Open access peer-reviewed chapter - ONLINE FIRST

Role of Feed Additives in Poultry Feeding under Marginal Environmental Conditions

Written By

Ahmed El-Baz and Raafat Khidr

Submitted: 20 May 2023 Reviewed: 07 June 2023 Published: 18 March 2024

DOI: 10.5772/intechopen.112130

Feed Additives - Recent Trends in Animal Nutrition IntechOpen
Feed Additives - Recent Trends in Animal Nutrition Edited by László Babinszky

From the Edited Volume

Feed Additives - Recent Trends in Animal Nutrition [Working Title]

Emeritus Prof. László Babinszky

Chapter metrics overview

21 Chapter Downloads

View Full Metrics

Abstract

Modern commercial breeding programs aim at maximizing productive performance, especially with modern broiler chicken strains, which are characterized by a high growth rate and a lower feed conversion factor. However, it is more sensitive to environmental stress, intensive rearing conditions, and high nutritional needs. Nutrition plays a key role in achieving the maximum amount of production while maintaining the health of the bird, in addition to reducing production costs by searching for unconventional feed ingredients or using some feed additives. Feed additives are mainly used in animal feed to help provide for the bird’s needs. In addition, it is used to enhance bird health, stimulate digestion, improve feed efficiency, and resistance to diseases by positive influence on the gastrointestinal tract, metabolism, and enhancement of the immune system, inhibiting pathogens, and improving intestinal integrity. In broiler nutrition, special attention should be paid to feed additives of modification of immunity and microbial content such as pre-and probiotics, nano compounds, herbs. In this chapter, we will elucidate the importance of feed additives from the point of marginal environmental conditions, which face many challenges concerning poultry feeding. Hence, feed additives will be a fruitful tool to cope with some of such challenges under those marginal conditions.

Keywords

  • poultry
  • feed additives
  • performance
  • heat stress
  • antibiotics
  • unconventional feed

1. Introduction

The poultry industry is one of the largest investments in the world. In particular, broiler chicken production, which attracted enormous investments for business profit, as it is characterized by low production costs and short production period. In addition to the increased demand for poultry meat due to its low-fat content and low consumer price compared to other meats (animals and fish). The consumption of poultry meat represents about 70% of the total meat consumed as about 66 billion birds are slaughtered annually, and the United States, China, and Brazil represent the largest poultry-producing countries. With this remarkable development in the broiler industry, it was necessary to use some feed additives to meet many challenges, including disease resistance, prevention of heat stress, improving the utilization of feed, and stimulating growth and production [1, 2, 3]. In this concern, feed additives are products used for specific purposes in animal feed, to meet the poultry nutritional requirements and improve the quality of feed, and enhance the animals performance and health, as well as the quality of food of animal origin (e.g., eggs and meat) [4, 5].

Global warming is one of the major challenges for animal breeding. High environmental temperatures negatively affect the poultry industry; thus, we have a fundamental interest in reducing the negative effects of climate change on poultry breeding. The important question is, what tools do we have to reduce the harmful impacts of high environmental temperatures? A solution for the prevention of heat stress in poultry includes developing technology devices (e.g., air conditioning and intensive ventilation); however, housing methods are more expensive and this makes it the biggest obstacle to its spread, especially in developing countries. Therefore, reducing the harmful effects of heat stress with different nutritional tools such as using a feed additive [6, 7]. Before selecting additions, we must be aware of the changes in the physiological and metabolism of broilers caused by heat stress to determine the type and role of each feed additive that can be used. Numerous studies have shown that the use of some feed additives (such as plant extract, probiotics, vitamins C, E, and A, zinc, and selenium) had a positive role in mitigating the harmful effects of heat stress [7, 8, 9].

It was reported that the use of antibiotics is necessary to fight pathogenic microbes, in particular, infectious pathologies (Clostridia and Coccidiosis), as well as growth promoters (regulation of the intestinal microflora, increased vitality, enhancement growth performance, and stimulation of the immune system) [10, 11]. Despite all these advantages, but as a result of the wrong use of antibiotics, led to the emergence of antibiotic-resistant bacterial strains with residues in animal meat, which affects human health. For this reason, the European Union in 2005 banned the use of antibiotics as a growth promoter to minimize health risks [12]. Nutritionists began searching for safe alternatives to antibiotics for animals and humans. In this concern, the use of some feed additives reduces the problems faced by the poultry sector, such as heat stress, and improves feed utilization, subsequently reducing production costs [13, 14, 15, 16]. Therefore, this chapter aims to summarize how various feed additives can reduce the use of antibiotics, the negative effects of heat stress, and improve the utilization of unconventional feed ingredients.

Advertisement

2. Using feed additives to eliminate harmful effects of heat stress on poultry

Heat stress is considered a critical holdback to coping with the poultry industry, particularly in a hot environment, triggering greater economic losses in the poultry industry [8, 17]. The bird begins to experience heat stress when the ambient temperature elevation is above the comfort zone (thermoneutral zone) leading to inducing stressful behavioral responses (higher respiratory rate, disorders in metabolism, and injuries intestinal integrity and morphology) to loss of excess heat that exceeds the critical temperature (Figure 1) [18, 19]. This means that there is more loss of heat (energy), which leads to less energy remaining for production (growth and egg production) and results in poultry performance deteriorating such as dehydration, high death, and altered meat quality characterized [6, 8]. Furthermore, developments in the genetic selection of broilers have led to rapid growth with a low feed conversion ratio and a high metabolic rate, which is accompanied by increased feed intake and causes a higher heat production level, this made him more sensitive to a hot environment [7]. Summarizing, it can be difficult to keep poultry in a thermoneutral zone in a hot environment, wherefore, it is important to use technical devices (ventilation and a cooling system), in addition to nutritional tools to reduce the negative effect of heat stress on birds. Therefore, the proper management practices can be complemented to keep health and performance by using some vital dietary doctrinaire (feed additives), so phytobiotics, probiotics, natural antioxidants, vitamins, electrolytes, and fat (Table 1 and Figure 2), in addition, to feed form, feed restriction, and drinking cold water [6, 7, 25].

Figure 1.

Physiological, behavioral, and growth performance changes during exposure to heat stress.

AdditivesFindingsReference
SeleniumEnhancing thyroid hormone metabolism, immunity, and antioxidative[20]
Nano-Selenium
  • Improvements in feed conversion ratio, weight gain, and feed intake. Peroxidase mRNA expression in liver.

  • Decreasing liver and breast muscle contents of malondialdehyde.

[6]
Zinc
  • Improving growth rate, FCR, and nutrient digestibility

  • Enhancing antioxidant enzymes and humoral immune response

[21]
Zinc, or magnesium, their combinations
  • Improving the quails performance

  • Enhancing humoral immunity

  • Decreasing of meat lipid peroxidation

[22]
Vitamin C
  • Improving the performance status.

  • Enhancing immunological traits, and behavior

[23]
Probiotic
  • Improving bacterial population of the cecal contents, and immune response

  • Improved daily weight gain and decreased mortality rate

[16]
Spirulina platensis as probiotic
  • Enhancing the productive performance

  • Enhancing the lipid profile, redox status, and humoral

  • immune response

[7]
Probiotic, citric acid, garlic powder or their combinations
  • Improving of body weight gain, feed conversion ratio, and reduction in abdominal fat.

  • Enhancing the feed utilization by highest crypt depth values

  • Improving of immune system by highest antibody level against NDV

[3]
Betaine
  • Better feed conversion ratio and performance efficiency factor.

  • Enhancing meat characteristics by improve breast fillets yield.

[24]
Herbs
  • Improving the immune system and antioxidative status

  • Stimulating digestive enzyme activity, and control pathogenic bacteria

[16]
Essential oil mixture (garlic and lemon)
  • Increasing digestive enzymes activities, and improving average body weight, feed conversion ratio

  • Enhancing intestinal microbial content, and intestinal histological status

[7]

Table 1.

Using feed additives to eliminate harmful effects of heat stress on poultry.

Figure 2.

The role of dietary supplements in mitigating the adverse effects of heat stress.

2.1 Oil or fats

Many studies indicated that the addition of fats in chicken diets enhanced the performance index, which was bred under high ambient temperatures [26, 27]. In general, energy is a limiting factor for high ambient temperature conditions, where a deficiency in energy intake could occur through reduced feed intake and appetite. Reduced feed intake during heat-stressed chickens causes the intake of protein and fat to be about 40% less than the needs required to maintain life and productivity [26], in addition to minimizing the heat production induced by feed digestion. Furthermore, chickens resort to panting for getting rid of the thermal burden, which depends on respiratory muscular activity, resulting in increased energy expenditure [28]. Therefore, chickens need to increase energy while obtaining an easy source to benefit from, for this reason, it was better to provide the required energy during the period of heat stress by adding oil or fats than using carbohydrates [8, 29]. Adding oil contributes to reducing heat production because the heat increment of carbohydrates or protein is higher than that of fat [30]. A significant improvement was observed in the performance and digestion coefficient of birds that received higher recommended levels of metabolizable energy during heat stress. Al-Harthi et al. [26] declared that heat-stressed broilers fed a high metabolizable energy diet showed an improvement in feed utilization and live body weight. Adding oil contributes to reducing heat production because the heat increment of carbohydrates or protein is higher than that of fat [30]. Moreover, fat-supplemented diets improved the palatability of poultry diets and physical characteristics, resulting in enhanced feed intake and performance [31]. In addition, many studies confirmed that oil supplementation in the poultry diet increases nutrient utilization by lowering the rate of food passage in the gut [32].

2.2 Minerals and vitamin

Minerals and vitamins play an important role in all vital processes in the body, including the basal metabolic rate, antioxidative properties, and protein composition, resulting in improved health and performance.

Selenium (Se) is one of the important elements that acts as a cofactor for antioxidant enzymes, as well as responsible for the conversion of thyroxin (T4) into active triiodothyronine (T3) and is involved in several biological functions. Several studies indicated that dietary supplementation of Se or Nano-Se enhanced BWG, FCR, and immune responsiveness in heat-stressed broilers [6, 33, 34]. Moreover, numerous studies have shown that adding Se to chicken diets reduces the negative effects of heat stress by enhancing thyroid hormone metabolism, immunity, and antioxidative status (elevated mRNA expression of GSH-Px in the liver), which resulted in improved productive performance [20, 34].

Zinc (Zn) is an essential element that contributes to bone formation, feather formation, and composition, and the function of more hundred enzymes linked to the metabolism of nucleic acid, energy, and protein [35]. Moreover, Zn is involved in the activity of the antioxidative enzymes (GSH-Px, SOD) by suppressing free radicals [36]. Numerous research also confirmed that the addition of zinc in its various forms (organic, inorganic, and nano) in chicken feed exposed to environmental heat stress led to improved growth rate, FCR, nutrient digestibility, minimized lipid peroxidation, and enhanced antioxidant enzymes and humoral immune response [21, 37]. Recently, mixing two or more elements had a positive effect in reducing the harmful effects of heat stress, such as mixing between magnesium (Mg) and zinc(Zn) diet increased BWG and dressing percentage in Japanese quail [22]. Moreover, the addition of an organic minerals mixture (Zn, Cu, and Mn) in heat-stressed laying hen feed, resulted in improved egg production, egg quality traits, minimized yolk lipid oxidation, and enhanced humoral immunity [37, 38].

Ascorbic acid (vitamin C) is one of the important antioxidant components (water-soluble) that attenuate the undesirable impacts of heat stress in poultry via safeguards cells against oxidative damage [39]. It is known as ascorbic acid and is endogenously synthesized in several bird species, however, necessary to be adding to the diet under conditions of heat stress. This can be explained by exposure to high ambient temperatures reducing the absorption of vitamin C and accelerating its destruction. Vitamin C is synthesized in poultry in the kidney from glucose, but in normal conditions, the birds are able to synthesize adequate amounts of vitamin C. A study showed a significant decrease in the level of ascorbic acid by 40% in the blood of Japanese quails under heat stress conditions compared with the control group [40], thus the increased requirements of this vitamin C during periods of heat stress [41]. Beside, vitamin C plays a role in improving feed efficiency by stimulating the thyroid gland, as well as enhancing Ca + 2 metabolism via participation in essential processes such as adrenaline, corticosterone release, and 1, 25-dihydroxy vitamin D biosynthesis [23]. In addition, it is necessary for immune system activation and body temperature regulation. Because of the increased intensity of heat stress on birds performance, many scientific studies that vitamin C supplementation in dietary stressed Japanese quails leads to improving the performance status, enhancing immunological traits, and behavior, and declines the metabolic rate and survival rate [25, 42]. Additionally, supplementation of the vitamin C diet decreased lipid peroxidation and improved the antioxidant status in Japanese quail exposed to heat stress [42].

2.3 Direct-fed microbials

Heat stress results in the impairment of gut integrity and function by impairing intestinal microflora balance, and mucus layer [43, 44]. This disruption of the intestinal barrier facilitates the translocation of pathogenic bacteria and their toxins into the host body (bird) and enhances inflammatory responses. Previous studies noted that acute heat stress leads to a significantly altered gut microbial community (increased opportunity for Salmonella attachment) and intestinal morphology [4345]. The strategy aims to use probiotics as a means to mitigate the negative effects of heat stress on the bird by modifying the microbial content to optimize gastrointestinal health. Probiotics or direct-fed microbials are microbial and are defined as live beneficial microbial feed supplements, including bacteria (Bifidobacteria, Bacilli, and Lactobacilli), fungi (Aspergillus awamori, and Aspergillus oryzae), and yeast cultures (Saccharomyces) that can intestinal microbial balance, intestinal health, and immune responses, results in improve poultry performance [3, 46]. Several studies summarized that probiotic supplemented in broiler diets improved daily weight gain and decreased mortality rate under hot environmental conditions [8, 47]. The inclusion of probiotics in broiler diets leads to enhanced growth performance, and immune response [16]. Therefore, it is extremely useful to equip poultry diets with probiotics levels that support intestinal integrity and improve feed utilization by increasing intestinal absorption surface by increasing the height of the villus (Figure 3) and enhancing the immune system. As indicated by a study by Abdel-Moneim et al., [15]; Elbaz et al., [3]; Li et al., [48] that the inclusion of Bacillus subtilis has the potential to produce some digestive enzymes, as well as, enhance intestinal development and function, and improve immune response. Moreover, Abdel-Moneim et al. [15]; Saleh et al., [49] indicated supplementation of B. subtilis in quail and broiler diets also improvement in feed efficiency and BWG, and raise muscle concentrations of unsaturated fatty acids. Many studies have also confirmed the important physiological role of probiotics in promoting the antioxidant defense system of heat-stressed broiler chickens via activating enzymes antioxidants [6]. For this reason, the positive role of adding probiotics can be emphasized in mitigating the negative effects of heat stress via enhancing intestinal integrity and improving feed utilization and antioxidant status.

Figure 3.

Photomicrographs of ileal villi showing how villus height of broiler chickens exposed to heat stress (G1) is shorter compared to other broiler-fed on some feed additive.

2.4 Medicinal plants and plant bioactives

Herbs, plant extract, and essential oils spice is widely used in herbal medicine to improve the immune system and enhance antioxidative status and antimicrobial. Volatile essential oils can stimulate digestive enzyme activity and control pathogenic bacteria [7, 50]. Heat stress disrupts the balance between oxidation and antioxidant defense systems, causing lipid peroxidation, and consequently DNA oxidative damage [33]. Plant bioactives are a type of chemical found in plants and certain foods with small amounts (such as vegetables, fruits, oils, and grains). Essential oils have the biological activity of substances with different chemical compositions and concentrations, which play of important in antioxidant activity, anti-inflammatory, and antimicrobial (thymol and carvacrol) [51, 52]. In addition, essential oils or organic acids, including lactic, citric, formic, and fumaric acids, generated from plants are to control harmful microorganisms in the digestive and respiratory organs of poultry via reducing pH in the gut [53]. Results of many research indicate that supplementation of thyme essential oil is a suitable strategy to improve the immune system and productive performance, decreased the mortality rate, and reduce the negative effects of heat stress [7, 54, 55]. Supplementation of essential oil broilers diet had reduced the adverse effects of heat stress on performance and immune responses [55] and can be a good alternative to improve the adverse impact of aflatoxin B1 contaminated in the broiler diet [56].

2.5 Betaine

Betaine is the amino acid glycine or trimethyl glycine and is greatly found in a variety of plants. Functionally, betaine plays an important role in mitigating the harmful effects of heat stress through its role as a methyl group donor for the methionine homocysteine cycle and as an organic osmolyte, as well as it is an antioxidant natural. It also plays an important role under conditions that inactivate cells (loss of water causes cells to die) via protecting cells from osmotic pressure, which allows them to continue normal metabolic activities. This confirms the evidence that biotin may be a feed material with positive effects on poultry performance, especially during heat stress through the high value [24, 57]. Many studies have confirmed that the addition of biotin improves broiler performance, carcass composition by changing lipid metabolism [58], immune response, lipid metabolism [59], and intestinal barrier function [60]. Furthermore, it has been suggested that improving the meat quality of broilers fed on betaine is due to its role as a natural antioxidant [61].

Advertisement

3. Use of feed additives as alternatives to antibiotics in poultry diets

For many decades, poultry breeders have been looking for a growth stimulant and protection for birds from intestinal and respiratory diseases, even using antibiotics. Several previous studies have shown that the addition of antibiotics in poultry feed improves productive performance by stimulating the immune system, increasing vitality and regulation of the intestinal microflora, and improving appetite and feed conversion efficiency [11, 62]. Despite all these desirable advantages, the incorrect use of antibiotics has led to increasing antimicrobial resistance bacteria and residues in animal products as a public health threat. For this reason, the European Union in 2005 banned the use of antibiotics as growth promoters. This motivated nutritionists to search for safe alternatives to antibiotics to maintain public health while increasing antibiotic-free broiler meat production. Therefore, this chapter part aimed to explain feeding strategies of different antibiotic alternatives, including prebiotics, probiotics, enzymes, and phytogenic groups (herbs, essential oils, and marine algae), [2, 3, 13, 16] in poultry production (Table 2 and Figure 4). Will be explained in the following points.

AdditivesTypeFindingsReference
ProbioticBifidobacterium
  • Increased body weight and weight gain and enhanced feed conversion ratio

  • Improved antioxidant status and immune response

  • Improved Ileal architecture by highest values of villus height

[5]
Multi-strain probiotic
  • Improved broiler growth performance

  • Reduced ileal enumeration of E. coli and total coliform and increased Lactobacillus count

  • Decreased abdominal fat and no effect on carcass weight

  • Enhanced immune response

[3]
B. subtilis
  • Improved live body weight and feed-to-gain ratio

  • Increased serum total protein and albumin levels

  • Triiodothyronine and thyroxine activities were significantly elevated

  • Promoted the antioxidative status and digestive enzymes activities

[5]
PrebioticsS. cerevisiae
  • Enhanced feed efficiency and performance

  • Improved gut morphological structure and reduced the number of pathogenic bacteria

  • Stimulation of the host adaptive immune system

[63]
Mannan oligosaccharides
  • Improved growth performance and intestinal oxidative status

  • Increased the relative weight of the bursa of Fabricius and jejunal immunoglobulin content,

  • Decreased cecal Salmonella colonies

[64]
Organic acidsCitric acid
  • Improved growth performance and decreased abdominal fat

  • Decreased serum concentrations of cholesterol, triglycerides and LDL, while HDL was elevated

  • Modification of the microbial content

[3]
Formic acid
  • Increased body weight gains and decreased feed consumption

  • Increased total fat and bursa weight

  • Decreased coliform counts and the pH

[65]
Butyric acid
  • Improved body weight gain and feed conversion ratio

  • Enhanced AMEN content and apparent ileal digestibility of amino acid

[66]
PhytogenicThyme oil
  • Better feed conversion ratio

  • Decreased the plasma AST and increased total protein

  • Increased antibody titer to infectious bursa disease

[54]
Curcumin
  • Enhanced performance and health status

  • Better carcass traits and decreased abdominal lipids

  • Improved Meat quality and cecal microbial counts

[67]

Table 2.

Use of feed additives as alternatives to antibiotics in poultry diets.

Figure 4.

The most important antibiotics alternative to enhance the general performance of chickens.

3.1 Probiotics

Probiotics are live strains of beneficial bacteria that confer a health benefit on the host by fighting pathogens in the gastrointestinal tract of chickens, enhancing immunity, and stimulating growth. In addition, it is providing feeding efficiency improvement, antioxidant capacity, the microbial profile of the cecum, and intestinal protection [5, 15]. Several strains of beneficial microbes have been identified in the bird’s gut for development and use as probiotics [3, 15]. The most used microorganisms as probiotics in poultry feed are bacterial strains (Gram-positive) such as Lactobacillus, Bifidobacterium, Bacillus, yeast (Saccharomyces), and fungi (Aspergillus). The main action of probiotics includes lowering the gut pH through the organic acids and volatile fatty acids produced during the fermentation process through probiotics [16]. As well low pH in the intestine inhibits the colonization effects of pathogens in the digestive tract. Probiotics work as well by secreting products that inhibit their development such as organic acids, bacteriocins, and hydrogen peroxide and competitive exclusion through competing with pathogenic bacteria for locations in the intestinal mucous membrane to adhere to nutrients [16, 68]. Other principal mechanisms of probiotics are also used to modulate immunomodulation and to improve intestinal integrity by modulating intestinal microbiota and competition for binding sites on the intestinal epithelium wall, which hinders competition and joining of pathogenic microorganisms, this higher concentration of the beneficial microbiota. The results of several studies showed that feeding poultry on probiotics enhanced fiber and protein digestion and enzymatic activity, resulting in efficient feed nutrient utilization [6769]. Some studies also confirmed that adding a mixture of beneficial microbes (B. subtilis and Lactobacillus) was more effective in performance in environmental stress conditions through promoting nutrient digestion and gut health and the immunity modulated by the microbiota [68, 69].

3.2 Prebiotics

Prebiotics are carbohydrates that can be utilized by useful gut microorganisms but are indigestible by the host animal. The most important sources of prebiotics are mannan oligosaccharides, fructooligosaccharide, oligofructose, inulin, galactan, galactooligosaccharides, and fiber components, which can extract from barley, oats, flax seeds, onion, and garlic, as well as green algae.

Feeding chickens on a diet containing prebiotics have been shown to gut microbiota modulation and improve immunity, which are antioxidant, and antibacterial properties [70]. The most common commercial feed nutrients in poultry feed are mannan oligosaccharides, D-mannose, and β-glucan, which are derived from the cell wall of Saccharomyces cerevisiae [63]. The positive role of adding probiotics can be explained by alterations of gut microorganisms that enable them to reduce pathogenic bacteria, increase their numbers of beneficial bacteria, maintain optimal intestinal pH, increase nutrients digestibility, and increase mineral and vitamin absorbability, which improved host health and performance [70, 71]. Modifying the intestine microbiota by promoting beneficial gut microbes that ferment them, leads to the production of short-chain fatty acids, or some antibacterial substances such as bacteriocins against pathogenic microbes [70]. These fermented products of beneficial microbes due to improving the integrity of intestinal epithelial cells [72] will be followed by increasing the absorption of nutrients and improving the growth performance of poultry. Numerous studies have demonstrated the effective role of establishing a healthy microbial community in the intestine of poultry by enhancing the abundance of Bifidobacteria and Lactobacilli and reducing harmful microbes such as coliform [64, 73]. In addition to stimulation of the immune system, improvement of the epithelium by regulation of the interaction among the host (birds) and the intestinal microbiota, thus improving the productive performance of poultry.

3.3 Organic acids

Organic acids (OC) are organic compounds with acidic properties (weak acids), classified based on the number of carboxylic acid groups (R-COOH) and antimicrobial effects in animal feeds. Organic acids are promising alternatives. Among these, are formic acid, citric acid, propionic acid, and acetic acid. Their inclusion in poultry feed has been shown to enhance growth and feed efficiency [74, 75]. Organic acids individually or in their combinations are usually considered safe and perform can function similarly to antibiotics [76], furthermore, used as feed preservatives due to their strong antifungal and antibacterial properties [74].

The antimicrobial mechanism of organic acid has been suggested for the lowering of the pH of the intestines, that way limiting the growth of the microbial less tolerant to acid pH. The magnitude of the antimicrobial activity of an acid depends upon its concentration and pH [3, 77]. The use of OC has been reported to protect poultry by competitive exclusion [70], and it can penetrate the bacteria cell wall and disrupt the normal physiology of certain types of bacteria, mostly pathogenic microbes (pathogenic bacteria reside at a pH close to 7) [65, 75, 77]. In addition to the antimicrobial activity, they reduce the pH of digesta, increase pancreatic secretion, and prevent damage to epithelial cells by reducing the production of toxic components via the bacteria and colonization of pathogens on the intestinal wall, thus enhancement of nutrient utilization and growth and feed conversion efficiency [3, 74]. Several studies have documented the positive effect of OC on improved growth and enhanced digestibility of nutrients and gut health by improved duodenal villus height, boost gastric proteolytic activity (activating the pepsin activity), enhanced absorption of the feed contents from the intestines, and the digestibility of minerals. Furthermore, an increase in antibody titer against Newcastle disease, and improved immunoglobulin status were significantly improved in broilers fed on organic acid supplementation [65, 78]. Similarly, the improved immune response has also been reported in response to organic acid supplementation in broilers could be due to the increased Lactobacillus spp. population in the gut, which has a positive effect on the host immune system [365]. For that can the use of organic acids as a sustainable and potent alternative to antibiotics, thus maximizing future production and health of poultry.

3.4 Phytogenic

Phytogenic are plant-origin extracted compounds that include herbs, spices, and essential oils. It also features less toxic, residue-free, and perfect feed additives for poultry production compared with synthetic antibiotics. Herbs also contain essential oils, organic acids, and a complex mixture of various compounds. Essential oils have many biological properties such as antimicrobial antioxidant enzymatic, anti-heat stress effects, activating the immune system, and stimulating digestion [7, 79, 80]. Organic acids, produced by plants, are which play an important role in controlling harmful microorganisms in poultry’s digestive and respiratory organs. The most important of them are lactic, citric, formic, and fumaric acids. The most critical role of organic acids is to reduce pH in the gastrointestinal tract and enhanced the immune responses of poultry [79]. Additionally, organic acids can preserve the microbial balance in the gastrointestinal tract by inhibiting microorganism growth in food and the gut. Many active components (flavonoids, hydrolyzable tannins, proanthocyanidins, phenolic acids, and phenolic terpenes) can prevent lipid peroxidation by the activation of antioxidant enzymes (glutathione reductase, superoxide dismutase, and catalase) or quenching free radicals [80, 81].

Numerous studies have shown that adding herbs or essential oils to chicken feed improves anti-oxidative and antimicrobial activities, reduces inflammation, enhances intestinal functions, and increases fiber and nitrogen retention digestibility [79, 82], which results in improving growth performance. Previous reports confirmed beneficial effects to improve performance and broiler health, which can be used as a good alternative to antibiotics.

Advertisement

4. Using feed additives to improve the utilization of some unconventional feed ingredients in poultry feeding

The major constraint in poultry feeding is the higher prices of conventional feedstuffs (mainly, corn and soybean), which are transported from many countries adding to the cost of production to a great extent. Moreover, these two feed ingredients are also high in demand by other humans (yellow maize) and animals (soybean meal). As a result, the availability of feed ingredients for poultry feed would become more competitive. Feed is one of the major constituents in poultry production, which represents about 80–85% of the total cost of poultry production. This caused an increase in the responsibility of nutritionists increasing the poultry production and research utilization of unconventional feed resources through strategic and applied research to bring down the cost of production. In addition, recently, corn has been used as a major source of produce biofuel, and this further poses a serious food security risk, especially in developing countries [83]. Currently, efforts are large to use alternative sources of energy and protein to be substituted for corn and soybean meal in monogastric animals [46, 84]. As produced a huge amount of alternative feedstuffs in some developing countries are considered as agro waste by-products such as cotton seed meal, olive cake, wheat bran, rice bran, canola meal, palm kernel cake, etc. [46, 85, 86, 87]. However, many of this agro-waste products are containing the presence of non-starch polysaccharides (NSPs) such as cellulose, hemicellulose, and lignin, as well as anti-nutritional factors [46, 87], which can negatively effect on productivity and health status of the chickens. Poultry is monogastric animals that lack fiber-degrading enzymes for the breakdown of complex carbohydrates [88].

So, there is a need to improve the utilization of these fibrous materials (unconventional feedstuffs) to incorporate such ingredients in poultry feed without any adverse effect on their health and production. In the following, we will throw some light on to use of some nonconventional feedstuffs with the potential to be replaced partially or totally with corn and soybean meal in poultry feeds, in addition to the importance of some additives to alleviate the secondary metabolites in such feedstuffs (Table 3).

AdditivesFindingsReference
Probiotic (fermentation)Canola meal (20%)
  • Improved body weight gain, and feed conversion ratio

  • Increased the population of Lactobacillus spp. and decreasing the E. coli

  • Enhanced body weight gain, and feed conversion ratio

[84]
Probiotic and enzymesCanola meal (20%)
  • Higher nutrient digestibility

  • Increased in the relative weight of the bursa of Fabricius

  • and antibody titer against Newcastle disease

  • Improved antioxidant capacity, and gut health.

[46]
EnzymesCanola meal (17.5%)
  • Higher final body weight and improved FCR

  • Highest levels of aspartate aminotransferase (AST).

  • Improved health status.

[89]
S. cerevisiaeOlive cake (10%)
  • Enhanced body weight gain, and feed conversion ratio.

  • The best European production efficiency index in broilers.

[90]
Citric acidOlive cake (20%)
  • Increased protein utilization.

  • Enhanced body weight gain, and increased feed intake

[91]
Probiotic (A. awamori)Olive pulp (15%)
  • Enhanced productive performance

  • Improved nutrient digestibilities.

[86]
Probiotic (fermentation)Rapeseed meal (10%)
  • Improved the production performance and maintain good health.

  • lower the intestinal pH and improve the intestinal barrier function

[92]
EnzymesCottonseed meal
  • Improved performance (lowered the FCR and increased BWG)

  • Enhanced the digestibility of amino acids, and starch

[93]
Probiotic (fermentation)Cottonseed meal
  • Decreased abdominal fat and hepatic triglycerides

  • Improves growth performance, gut microbes,

  • Strengthening the immune system and reinforcing stress fighting capabilities

[94]
EnzymesSunflower meal
  • Improved growth performance

  • Increasing nutrient digestibility

[95]

Table 3.

Using feed additives to improve the utilization of some unconventional feed ingredients in poultry feeding.

4.1 Canola meal

Canola meal (CM) is the by-product of oil extraction. It has a higher crude protein content of approximately 35–40% and sulfur-containing amino acids are higher than that of soybean meal, while lysine content is less than that of soybean meal. The problem with using CM in poultry feeds is the containing of glucosinolate, fibers, sinapine, tannins, and phytate, as well as it has low metabolizable energy [7986]. Many methods help to reduce anti-nutritional factors, one of these methods is adding some feed additive, fermentation, etc. [79, 88]. Many studies have shown that adding probiotics, extrusion, exogenous enzymes, or using the fermentation process for some dietary ingredients has improved performance, increased nutrient digestibility, and reduced the effects of antinutritional [96, 97]. Therefore, it was reported that canola meal can be incorporated in poultry diets up to 5–8% without any feed additive, and broiler chickens were fed on a diet containing 20% of fermented CM, which did not negatively affect performance [84]. The fermentation process leads to reducing pathogens such as Escherichia coli, and Clostridium perfringens, resulting in enhanced gut health [85, 96]. Furthermore, the addition of exogenous enzymes is important to degrade complex fibers (non-starch polysaccharides, NSP) to improve the nutritional value of unconventional feed ingredients [85]. Enzymes play an influential role in improving feed digestion and utilization. Moreover, exogenous enzymes improved nutrient digestibility in poultry leading to lowering nutrient excretion in excreta such as excess nitrogen, phosphorus, and zinc, which reduces environmental pollution and improves feed utilization, in addition, reduced the effect of anti-nutrients and improved productive performance. Previous studies indicated that the fermentation broiler feed by Aspergillus resulted in an increase in nutrient solubility and digestibility, reduced phosphorus excretion, and improved broiler growth and feed utilization compared to the control group [89]. However, positive effects were observed when the addition of enzymes in broiler diets containing canola meal (17.5%) on the overall performance of broilers [95]. It was reported that CM can be incorporated in poultry diets up to 20–25% fermented CM-based with exogenous enzymes in broilers fed [46, 85].

4.2 Sunflower meal

Sunflower meal, a by-product from the oil extraction industry, is available in significantly high quantities throughout the year at a lower cost than soybean. Sunflower meal has protein levels ranging between 30 and 37%, it is a good source of protein with amino acid availabilities similar to those of soybean meal [95]. One of the important characteristics of sunflower meal is that it does not have anti-nutritional factors like those found in soybean. Despite this, its addition to poultry feed does not exceed 15% because it contains a high concentration of non-starch polysaccharides, in addition to low metabolizable energy and lysine levels [98, 99]. Some studies recommended the sunflower meal up to 15% in broiler diets without negative effects on performance [98]. Many studies reported that sunflower meal can be used at higher levels with no negative effects on the utilization and growth performance of broiler chickens with the addition of enzymes [95]. Supplementation of exogenous enzymes in poultry diets can decrease their deleterious effects on high concentrations of fiber and stimulate fiber digestion. Supplementation of exogenous enzymes functions in the breakdown of NSPs and reduction of gut viscosity, thus improving nutrients digestibility and gut performance. In some studies, an improvement in growth performance (LBW and FCR) was observed in the birds fed SFM supplemented with exogenous enzymes compared to the control diet [100, 101] maybe as a result of the enhancement of other physiological and metabolic processes such as depolymerize complex NSPs and increasing nutrient digestibility that has prebiotic effects on health-promoting bacterial proliferation by releasing fermentable manno-, galacto-, xylo-, or gluco-oligomers during cracking of fiber [95]. In addition, it increases energy concentration and enhances nutrient utilization and absorption [100, 101]. From that, sunflower meal up to 25–30% can be used with some feed additives as a soybean meal substitute.

4.3 Cottonseed meal

Cottonseed meal is a potentially good source of protein (41–44%) and metabolizable energy as a substitute for soybean in poultry diets, the protein percentage varies based on the degree of dehulling before oil extraction. However, using cottonseed meal as an ingredient in poultry feeds presents numerous challenges and limitations, including high fiber content, as well as high presence of gossypol (a toxic polyphenolic pigment) and unbalanced amino acids such as low lysine content. Many reports have shown various ways to optimize the use of cottonseed meal in poultry feed such as proper processing, supplementation with lysine, other feed additives, or a particular combination of feed additives [102]. Gossypol inhibits the activity of pepsin and trypsin in the gut, thereby reducing the digestibility of protein [94, 103]. One of the factors that can impede protein utilization and nutrient digestibility is the presence of non-starch polysaccharides (NSP), which the bird cannot digest. It is well established that supplementing exogenous enzymes in poultry feed, such as β-glucanase, xylanase, and pectinase, leads to improved digestibility by potentially lower intestinal content viscosity [102]. Several studies confirmed that adding a mixture of enzymes (β-glucanase and xylanase) to the poultry diet that contained cottonseed meal led to an improvement in performance (lowered the FCR and increased BWG) through improving the digestibility of amino acids, and starch [94]. The improvement in nutrient digestion may be due to the role of enzyme supplementation (β-glucanase and xylanase) in the removal of nutrient encapsulation of cell walls existing in many dietary ingredients, which leads to nutrient release and digestibility of dietary nutrients [93, 100]. Nevertheless in a previous study, the fermentation process was found very effective in detoxifying free gossypol, resulting in the improvement of the nutritional value of cottonseed meal [94]. Microbial fermentation is currently considered one of the most effective ways improvement of the nutritional value of unconventional feed via reducing anti-nutritional factors such as free gossypol [94, 102], thus enhancing the growth and health of poultry. In addition, the metabolic activities of probiotics microbials during fermentation lead to produce enzymes, vitamins, oligosaccharides, organic acids, and some other compounds, which help in improving growth performance, as well as enhancement of the nutritional value of cottonseed meal [94, 102]. Furthermore, fermentation could improve intestinal digestive enzyme activity, bacterial ecology, and intestinal morphology in broilers [85, 102]. From this, we can recommend that the fermentation process increases the amount of cottonseed meal that can be substituted for soybeans meal.

4.4 Olive pulp

Olive pulp (OP) is one of the olive oil extraction products, especially since it is rich in fatty acids (oleic, linoleic, and linolenic), crude protein, calcium, and copper [104, 105], as well as some biologically active compounds (polyphenol) that have an antioxidant, anti-inflammatory, and antibacterial properties [93]. However, OP has low nutritional value due to its low energy and indigestible proteins, in addition to containing high fiber content and lignin [105, 106]. It was necessary to use some feed supplements in chicken diets containing these by-products (such as OP) to reduce anti-nutritional factors, thereby reducing their negative influence on chicken production performance.

Some studies reported that the inclusion of up to 5% of olive pulp in the diet of broiler chickens did not have a negative effect on productive performance [107]. However, the addition of 10–15% olive pulp to the broilers had a detrimental effect on the health and performance of the bird [100]. This may be due to the anti-nutritional factors in olive pulp, especially the high fiber content (NSPs), which negatively influence gut ecology and thus health in monogastric animals, beside its high content of lignin which hinders the digestibility coefficients of nutrients.

Several studies have proven that the use of some feed additives has an effective effect in improving the nutritional value of olive pulp in poultry feed such as exogenous enzymes, probiotics, organic acid, etc. [103, 105, 106]. Some previous studies results indicated that adding A. awamori as a probiotic enhanced the nutritional value of the OP in the diet, leading to an improved broiler growth performance [87]. This improvement might be due to the reduction in the anti-nutritional factor of the feed and the improvement in gut health, by the activation of several health-promoting bacteria, improving the intestinal epithelial cells structure, and selectively stimulating their growth and immune system [87], as well as stimulating the activity of some enzymes (active amylase, glucoamylase, and protease) in the digestive system [108], leading to an improvement in the metabolism of protein and carbohydrates. Likewise, several studies reported that the inclusion of citric acid in rabbits’ diets enhanced nutrient digestibility [108]. Organic acids contribute to improving nutrient digestibility by reducing antinutrients and adjusting gut pH, which stimulates the activity of beneficial microbes, reduces the number of pathogenic microbes, and reduces inflammation, thus contributing to the availability of nutrients [3, 91]. In addition, citric acid has been reported to enhance the utilization of protein and some minerals [108]. As a previous study indicated, feeding broiler chickens a diet containing olive cake (20%) and citric acid (1 g/kg) resulted in a positive effect on growth performance compared to chickens that were fed 20% olive cake without additives or control [91]. Previous studies indicate that combining olive pulp with enzymes, probiotics, or organic acids led to improves the nutritional value of olive pulp, this supports the possibility of replacing part of the diet with olive pulp.

Advertisement

5. Conclusion

This chapter confirms that the use of feed additives plays an important role in poultry feeding as safe alternatives to antibiotics and as improvements to the bird’s performance under conditions of heat stress. Beside their importance to improve and enhance the utilization of feed, especially nonconventional feed materials. Based on the scientific findings, which have been mentioned, the following important conclusions could be summarized as follows:

  • Using feed additives in the poultry diets can reduce the negative impact of heat stress on poultry via reduced heat production (fat and betaine), capable of reacting with free radicals (Vitamins A, E, and C) leading to reducing lipid peroxidation, improved antioxidant parameters (Vitamin E, C, and Zn and Se), increased antioxidant enzyme activity (plant extracts, e.g., oregano and lemon), a modulating the gut microflora (probiotic and plant extracts).

  • Antibiotic alternatives have analogous advantages to antibiotics to enhance the well-being and the production performance of broiler chickens without human health challenges. The major provided effects of alternative feed additives include enhance digestion, increase absorbability of nutrients, improved nutrient availability, antioxidant activity, immune-modulating, antimicrobial, improve intestinal health by enhancement of gut integrity, modulating the host gut microflora, and intestinal barrier function. Moreover, it increases body weight and carcass weight, enhances feed conversion ratio, and the gut health of broilers.

  • The use of nonconventional feed materials is necessary to reduce the costs of poultry feed, but some feed additives must be used to reduce the anti-nutrition factors that hinder their use in feeding poultry. This study confirmed that feed additives improved the nutritional value of many unconventional raw materials that have been already in poultry feeding under the Egyptian and marginal environmental conditions of Egypt.

Further studies must be carried out on the use of feed additives concerning their role in poultry thriftiness and the physiological responses of poultry stocks under heat-stress conditions. The recent approaches of biotechnology and its role in feed additives and the importance of food processing should also be considered.

Advertisement

Abbreviations

CM

canola meal

FCR

feed conversion ratio

GSH-Px

glutathione peroxidase

LBW

live body weight

NSPs

non-starch polysaccharides

OC

organic acids

OP

olive pulp

Se

selenium

SOD

superoxide dismutase

T4

thyroxin

T3

triiodothyronine

Zn

zinc

References

  1. 1. Rahman MA, Parvin MS, Sarker RR, Islam MT. Effects of growth promoter and multivitamin-mineral premix supplementation on body weight gain in broiler chickens. Journal of the Bangladesh Agricultural University. 2012;10(2):245-248
  2. 2. Perić L, Žikić D, Lukić M. Application of alternative growth promoters in broiler production. Biotechnology in Animal Husbandry. 2009;25(5-6-1):387-397
  3. 3. Elbaz AM, Ibrahim NS, Shehata AM, Mohamed NG, Abdel-Moneim AME. Impact of multi-strain probiotic, citric acid, garlic powder or their combinations on performance, ileal histomorphometry, microbial enumeration and humoral immunity of broiler chickens. Tropical Animal Health and Production. 2021;53:1-10
  4. 4. Morsy AS. Effect of zeolite (Clinoptilolite) as a salinity stress alleviator on semen quality and hemato-biochemical parameters of Montazah cocks under South Sinai conditions. Research Journal of Animal and Veterinary Sciences. 2018;10(2):9-17
  5. 5. Abdel-Moneim AE, Elbaz AM, Khidr RE, Badri FB. Effect of in ovo inoculation of Bifidobacterium spp. on growth performance, thyroid activity, ileum histomorphometry and microbial enumeration of broilers. Probiotic Antimicrobial Proteins. 2020;12:873-882
  6. 6. Abdel-Moneim AME, Shehata AM, Mohamed NG, Elbaz AM, Ibrahim NS. Synergistic effect of Spirulina platensis and selenium nanoparticles on growth performance, serum metabolites, immune responses, and antioxidant capacity of heat-stressed broiler chickens. Biological Trace Element Research. 2022;200(2):768-779
  7. 7. Elbaz AM, Ashmawy ES, Salama AA, Abdel-Moneim AME, Badri FB, Thabet HA. Effects of garlic and lemon essential oils on performance, digestibility, plasma metabolite, and intestinal health in broilers under environmental heat stress. BMC Veterinary Research. 2022;18(1):1-12
  8. 8. Abdel-Moneim AME, Shehata AM, Khidr RE, Paswan VK, Ibrahim NS, El-Ghoul AA, et al. Nutritional manipulation to combat heat stress in poultry–A comprehensive review. Journal of Thermal Biology. 2021;98:102915
  9. 9. Elbaz AM, Ahmed AM, Abdel-Maksoud A, Badran AM, Abdel-Moneim AME. Potential ameliorative role of Spirulina platensis in powdered or extract forms against cyclic heat stress in broiler chickens. Environmental Science and Pollution Research. 2022;29(30):45578-45588
  10. 10. Hakimul H, Subir S, Shariful I, Aminul I, Rezaul K, Mohammad EHK. Sustainable antibiotic-free broiler meat production: Current trends, challenges, and possibilities in a developing country perspective. Biology. 2020;9:1-24
  11. 11. Mehdi Y, Létourneau-Montminy MP, Gaucher ML, Chorfi Y, Suresh G, Rouissi T, et al. Use of antibiotics in broiler production: Global impacts and alternatives. Animal Nutrition. 2018;4(2):170-178
  12. 12. Amaechi N, Amaeze PN. Effect of dietary chloroacetic acid as antibiotic replacer on the gastrointestinal microflora and gut morphology of weanling pigs. Research Opinions in Animal and Veterinary Sciences. 2012;2:494-498
  13. 13. Jet SM, Florencia NS. Phytogenic feed additives as an alternative to antibiotic growth promoters in poultry nutrition. Advanced studies in the 21st century. Animal Nutrition. 2021;8:1-18
  14. 14. Abdel-Moneim AME, Shehata AM, Alzahrani SO, Shafi ME, Mesalam NM, Taha AE, et al. The role of polyphenols in poultry nutrition. Journal of Animal Physiology and Animal Nutrition. 2020;104:1851-1855
  15. 15. Abdel-Moneim A-ME, Selim DA, Basuony HA, Sabic EM, Saleh AA, Ebeid TA. Effect of dietary supplementation of Bacillus subtilis spores on growth performance, oxidative status and digestive enzyme activities in Japanese quail birds. Tropical Animal Health and Production. 2020;52:671-680
  16. 16. Abd El-Hack ME, El-Saadony MT, Shafi ME, Qattan SY, Batiha GE, Khafaga AF, et al. Probiotics in poultry feed: A comprehensive review. Journal of Animal Physiology and Animal Nutrition. 2020;104:1835-1850
  17. 17. Thornton PK, J.van de Steeg, A. Notenbaert, M. Herrero. The impacts of climate change on livestock and livestock systems in developing countries: A review of what we know and what we need to know. Agricultural Systems. 2009;101:113-127
  18. 18. Daghir NJ. Nutritional strategies to reduce heat stress in broilers and broiler breeders. Lohmann Information. 2009;1:6-15
  19. 19. DEFRA (Department for Environment, Food and Rural Affairs). Heat stress in poultry, solving the problem. UK. Nobel House 17 Smith Square London SW1P 3JR. 2005
  20. 20. Attia Y, Abdalah A, Zeweil H, Bovera F, El-Din AT, Araft M. Effect of inorganic or organic selenium supplementation on productive performance egg quality and some physiological traits of dual-purpose breeding hens. Czech Journal of Animal Science. 2010;55:505-519
  21. 21. Rao SR, Prakash B, Raju M, Panda A, Kumari R, Reddy EPK. Effect of supplementing organic forms of zinc, selenium and chromium on performance, anti-oxidant and immune responses in broiler chicken reared in tropical summer. Biological Trace Element Research. 2016;172:511-520
  22. 22. Kucuk O. Zinc in a combination with magnesium helps reducing negative effects of heat stress in quails. Biological Trace Element Research. 2008;123:144-153
  23. 23. Panda A, Ramarao S, Raju M, Chatterjee R. Effect of dietary supplementation with vitamins E and C on production performance, immune responses and antioxidant status of white Leghorn layers under tropical summer conditions. British Poultry Science. 2008;49:592-599
  24. 24. Abudabos AM, Suliman GM, Al-Owaimer AN, Sulaiman ARA, Alharthi AS. Effects of nano emulsified vegetable oil and betaine on growth traits and meat characteristics of broiler chickens reared under cyclic heat stress. Animals. 2021;11(7):1911
  25. 25. Attia YA, Abd El AE-HE, Abedalla AA, Berika MA, Al-Harthi MA, Kucuk O, et al. Laying performance, digestibility and plasma hormones in laying hens exposed to chronic heat stress as affected by betaine, vitamin C, and/or vitamin E supplementation. Springer Plus. 2016;5:1619
  26. 26. Attia YA, Al-Harthi MA, ShElnaggar A. Productive, physiological and immunological responses of two broiler strains fed different dietary regimens and exposed to heat stress. Italian Journal of Animal Science. 2018;17:686-697
  27. 27. Al-Harthi M, El-Deek A, Al-Harbi B. Interrelation ships among triiodothyronine (T3), energy and sex on nutritional and physiological responses of heat stressed broilers. Egyptian Poultry Science. 2002;22:349-385
  28. 28. Habashy WS, Milfort MC, Fuller AL, Attia YA, Rekaya R, Aggrey SE. Effect of heat stress on protein utilization and nutrient transporters in meat-type chickens. International Journal of Biometeorology. 2017;61:2111-2118
  29. 29. Babinszky L, Horváth M, Remenyik J, Verstegen MWA. The adverse effects of heat stress on the antioxidant status and performance of pigs and poultry and reducing these effects with nutritional tools. In: Hendriks WH, Verstegen MWA, Babinszky L, editors. Poultry and Pig Nutrition. Challenges of the 21st Century. Wageningen: Wageningen Academic Publishers; 2019. pp. 187-208
  30. 30. Musharaf NA, Latshaw JD. Heat increment as affected by protein and amino acid nutrition. World’s Poultry Science Journal. 1999;55:233-240
  31. 31. Pursey KM, Davis C, Burrows TL. Nutritional aspects of food addiction. Current Addiction Reports. 2017;4:142-150
  32. 32. Ghazalah A, Abd-Elsamee M, Ali A. Influence of dietary energy and poultry fat on the response of broiler chicks to heat therm. International Journal of Poultry Science. 2008;7:355-359
  33. 33. El-Deep MH, Ijiri D, Ebeid TA, Ohtsuka A. Effects of dietary nanoselenium supplementation on growth performance, antioxidative status, and immunity in broiler chickens under thermoneutral and high ambient temperature conditions. The Journal of Poultry Science. 2016;53(4):274-283
  34. 34. Habibian M, Ghazi S, Moeini MM. Effects of dietary selenium and vitamin E on growth performance, meat yield, and selenium content and lipid oxidation of breast meat of broilers reared under heat stress. Biological Trace Element Research. 2016;169:142-152
  35. 35. Sahin K, Sahin N, Kucuk O, Hayirli A, Prasad A. Role of dietary zinc in heat-stressed poultry: A review. Poultry Science. 2009;88:2176-2183
  36. 36. Lee SR. Cr itical role of zinc as either an antioxidant or a Prooxidant in cellular systems. Oxidative Medicine and Cellular Longevity. 2018;2018
  37. 37. Saleh AA, Eltantawy MS, Gawish EM, Younis HH, Amber KA, Abd El-Moneim AE-ME, et al. Impact of dietary organic mineral supplementation on reproductive performance, egg quality characteristics, lipid oxidation, ovarian follicular development, and immune response in laying hens under high ambient temperature. Biological Trace Element Research. 2020;195:506-514
  38. 38. Baxter MF, Greene ES, Kidd MT, Tellez-Isaias G, Orlowski S, Dridi S. Water amino acid-chelated trace mineral supplementation decreases circulating and intestinal HSP70 and proinflammatory cytokine gene expression in heat-stressed broiler chickens. Journal of Animal Science. 2020;98:skaa049
  39. 39. Abidin Z, Khatoon A. Heat stress in poultry and the beneficial effects of ascorbic acid (vitamin C) supplementation during periods of heat stress. World's Poultry Science Journal. 2013;69:135-152
  40. 40. Sahin N, Onderci M, Sahin K, Gursu M, Smith M. Ascorbic acid and melatonin reduce heat-induced performance inhibition and oxidative stress in Japanese quails. British Poultry Science. 2004;45:116-122
  41. 41. Daghir N. Broiler feeding and management in hot climates. Poultry Production in Hot Climate. 2008:227-260
  42. 42. Sahin K, Sahin N, Kucuk O. Effects of chromium, and ascorbic acid supplementation on growth, carcass traits, serum metabolites, and antioxidant status of broiler chickens reared at a high ambient temperature (32°C). Nutrition Research. 2003;23:225-238
  43. 43. Burkholder K, Thompson K, Einstein M, Applegate T, Patterson J. Influence of stressors on normal intestinal microbiota, intestinal morphology, and susceptibility to Salmonella enteritidis colonization in broilers. Poultry Science. 2008;87:1734-1741
  44. 44. Varasteh S, Braber S, Akbari P, Garssen J, Fink-Gremmels J. Differences in susceptibility to heat stress along the chicken intestine and the protective effects of galacto-oligosaccharides. PLoS One. 2015;10(9):e0138975
  45. 45. Abd El-Hack ME, Abdel-Moneim A-ME, Mesalam NM, Mahrose KM, Khafaga AF, Taha AE, et al. Nigella Sativa Seeds and its Derivatives in Poultry Feed, Black Cumin (Nigella Sativa) Seeds: Chemistry, Technology, Functionality, and Applications. Springer; 2021. pp. 265-296
  46. 46. Elbaz AM, El-sheikh SE, Abdel-Maksoud A. Growth performance, nutrient digestibility, antioxidant state, ileal histomorphometry, and cecal ecology of broilers fed on fermented canola meal with and without exogenous enzymes. Tropical Animal Health and Production. 2023;55:46
  47. 47. Ebeid T, Fathi M, Al-Homidan I, Ibrahim Z, Al-Sagan A. Effect of dietary probiotics and stocking density on carcass traits, meat quality, microbial populations and ileal histomorphology in broilers under hot-climate conditions. Animal Production Science. 2019;59:1711-1719
  48. 48. Li W, Bai J, Li Y, Qin Y, Yu D. Effects of Bacillus subtilis on meat quality, nutrient digestibility and scrum biochemical index of broilers. Chinese Journal of Veterinary Science. 2014;34:1682-1685
  49. 49. Saleh AA, Shukry M, Farrag F, Soliman MM, Abdel-Moneim A-ME. Effect of feeding wet feed or wet feed fermented by bacillus licheniformis on growth performance, histopathology and growth and lipid metabolism marker genes in broiler chickens. Animals. 2021;11:83
  50. 50. Abd El-Hack ME, Abdelnour SA, Taha AE, Khafaga AF, Arif M, Ayasan T, et al. Herbs as thermoregulatory agents in poultry: An overview. Science of the Total Environment. 2020;703:134399
  51. 51. Aljabeili HS, Barakat H, Abdel-Rahman HA. Chemical composition, antibacterial and antioxidant activities of thyme essential oil (Thymus vulgaris). Food and Nutrition Sciences. 2018;9:433
  52. 52. Toghyani M, Tohidi M, Gheisari AA, Tabeidian SA. Performance, immunity, serum biochemical and hematological parameters in broiler chicks fed dietary thyme as alternative for an antibiotic growth promoter. African Journal of Biotechnology. 2010;9:6819-6825
  53. 53. Sigolo S, Milis C, Dousti M, Jahandideh E, Jalali A, Mirzaei N, et al. Effects of different plant extracts at various dietary levels on growth performance, carcass traits, blood serum parameters, immune response and ileal microflora of Ross broiler chickens. Italian Journal of Animal Science. 2021;20:359-371
  54. 54. Attia YA, Bakhashwain AA, Bertu NK. Thyme oil (thyme vulgaris L.) as a natural growth promoter for broiler chickens reared under hot climate. Italian Journal of Animal Science. 2017;16(2):275-282
  55. 55. Khafar K, Mojtahedin A, Rastegar N, Kalvani Neytali M, Olfati A. Dietary inclusion of thyme essential oil alleviative effects of heat stress on growth performance and immune system of broiler chicks. Iranian Journal of Applied Animal Science. 2019;9:509-517
  56. 56. Nazarizadeh H, Mohammad Hosseini S, Pourreza J. Effect of plant extracts derived from thyme and chamomile on the growth performance, gut morphology and immune system of broilers fed aflatoxin B1 and ochratoxin A contaminated diets. Italian Journal of Animal Science. 2019;18:1073-1081
  57. 57. Alirezaei M, Gheisari HR, Ranjbar VR, Hajibemani A. Betaine: A promising antioxidant agent for enhancement of broiler meat quality. British Poultry Science. 2012;53:699-707
  58. 58. He S, Zhao S, Dai S, Liu D, Bokhari SG. Effects of dietary betaine on growth performance, fat deposition and serum lipids in broilers subjected to chronic heat stress. Animal Science Journal. 2015;86:897-903
  59. 59. Nasiroleslami M, Torki M, Saki AA, Abdolmohammadi AR. Effects of dietary guanidinoacetic acid and betaine supplementation on performance, blood biochemical parameters and antioxidant status of broilers subjected to cold stress. Journal of Applied Animal Research. 2018;46:1016-1022
  60. 60. Liu W, Yuan Y, Sun C, Balasubramanian B, Zhao Z, An L. Effects of dietary betaine on growth performance, digestive function, carcass traits, and meat quality in indigenous yellow-feathered broilers under long-term heat stress. Animals. 2019;9:506
  61. 61. Dos Santos TT, Dassi SC, Franco CR, Da Costa CR, Lee SA, Da Silva AVF. Influence of fibre and betaine on development of the gastrointestinal tract of broilers between hatch and 14 d of age. Animal nutrition. 2019;5:163-173
  62. 62. United states Department of Agriculture. Restrictions on Antibiotic Use for Production Purposes in U.S. Livestock Industries Likely To Have Small Effects on Prices and Quantities. Economic Research Service. 2019
  63. 63. Elghandour MMY, Tan ZL, Abu Hafsa SH, Adegbeye MJ, Greiner R, Ugbogu EA, et al. Saccharomyces cerevisiae as a probiotic feed additive to non and pseudo-ruminant feeding: A review. Journal of Applied Microbiology. 2020;128(3):658-674
  64. 64. Zhou M, Tao Y, Lai C, Huang C, Zhou Y, Yong Q. Effects of mannanoligosaccharide supplementation on the growth performance, immunity, and oxidative status of partridge shank chickens. Animals. 2019;9(10):817
  65. 65. Mahmoud H, Afiffy O, Mahrous M. Effect of using formic acid on growth performance and some blood parameter of broiler chicken. Assiut Veterinary Medical Journal. 2020;66(164):140-154
  66. 66. Kaczmarek SA, Barri A, Hejdysz M, Rutkowski A. Effect of different doses of coated butyric acid on growth performance and energy utilization in broilers. Poultry Science. 2016;95(4):851-859
  67. 67. Abd El-Hack ME, Alaidaroos BA, Farsi RM, Abou-Kassem DE, El-Saadony MT, Saad AM, et al. Impacts of supplementing broiler diets with biological curcumin, zinc nanoparticles and bacillus licheniformis on growth, carcass traits, blood indices, meat quality and cecal microbial load. Animals. 2021;11(7):1878
  68. 68. Al Fatah MA. Probiotic modes of action and its effect on biochemical parameters and growth performance in poultry. Iranian Journal of Applied Animal Science. 2020;10:9-15
  69. 69. Celina EB, Tamiris NSS. Probiotics as a promising additive in broiler feed: Advances and limitations. In: Advances in Poultry Nutrition Research. IntechOpen; 2021
  70. 70. Kaur AP, Bhardwaj S, Dhanjal DS, Nepovimova E, Cruz-Martins N, Kuča K, et al. Plant prebiotics and their role in the amelioration of diseases. Biomolecules. 2021;11(3):440
  71. 71. Yaqoob M, Abd El-Hack ME, Hassan F, El-Saadony MT, Khafaga A, Batiha G, et al. The potential mechanistic insights and future implications for the effect of prebiotics on poultry performance, gut microbiome, and intestinal morphology. Poultry Science. 2021;100(7):101143
  72. 72. Indikova I, Humphrey TJ, Hilbert F. Survival with a helping hand: campylobacter and microbiota. Frontiers in Microbiology. 2015;6:1-6
  73. 73. Chee SH, Iji PA, Choct M, Mikkelsen LL, Kocher A. Characterization and response of intestinal microflora and mucins to manno-oligosaccharide and antibiotic supplementation in broiler chickens. British Poultry Science. 2010;51:368-380
  74. 74. Partanen KH, Morz Z. Organic acids for performance enhancement in pig diets. Nutrition Research Reviews. 1999;12:117-145
  75. 75. Christian L, Mellor S. The use of organic acids in animal nutrition, with special focus on dietary potassium deformity under European and Austral-Asian conditions. Recent Advances in Animal Nutrition – Australia. 2011;4:123-130
  76. 76. Adil S, Banday MT, Bhat GA, Mir MS, Rehman M. Effect of dietary supplementation of organic acids on performance, intestinal histomorphology, and serum biochemistry of broiler chicken. Veterinary Medicine International. 2010;8:1-7
  77. 77. Hassan HMA, Mohamed MA, Youssef AW, Hassan ER. Effect of using organic acids to substitute antibiotic growth promoters on performance and intestinal microflora of broilers. Asian Australasian Journal of Animal Sciences. 2010;23:1348-1353
  78. 78. Chowdhury R, Islam KMS, Khan MJ, Karim MR, Haque MN, Khatun M, et al. Effect of citric acid, avilamycin, and their combination on the performance, tibia ash, and immune status of broilers. Poultry Science. 2009;88(8):1616-1622
  79. 79. Madhupriya V, Shamsudeen P, Raj Manohar G, Senthilkumar S, Soundarapandiyan V, Moorthy M. Phyto feed additives in poultry nutrition - A review. International Journal of Science, Environment and Technology. 2018;7:815-822
  80. 80. Li HL, Zhao PY, Lei Y, Hossain MM, Kim IH. Phytoncide, phytogenic feed additive as an alternative to conventional antibiotics, improved growth performance and decreased excreta gas emission without adverse effect on meat quality in broiler chickens. Livestock Science. 2015;181:1-6
  81. 81. Miguel MG. Antioxidant and anti-inflammatory activities of essential oils: A short review. Molecules. 2010;15:9252-9287
  82. 82. Joshua JF, Bhaskar G, Sami D. Phytogenic feed additives improve broiler feed efficiency via modulation of intermediary lipid and protein metabolism–related signaling pathways. Poultry Science. 2021;100:1-11
  83. 83. Elbaz AM, Salama AA, Ashmawy ES, Thabet HA, Badri FBA. Effect of dietary inclusion of corn distillers dried grains with solubles on productive performance, nutrient digestibility, immune status, Ileal Histometric and microbiota of broiler chickens. Egyptian Journal of Nutrition and Feeds. 2022;25(3):369-376
  84. 84. Elbaz AM. Effects of the diet containing fermented canola meal on performance, blood parameters, and gut health of broiler chickens. Journal Worlds Poultry Research. 2021;11(1):1-7
  85. 85. Abdel-Moneim A-ME, Sabic E, Abu-Taleb A, Ibrahim N. Growth performance, hemato-biochemical indices, thyroid activity, antioxidant status, and immune response of growing Japanese quail fed diet with full-fat canola seeds. Tropical Animal Health and Production. 2020;52:1853-1862
  86. 86. Abd El-Moneim AE, Sabic EM. Beneficial effect of feeding olive pulp and aspergillus awamori on productive performance, egg quality, serum/yolk cholesterol and oxidative status in laying Japanese quails. Journal of Animal and Feed Sciences. 2019;28:52-61
  87. 87. Abd El-Moneim AE, Sabic EM, Abu-Taleb AM. Influence of dietary supplementation of irradiated or non-irradiated olive pulp on biochemical profile, antioxidant status and immune response of Japanese quails. Biological Rhythm Research. 2019;53:519-534
  88. 88. Alshelmani MI, Loh TC, Foo HL, Sazili AQ , Lau WH. Effect of feeding different levels of palm kernel cake fermented by Paenibacillus polymyxa ATCC 842 on nutrient digestibility, intestinal morphology, and gut microflora in broiler chickens. Animal Feed Science and Technology. 2016;216:216-224
  89. 89. Disetlhe ARP, Marume U, Mlambo V. Humic acid and enzymes inclusion in canola-based diets generate different responses in growth performance, protein utilization dynamics, and hemato-biochemical parameters in broiler chickens. Poultry Science. 2018;97(8):2745-2753
  90. 90. Al-Harthi MA. The efficacy of using olive cake as a by-product in broiler feeding with or without yeast. Italian Journal of Animal Science. 2016;15(3):512-520
  91. 91. Al-Harthi MA, Attia YA. Effect of citric acid on the nutritive value of olive cake in broiler diets. European Poultry Science. 2016;80:1-14
  92. 92. Wu Z, Chen J, Ahmed Pirzado S, Haile TH, Cai H, Liu G. The effect of fermented and raw rapeseed meal on the growth performance, immune status and intestinal morphology of broiler chickens. Journal of Animal Physiology and Animal Nutrition. 2022;106(2):296-307
  93. 93. Saki AA, Pournia K, Tabatabaie MM, Zamani P, Haghighat M, Salary J. Effects of cottonseed meal supplemented with lysine and enzyme (Hydroenzyme XP) on egg quality and performance of laying hens. Revista Brasileira de Zootecnia. 2012;41:2225-2231
  94. 94. Nie CX, Zhang WJ, Wang YQ , Liu YF, Ge WX, Liu JC. Tissue lipid metabolism and hepatic metabolomic profiling in response to supplementation of fermented cottonseed meal in the diets of broiler chickens. Journal of Zhejiang University. Science. B. 2015;16:447-455
  95. 95. Mbukwane MJ, Nkukwana TT, Plumstead PW, Snyman N. Sunflower meal inclusion rate and the effect of exogenous enzymes on growth performance of broiler chickens. Animals. 21 Jan 2022;12(3):253
  96. 96. Jazi V, Boldaji F, Dastar B, Hashemi SR, Ashayerizadeh A. Effects of fermented cottonseed meal on the growth performance, gastrointestinal microflora population and small intestinal morphology in broiler chickens. British Poultry Science. 2017;58:402-408
  97. 97. Chiou PWS, Chen C, Yu B. Effects of Aspergillus oryzae fermentation extract on in situ degradation of feedstuffs. Asian-Australasian Journal of Animal Sciences. 2000;13(8):1076-1083
  98. 98. Rama Rao S, Raju M, Panda A, Reddy M. Sunflower seed meal as a substitute for soybean meal in commercial broiler chicken diets. British Poultry Science. 2006;47:592-598
  99. 99. Nassiri Moghaddam H, Salari S, Arshami J, Golian A, Maleki M. Evaluation of the nutritional value of sunflower meal and its effect on performance, digestive enzyme activity, organ weight, and histological alterations of the intestinal villi of broiler chickens. Journal of Applied Poultry Research. 2012;21:293-304
  100. 100. Horvatovic M, Glamocic D, Zikic D, Hadnadjev T. Performance and some intestinal functions of broilers fed diets with different inclusion levels of sunflower meal and supplemented or not with enzymes. Brazilian Journal of Poultry Science. 2015;17:25-30
  101. 101. Tüzün AE, Olgun O, Yıldız AÖ, Sentürk ET. Effect of different dietary inclusion levels of sunflower meal and multi-enzyme supplementation on performance, meat yield, ileum Histomorphology, and pancreatic enzyme activities in growing quails. Animals. 2020;10:680
  102. 102. Niu JL, Wei LQ , Luo YQ , Yang WT, Lu QC, Zheng XX, et al. Fermented cottonseed meal improves production performance and reduces fat deposition in broiler chickens. Animal Bioscience. 2021;34(4):680
  103. 103. Zhang WJ, Xu ZR, Zhao SH, Sun JY, Yang X. Development of a microbial fermentation process for detoxification of gossypol in cottonseed meal. Animal Feed Science and Technology. 2007;135:176-186
  104. 104. Elbaz AM, Thabet HA, Gad GG. Productive and physiological performance of broilers fed diets containing different levels of olive pulp. Journal of Animal and Poultry Production. 2020;11(11):435-439
  105. 105. Al-Harthi MA. The chemical composition and nutrient profiles and energy values of olive cake for poultry diets. Life Science Journal. 2014;11(9):159-165
  106. 106. Zarei M, Ehsani M, Torki M. Productive performance of laying hens fed wheat-based diets included olive pulp with or without a commercial enzyme product. African Journal of Biotechnology. 2011;10:4303-4312
  107. 107. Ibrahim NS, Sabic EM, Abu-Taleb AM. Effect of inclusion irradiated olive pulp in laying quail diets on biological performance. Journal of Radiation Research and Applied Sciences. 2018;11(4):340-346
  108. 108. Nourmohammadi R, Khosravinia H, Afzali N. Effects of high dietary levels of citric acid on productive performance, serum enzyme activity, calcium and phosphorus retention and immune response in broiler chickens. European Poultry Science. 2015;79:1-9

Written By

Ahmed El-Baz and Raafat Khidr

Submitted: 20 May 2023 Reviewed: 07 June 2023 Published: 18 March 2024