Decreased heart weight [29]
Garlic powder 0.5% of feed Increased live BWG [30]
Garlic powder 3% and 5% of diet Increased breast weight (3%)
Low BW (5%)
[31]
A mixture of ginger and garlic (1:1 ratio) 50ml/liter of the drinking water Improved BW, BWG, FI, and FCR [32]
Garlic bulb 5, 10, or 15 g/kg meal Decreased BW (high dose and standard temperature)
No effect on the FCR
[33]
The 5 g/kg garlic powder+1 g/kg black pepper powder and 10 g/kg garlic powder+2 g/kg black pepper powder Improved WG and FCR [34]
Fresh garlic paste 0.2, 0.4, 0.6, and 0.8%/ liter of drinking water No effect on BWG or FCR
Decreased mortality
[35]
Garlic powder 3% in diet and a mixture of garlic powder 1.5% plus turmeric powder 0.25% mproved BWG, FI, FCR, performance index, and protein efficiency ratio [36]
Garlic paste 0.25 % and 0.50% with basal diet Improved BWG, FCR, and livability
No influence on carcass attributes
[37]
Garlic 5g/kg feed, black cumin 5g /kg, or their combination No difference in BWG, FI, FCR, and relative organ weights [38]
A basal diet plus 0.25, 0.50, and 0.75 g garlic powder/kg diet Increased BW and BWG at 21 and 42 days of age
High length and average width of small intestine
[12]
Garlic essential oil (200 mg/kg diet) alone/or combination with lemon essential oil (200 mg/kg diet) under heat stress Enhancement in BW, FCR, carcass dressing, and increasing the digestive enzymes
Decreasing mortality rate and abdominal fat content
[23]
Garlic powder 3% of feed Improved BWG and final BW [39]
Feed intake= FI; Body weight= BW; Body weight gain= BWG; FCR= Feed conversion ratio.
Table 2. The different effects dietary garlic on the production performance parameters of layers.
Table 2. The different effects dietary garlic on the production performance parameters of layers.
Dose/route Effects Reference
1 or 3% garlic meal Decreased egg yolk cholesterol [40]
Garlic paste (3.8%), solvent fractions, or garlic oil equal to this quantity in feed No effect on daily FI [24]
Garlic oil 0.02% in meal No effect on egg production, egg mass, body weight, feed consumption, and feed efficiency [41]
Garlic powder 3% in diet No differences in color and flavor of eggs
No change in yolk cholesterol concentrations
[42]
Sun-dried garlic paste 0, 2, 4, 6, 8, or 10% of diet No effect on egg weight, egg mass, feed consumption, and feed efficiency among diets or birds’ strain
Increased Yolk weight with increasing levels of dietary garlic
Decreased yolk cholesterol concentrations
[43]
Garlic powder 0, 5, 10, and 15 g/kg feed Decreased yolk weight [44]
Garlic powder 0.5 and 10 g/kg feed Increased egg weight
Decreased egg yolk cholesterol triglyceride
No effect on performance or egg albumin index, eggshell index, and egg Haugh unit
[45]
Garlic powder 0, 2, 6, or 8% in feed Increased egg production [46]
Garlic 2% and fenugreek 2% No effect on FI, FCR, BW, BWG, egg rate, egg weight, and egg mass
Increased yolk weight and color and Haugh units
Decreased albumen weight
[47]
Garlic powder 8% in feed Better egg production
No effect on egg mass and egg weight
[48]
Garlic powder 1, 2, and 4% in feed Increased egg production
No effect on egg weight, yolk index, shell weight, shell thickness, yolk weight (1% garlic)
Decreased eggshell index and Haugh unit (4% garlic)
[49]
Garlic juice at 0.25, 0.50, and 1% Improved egg albumin, yolk and shell weight, albumin height, and Haugh unit [50]
Garlic powder 1%, fenugreek 1%, and garlic powder 1% + fenugreek 0.5% No effect on laying hens’ performance [51]
Garlic 1, 2, and 3% of ration No effect on BWG, FCR, egg production, egg mass, albumen weight, albumen height, Haugh unit, yolk index, yolk height, egg weight, fertility, hatchability, embryonic mortality, chick weight and chick visual score, shell thickness, and shell weight
An improvement in yolk diameter, yolk weight, chick length and yolk color
[52]
A mixture of lemon, onion, and garlic juice at portions 1.00, 1.00, and 0.125/liter of the drinking water, respectively Improved FCR
Increased number of eggs/hen, percentage of egg production, and egg mass/hen
Enhanced yolk color and yolk percentage
[53]
Feed intake= FI; Body weight= BW; Body weight gain= BWG; FCR= Feed conversion ratio.

2.1.2. Intestinal architecture

The addition of eugenol and garlic tincture could improve the intestinal integrity and enhance the mucin-producing goblet cell numbers as a defensive response to the birds against necrotic enteritis [59]. Administration of garlic increased the villus height and crypt depth but decreased epithelial thickness and goblet cell numbers in the intestine of broiler chickens [60]. Furthermore, the highest capacity of crypt and villi of small intestines was detected following dietary addition of garlic in coccidiosis infected broilers [61]. Allicin can regenerate and improve and the physiological structure epithelium layer of the intestine, increase the crypt’s depth and villus height, which eventually support the digestive capacity via increasing the nutrients absorption and assimilation. A longer villi and deeper crypt is considered a sign of a healthy intestine architecture, and consequently a good digestive capacity and the pancreatic enzyme activity. Moreover, the antioxidant characters of garlic can enhanced the overall gut function and improved the nitrogen energy utilization [62]. Yang et al. [63] reported that feeding of broilers on garlic reduces the pH of digesta which was resulted in an increase in the production of the volatile fatty acid and the proliferation of beneficial bacteria. Dietary addition of 0.5% garlic efficiently reduced the systemic hypertension and the prevalence of ascites, but had no negative influences on broilers performance [33]. Inulin component of garlic decreases the digesta pH of birds and increases the volatile fatty acids production which may help in enhancing the beneficial bacterial colonization [64].
Others showed that garlic supplementation has no effect on feed efficiency or growth performance of broilers and layers [41,43,52,65].This discrepancy might be resulted from the differences in the experiment duration, birds’ genetic and health status, or the type, processing, and quality of garlic products components.

2.2. Immunity

The effect of garlic on the immunity of birds is illustrated in Table (3). It has been found that the different forms of dietary garlic alone or in combination with other aromatic phytobiotics can enhance the immune response in terms of enhancing the antibody titers against and increasing the immune organ/ body weight ratio [12,23,35].
The improvement in immune response may be related to the characters of biologically active compounds in essential oils as antimicrobial, antioxidant, and anti-inflammatory, which provide essential nutrients the development of the immune cells. In addition, promoting the proliferation of lymphocytes in the primary immune organs and improving intestinal integrity could stimulating the production of immunoglobulin (Ig) such as IgG, IgM, and IgA which is associated with increasing the relative weight of the immune organs. Many immuno-stimulators compounds are present in garlic, including the lectin family, which is known to interact with pathogen recognition receptors on immune cell surfaces [72]. Garlic is one of the impressive conductors of the body’s immune system; which stimulates immune function by making macrophages or killer cells more active. Moreover, garlic can improve the humoral immune cell functions via enhancement of the cytokine production and/or antigen presenting cells phagocytic capacity [67]. Dorhoi et al. [73] demonstrated that a high dose of garlic extract (200 mg/ml) on to a macrophage culture of laying chickens could impair the phagocyte function and inhibit phagocytosis, whereas a low dose (50 mg/ml) increased the sheep red blood cell uptake. Inoculation of garlic extract or its protein fraction increased the destruction in peritoneal macrophages and engulfment of parasites in Leishmanial major-infected Balb [74].
An in-vitro study showed that garlic extract increased concanavalin A (ConA)-induced splenocytes, thymocytes proliferations, and gene expression of interleukin (IL)-2 and interferon gamma (INF-γ) [75]. Further, addition of garlic extract to a culture augmented the production of IL-2 and IL-12, INF-γ, and tumor necrosis factor α in stimulated splenocytes [76]. Low concentrations of diallyl trisulfide (3-12.5 mg/ml) of garlic increased the proliferative responses in a culture, while higher concentration (50 mg/ml) inhibited T-lymphocyte proliferation in mice [77]. Aged garlic extract stimulated the proliferation and increased activity of T-cells and natural killer cells as well as enhanced phagocytosis and cytokine release [78,79].
Garlic supplementation increased the relative weights of immune organs such as spleen, thymus, and bursa of Fabricius, the white blood cells counts, as well as lymphocytes, splenocyte, and thymocyte proliferations [67]. In addition, the titers of antibodies against Newcastle disease virus, sheep red blood cells count, and Brucella abortus have been increased following administration of garlic in laying chickens [67].
It has been demonstrated that the anti-oxidative stress of garlic is a potential factor to enhance the immune response [80]. Supplementation with garlic extract at 4 and 8 mg/ml revealed that macrophages may display antimicrobial activity and enhance the production of reactive oxygen species.
Table 3. The effect of dietary garlic on the immune response of poultry.
Table 3. The effect of dietary garlic on the immune response of poultry.
Dose/route Type of production Effects Reference
Garlic powder 1% or 3% garlic Broiler chickens No effect on antibody production against NDV and leukocyte count [66]
Garlic 10 and 30 g/kg diet White Leghorn chickens Enhanced antibodies against NDV, SRBCs, and BA
Augmented splenocyte and thymocyte proliferations
Reduced CD4+, but increasing CD4: CD8- lymphocyte ratios and WBCs count
Increased relative weights of immune organs (spleen, thymus glands, and bursa of Fabricius)
[67]
Garlic 0.5%, 1.0%, and 3% Broiler chickens Lower weights of bursa of Fabricius and spleen [29]
Garlic powder 0.1% Broiler chickens Improved relative weight of bursa of Fabricius without effect on the spleen weight
No effect on NDV vaccine (LaSota) antibody response
[68]
Garlic powder 3% and 5% of diet Broiler chickens No influence on bursa of Fabricius and thymus weights
Decrease spleen weight
[31]
A mixture of ginger and garlic (1:1 ratio) 50ml/liter of the drinking water Marshal broiler chickens Increased total protein, albumin, and globulin [32]
Garlic extract (allicin) 25, 50, 75, or 100 mg/kg diet Broiler chickens Increased total protein and albumin concentrations by about 4.7 and 5.9%, respectively (50 mg/kg)
No effect on total protein, albumin or globulin concentrations (25, 75, or 100 mg/kg)
[69]
Fresh garlic paste 0.2, 0.4, 0.6, and 0.8%/ liter of drinking water Broiler chickens Increased antibody titer against NDV [35]
Garlic-meal 0.125% of feed. Broiler chickens Reducing scores of IBDV signs
Higher mortality rate
High antibody response to IBDV
[70]
Garlic essential oil 0.06 mL/L drinking water Broiler chickens Improved immune organ index, IgM, IgG, and IgA [71]
A basal diet plus 0.25, 0.50, and 0.75 g garlic powder/kg diet Broiler chickens Increasing total protein, globulin, IgM, and IgG
Improved liver and immune related organs weight
[12]
Garlic essential oil (200 mg/kg diet) alone/or combination with lemon essential oil (200 mg/kg diet) under heat stress Broiler chickens Increasing the relative weight of bursa of Fabricius and the serum antibody titer against NDV
No changes in relative weights of spleen and thymus glands, and antibody titer against AIV
[23]
NDV= Newcastle disease virus; AIV= Avian influenza virus; BA= Brucella abortus.SRBC= Sheep red blood cells; Ig= Immunoglobulin; CD= Cluster of differentiation; IBDV= Infectious bursal disease virus

2.3. Gut health

2.3.1. Antibacterial

The strong antimicrobial effects of garlic have been reported [37,55,81,82]. It has been reported that garlic extracts exert a differential inhibition between beneficial intestinal microflora and potentially harmful enterobacteria [83]. Garlic could reduce the number of gut pathogenic bacterial populations such as Escherichia coli (E. coli). Garlic showed an ability to inhibit E. coli 10 times greater than that seen in Lactobacillus casei [84]. Rahimi et al. [68] demonstrated that E. coli count was significantly reduced in the digesta of ileo-cecum of broiler chickens supplemented by a blend of garlic, thyme, and coneflower. Recently, Elbaz et al. [20] (2021) found that garlic treatment could reduce the ileal enumeration of E. coli and total coliform, but increase the Lactobacillus count. In addition, the positive influences of eugenol and garlic mixture on broilers performance and intestinal health status under necrotic enteritis condition have been reported [82]. Microencapsulated eugenol and garlic tincture modulated the microbiota balance by inhibiting pathogenic while promoting beneficial microbial growth, as well as reduced the severity of the intestinal lesions of broilers with necrotic enteritis [59]. The antimicrobial and the bacteriostatic properties of garlic extract is associated with the presence of allicin active compound [13]. Allicin exhibited bacteriostatic effect on some vancomycin-resistant enterococci. Besides, allicin exhibits SH group reactivity on cysteine residues of pathogen enzymes causing deactivation and suppression of specific thiol-containing enzymes in pathogens [85]. This activity resulted in the inactivation and inhibition of specific thiol-containing enzymes in microorganisms [21,86]. Garlic is a nucleophilic agent that has the ability to counteract the impact of electrophilic substances on microorganisms [87].

2.3.2. Anti-parasitic

The in-vitro and in-vivo anticoccidial activities of different processed extract forms of garlic have been documented [88-96]. The study of Ali et al. [97] found that supplementing coccidiosis infected broiler chickens with garlic at 15 g/kg feed reduced the oocysts shedding and lesion score, but improved the histopathology of the small intestines. In the same context, continuous feeding of Eimeria tenella infected broiler chickens on natural garlic essential oil (0.06 mL/L drinking water) significantly reduced the clinical signs, cecal lesions score, the oocysts shedding, but increased the weight of diseased chickens, and effectively improve the intestinal functions [71]. In comparison with ginger oil, garlic oil (150μL/100 mL) showed superior efficacy against Eimeria species infection of quails in terms of improved activity level with better health, increased feed intake, and complete recovery from oocysts on day 15 post-infection [98].
Allen et al. [99] reported that the antioxidant properties of garlic causes oxidative stress against parasites and neutralize oxygen reactive species. In furtherance of this, Pourali et al. [100] have owed the anticoccidial activity of garlic to its immunomodulatory activity. Similarly, Kim et al. [101] revealed improved resistance against Eimeria acervulina infection in chickens after dietary treatment with garlic metabolites [101]. Propyl thiosulphinate oxide and propyl thiosulphinate active ingredients of garlic reduced the faecal oocysts shedding and enhanced the antibody response against coccidial infection [101]. Likewise, the aqueous garlic extract is rich in phenols, flavonoids, and varying sulphur compounds [14]. The phenolic compounds change the permeability of the cytoplasmic membrane to many cations, inhibit the physiological functions, and consequently resulting in loss of membrane potential, allowing vital cellular substances to leak out, protein and ATP production to be inhibited and cellular death to occur [102].
Allicin induces changes in the intestinal microbiota, exerts antioxidant effect on Eimeria oocysts, and stimulates the immunity through enhancing the antibody response which directly destruct sporozoites [54,103]. Additionally, phenolic component in garlic acts on the cytoplasmic membrane of Eimeria species and make changes in their cation permeability, leading to the death of Eimeria [104]. Further, allicin can interact with the intestinal cytoplasmic membranes and alters cations permeability, resulting in the disruption of vital processes in the parasite cells and, eventually, their death [105]. The ability of allicin and alcoholic garlic extract to eliminate Eimeria tenella oocysts makes them superior to chemical disinfectants [22]. Eimeria oocysts sporulated in allicin-containing media displayed the lowest in-vivo gross lesion score and oocyst count shedding compared to those sporulated in alcoholic garlic extract and potassium hydroxide [22]. Garlic extracts at 360 mg/mL and Allicin at 180 mg/mL significantly decreased the number of oocysts by 73.5 and 88.3%, respectively [22].
Moreover, the garlic crude extract proved great activities against worms and protozoon parasites Cryptosporidium spp in different animals’ model [106-108].

2.4. Antioxidant status

Garlic exhibited a strong antioxidant activity in birds (Table 4). The imbalance between the oxidation and reduction in the host’s cells induces a significant destruction of them with a subsequent oxidative stress. However, the antioxidant enzymes can prevent the free radicals to attack the cell membranes [117]. Essential oils present in different aromatic plants contain several natural antioxidants [12]. Garlic and/or garlic tocopherol induced a much higher antioxidant effect with reducing the free radicals production [12,43], especially in birds under heat stress conditions [23].
Decreased activities of hydroxymethylglutaryl coenzyme A reductase, cholesterol 7 α-hydroxylase, and fatty acid synthetase have been demonstrated after administration of garlic powder polar fractions (garlic equivalent to 1, 2, 4, 6, and 8% fresh garlic paste) [118]. The diallyl polysulfides from an aged garlic extract could protect the cell membranes from lipid peroxidation [119]. Besides, essential oils present in garlic and other plants are able to remove the oxygen free radicals through reducing the level of malondialdehyde (MDA), and enhancing the levels of superoxide dismutase (SOD) and glutathione peroxidase (GPx) [100,120,121].

2.5. Blood parameters

The influence of dietary addition of garlic addition on the different blood parameters of poultry is shown in Table (4).
Many studies showed the hypo-cholesteric effect of garlic in broilers and layers [12,23,51,53,114]. Garlic containing enzymes may have a role in regulating the metabolism of lipid and enhancing enzymes activities that stimulates the biliary cholesterol secretion and lowers the fractional absorption of dietary cholesterol [20]. Moreover, inhibition of acetyl CoA synthetase and 3-hydroxyl-3-methylglutaryl-CoA reductase enzymes, that are required for cholesterogenesis and the biosynthesis of fatty acids, can reduce the blood cholesterol level [122]. Similarly, the potential effect of garlic on the lipid metabolism in layers may be attributed to depressing of lipogenic and cholesterogenic activity of the liver enzymes such as fatty acid synthase, glucose 6 phosphatase dehydrogenase, and malic enzyme, consequently, the mechanism of hypocholesterol and hy polipid syntheses [50]. Lower serum and liver cholesterol [118] inhibits bacterial growth [123], reduces platelet formation, and decreases oxidative stress [119].
Additionally, the effect of garlic on the hematological parameters such as red blood cells (RBCs) and white blood cells (WBCs) counts, haemoglobin, and packed cell volume have been reported [12,31,32]. The hemolytic bioactives and their metabolites in garlic may be responsible for these effects. Increasing in erythrocytes count with garlic supplementation could be owing to the end- product pro duced from garlic metabolism possible stimulates the formation and secretion of erythropoietin in the kidney causing synthesis of RBCs [124]. Moreover, addition of garlic extract to laying hens diet could enhance spleen RBCs uptake [73].

3. Conclusion

The supplementation of garlic to broiler and layers poultry species mostly shows improvement in the performance and production efficiency, enhances the immune response, maintains the gut health, reduces the exudative stress, and modulates many important blood parameters. However, the different mode of actions of garlic are is indefinite. Therefore, further studies should focus on establishing the mechanisms of actions of garlic and its derivatives.

Author Contributions

WAA designed and reviewed the literatures, wrote, and submitted the article.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All prepared data are presented in the present article.

Conflicts of Interest

The author provides the publisher a copyright license, granting the publisher the exclusive right to publish and sell the study findings in whole or in part in any language. The authors have no relevant financial or non-financial interests to disclose.

References

  1. Saleha, A.A.; Myaing, T.T.; Ganapathy, K.K.; Zulkifli, I.; Raha, R. , Arifah, K. Possible effect of antibiotic supplemented feed and environment on the occurrence of multiple antibiotic resistant Escherichia coli in chickens. Int. J. Poult. Sci; 2009; 8, pp. 28–31. [Google Scholar] [CrossRef]
  2. Abd El-Ghany, W.A. (2020). Phytobiotics in poultry industry as growth promoters, antimicrobials and immunomodulators – A review. J. World’s Poult. Res. 2020, 10, 571–579. [Google Scholar] [CrossRef]
  3. Navidshad, B.; Darabighane, B.; Malecky, M. 2018. Garlic: An alternative to antibiotics in poultry production, a review. Iran. J. Appl. Anim. Sci. 2018, 8, 9–17. [Google Scholar]
  4. Ur Rahman, S.; Khan, S.; Chand, N.; Sadique, U.; Khan, RU. In vivo effects of Allium cepa L. on the selected gut microflora and intestinal histomorphology in broiler. Acta Histochem. [CrossRef]
  5. Ezeorba, T.P.C.; Chukwudozie, K.I.; Ezema, C.A.; Anaduaka, E.G.; Nweze, E.J.; Okeke, E.S. Potentials for health and therapeutic benefits of garlic essential oils: Recent findings and future prospects. Pharmacol. Res. Mod. Chin. Med. 2022, 3, 100075. [Google Scholar] [CrossRef]
  6. Najda, A.; Błaszczyk, L.; Winiarczyk, K.; Dyduch, J.; Tchórzewska, D. Comparative studies of nutritional and health-enhancing properties in the “garlic-like” plant Allium ampeloprasum var. ampeloprasum (GHG-L) and A. sativum. Sci. Hortic. 2016, 201, 247–255. [Google Scholar] [CrossRef]
  7. Ozma, M.A.; Abbasi, A.; Ahangarzadeh Rezaee, M.; Hosseini, H.; Hosseinzadeh, N.; Sabahi, S.; Noori, S.M.A.; Sepordeh, S.; Khodadadi, E.; Lahouty, M.; Kafil, H. S. A critical review on the nutritional and medicinal profiles of garlic’s (A. sativum L.) bioactive compounds. Food Rev. Int. [CrossRef]
  8. Puvača, N.; Kostadinović, L. ; Ljubojević D, Lukač D, Lević J, Popović S, Novakov N, Vidović B, Đuragić O. Effect of garlic, black pepper and hot red pepper on productive performances and blood lipid profile of broiler chickens. Eur. Poult. Sci. [CrossRef]
  9. Saleem, Z.M.; Al-Delaimy, K.S. Inhibition of Bacillus aurous by garlic extracts. J. Food Prot. 1982, 45, 1007–1009. [Google Scholar] [CrossRef] [PubMed]
  10. Chang, K.J.; Cheong, S.H. Volatile organosulfur and nutrient compounds from garlic by cultivating areas and processing methods. Fed. Am. Soc. Exp. Bio. J. 2008, 22, 1108–1112. [Google Scholar] [CrossRef]
  11. Bordia, A. Effect of garlic on blood lipids in particles with coronary heart disease. Am. J. Clin. Nutr. 1981, 34, 2100–2103. [Google Scholar] [CrossRef]
  12. Ismail, I.E.; Alagawany, M.; Taha, A. E; Puvača, N; Laudadio, V.; Tufarelli, V. Effect of dietary supplementation of garlic powder and phenyl acetic acid on productive performance, blood haematology, immunity and antioxidant status of broiler chickens. Anim. Biosci. 2021, 34, 363. [CrossRef]
  13. Sivam, G.P. Protection against Helicobacter pylori and other bacterial infections by garlic. J. Nutr. 2001, 131, 1106S–1108S. [Google Scholar] [CrossRef]
  14. Jang, H.J.; Lee, H.J.; Yoon, D.K.; Ji, D.S.; Kim, J.H.; Lee, C.H. Antioxidant and antimicrobial activities of fresh garlic and aged garlic by-products extracted with different solvents. Food Sci, Biotechnol, 27. [CrossRef]
  15. Morioka, N.; Sze, L.L.; Morton, D.L.; Irie, R.F. A protein fraction from aged garlic extract enhances cytotoxicity and proliferation of human lymphocytes mediated by interleukin-2 and concanavalin A. Cancer Immunol Immunother. 1993, 37, 316–322. [Google Scholar] [CrossRef]
  16. Agarwal, K.C. Therapeutic actions of garlic constituents. Med. Res. Rev. 1996, 16, 111–124. [Google Scholar] [CrossRef]
  17. Ariga, T.; Seki, T. Antithrombotic and anticancer effects of garlic derived sulfur compounds. BioFactors. 2006, 26, 93–103. [Google Scholar] [CrossRef] [PubMed]
  18. Makwana, R.B.; Raval, A.P.; Chauhan, H.D. , Kulkarni, R.C., Srivastava, A.K.; Bhagwat, S.R.; Rajgor, B.B. Effects of garlic (Allium sativum) supplementation on growth performance, carcass characteristics and economics of broilers. J. Anim. Res. [CrossRef]
  19. Al-Massad, M.; Al-Ramamneh, D.; AL-Sharafat, A.; Abdelqader, A.; Hussain, N. Effect of using garlic on the economical and physiological characteristics of broiler chickens. Russ. Agric. Sci. 2018, 44, 276–281. [Google Scholar] [CrossRef]
  20. Elbaz, A.M.; Ibrahim, N.S.; Shehata, A.M.; Mohamed, N.G.; Abdel-Moneim, A.M. Impact of multi-strain probiotic, citric acid, garlic powder or their combinations on performance, ileal histomorphometry, microbial enumeration and humoral immunity of broiler chickens. Trop. Anim. Health Prod. 2021, 53. [Google Scholar] [CrossRef]
  21. Bhatwalkar, S.B.; Mondal, R.; Krishna, S.B.N.; Adam, J.K.; Govender, P.; Anupam, R. Antibacterial properties of organosulfur compounds of garlic (Allium sativum). Front. Microbiol. 2021, 12, 613077. [Google Scholar] [CrossRef] [PubMed]
  22. Abd-ELrahman, S.M.; Mohamed, S.A.-A.; Mohamed, S.E.; El-Khadragy, M.F.; Dyab, A.K.; Hamad, N.; Safwat, M.M.; Nasr, A.A.E.; Alkhaldi, A.A.M.; Gareh, A.; Elmahallawy E., K. Comparative effect of allicin and alcoholic garlic extract on the morphology and infectivity of Eimeria tenella oocysts in chickens. Animals. 2022, 12, 3185. [Google Scholar] [CrossRef] [PubMed]
  23. Elbaz, A.M.; Ashmawy, E.S.; Salama, A.A.; Abdel-Moneim, A.E.; Badri, F.B.; Thabet, H.A. Effects of garlic and lemon essential oils on performance, digestibility, plasma metabolite, and intestinal health in broilers under environmental heat stress. BMC Vet. Res. 2022, 18, 430. [Google Scholar] [CrossRef] [PubMed]
  24. Qureshi, A.A.; Din, Z.Z. .; Abuirmeileh, N., Burger, W.C., Ahmad, Y, Eds.; Elson, C.E. Suppression of avian hepatic lipid metabolism by solvent extracts of garlic: impact on serum lipids. J. Nutr. 1983, 113, 1746-1755. [Google Scholar] [CrossRef]
  25. Horton, G.M.J.; Fennell, M.J.; Prasad, B.M. Effects of dietary garlic (Allium sativum) on performance, carcass composition and blood chemistry changes in broiler chickens. Canadian J. Anim. Sci. 1991, 71, 939–942. [Google Scholar] [CrossRef]
  26. Tollba, A.A.H.; Hassan, M.S.H. Using some natural additives to improve physiological and productive performance of broiler chicks under high temperature conditions. 2. Black cumin (Niglla sativa) or garlic (Allium sativum). Egypt. Poult. Sci J.
  27. Ashayerizadeh, O.; Dastar, B.; Shargh, M.S.; Ashayerizadeh, A. ; Rahmatnejad. E.; Hossaini, S.M.R. Use of garlic (Allium sativum), black cumin seeds (Nigella sativa L.) and wild mint (Mentha longifolia) in broiler chickens diets. J. Anim. Vet. Adv.
  28. Choi, H.; Park, W.Y.; Kim, Y.J. Effects of dietary garlic powder and α-tocopherol supplementation on performance, serum cholesterol levels, and meat quality of chicken. Poult. Sci. 2010, 89, 1724–1731. [Google Scholar] [CrossRef] [PubMed]
  29. Raeesi, M. , Hoseini Aliabad, S.A., Roofchaee, A., Zare Shahneh, A., Pirali, S. Effect of periodically use of garlic (Allium sativum) powder on performance and carcass characteristics in broiler chickens. World Acad. Sc. Eng. Technol.
  30. Suriya, R.; Zulkifli, I.; Alimon, A.R. The effect of dietary inclusion of herbs as growth promoter in broiler chickens. J. Anim. Vet. Adv. [CrossRef]
  31. Elagib, H.A.A.; El-Amin, W.I.A; Elamin, K.M. , Malik, H.E.E. Effect of dietary garlic (Allium sativum) supplementation as a feed additive on broiler performance and blood profile. J. Anim. Sci. Adv.
  32. Oleforuh-Okoleh, V.U.; Harrie, M.; Solomon, N.F.; Olorunleke, O.; Joesph, U. Evaluation of growth performance, hematological and serum biochemical response of broiler chickens to aqueous extract of ginger and garlic. J. Agric. Sci. 2015, 7, 167–173. [Google Scholar] [CrossRef]
  33. Varmaghany, S.; Torshizi, M.A.K.; Rahimi, S.; Lotfollahian, H.; Hassanzadeh, M. The effects of increasing levels of dietary garlic bulb on growth performance, systolic blood pressure, hematology, and ascites syndrome in broiler chickens. Poult. Sci. 2015, 94, 1812–1820. [Google Scholar] [CrossRef]
  34. Kirubakaran, A.; Moorthy, M.; Chitra, R.; Prabakar, G. Influence of combinations of fenugreek, garlic, and black pepper powder on production traits of the broilers. Vet. World 2016, 9, 470. [Google Scholar] [PubMed]
  35. Gautam, G.; Nabaraj Shishir, B. Effect of Allium sativum on immune status against Newcastle disease virus and the productive performance of broiler chickens. J. Poult. Sci. 2017, 16, 515–521. [Google Scholar] [CrossRef]
  36. Ratika, K.; James, S.R.K; Kumar, S.R. , Singh, M. Weekly assessment of growth performance of broilers fed a diet supplemented with garlic and turmeric powder and their combination. Int. J. Curr. Microbiol. Appl. Sci. 2018, 7, 1373–1381. [Google Scholar] [CrossRef]
  37. Sangilimadan, K. , Churchil, R.R., Premavalli, K., Omprakash, A.V. Effect of garlic (Allium sativum) on production performances and carcass traits of Nandanam broiler-2. Int. J. Curr. Microbiol. Appl. Sci. 2538. [Google Scholar] [CrossRef]
  38. Aydogan, I.; Yildirim, E.; Kurum, A.; Bolat, D.; Cinar, M.; Basalan, M.; Yigit, A. The effect of dietary garlic (Allium Sativum), black cumin (Nigella Sativa) and their combination on performance, intestine morphometry, serum biochemistry and antioxidant status of broiler chickens. Braz. J. Poult. Sci. 2020, 22. [Google Scholar] [CrossRef]
  39. Tanti, A.; Retnani, Y.; Soesanto, I.R.H. Effect of supplementation garlic (Allium sativum) by various processing on performances of broiler. IOP Conf. Ser.: Earth Environ. Sci.
  40. Sharma, R.K.; Singh, R.A.; Pal, R.N.; Aggarwal, C.K. Cholesterol contents of chicken eggs as affected by feeding garlic, sarpagandha and nicotinic acid. Haryana Agric. Univ. J. Res. 1979, 9, 263–265. [Google Scholar]
  41. Reddy, R.V.; Lightest, S.F.; Maurice, D.V. Effect of feeding garlic oil on performance and egg yolk cholesterol concentration. Poult Sci. 1991, 70, 2006–2009. [Google Scholar] [CrossRef]
  42. Birrenkott, G.; Brockenfelt, G.E.; Owens, M.; Halpin, E. Yolk and blood cholesterol levels and organoleptic assessment of eggs from hens fed a garlic-supplemented diet. Poult. Sci. 2000, 79, 75–82. [Google Scholar]
  43. Chowdhury, S.R.; Chowdhury, S.D.; Smith, T.K. Effects of dietary garlic on cholesterol metabolism in laying hens. Poult. Sci. 2002, 81, 1856–1862. [Google Scholar] [CrossRef]
  44. Mottaghitalab, M.; Taraz, Z. Effects of garlic (Allium sativum) on egg yolk and blood serum cholesterol in Aryan breed laying hens. Br. Poult. Sci. 2002, 43, S42–S43. [Google Scholar]
  45. Yalcin, S.; Onbasilar, E.E.; Reisli, Z.; Yalcin, S. Effects of garlic powder on the performance, egg traits and blood parameters of laying hens. J. Sci. Food Agric. 2006, 86, 1336–1339. [Google Scholar] [CrossRef]
  46. Khan, S.H.; Sardar, R.; Anjum, M.A. Effects of dietary garlic on performance and serum and egg cholesterol concentration in laying hens. Asian Aust. J. Anim. Sci. 2007, 21, 22–27. [Google Scholar] [CrossRef]
  47. Saffa, H.M. Effect of dietary garlic or fenugreek on cholesterol metabolism in lying hens. Egypt. J. Poult. Sci. 2007, 27, 1207–1221. [Google Scholar]
  48. Khan, Q.S.H.; Hassan, S.; Sardar, R.; Anjum, M.A. Effects of dietary garlic on cholesterol concentration in native Desi laying hens. Am. J. Food Technol. 2008, 3, 207–213. [Google Scholar]
  49. Canogullari, S.; Baylan, M.; Erdogan, Z.; Duzguner, V.; Kucukgul, A. The effects of dietary garlic powder on performance, egg yolk and serum cholesterol concentrations in laying quails. Czech. J. Anim. Sci. 2010, 55, 286–293. [Google Scholar] [CrossRef]
  50. Mahmoud, K.Z.; Saad, M.; Gharaibeh, H.; Zakaria, A.; Amer, M. Garlic (Allium sativum) supplementation: influence on egg production, quality and yolk cholesterol level in laying hens. Asian Australs. J. Anim. Sci. 2010, 23, 1503–1509. [Google Scholar] [CrossRef]
  51. Motamedi, S.M.; Taklimi, S.M. Investigating the effect of fenugreek seed powder and garlic powder in the diet on immune response of commercial laying hens’ egg. Indian J. Sci. Res. 2014, 3, 277–283. [Google Scholar]
  52. Asrat, M.; Zeryehun, T.; Amha, N.; Urge, M. Effects of supplementation of different levels of garlic (Allium sativum) on egg production, egg quality and hatchability of White Leghorn chicken. Livest. Res. Rural Dev. 2018, 30. [Google Scholar]
  53. Omer, H.A.A.; El-Mallah, G.M.H.; Abdel-Magid, S. S. Impact of adding natural bioactive mixture composed of lemon, onion, and garlic juice at different levels on productive performance, egg quality, and some blood parameters of commercial laying hens. Bull. Natl. Res. Cent. 2019; 43. [Google Scholar] [CrossRef]
  54. Khan, R.U.; Nikousefat, Z.; Tufarelli, V.; Naz, S.; Javdani, M.; Laudadio, V. Garlic (Allium sativum) supplementation in poultry diets: effect on production and physiology. Worlds Poult. Sci. J. [CrossRef]
  55. Ziarlarimi, A.; Irani, M.; Gharahveysi, S.; Rahmani, Z. Investi gation of antibacterial effects of garlic (Allium sativum), mint (Menthe spp.) and onion (Allium cepa) herbal extracts on Escherichia coli isolated from broiler chickens. Afr. J. Biotechnol. [CrossRef]
  56. Ross, Z.M.; O’Gara, E.A.; Hill, D.J.; Sleightholme, H.V.; Maslin, D.J. Antimicrobial properties of garlic oil against human enteric bacteria: evaluation of methodologies and comparisons with garlic oil sulfides and garlic powder. Appl. Environ. Microbiol. [CrossRef]
  57. Olukosi, O.A.; Dono, N.D. Modification of digesta pH and intestinal morphology with the use of benzoic acid or phytobiotics and the effects on broiler chicken growth performance and energy and nutrient utilization. J. Anim. Sci. 2014, 92, 3945–3953. [Google Scholar] [CrossRef]
  58. Nusairat, B.M. Dietary supplementation of garlic (Allium sativum): influence on performance parameters, meat quality and humoral immune response in broiler chicks. M.S. Thesis, . Jordan University of Science and Technology, Irbi, 2007. [Google Scholar]
  59. Kumar, A.; Kheravii, S.K.; Ionescu, C.; Blanchard, A.; Barekatain, R.; Bajagai, Y.S.; Wu, S.B. A microencapsulated mixture of eugenol and garlic tincture supplementation mitigates the effect of necrotic enteritis on intestinal integrity and increases goblet cells in broilers. Microorganisms. 2021, 9, 1451. [Google Scholar] [CrossRef]
  60. Adibmoradi, M.; Navidshad, B.; Seifdavati, J.; Royan, M. Effect of dietary garlic meal on histological structure of small intestine in broiler chickens. J. Poult. Sci. 2006, 43, 378–383. [Google Scholar] [CrossRef]
  61. Gotep, J.G.; Tanko, J.T.; Forcados, G.E.; Muraina, I.A.; Ozele, N.; Dogonyaro, B.B.; Oladipo, O.O.; Makoshi, M.S.; Akanbi, O.B.; Kinjir, H.; Samuel, A.L. Onyiche, T.E.; Ochigbo, G.O.; Aladelokun, O.B.; Ozoani, H.A.; Viyoff, V.Z.; Dapuliga, C.C.; Atiku, A.A.; Okewole, P.A.; Shamaki, D.; Ahmed, M.S.; Nduaka, C.I. Therapeutic and safety evaluation of combined aqueous extracts of Azadirachta indica and Khaya senegalensis in chickens experimentally infected with Eimeria oocysts. J. Parasitol. Res. 2016, 2016, 4692424. [Google Scholar] [CrossRef]
  62. Halliwell, B.; Zhao, K.; Whiteman, M. The gastrointestinal tract: A major site of antioxidant action? Free Radic. Res. 2000, 33, 819–830. [Google Scholar] [CrossRef] [PubMed]
  63. Yang, Y.; Iji, P.A.; Choct, M. Dietary modulation of gut microflora in broiler chickens: A review of the role of six kinds of alternatives to in-feed antibiotics. Worlds Poult. Sci. J. 2009, 65, 97–114. [Google Scholar] [CrossRef]
  64. Grajek, W.; Olejnik, A.; Sip, A. Probiotics, prebiotics and antioxidants as functional foods. Acta. Biochim. Pol. 2005, 52, 665–671. [Google Scholar] [CrossRef] [PubMed]
  65. Yalcin, S.; Onbaşilar, Ĺ.; Şehu, A.; Yalcin, S. The effects of dietary garlic powder on the performance, egg traits and blood serum cholesterol of laying quails. Asian-Australas. J. Anim. Sci. [CrossRef]
  66. Jafari, R.; Razi, M.; Ghorbanpoor, M.; Marashian, S. Effect of dietary garlic on immune response of broiler chicks to live Newcastle disease vaccine. Pak. J. Biol. Sci. 2008, 11, 1848–1851. [Google Scholar] [CrossRef]
  67. Hanieh, H.; Narabara, K.; Piao, M.; Gerile, C.; Abe, A.; Kondo, Y. Modulatory effects of two levels of dietary Alliums on immune response and certain immunological variables, following immunization, in White Leghorn chickens. Anim Sci J. 2010, 81, 673–380. [Google Scholar] [CrossRef]
  68. Rahimi, S.; Teymouri Zadeh, Z.; Karimi Torshizi, M.A.; Omidbaigi, R.; Rokni, H. Effect of the three herbal extracts on growth performance, immune system, blood factors and intestinal selected bacterial population in broiler chickens. J. Agric. Sci. Technol.
  69. El-katcha, M.I.; Soltan, M.A.; Sharaf, M.M.; Hasen, A. Growth performance, immune response, blood serum parameters, nutrient digestibility and carcass traits of broiler chicken as affected by dietary supplementation of garlic extract (allicin). Alex. J. Vet. Sci. 2016, 49, 50–54. [Google Scholar] [CrossRef]
  70. Oladele, O.; Esan, O.; Akpan, I.; Enibe, F. Garlic feed inclusion and susceptibility of broiler chickens to infectious bursal disease. J. Adv. Vet. Anim. Res. 2018, 5, 275–281. [Google Scholar] [CrossRef]
  71. Chang, L.Y; Di, K.Q.; Xu, J.; Chen, Y.F.; Xi, J.Z.; Wang, D.H.; Hao, E.Y.; Xu, L.J.; Chen, H.; Zhou, R.Y. Effect of natural garlic essential oil on chickens with artificially infected E. tenella. Vet. Parasitol. 2021, 300, 109614. [Google Scholar] [CrossRef]
  72. Susan, S.P. Aged garlic extract modifies human immunity. J. Nutr. 2016, 146, 433S–436S. [Google Scholar] [CrossRef]
  73. Dorhoi, A.; Dobrean, V.; Zahan, M.; Virag, P. Modulatory effects of several herbal extracts on avian peripheral blood cell immune responses. Phytother. Res. 2006, 20, 352–358. [Google Scholar] [CrossRef] [PubMed]
  74. Ghazanfari, T.; Hassan, Z.; Ebtekar, M.; Ahamdiani, A.; Naderi, G. Azar, A. Garlic induces a shift in cytokine pattern in Leishmania major-infected Balb/c mice. Scand. J. Immunol. [CrossRef]
  75. Hanieh, H.; Narabara, K. ; Tanaka, Y; Gu, Z.; Abe, A.; Kondo, Y. Immunomodulatory effects of Alliums and Ipomoea batata extracts on lymphocytes and macrophages functions in White Leghorn chickens: In vitro study. Anim. Sci. J. [CrossRef]
  76. Kyo, E.; Uda, N.; Ushijima, M.; Kasuga, S.; Itakura, Y. Prevention of psychological stress-induced immune suppression by aged garlic extract. Phytomedicine. 1999, 6, 325–330. [Google Scholar] [CrossRef] [PubMed]
  77. Feng, Z.; Zhang, G.; Hao, T.; Zhou, B.; Zhang, H.; Jiang, Z. Effect of diallyl trisulfide on the activation of T cell and macrophage-mediated cytotoxicity. J. Tongii Med. Univ. 1994, 14, 142–147. [Google Scholar] [CrossRef]
  78. Nantz, M.P.; Rowe, C.A.; Muller, C.E.; Creasy, R.A.; Stanika, J.M.; Percival, S.S. Supplementation with aged garlic improves both NK and –T cell function and reduces the severity of cold and flu symptoms: a randomized, double-blind placebo-controlled nutrition intervention. Clin. Nutr. 2012, 31, 337–344. [Google Scholar] [CrossRef] [PubMed]
  79. Percival, SS. Aged garlic extract modifies human immunity. J. Nutr. 2016, 146, 433S–436S. [Google Scholar] [CrossRef] [PubMed]
  80. Costantini, D.; Møller, A. Does immune response cause oxidative stress in birds? A meta-analysis. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 2009, 153, 339–344. [Google Scholar] [CrossRef] [PubMed]
  81. Karangiya, V.; Savsani, H.; Patil, S.S.; Garg, D.; Murthy, K.; Ribadiya, N.; Vekariya, S. Effect of dietary supplementation of garlic, ginger and their combination on feed intake, growth performance and economics in commercial broilers. Vet. World. 2016, 9, 245. [Google Scholar] [CrossRef] [PubMed]
  82. Pirgozliev, V.; Rose, S.; Catherine, I.; Blanchard, A. Phytogenic feed additives can alleviate the negative impact of necrotic enteritis in broilers; Proc. 6th Int. Conf. Poult. Intest. Health, Rome, Italy. 3-5 April, 2019.
  83. Rees, L.P.; Minney, S.F.; Plummer, N.T.; Slater, J.H.; Skyrme, D.A. A quantitative assessment of the antimicrobial activity of garlic (Allium sativum). World J. Microbiol. Biotechnol. 1993, 9, 303–307. [Google Scholar] [CrossRef]
  84. Skyrme, D.A. The antimicrobial activity of Allium sativum. Ph.D. Thesis, Cardiff University, 1997.
  85. Elmahallawy, E.K. , Fehaid, A., El-Shewehy, D.M., Ramez, A.M., Alkhaldi, A.A., Mady, R., Nasr, N.E., Arafat, N., Hassanen, E.A., Alsharif, K.F., Abdo, W. S-methylcysteine ameliorates the intestinal damage induced by Eimeria tenella infection via targeting oxidative stress and inflammatory modulators. Front. Vet. Sci. 2022, 8, 754991. [Google Scholar] [CrossRef]
  86. Müller, A.; Eller, J.; Albrecht, F.; Prochnow, P.; Kuhlmann, K.; Bandow, J.E.; Slusarenko, A.J.; Leichert, L.I.O. Allicin induces thiol stress in bacteria through S-allylmercapto modification of protein cysteines. J. Biol. Chem. 2016, 291, 11477–11490. [Google Scholar]
  87. Becerra-Torres, S.; Soria Fregozo, C.; Jaramillo-Juarez, F.; Moreno-Hernandez-Duque, J. Allium sativum aqueous extract prevents potassium dichromateinduced nephrotoxicity and lipid oxidation in rats. J. Pharm. Pharmac. Res. 2014, 2, 45–52. [Google Scholar] [CrossRef]
  88. Abou-Elkhair, R.; Gaafar, K.M.; Elbahy, N.M.; Helal, M.A.; Mahboub, H.D.; Sameh, G. Bioactive effect of dietary supplementation with essential oils blend of oregano, thyme and garlic oils on performance of broilers infected with Eimeria species. Global Vet. 2014, 13, 977–985. [Google Scholar] [CrossRef]
  89. El-Khtam, A.; Shata, A.; El-Hewaity, M.H. Efficacy of turmeric (Curcuma longa) and garlic (Allium sativum) on Eimeria spp in broilers. Int. J. Bas. Appl. Sci. 2014, 3, 349–356. [Google Scholar] [CrossRef]
  90. El Dakroury, M.F.; Reda, S.F.; Baz, G.M. A study of the anticoccidial effects of clopidol and garlic powder on Eimeria-infected broilers. Assiut. Vet. Med. J. 2016, 62, 84–89. [Google Scholar]
  91. Kefyalew, D.; Sibhat, B.; Cheru, H. Anticoccidial effect of garlic on leghorn chickens. Biomed. Nurs,.
  92. Udo, E.J.; Abba, A.M. Comparative study of in-vitro anticoccidial efficacy of Allium sativum and Carica papaya. J. Zool. Res. 2018, 2, 10–14. [Google Scholar] [CrossRef]
  93. Al-Shaibani, I.R.M.; Al-Khadher, A.M.A.; AlHibah, A.Z.H. Anticoccidial activity of Allium sativum and Punica granatum against experimentally induced Eimeria tenella infection in broiler chickens. Asian J. Res. Anim. Vet. Sci. 2020, 5, 20–29. [Google Scholar] [CrossRef]
  94. Sidiropoulou, E.; Skoufos, I.; Marugan-Hernandez, V.; Giannenas, I.; Bonos, E.; Aguiar-Martins, K.; Lazari, D.; Blake, D.P.; Tzora, A. In vitro anticoccidial study of oregano and garlic essential oils and effects on growth performance, fecal oocyst output, and intestinal microbiota in vivo. Front. Vet. Sci. 2020, 7, 420. [Google Scholar] [CrossRef] [PubMed]
  95. Hussein, S.H.; Soad, M.; Mervat, A.A.; Gehan, N.A.; Rania, A.A. Comparative biochemical and pathological studies between toltrazuril and garlic supplementation in chickens experimentally infected with coccidiosis. Egypt. J. Anim. Health. 2021, 1, 65–80. [Google Scholar] [CrossRef]
  96. Adjei-Mensah, B.; Atuahene, C.C. Avian coccidiosis and anticoccidial potential of garlic (Allium sativum L.) in broiler production: a review. J. Appl. Poult. Res. [CrossRef]
  97. Ali, M.; Chand, N.; Khan, R.U.; Naz, S. ; Gul. S. Anticoccidial effect of garlic (Allium sativum) and ginger (Zingiber officinale) against experimentally induced coccidiosis in broiler chickens. J. Appl. Anim. Res. [CrossRef]
  98. Asghar, M.; Durrani, U.F.; Hussain, R.; Matloob, K.; Mahmood, A.K. , Anees, M. et al. Comparative efficacy of amprolium, garlic oil (A. sativum) and ginger oil (Zingiber officinale) against coccidiosis in common quail (Coturnix coturnix). J. Hellen. Vet. Med. Soc. [CrossRef]
  99. Allen, P.C.; Danforth, H.D.; Augustine, P.C. Diet modulation of avian coccidiosis. Int. J. Parasitol. 1998, 28, 1131–1140. [Google Scholar] [CrossRef]
  100. Pourali, M.; Kermanshahi, H.; Golian, A.; Razmi, G.R.; Soukhtanloo, M. Antioxidant and anticoccidial effects of garlic powder and sulfur amino acids on Eimeria infected and uninfected broiler chickens. Iran. J. Vet. Res. [CrossRef]
  101. Kim, D.K.; Lillehoj, H.S.; Lee, S.H.; Lillehoj, E.P.; Bravo, D. Improved resistance to Eimeria acervulina infection in chickens due to dietary supplementation with garlic metabolites. Br. J. Nutr. 2013, 109, 76–88. [Google Scholar] [CrossRef]
  102. Christaki, E.; Florou-Paneri, P.; Giannenas, I.; Papazahariadou, M.; Botsoglou, N.A.; Spais, A.B. Effect of a mixture of herbal extracts on broiler chickens infected with Eimeria tenella. Anim. Res. 2004, 53, 137–144. [Google Scholar] [CrossRef]
  103. Jamil, M.; Aleem, M.T.; Shaukat, A.; Khan, A.; Mohsin, M.; Rehman, T.U.; Abbas, R.Z.; Saleemi, M.K.; Khatoon, A.; Babar, W.; Yan, R.; Li, K. Medicinal plants as an alternative to control poultry parasitic diseases. Life (Basel). 2022, 12, 449. [Google Scholar] [CrossRef] [PubMed]
  104. Tanweer, A.J.; Saddique, U.; Bailey, C.A.; Khan, R.U. Antiparasitic effect of wild rue (Peganum harmala L.) against experimentally induced coccidiosis in broiler chicks. Parasitol. Res. 2960. [Google Scholar] [CrossRef]
  105. El-Saber Batiha, G.; Magdy Beshbishy, A.; Wasef, L.G.; Elewa, Y.H. ; A. Al-Sagan, A.; Abd El-Hack, M.E.; Taha, A.E.; M. AbdElhakim, Y.; Prasad Devkota, H. Chemical constituents and pharmacological activities of garlic (Allium sativum L.): A review. Nutrients.
  106. Ayaz, E.; Turel, I.; Gul, A.; Yilmaz, O. Evaluation of the anthelmentic activity of garlic (Allium sativum) in mice naturally infected with Aspiculuris tetraptera. Rec. Pat. Antiinfect. Drug Discov. 2008, 3, 149–152. [Google Scholar] [CrossRef] [PubMed]
  107. Dkhil, M.A.; Abdel-Baki, A.S.; Wunderlich, F.; Sies, H.; AlQuraishy, S. Anticoccidial and antiinflammatory activity of garlic in murine Eimeria papillata infections. Vet. Parasitol. 2011, 175, 66–72. [Google Scholar] [CrossRef] [PubMed]
  108. Sadek, H.A.; Abdel-Rahman, S.M.; Bakir, H.Y.; Arafa, M.I.; Ahmed, A.A.; Gaber, M.M. The potential convention of garlic and black seed different extracts as an effective treatment of Cryptosporidium spp.: An experimental study. J. Egypt. Soc. Parasitol. [CrossRef]
  109. Sklan, D.; Berner, Y.N.; Rabinowitch, H.D. The effect of dietary onion and garlic on hepatic lipid concentrations and activity of antioxidative enzymes in chicks. J. Nutr. Biochem. 1992, 3, 322–325. [Google Scholar] [CrossRef]
  110. Konjufca, V.H.; Pesti, G.M.; Bakalli, R.I. Modulation of cholesterol levels in broiler meat by dietary garlic and copper. Poult. Sci. 1997, 76, 1264–1271. [Google Scholar] [CrossRef] [PubMed]
  111. Lim, K.S.; You, S.J.; An, H.K.; Kang, C.W. Effects of dietary garlic powder and copper on cholesterol content and quality characteristics of chicken eggs. Asian-Australas. J. Anim. Sci. 2006, 19, 582-586. [CrossRef]
  112. Azeke, M.; Ekpo, K.E. Egg yolk cholesterol lowering effects of garlic and tea. J. Biol. Sci. 2008, 8, 456–460. [Google Scholar] [CrossRef]
  113. Kim, Y.J.; Jin, S.K.; Yang, H.S. Effect of dietary garlic bulb and husk on the physicochemical properties of chicken meat. Poult. Sci. 2009, 88, 398–405. [Google Scholar] [CrossRef] [PubMed]
  114. Ao, X.; Yoo, J.S.; Lee, J.H.; Jang, H.D.; Wang, J.P.; Zhou, T.X.; Kim, I.H. Effects of fermented garlic powder on production performance, egg quality, blood profiles and fatty acids composition of egg yolk in laying hens. Asian Australs. J. Anim. Sci. 2010, 23, 786–791. [Google Scholar] [CrossRef]
  115. Ghasemi, R.; Zarei, M.; Torki, M. Adding medicinal herbs including garlic (Allium sativum) and thyme (Thymus vulgaris) to diet of laying hens and evaluating productive performance and egg quality characteristics. Am. J. Anim. Vet. Sci. 2010, 5, 151–154. [Google Scholar] [CrossRef]
  116. Issa, K.J.; Omar, J.M.A. Effect of garlic powder on performance and lipid profile of broilers. Open J. Anim. Sci. [CrossRef]
  117. Ojo, O.O.; Kabutu, F.R.; Bello, M.; Babayo, U. Inhibition of paracetamol-induced oxidative stress in rats by extracts of lemongrass (Cymbropogon citratus) and green tea (Camellia sinensis) in rats. Afr. J. Biotechnol. 2006, 5, 1227–1232. [Google Scholar]
  118. Qureshi, A.A.; Abuirmeileh, N.; Din, Z.Z.; Elson, C.E.; Burger, W.C. Inhibition of cholesterol and fatty acid biosynthesis in liver enzymes and chicken. Hepatocytes by polar fractions of garlic. Lipids. 1983, 18, 343–348. [Google Scholar] [CrossRef] [PubMed]
  119. Horie, T.; Awazu, S.; Itakura, Y.; Fuwa, T. Identified diallyl polysulfides from an aged garlic extract which protects the membranes from lipid peroxidation. Planta Med. 1992, 58, 468–469. [Google Scholar] [CrossRef] [PubMed]
  120. Chen, C.H.; Chan, H.C.; Chu, Y.T.; Ho, H.Y.; Chen, P.Y.; Lee, T.H.; Lee, C.K. Antioxidant activity of some plant extracts towards xanthine oxidase, lipoxygenase and tyrosinase. Molecules. 2009, 14, 2947–2958. [Google Scholar] [CrossRef]
  121. Lin, W.C.; Lee, M.T.; Chang, S.C.; Chang, Y.L.; Shih, C.H.; Yu, B.; Lee, T.T. Effects of mulberry leaves on production performance and the potential modulation of antioxidative status in laying hens. Poult. Sci. 2017, 96, 1191–1203. [Google Scholar] [CrossRef]
  122. Pourakbari, M.; Seidavi, A.; Asadpour, L.; Martínez, A. Probiotic level effects on growth performance, carcass traits, blood parameters, cecal microbiota, and immune response of broilers. An. Acad. Bras. Ciênc. 1011. [Google Scholar] [CrossRef]
  123. Cavallito, C.J.; Bailey, J.H. Allicin, the antibacterial principle of Allium sativum. I. Isolation, physical properties and antibacterial action. J. Am. Chem. Soc. 1951. [Google Scholar] [CrossRef]
  124. Rehman, Z.U.; Munir, M.T. Effect of garlic on the health and performance of broilers. Veterinaria. 2015, 3, 32-3 9.
Table 4. The effect of dietary garlic on the antioxidant status and blood parameters of poultry.
Table 4. The effect of dietary garlic on the antioxidant status and blood parameters of poultry.
Dose/route Type of production Effects Reference
Garlic paste (3.8%), solvent fractions, or garlic oil equal to this quantity in feed Broiler chickens
Leghorn laying pullets
Decreasing serum cholesterol by 18 and 23% in broilers and Leghorn pullets, respectively [24]
Garlic oil 0.02% in meal Babcock B-300 strain of laying hens No effect on serum cholesterol [41]
Garlic 2% in feed Broiler chickens Lowering in hepatic cholesterol concentrations [109]
Garlic 3% in meal Broiler chickens Decreased plasma cholesterol and breast and thigh muscle cholesterol [110]
Garlic powder 3% in diet Laying hens No change in serum cholesterol concentrations [42]
Sun-dried garlic paste 0, 2, 4, 6, 8, or 10% of diet Hisex Brown, Isa Brown, Lohmann, Starcross, Babcock, and Starcross-579 strains of laying hens Decreased serum cholesterol concentrations [43]
Garlic 0, 1, 3, or 5% in meal Laying hens No change in HDL level [111]
Garlic powder 0.5 and 10 g/kg feed Laying hens Decreased serum triglyceride [45]
Garlic 2% and fenugreek 2% Lohmann Brown laying hens Increased HDL
Reduced serum cholesterol and LDL
[47]
Garlic powder 1% or 3% garlic Broiler chickens No effect on leukocyte count [66]
Garlic powder 10 and 20 g kg−1 Laying hens Reduced total cholesterol, triglyceride, LDL, and HDL [112]
Garlic powder 5-20 g kg−1 Broiler chickens Decreased plasma LDL cholesterol No effect on HDL cholesterol [113]
Fermented garlic powder 3% in diet Laying hens Decreased serum cholesterol [114]
Garlic powder 1, 2, and 4% in feed Laying hens Increased plasma HDL and LDL (1, 2, and 4%). [49]
Garlic 1, 3, and 5% and 3% garlic powder + 200 IU of α-tocopherol/kg of feed Broiler chickens Reduced the total and LDL levels
Increased the HDL levels
[28]
A mixture of garlic and thyme powder 0.1 and 0.2 g kg−1 Laying hens No effect on cholesterol, triglyceride, HDL, and LDL [115]
Garlic powder 0.1% Broiler chickens Decreased tri glycerides, total cholesterol, and LDL
Increased HDL
[68]
Garlic powder at 0.2% and 0.4% of feed Cobb broiler chickens Reduced tri glycerides, cholesterol, and LDL
Increased HDL
[116]
Garlic powder 3% and 5% of diet Broiler chickens Decrease spleen weight, RBCs, WBCs, and packed cells volume [31]
Garlic powder 1%, fenugreek 1%, and garlic powder 1% + fenugreek 0.5%
Garlic and fenugreek 2%
Laying hens Decreased LDL
Beneficial effects on cholesterol metabolism
[51]
A mixture of ginger and garlic (1:1 ratio) 50ml/liter of the drinking water Marshal broiler chickens Increased haemoglobin, packed cell volume, WBCs, RBCs, total protein, albumin, and globulin
Decreased cholesterol
[32]
A mixture of lemon, onion, and garlic juice at portions 1.00, 1.00, and 0.125/liter of the drinking water, respectively Bovan Brown layer chickens Decreasing total plasma cholesterol content, GPT, GOT, and creatinine [53]
Garlic 5g/kg feed, black cumin 5g /kg, or their combination Ross-308 broiler chickens Increasing total protein
Reduced GOT
[38]
Probiotic, citric acid, and garlic supplemented with 0.5 g kg−1 multi-strain probiotic mixture, citric acid and garlic powder, respectively. Probiotic-citric and probiotic-garlic groups treated with 0.5 g kg−1 multi-strain probiotic mixture, and 0.5 g kg−1 citric acid and garlic powder, respectively, while citric-garlic group fed diet with 0.5 g kg−1 of citric acid and garlic powder. Broiler chickens Decreased cholesterol, triglycerides, and LDL
Elevated HDL
[20]
A basal diet plus 0.25, 0.50, and 0.75 g garlic powder/kg diet Broiler chickens Increasing RBCs, hemoglobin HDL, SOD, and total anti oxidant capacity
Decreasing total cholesterol, LDL, GOT, and AMD
[12]
Garlic essential oil (200 mg/kg diet) alone/or combination with lemon essential oil (200 mg/kg diet) under heat stress Broiler chickens Reducing MDA, triglycerides, cholesterol, and LDL
Increasing HDL, SOD, and GPx
[23]
WBCs= White blood cells; RBCs-= Red blood cells; MDA= Malondialdehyde; GPT= Glutamic-pyruvic transaminase; GOT= Glutamic-oxaloacetic transaminase; HDL= High density lipoprotein; LDL= Low density lipoprotein; SOD= Superoxide dismutase; GPx= Glutathione peroxidase
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