Next Article in Journal
MOB: Pivotal Conserved Proteins in Cytokinesis, Cell Architecture and Tissue Homeostasis
Previous Article in Journal
First De Novo Transcriptome of the Copepod Rhincalanus gigas from Antarctic Waters
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Sustainable Antibiotic-Free Broiler Meat Production: Current Trends, Challenges, and Possibilities in a Developing Country Perspective

by
Md. Hakimul Haque
1,*,
Subir Sarker
2,*,
Md. Shariful Islam
1,
Md. Aminul Islam
3,
Md. Rezaul Karim
4,
Mohammad Enamul Hoque Kayesh
5,
Muhammad J. A. Shiddiky
6 and
M. Sawkat Anwer
7
1
Department of Veterinary and Animal Sciences, Faculty of Agriculture, Rajshahi University, Rajshahi 6205, Bangladesh
2
Department of Physiology Anatomy and Microbiology, School of Life Sciences, La Trobe University, Bundoora, VIC 3086, Australia
3
Department of Medicine, Faculty of Veterinary Medicine and Animal Science, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur 1706, Bangladesh
4
Livestock Research Institute, Savar, Dhaka 1341, Bangladesh
5
Department of Microbiology and Public Health, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Barishal 8210, Bangladesh
6
School of Environment and Science (ESC), and Queensland Micro- and Nanotechnology Centre (QMNC), Griffith University, Nathan Campus, 170 Kessels Road, QLD 4111, Australia
7
Department of Biomedical Sciences, Cummings School of Veterinary Medicine, Tufts University, 200 Westboro Road, North Grafton, MA 01536, USA
*
Authors to whom correspondence should be addressed.
Biology 2020, 9(11), 411; https://doi.org/10.3390/biology9110411
Submission received: 16 October 2020 / Revised: 13 November 2020 / Accepted: 19 November 2020 / Published: 23 November 2020

Abstract

:

Simple Summary

Chickens are raised with the assistance of the regular use of antibiotics, not only for the prevention and treatment of diseases but, also, for body growth. Overuse and misuse of antibiotics in animals are contributing to the rising threat of antibiotic resistance. Therefore, antibiotic-free broiler meat production is becoming increasingly popular worldwide to meet consumer demand. However, numerous challenges need to be overcome in producing antibiotic-free broiler meat by adopting suitable strategies regarding food safety and chicken welfare issues. This review focuses on the current scenario of antibiotic use, prospects, and challenges in sustainable antibiotic-free broiler meat production. We also discuss the needs and challenges of antibiotic alternatives and provide a future perspective on antibiotic-free broiler meat production.

Abstract

Antibiotic-free broiler meat production is becoming increasingly popular worldwide due to consumer perception that it is superior to conventional broiler meat. Globally, broiler farming impacts the income generation of low-income households, helping to alleviate poverty and secure food in the countryside and in semi-municipal societies. For decades, antibiotics have been utilized in the poultry industry to prevent and treat diseases and promote growth. This practice contributes to the development of drug-resistant bacteria in livestock, including poultry, and humans through the food chain, posing a global public health threat. Additionally, consumer demand for antibiotic-free broiler meat is increasing. However, there are many challenges that need to be overcome by adopting suitable strategies to produce antibiotic-free broiler meat with regards to food safety and chicken welfare issues. Herein, we focus on the importance and current scenario of antibiotic use, prospects, and challenges in the production of sustainable antibiotic-free broiler meat, emphasizing broiler farming in the context of Bangladesh. Moreover, we also discuss the need for and challenges of antibiotic alternatives and provide a future outlook for antibiotic-free broiler meat production.

1. Introduction

There is a worldwide movement to support a sustainable agricultural system that involves sustaining farmers, resources, and societies. It is expected that this can be achieved by upgrading farming practices that are profitable, environmentally sound, good for communities, and antibiotic-free. However, raising animals without antibiotics is a challenge, and especially, antibiotic-free broiler meat production is a growing challenge in many developing countries, including Bangladesh, where antibiotics are used injudiciously [1]. Broiler chickens are reared particularly for meat production because of their typical soft, tender meat, low-fat content, and short production period. Broilers take the place of valuable food animals globally by notably contributing to food security, protein supply, and people’s employment [2]. Sustainable broiler production not only requires maximum productivity but, also, includes bird and human welfare and environmental protection. In addition, consumers are concerned about antibiotic residue and antimicrobial resistance, as well as pesticide residues, additives, nutritional content, flavor, traceability, regional production, genetically modified organisms, social justice, etc., with regards to broiler meat production. Therefore, broiler meat production without using antibiotics is crucial in the battle of antimicrobial resistance to save poultry, animals, and public health.
Broiler meat production has undergone exponential growth for global consumption and business profit. Low production costs and rapid economic progress are pivotal in its expansion [3]. Though commercial poultry farming is a profitable business, it faces a number of challenges. Among them, the occurrence of infectious and noninfectious diseases is a major challenge due to poor biosecurity and husbandry practices. Over several decades, some antibiotics have been used in broiler feed to control, prevent, and treat diseases and boost performance and feed efficacy [4,5]. This inappropriate antibacterial use favors antimicrobial resistance. The most common pathway for bacteria to gain resistance is through mobile genetic components, including bacteriophages, plasmids, naked DNA, or transposons. Plasmid-mediated gene transfer facilitates the flow of resistant genes between bacteria, accelerating antibiotic resistance [6]. Bacteria can also develop antibiotic resistance through sequential mutations in the chromosome, as happens in fluoroquinolone resistance. Using normal genetic variations, bacterial populations mutate to render antibiotics ineffective against them [7]. Indeed, antibiotic resistance begins with the interaction between bacteria and antibiotic, leading to the removal of sensitive bacteria and selection of resistant populations. However, the distribution and assortment of resistance are complicated matters that pose a severe public health problem [8]. The indiscriminant use of antibiotics in nonbacterial infections like influenza and other viral infections facilitates antibiotic resistance [9].
In Bangladesh, commercial poultry farmers extensively utilize antibiotics without any veterinary advice and often do not follow withdrawal period guidelines [10]. A lack of both easily accessible veterinary facilities and adequate knowledge combined with a high-profit motive are some of the factors that drive local producers to inappropriate and, at times, illegal use of antimicrobial agents [11]. The cost-effective production of broilers may act as a driver for the practice of using growth-promoting medicines, including antibiotics, for the overall growth performance [12,13]. These agents get stored in various body parts and tissues, resulting in antibiotic residues for unintended exposure to consumers. Sattar et al. [14] reported antibiotic residues mostly in the liver, kidney, thigh meat, and breast meat of broilers. Easy access to antibiotics from registered veterinarians by farmers without prescriptions contributes to the indiscriminant use of antibiotics, which can result in antimicrobial resistance from food animals [11]. Although antibiotic resistance has always been present in nature, antibiotic pressure due to inappropriate use facilitated the rapid and widespread emergence of drug-resistant pathogenic bacteria [15]. As several antibiotics frequently consumed by livestock are identical to those used in humans, there is worldwide fear that antibiotic-resistant bacteria may be transferred from animals to humans, leading to severe public health concerns [16]. Resistant bacteria with resistant genes can quickly spread among humans, animals, and the ecological community. Therefore, new approaches should be considered for antibiotic-free broiler production so they can be sustainably raised and marketed. Therefore, this review highlights the current scenario of antibiotic use in broiler meat production, as well as the global challenges, prospects, and approaches of antibiotic-free production, particularly in the context of Bangladesh.

2. Economic and Clinical Importance of Antibiotic-Free Broiler Meat Production

The fast growth of the poultry industry has been attained through the effective implementation of high-yielding strains of meat-type chickens and the availability of nutritionally balanced feed. Broiler farming plays a central role in enhancing income, improving food safety, and mitigating scarcity in the countryside and in semi-urban communities in developing countries. For a couple of decades, the poultry industry has played a critical role in the economic development of Bangladesh by providing job opportunities, food security, and good-quality protein. The poultry industry has assisted in changing living and food habits by moderating animal protein sources such as beef and mutton. For instance, about 44% of the protein for everyday human consumption comes from poultry and animal products [17]. As a primary portion of production, this industry’s ability to furnish the country with affordable and nourishing protein in the form of meat and eggs is encouraging [18]. There are over a million small and large poultry farms, 80 grandparent (GP) stock farms, 130 parent stock farms and hatcheries, and over 50 feed mills across the country, making up a USD 2.36 billion industry. About five million people are employed in the industry directly and indirectly. A study estimated that around 150,000 poultry farms in Bangladesh are producing 570 million tons of meat and 7.334 billion eggs annually, and about 68.17% of animal protein consumed comes from poultry meat [19]. A significant number of pastoral individuals depend on this business for their income. The poultry industry has made up one-third of the entire agronomic contribution to the Gross Domestic Product (GDP) (18.60%) in recent years [20].
In food animal production, antibiotics are also exploited, albeit unwisely, to advance animal growth and feed efficiency [21,22]. Generally, farmers in developing countries use antibiotics deliberately to promote growth without any veterinary consultation. Additionally, shockingly, 88% of producers did not adhere to the required antibiotic withdrawal time before marketing [22]. On the other hand, only 10% of farmers stopped using antibiotics before marketing, and only 2% of farmers withdrew antibiotics at least seven days before marketing. Still, they did not always follow this withdrawal protocol [23]. Generally, excessive and unnecessary use of medicines affects the total cost of production. A study on the antibiotic usage patterns in Bangladesh concluded that the use of antibiotics has an economic effect on broiler production [11]. Another study revealed that the cost of antibiotic usage could be 3.53% of the overall production rate based on responses from 84% of farmers [23]. The cost of antibiotics varies from farm to farm due to the presence and severity of diseases and their use as growth promoters. Removing antibiotics from broilers can lower the production cost and, thereby, decrease the market price of broiler meat.
The nontherapeutic use of antibiotics increases the residual accumulation more than medically necessary to use and, thereby, increases the incidence of antimicrobial resistance. The consumption of residual medicines through animal food products (e.g., meat, milk) is assumed to initiate resistance development in humans. Besides, commensal bacteria of livestock are often present in fresh meat, which can serve as reservoirs of resistant genes to be relocated to pathogenic bacteria in humans [7]. Studies have shown that antibiotic residues were present in more than 50% of samples of broiler and layer meat collected in different regions of Bangladesh [14,22]. Another study by Faiz and Bashe (2011) reported that some pathogenic bacteria, such as Pseudomonas aeruginosa and Salmonella typhi, are resistant to commonly used antibiotics [24]. The high degree of antibiotics resistance in Bangladesh poses a regional and global threat [25]. In Bangladesh, diarrhea accounts for around 230,000 child deaths annually, and a significant portion is due to antibiotic-resistant bacterial infection [19].

3. Prospects of Antibiotic-Free Broiler Meat Production

In veterinary practice, antibiotics are used for prophylactic, therapeutic, and growth-promoting purposes. The purchase of medicines without a prescription is common in developing countries like Bangladesh. This can lead to an inadequate course of treatment, incorrect antibiotic selection, indiscriminant and excessive use, and enhanced residual deposition in animal bodies. A recent study with 160 poultry samples from different regions in Bangladesh identified antibiotics in more than 50% of the samples [22]. Producing a sufficient amount of food for a growing population is a great challenge for any country. Of the 17 Sustainable Development Goals (SDGs), 14 are connected to the poultry sector in some way or other. According to data from the Bangladesh Poultry Industries Central Council (BPICC), the annual commercial production of eggs and poultry meat is about to 1022 crore pieces and 14.6 lakh tons, respectively. Thus, the poultry industry appears to be a big sector, worth about USD 353.88 crore [26]. Nowadays, consumers are refusing to consume antibiotic-treated chicken and demanding safe, antibiotic-free beef. Therefore, there is a large market for antibiotic-free chicken in Bangladesh. The challenge is to find a way to produce them. One option would be to use medicinal plants instead of antibiotics as growth promoters. Bangladesh is rich in medicinal plants, and many such plants have been shown to have antibacterial activities, such as Abutilon indicum L., Caesalpinia bonduc L., Ixora nigricans L., etc. Many natural foods also have antibacterial actions, such as broccoli (Brassica oleracea), guava (Psidium guajava), garlic (Allium sativum), and okra (Abelmoschus esculentus) [27,28,29,30]. Based on antibacterial medicinal plants and natural foods, a safe antibacterial preparation could be developed to use in food animals as an alternative to antibiotics for growth promotion and feeding efficiency.

4. Significant Challenges for Sustainable Antibiotic-Free Broilers Production

Bangladesh is a developing country, and its seasonal variations are very distinct, categorized by extreme temperatures, excessive humidity, and heavy rainfall. The environment is beneficial for the survival and growth of various microorganisms and makes them ubiquitous and fastidious. Most poultry farmers are not well-educated or well-trained for modern scientific farming. It is estimated that about 80% of farmers lack adequate knowledge about rearing current high-yielding strains [23]. Moreover, farmers in Bangladesh can quickly get antibiotics from local vendors without a veterinarian’s prescription. Biosecurity measures are also terrible; thus, the entry of microorganisms on most farms is common, affecting the production performance of flocks. The commercial livestock sector is multiplying and conveying a lot of diseases with it. Thus, biosecurity must be implemented without fail [26]. Newcastle disease, Gumboro or infectious bursal disease, Marek’s disease, duck plague, fowl pox, fowl cholera, leucosis, and infectious bronchitis are among the most common infectious diseases in the poultry sector [26]. It is therefore essential to control primary and secondary infections for successful poultry farming in Bangladesh. One of the most critical factors in antibiotic-free broiler production is the economic challenge, i.e., cost management. The most critical challenges in producing antibiotic-free broilers in Bangladesh and abroad (Figure 1) are addressed below.

4.1. Environment

Whatever system is followed in any corner of the world, none can deny that environmental pollution is a part of broiler production. Disease and mortality are likely to increase due to polluted and hazardous environments. Increased clinical and subclinical necrotic enteritis (NE) and related disorders, including cholangiohepatitis, on poultry farms are the likely consequences. Therefore, it is vital to keep the level of pollution to a minimum for the well-being of both birds and humans. To achieve this goal, farmers should prioritize proper carcass disposal and waste management during farm operations. While about 70% of all agricultural land globally is occupied by livestock [31], poultry farming’s effect on agricultural land loss is minimal [32]. However, another study suggested that feed production, processing, and transport result in a greater overall environmental impact than any other part of broiler production [33,34]. Therefore, farmers must follow the principles of poultry production, upholding public interest, as well as a hazard-free environment, thereby ensuring sustainable antibiotic-free poultry meat production.

4.2. Resource Management

Resource management is the process by which farm owners effectively utilize their tangible and intangible resources. It involves effective planning to ensure that the right resources are assigned to the right tasks. Broiler meat production without the use of antibiotics requires farmers to decrease the stocking density, raise the downtime, clean rapidly and frequently, maintain the correct temperature, provide rigorous biosecurity, reduce hassle, select the best breed, etc. Therefore, it is a significant undertaking for the efficient utilization of limited resources in broiler farming management. Broiler production and meat processing require an adequate supply of water. Thus, inadequate water availability is a significant obstacle to sustainable antibiotic-free broiler meat production [35]. Another relevant aspect of resource management is feeding the poultry. There is competition between poultry and humans for quality proteins. This creates a challenge when a protein-rich foodstuff (wheat and maize) needs to be included in the supplied ration [36,37].

4.3. Antibiotics

Despite increasing concerns, antibiotics are used worldwide on poultry farms, particularly broiler farms, to treat and prevent diseases and as growth promoters to improve meat production [38,39,40]. Antibiotics are commonly used to treat intestinal infections caused by Salmonella, Escherichia coli (E. coli), or Clostridium spp. These pathogens can negatively impact poultry farming and farmers’ profit. A recent study demonstrated the patterns of antibiotic use at selected broiler farms in Bangladesh, with reported use for therapy (43.8%), prevention (31.5%), or both (47.9%), and for promoting growth (8.2%) [11]. However, antibiotic use varies from nation to nation depending on several factors, including knowledge, economy, management system, and farming practices [41]. Although the monitoring of antibiotic use is essential, it is poorly implemented around the world, including in Bangladesh [40]. According to a recent estimate, the average annual global consumption of antimicrobials per kilogram of chicken production was 148 mg [42]. Furthermore, a rise of the antimicrobial consumption by 67% was projected [42]. The widespread use of antibiotics on broiler farms could encourage antibiotic resistance, ultimately causing a global public health threat [43]. Alternative approaches should be investigated to replace growth-promoting antibiotics to maintain and ensure gut health and good-quality meat production. However, producing quality broiler meat at consumer-friendly prices without antibiotics will be a challenge.

4.4. Breed Diversity

In the modern period, it is evident that there is minimal breed and genetic variability among commercial birds. Researchers have found that the breed or genetic diversity of commercial chicken farms has declined in the developed world. This is mainly because modern industrialized agriculture depends, in no small degree, on uniformity. There are hundreds of breeds of poultry that are well-recognized and registered. Most of these poultry breeds and varieties are locally adapted for multiple purposes and suited to various farming enterprises. They are mostly reared under small-hold production systems and are a large part of poultry meat production worldwide. On the contrary, modern chicken strains are raised for either meat or eggs, and only limited high-producer strains are employed. However, such top-yielding hybrids are more susceptible because of their compromised immune capacity [44]. Not cultivating other breeds means not only sacrificing the natural genetic diversity but, also, decreasing the birds’ potential to adapt to new conditions and circumstances, such as climate changes [45]. It is noteworthy that genetic uniformity or a lack of genetic diversity makes birds more vulnerable to many diseases. While it is convenient and profitable to mass-produce a particular breed, the loss of diversity makes it more challenging to adapt to changes [46].

4.5. Social Aspects

Two social issues, working environments and human health, and the impartiality of job agreements, including health care, fair wages, and cooperative trading rights, are significant matters in sustainable broiler production. Poultry farmers and their family members risk becoming contaminated with antibiotic-resistant bacteria and developing antibiotic allergies. Health ailments in farm workers due to exposure to dust, litter, and feathers are quite common [47] and should receive attention to assure production continuity. According to Quandt et al. [48], “chicken grabbing” in the USA is characterized by a working atmosphere and work organization that encourages accidents and illness and is closely connected to the risk of disease, human rights, and overall working environments. Workers are exploited disproportionately in food-producing industries such as the poultry sector. For example, healthy working conditions are not maintained in order to keep the direct costs of production low. Besides, the terms and conditions with contract growers vary greatly and, in some cases, are grossly unreasonable [49,50].

4.6. Gender Issue

Among the 17 Sustainable Development Goals established by the United Nations in 2015, promoting gender egalitarianism and empowering women is noteworthy. Commercial poultry production on an industrial scale does not firmly follow this gender goal. However, small-scale family poultry production with low input is mostly run by women in most Asian and African countries. Such a production system supplies much-needed poultry meat and eggs for the proper nutrition of millions of people worldwide and helps reduce poverty and improve incomes in rural areas. Dolberg et al. [51] reported that women are actively involved in various aspects of small-scale poultry production in rural households. While women are often responsible for taking care of poultry, they usually face more critical challenges than men. Women have less access to and influence over property, credit, labor, technology, and the facilities required to take advantage of development opportunities. In some instances, they do not have full control or decision-making authority over the birds or the revenue from their sale [52]. Further, the keeping of family poultry (FP) is typically the responsibility of women. Unfortunately, there is a lack of knowledge of women’s and men’s particular roles in FP production; this results in gender blindness. Therefore, the contribution of women to this subsector of poultry remains invisible [53]. Thus, the gender issue is a massive challenge in sustainable antibiotic-free broiler meat production in Bangladesh.

4.7. Animal Welfare

It is imperative that we look after the welfare of animals that serve us in so many ways. Humanity demands it. With the advancement of time, the animal welfare issue has become a matter of great concern. The suffering of poultry caused intentionally or unintentionally cannot be justified in any production [54]. The Animal Welfare Standards research project funded by the EU laid down 12 standards for animal protection. For example, poultry should not be stressed from excessive hunger or thirst, should have room for free movement, and should show usual nonharmful behavior. Poultry producers should promote positive emotions and avoid negative emotions, such as fear, distress, frustration, and apathy. These criteria are currently not fulfilled by many producers, and some poultry production systems may cause suffering [55]. Skipping a day of feeding broiler breeders to control their body weight affects the chickens’ welfare under the modern husbandry system. This practice needs the attention of researchers to ensure the sustainability of production in the future. It is interesting to note that some studies recommend providing low-density feeds to increase female broiler breeders as an alternative to feeding constraints [56]. Any improvement in animal welfare also upgrades the sustainability and is less harmful to the environment. Nevertheless, it is challenging to balance the relationship between poultry production, animal welfare, and the impact of production on the ground. Organic animal production is often set in with sustainability, which can lead consumers to think that animals raised organically have better welfare. Although some organic poultry systems uphold high levels of interest, it can be challenging to maintain good health and well-being on organic poultry farms [57].

4.8. Institutional Aspects

The institutional dimensions of sustainability comprise the management and governance of global processes and ensure that organizations are responsible, accountable, and transparent to their members and representatives. Indeed, a few breeding corporations dominate a significant part of the industry, making it hard for small businesses to start up. The producer should balance the multiple interests inherent in the principle of sustainability with the management of operations. Although Bangladesh’s government has many policies to meet the SDGs to tackle the economic, environmental, and social aspects, there is still no poultry policy to coordinate with other enterprises. One policy in a field often hampers advancement in another. Solutions to difficult problems are sometimes in the hands of policymakers in different industries or at various government levels. It is a significant cause of many unsustainable long-term patterns [46]. The sustainability of poultry production involves producing sufficient outputs to provide satisfactory products for consumers and income for farmers and constant availability of the required inputs such as raw materials, labor, and capital in the long term. On a biological basis, the production of village-based poultry in Bangladesh is almost sustainable. Almost all of the necessary feed is found through scavenging, and home-grown grain and byproducts serve as feed supplements. Although poultry meat and egg productivity has increased continuously during the last decades, it is questionable whether the consequent rapidly rising need for poultry products will be fulfilled in the future. The challenges of small-scale and comprehensive poultry production have been discussed previously [58]. In recent years, Bangladesh’s action plan to train vast numbers of rural extension staff and coordinate the supply of vaccines at the rural level has been useful. There is also a need to ensure the long-term viability of the organizational structure and training programs.

4.9. Consumption Pattern and Demand for Poultry Products

The requirements for poultry products will be doubled in 2050 based on the rising usage in recent decades [49]. It is believed that today’s food insecurity problems are not due to a shortage of food but, rather, to poor people’s ability to afford it. Increasing consumption patterns in some countries will demand increased production. In contrast, as people grow wealthier, the demand for healthier “green” diets or organic foods will increase in some other countries [46]. On the other hand, the indiscriminate use of antibiotics or other harmful substances in the production chain negatively affects consumers’ trust in broiler meat. These results negatively impact market demand, as observed recently in Bangladesh. A lack of confidence in the product threatens sustainable production, causing colossal loss to the industry. Farmers must balance order, supply, and consumption patterns in a transparent and healthy competitive environment. Further, the quality of feeds and feeding programs is also a component of sustainable broiler production. The purpose of a feeding program is to feed the chickens and not the bacteria. A successful feeding program is essential in antibiotic-free broiler production. Poor-quality feed ingredients, rancid animal byproducts in the feed, and mycotoxin contamination can damage gut health and the intestinal epithelium. Therefore, excellent feed ingredients are essential to keep proper gut health, as well as better flock health. However, these ingredients will increase the production cost unless the savings from not using antibiotics can offset the cost of quality feed. This is an important consideration, since consumers in Bangladesh are demanding high-quality products but are unwilling to pay more. Therefore, it may be a significant challenge to supply antibiotic-free broiler meat at a price desired by consumers.

5. Possibilities of Antibiotic-Free Broiler Production

Superior output and biosecurity management practices are essential components in raising chicken without antibiotics. Some general approaches for antibiotic-free broiler production are shown in Table 1 and discussed below.

5.1. Strict Downtime between Placements

It is a quick, simple management procedure to raise antibiotic-free broilers. In this case, new flock entry should be restricted to a minimum of 14 days (downtime) with good cleanout (clearing out birds and removing the litter cake). The downtime should start when birds are out of the house production site.

5.2. Optimum Stocking Density

The stocking density is a crucial concern for profitable broiler farming. As the stocking density increases, so does the stress level of birds. Increased stress is associated with compromised immunity and, consequently, an increased susceptibility to disease. Thus, decreasing stress by increasing the stock density can help reduce the risk of disease and the need for antibiotics. A reduced stocking density is also an excellent option to help keep litter moisture at a minimum compared to the current conventional program. Farmers should decrease the stocking density, which, in turn, reduces the shedding of cocci oocyst and pathogenic bacteria. This practice also helps in proper ventilation and aeration and, thus, reduces stress. However, the ideal stock density is still being debated. Bilgili and Hess [59] reported a significant improvement of the overall growth performance, carcass quality, and mortality with a decreased stock density. In Bangladesh, usually 1- to 1.5-square-feet of floor space is assigned to each bird. However, in antibiotic-free broiler production, providing more space than required is an important factor.

5.3. Good Litter Management

Keeping the litter dry is critical in the overall management of any poultry farm, as it influences the bird performance by decreasing the ammonia level and, thereby, the growers’ profits. Dry waste and low ammonia levels are the keys to success in raising poultry. The negative impact of ammonia on bird performance is well-documented [60,61]. Dry litter controls the ammonia levels and provides a better flock atmosphere and reduces disapproval due to contact dermatitis and inflamed bursa. When unused bedding materials start to hold moisture, it will clump together to form caking, leading to increased ammonia formation. Caking is mainly due to moisture in the litter and can be prevented by having adequate ventilation. Broilers drink approximately two pounds of water for every pound of feed they consume. About 20% of the water is used for growth, while most of it eventually reaches the litter as waste. Therefore, there must be adequate ventilation to remove moisture within the waste to prevent caking. Generally overventilation is needed to fix the problem once caking has started. Growers should attend to litter sanitation and treatment at regular intervals. It is a great idea to monitor the ammonia levels regularly, and handheld sensors can accurately manage them. Amending the litter and providing adequate ventilation are the most practical ways to control ammonia and improve litter quality [62]. Preventive fan maintenance can aid in keeping the ventilation program effective. A total litter cleanout at least once a year is highly recommended.

5.4. Control Environment Housing

Producers can reduce bacterial growth and antibiotic use by maintaining the adequate ventilation of poultry housing facilities. A study reported the presence of antibiotic-resistant bacteria in the air of broiler chicken facilities [63]. Dust is an excellent carrier of bacteria, while mold is a potential source of infection. For appropriate airing, heat, relative moisture, and light, an environmentally controlled structure should be built oriented in the east-to-west direction longitudinally, with large exhaust fans on the west side and evaporative chilling plugs on the east side, accompanied by programmed feeding and drinking methods inside [64]. Chick suppliers can provide useful information on the ideal temperature, humidity, and air quality for raising broilers. Airborne dispersion of antibiotic-resistant bacteria should not be underestimated, considering the respiratory health of chickens and poultry workers. Farmers should follow the standard guidelines for maintaining adequate ventilation [64].

5.5. Pre-Starter Feed

Pre-starter feed is crucial in establishing good gut microbe populations. To achieve a balance in gut microbiota for nutritional enhancement of the gastrointestinal (GI) tract, boost the immune development, and facilitate nutrient absorption, it is useful to include probiotics, prebiotics, organic acids, short- and medium-chain fatty acids, and phytogenic feed. The broiler industry has achieved noteworthy advances in productivity by prioritizing the hereditary selection, diet, and controlling procedures. The nutrition for broilers is focused on the need to get to the market weight as quickly as possible. There is a growing interest in a specifically designed pre-starter feed for 10–14 days of broiler growth, since this represents more than 20% of the growth time [65]. A specialized formulation should ensure that the feed is easily digestible and meets the broiler’s nutritional needs. The efficacy of pre-starter diets relies on the potential carryover effect to increase the bird performance until market age. The nutrient requirements, particularly digestible amino acids, are crucial in the broiler’s first 10 days. Rice and its lower non-starch polysaccharide substance may be a better option than corn or wheat for pre-starter diets. Additionally, the addition of fibrous components in low-fiber feeds at earlier stages may enhance the gut development and improve nutrient absorption, eventually enhancing the overall growth performance. Finally, the manufacturer should concentrate on feed formulations to remove antibiotic growth promoters from all broiler diets. This will ensure sustainable growth and gain consumer acceptance. Broiler feed should receive particular attention by providing the particle size, protein and fat qualities, and specific additives.

5.6. Water Quality and Sanitation

A good water sanitation program is key to healthy poultry production. Water is essential for birds. A routine water quality analysis for bacteria, pH, hardness, minerals, and total dissolved solids should be conducted annually. Flushing and disinfecting between flocks with suitable quality disinfectants should be done to remove biofilm from the pipeline. Biofilm is a sticky film that can exist inside water lines, regulators, and nipple drinkers and can be composed of bacteria and other organisms [66]. Chlorine is the most popular sanitizer; other well-documented sanitizers include hydrogen peroxide, chlorine dioxide, and ozone. In addition, acidifiers can improve the sanitizer’s effectiveness and reduce bacterial growth in water lines [67].

5.7. Antibiotic Alternatives

Over the past two decades, producers have extensively used antibiotics for broiler weight gain. Including antibiotics in broiler production enhances the food conversion ratio by 4% [68]. Thus, measures need to be in place to offset this loss and any undesirable growth performance in immunocompromised broilers [68]. Additionally, withdrawing antibiotic feed additives could raise necrotic enteritis in the flocks. Although removing antibiotic feed additives from the diet would enhance the production cost, this increased cost can be recovered from the expected increase in broiler meat prices [69]. It should be noted that the effect on broiler growth and weight from the withdrawal of growth-promoting medicines may occur only after the first year [70]. Thus, the campaign for an alternative to antibiotics should focus on antimicrobial stewardship [71]. These alternatives should provide a low mortality rate and an adequate level of yield while preserving the environment and consumer health. Much research has been conducted to explore natural agents with beneficial effects similar to growth-promoting antibiotics. In addition, several nontherapeutic alternatives can be substituted for antibiotics. The most popular options are probiotics, prebiotics, enzymes, organic acids, immunostimulants, bacteriocins, bacteriophages, phytogenic feed additives, nanoparticles, and essential oils (Table 2), and these alternatives will be discussed in detail below.

5.7.1. Probiotics and Prebiotics

Probiotics are yeasts and live bacteria that confer beneficial effects on the health if administered in adequate doses (WHO, 2001). Probiotics can replace antibiotics by changing the intestinal microbiome, thereby producing some of the effects of antibiotics. For example, feed supplementation with probiotics improves the feed efficiency and intestinal health and, ultimately, facilitates the faster growth of broilers by reducing the intestinal pH, altering the intestinal bacterial composition, and improving digestive activity [72,73]. Probiotics stimulate endogenous enzyme production, which reduces the production of toxic substances and increases vitamins and/or antimicrobials such as bacteriocins [74]. It has been reported that bacteriocins inhibit the production of toxins and the adhesion of pathogenic microbes [75]. Probiotics decrease colonization by intestinal bacteria and, ultimately, stimulate the immune response [74]. The administration of Enterococcus faecium, Streptomyces spp., and Bacillus spp. in chicken feed triggers antibacterial effects on other pathogenic bacteria in the small intestine (Figure 2) [76,77,78]. Broiler feed supplemented with B. subtilis increased the body weights by 4.4% [78]. The H2S and NH3 concentrations in chicken excretions were also reduced after treating chickens with probiotics, leading to less odor. Probiotics increased the meat quality of poultry by affecting the fat and protein contents [74,79]. They are essential in improving the water-holding capacity, color, pH, oxidation stability, and the chemical composition of meat, such as the fatty acid content [79]. Feed supplemented with B. licheniformis improves the juiciness, flavor, and color of broiler chicken meat [80], which is appreciated by consumers [81]. Probiotic supplementation also lessens parasitic infestation in chickens [73]. Probiotics exert coccidiostatic effects on Eimeria tenella, maintain intestinal health, and reduce the spread and risk of coccidiosis in broiler production systems [81].
The nondigestible components of feed that exert potential beneficial effects on the health are known as prebiotics. Most prebiotics are fermentation products consisting of oligosaccharides and short-chain polysaccharides [82]. Their fermentable properties stimulate the growth and activity of beneficial bacteria in the ileum and cecum and contribute to a healthy intestinal tract and, ultimately, increase poultry productivity [83,84]. They are also considered as excellent alternatives to antibiotics. Prebiotics alter cecal proteobacteria composition and increase broiler growth [85]. Products containing high levels of mannose and mannoprotein in the feed tend to increase villus cell numbers in the intestines [86] and are essential for improving intestinal health, thereby producing healthier poultry. Adding 0.2% mannan oligosaccharides to the chicken diet improves the intestinal health more than antibiotics by reducing harmful pathogenic bacteria and increasing potentially beneficial bacteria [87].

5.7.2. Organic Acids

Organic acids are conservation agents widely known for protecting feed from microbial spoilage and improving the nutrient digestibility in poultry [88]. Organic acids include carboxylic acids that carry a hydroxyl group on the alpha-carbon, such as malic, lactic, and tartaric acids, and pure monocarboxylic acids, including acetic, formic, butyric, and propionic acids. Organic acids can inhibit the microbial growth by disrupting bacterial enzymatic reactions and decreasing the transport of acidic compounds by nonionic diffusion through the membrane [89]. It has been reported that adding organic acids to feed may improve the growth, feed conversion rate, and feed utilization of broilers [90,91,92]. While drinking water is a risk factor for spreading campylobacter infection in broilers, Chaveerach et al. demonstrated that organic acid-treated drinking water can potentially prevent campylobacter infection in broiler flocks without any damage to gut epithelial cells [93]. Blends of formic and propionic acids in drinking water for chickens can generate homogeneous and distinct populations in the intestinal microbiota and increase Lactobacillus spp. colonization in the ileum [91], which can be a substitute for antibiotics used to reduce pathogenic bacteria in the gastrointestinal tract (GIT). These changes in the intestinal microbiota and increased Lactobacillus populations suggest that organic acids can substitute for antibiotics such as bacitracin to reduce pathogenic bacteria in the GIT [91]. Additionally, organic acids have the potential to inhibit E. coli infection [94], and a supplementation with 2% citric acid can improve the gut health [95]. It has been reported that formic acid, an extensively studied organic acid, can limit Salmonella infection and other foodborne pathogens when used in a poultry diet [96]. Several organic acids may also play beneficial roles in digestion. For example, when butyric acid is used as a feed additive, it improves the digestibility of ileal proteins from poorly digestible protein sources [92]. Butyric acid, a saturated carboxylic acid, is produced in the cecum and colon by fermenting carbohydrates such as dietary fiber and unabsorbed starch [97]. Moreover, butyric acid is a readily available energy source for intestinal epithelial cells and stimulates their multiplication and differentiation, thereby improving the feed efficiency and growth performance of chickens [82,92,98].

5.7.3. Amino Acids and Enzymes

Broiler feeds are supplemented with amino acids and enzymes to increase the feed conversion [81]. These enzymes are produced by fermenting fungi and bacteria. Enzymes enhance the digestibility of the feed by facilitating the degradation of proteins, phytates, and glucan. For example, it has been reported that broiler diets of wheat and barley supplemented with endo-b-1-4-xylanases and b-1-3, 1-4-glucanases can improve the digestibility of the feed [99]. Another study reported that a phytase enzyme improved daily weight gain by increasing the villus width and decreasing the crypt depth [95]. Lysins are bacteriophage endolysins that could be an alternative therapeutic option instead of antibiotics. Lysins are phage-encoded peptidoglycan hydrolases that cause lysis of bacteria by cleaving peptidoglycan when applied exogenously to Gram-positive bacteria [100,101]. The antibacterial efficacy of several lysins has been reported; for example, peptidases, amidases, and lysozymes showed antimicrobial potential against C. perfringens in poultry [102].

5.7.4. Phytogenic Feed Additives

Phytogenic feed additives (PFAs), also known as phytobiotics or botanicals, are derived from plants, herbs, and spices and can improve animal health. PFAs are reported to positively affect growth by improving the feed conversion ratio (FCR), boosting the immune system, and reducing stress. Several recent studies also showed that phytogenic feed additives promoted broiler chicken growth and could be used as an alternative to antibiotics [72,103,104,105,106]. Another study demonstrated that including Lippia javanica in broiler feed at 5 g/kg enhanced the broilers’ daily gain and slaughter weight. Phytogenic extracts of Lippia javanica leaf can stimulate glycolysis and increase energy production utilization and, thus, growth [107]. They can also improve the fatty acid profile of broiler chicken meat [107]. It has been reported that the use of garlic (5 g/kg) and black pepper powder (1 g/kg) in broiler feed could enhance broiler chickens’ weight gain and consumption index [108]. Thus, PFAs have the potential to replace antibiotics in the poultry industry. On the other hand, there are also essential oils, the hydrophobic concentrated liquid of odoriferous and volatile aromatic compounds, which can be of plant origin (natural) or synthetic. The crucial vital oils in broiler production are trans-cinnamaldehyde, thymol, eugenol, and carvacrol. They interfere with the bacterial enzymatic system and modulate inflammation and immune responses. They are excellent alternatives to growth-promoting antibiotics such as Avilamycin for increasing chicken production [109,110,111]. Essential oils also have a significant role in preventing and controlling necrotic enteritis in chickens [112]. Furthermore, it was reported that supplementing with essential oils such as oregano (Origanum genus) in broiler feed at 300–600 g/kg increased the average daily gain of broiler chickens [110]. Therefore, essential oils should be used as an alternative to antibiotics in the poultry industry.

5.7.5. Nanoparticles as Feed Additives

Nanoparticles (NPs) used as supplements in broiler chicken feed are favorable for optimizing the overall health and FCR. Some NPs have been used in poultry feed to decrease harmful bacteria and stimulate beneficial bacteria in the chicken microbiota [113]. The impact of NPs on birds has been studied worldwide to better understand the overall health and growth performance, immune response, and antibacterial prospects [114]. Gangadoo et al. [114] noted that the most commonly used silver nanoparticles in commercial chicken feed were shown to boost chickens’ microbiota. However, silver nanoparticles seem to have a somewhat elevated toxicity in birds. To avoid the toxic side effects, scientists have investigated other nanoparticles that can safely contribute to the positive impact on health and productivity. A study showed that selenium NPs at concentrations ranging from 0.15 to 1.20 ppm could enhance broilers’ average daily gains [115]. Others showed that selenium NPs had a positive influence on chicken bodies, with reduced toxicity achieved at low concentrations from 0.3 to 0.5 ppm [116,117,118,119,120]. Meanwhile, similar concentrations of copper NPs as a supplement in poultry feed could have positive or negative health consequences. For example, a concentration of 50 ppm of copper at sizes 2–15 nm produced a decreased metabolic rate, oxygen consumption, and heat production and resulted in reduced embryonic development [121], whereas others showed that including copper NPs in poultry feed could boost breast and leg muscle growth, along with decreased mortality in broiler chicks [121]. Various other metals have been synthesized as NPs as supplements to poultry feed. For example, studies using metal NPs such as zinc oxide, zirconium dioxide, and platinum showed that they had a positive influence on the antibacterial activity against Salmonella spp. and Staphylococcus aureus [122,123,124]. On the other hand, Zn-bearing zeolite clinoptilolite NPs were shown to improve broilers’ growth and feed intake ratio [125]. In addition, NPs combined with extracts of natural antibacterial products, such as certain herbs and oils, could be utilized to upgrade the overall performance of broiler feed. For instance, a study using a turmeric extract in nanocapsules showed improved meat quality without affecting broiler performance.
Nanosuspensions of clay minerals improved the antibody protection against a number of infectious diseases in chickens, including Newcastle disease, infectious bronchitis, and infectious bursal disease [126]. However, more research is needed on the benefits of using nanoparticles with poultry feed as an alternative to antibiotics.

6. Research Gap, Status, and Future Trends

The global poultry industry has dramatically expanded to meet the increasing need for animal proteins for human consumption. The Food and Agriculture Organization projected that annual meat production by 2050 will be 200 million tons due to the global need [127]. Therefore, there is an urgent need to find strategies by conducting relevant research to improve the growth rate, feed efficiency, and health status and reduce the pathogen burden to meet the increased demand. It is possible to use feed formulations to improve the FCR, resulting in lower feed requirements to attain market weight. Feed additives such as vitamins and minerals are usually combined with typical diets to support a rapid growth and favorable FCR. Recently, various nanoparticles have been added to feed to improve the overall health performance and FCR. More studies determining the influence of NPs on the intestinal microbiota of chickens would allow scientists to understand their role in the production of beneficial gut microbes and metabolites. Recent advances in sequencing technology could allow a much-needed understanding of the interactions between NPs and intestinal bacteria. Further research that includes the toxicology, histology, and the residual effects of NPs on broiler weight and egg production is warranted before any wide adoption of NPs in feed could occur [128].
In contrast, the global consumption of antimicrobials in food animal production is anticipated to increase by two-thirds by 2030 due to rises in production and the demand for animal products. [129] Although most antibiotic use occurs in the agricultural sector, relatively little research has been done on how antibiotic use in food animals contributes to the overall problem of antibiotic resistance. There is a notable lack of quantitative monitoring data on antibiotic use in broilers in most large poultry-producing countries [40]. An increase in the progression and spread of antibiotic resistance has become a significant concern. Over the past few decades, no new major types of antibiotics have been developed and almost all known antibiotics are increasingly losing their curative sensitivity against pathogenic microorganisms. A single health approach that highlights the connections among humans, animals, and the environment is required to tackle antibiotic resistance in an integrated manner. This viewpoint entails a pledge of cooperation among professionals in several disciplines, including physicians, veterinarians, food safety practitioners, and environmental health experts.

7. Conclusions

Antibiotic-free poultry meat production is an old issue in developed countries; however, it is at the beginning stage in Bangladesh. Although consumers are becoming more interested in antibiotic-free poultry, it is not easy to produce quality antibiotic-free meat while maintaining animal welfare and making farming profitable. There is still a long way to go for sustainable antibiotic-free broiler meat production, particularly in developing countries like Bangladesh. The aspects related to broiler meat production and marketing should be ensured through improved management systems, proper legislation, and implementation. It is difficult to achieve sustainable production if there is any interruption of the supply chain, such as the supply of day-old chicks from hatcheries or feed from feed mills, or other support. As such, producing sustainable broiler meat without antibiotics is an ongoing challenge for the food industry in Bangladesh. To overcome this challenge, good management practices, including strict biosecurity measures, should be ascertained. Moreover, access to antibiotics without a prescription by veterinarians should be strictly enforced. In addition, for fighting against antimicrobial resistance, awareness-building programs as recommended by the World Organisation for Animal Health (OIE) (https://oie-antimicrobial.com/) should be implemented for raising awareness among poultry farm workers, marginal poultry farmers, and poultry consumers to highlight the dangers of antibiotic resistance and the benefits of consuming antibiotic-free poultry meat. As policymakers and local poultry industries are aiming to produce safe meat without using antibiotics by 2024, alternative approaches to antibiotics and active participation by farmers and consumers will be required to achieve this.

Author Contributions

Conceptualization, M.H.H. and S.S.; writing—original draft preparation, M.H.H., M.S.I., and S.S.; and writing—review and editing, M.H.H., M.S.I., S.S., M.A.I., M.R.K., M.E.H.K., M.J.A.S. and M.S.A. All authors have read and agreed to the published version of the manuscript.

Funding

The study was supported by research funding from the government of the People’s Republic of Bangladesh, Ministry of Science and Technology (MOST). Sarker is the recipient of an Australian Research Council Discovery Early Career Researcher Award (grant number DE200100367) funded by the Australian government.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Masud, A.A.; Rousham, E.K.; Islam, M.A.; Alam, M.U.; Rahman, M.; Mamun, A.A.; Sarker, S.; Asaduzzaman, M.; Unicomb, L. Drivers of Antibiotic Use in Poultry Production in Bangladesh: Dependencies and Dynamics of a Patron-Client Relationship. Front. Vet. Sci. 2020, 7, 78. [Google Scholar] [CrossRef] [PubMed]
  2. Kryger, K.N.; Thomsen, K.; Whyte, M.; Dissing, M. Smallholder Poultry Production: Livelihoods, Food Security and Sociocultural Significance; Series FAO Smallholder Poultry Production; FAO: Rome, Italy, 2010; p. 4. [Google Scholar]
  3. Najeeb, A.; Mandal, P.; Pal, U. Efficacy of fruits (red grapes, gooseberry and tomato) powder as natural preservatives in restructured chicken slices. Int. Food Res. J. 2014, 21, 2431–2436. [Google Scholar]
  4. Tollefson, L.; Miller, M.A. Antibiotic use in food animals: Controlling the human health impact. J. AOAC Int. 2000, 83, 245–254. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Gaskins, H.; Collier, C.; Anderson, D. Antibiotics as growth promotants: Mode of action. Anim. Biotechnol. 2002, 13, 29–42. [Google Scholar] [CrossRef] [PubMed]
  6. Davies, J.; Davies, D. Origins and evolution of antibiotic resistance. Microbiol. Mol. Biol. Rev. 2010, 74, 417–433. [Google Scholar] [CrossRef] [Green Version]
  7. Landers, T.F.; Cohen, B.; Wittum, T.E.; Larson, E.L. A Review of Antibiotic Use in Food Animals: Perspective, Policy, and Potential. Public Health Rep. 2012, 127, 4–22. [Google Scholar] [CrossRef] [Green Version]
  8. Diaz-Sanchez, S.; Moscoso, S.; Solís de los Santos, F.; Andino, A.; Hanning, I. Antibiotic use in poultry; A driving force for organic poultry production. Food Prot. Trends 2015, 35, 440–447. [Google Scholar]
  9. Marshall, B.M.; Levy, S.B. Food Animals and Antimicrobials: Impacts on Human Health. Clin. Microbiol. Rev. 2011, 24, 718–733. [Google Scholar] [CrossRef] [Green Version]
  10. Hoque, R.; Ahmed, S.M.; Naher, N.; Islam, M.A.; Rousham, E.K.; Islam, B.Z.; Hassan, S. Tackling Antimicrobial Resistance in Bangladesh: A Scoping Review of Policy and Practice in Human, Animal and Environment Sectors. PLoS ONE 2020, 15, e0227947. [Google Scholar] [CrossRef] [Green Version]
  11. Saiful, I.K.B.M.; Shiraj-Um-Mahmuda, S.; Hazzaz-Bin-Kabir, M. Antibiotic Usage Patterns in Selected Broiler Farms of Bangladesh and their Public Health Implications. J. Public Health Dev. Ctries. 2016, 2, 276–284. [Google Scholar]
  12. Stutz, M.W.; Lawton, G.C. Effects of diet and antimicrobials on growth, feed efficiency, intestinal Clostridium perfringens, and ileal weight of broiler chicks. Poult. Sci. 1984, 63, 2036–2042. [Google Scholar] [CrossRef] [PubMed]
  13. Sirdar, M.M.; Picard, J.; Bisschop, S.; Gummow, B. A questionnaire survey of poultry layer farmers in Khartoum State, Sudan, to study their antimicrobial awareness and usage patterns. Onderstepoort J. Vet. Res. 2012, 79, 1–8. [Google Scholar] [CrossRef] [PubMed]
  14. Sattar, S.; Hassan, M.M.; Islam, S.K.M.A.; Alam, M.; Faruk, M.S.A.; Chowdhury, S.; Saifuddin, A.K.M. Antibiotic residues in broiler and layer meat in Chittagong district of Bangladesh. Vet. World 2014, 7, 738–743. [Google Scholar] [CrossRef] [Green Version]
  15. D’Costa, V.M.; King, C.E.; Kalan, L.; Morar, M.; Sung, W.W.L.; Schwarz, C.; Froese, D.; Zatula, G.; Camels, F.; Debruyme, R.; et al. Antibiotic resistance is ancient. Nat. Lett. 2011, 477, 457–461. [Google Scholar] [CrossRef] [PubMed]
  16. Laxminarayan, R.; Van Boeckel, T.; Teillant, A. The Economic Costs of Withdrawing Antimicrobial Growth Promoters from the Livestock Sector. OECD Food Agric. Fish. 2015. [Google Scholar] [CrossRef]
  17. Islam, M.K.; Uddin, M.F.; Alam, M.H. Challenges and Prospects of Poultry Industry in Bangladesh. Eur. J. Bus. Manag. 2014, 6, 116–127. [Google Scholar]
  18. Akter, S.; Uddin, M. Bangladesh poultry industry. J. Bus. Technol. 2009, 4, 97–112. [Google Scholar]
  19. Al-Mamun, M.; Islam, M.; Rahman, M.M. The occurrence of poultry diseases at Kishoregonj district of Bangladesh. MOJ Proteom. Bioinform. 2019, 8, 7–12. [Google Scholar]
  20. Khaled, S.M.S. Poultry Industry: Realities and Prospects. The Financial Express, International Publication Limited. Available online: http://www.thefinancialexpress-bd.com (accessed on 26 April 2014).
  21. Hao, H.; Sander, P.; Iqbal, Z.; Wang, Y.; Cheng, G. The Risk of Some Veterinary Antimicrobial Agents on Public Health Associated with Antimicrobial Resistance and their Molecular Basis. Front. Microbiol. 2016, 7, 1626. [Google Scholar] [CrossRef] [Green Version]
  22. Sarker, Y.A.; Hasan, M.M.; Paul, T.K.; Rashid, S.Z.; Alam, M.N.; Sikder, M.H. Screening of antibiotic residues in chicken meat in Bangladesh by thin layer chromatography. J. Adv. Vet. Anim. Res. 2018, 5, 140–145. [Google Scholar] [CrossRef]
  23. Sultan, S.; Begum, R.; Rahman, M.A.; Ahmed, M.J.U.; Islam, M.M.; Haque, S. Economic analysis of antibiotics use and vaccine program in commercial broiler farming of Tangail district in Bangladesh. Prog. Agric. 2016, 27, 490–501. [Google Scholar] [CrossRef] [Green Version]
  24. Faiz, M.A.; Bashe, A. Antimicrobial resistance: Bangladesh experience. Reg. Health Forum. 2011, 15, 1–8. [Google Scholar]
  25. Ahmed, I.; Rabbi, M.B.; Sultana, S. Antibiotic resistance in Bangladesh: A systematic review. Int. J. Infect. Dis. 2019, 80, 54–56. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Saleque, M.A. Poultry Industry in Bangladesh: Current Status and Its Challenges and Opportunity in the Emerging Market Environment. In Poul Business. Directory 2007; Khamar Bichitra: Dhaka, Bangladesh, 2007. [Google Scholar]
  27. Sibi, G.; Shukla, A.; Dhananjaya, K.; Ravikumar, K.R.; Mallesha, H. In vitro antibacterial activities of Broccoli (Brassica oleracea L.var italica) against food borne bacteria. J. App. Pharm. Sci. 2013, 3, 100–103. [Google Scholar]
  28. Farhana, J.A.; Hossain, M.F.; Mowlah, A. Antibacterial effects of guava (Psidium guajava L.) extracts against food borne pathogens. Int. J. Nutr. Food Sci. 2017, 6, 1–5. [Google Scholar] [CrossRef] [Green Version]
  29. Carvalho, C.C.R.; Cruz, P.A.; Fonseca, M.M.R.; Xavier-Filho, L. Antibacterial properties of the extract of Abelmoschus esculentus. Biotechnol. Bioproc. Eng. 2011, 16, 971. [Google Scholar] [CrossRef]
  30. Tijjani, A.; Musa, D.D.; Aliyu, Y. Antibacterial Activity of Garlic (Allium sativum) on Staphylococcus aureus and Escherihia coli. Int. J. Curr. Sci. Stud. 2017, 1, 1410–1703. [Google Scholar]
  31. Steinfeld, H.; Gerber, P.; Wassenaar, T.; Castel, V.; Rosales, M.; De Haan, C. Livestock’s Long Shadow—Environmental Issues and Options; FAO: Rome, Italy, 2006; p. 390. [Google Scholar]
  32. De Vries, M.; de Boer, I. Comparing environmental impacts for livestock products: A review of life cycle assessments. Livest. Sci. 2010, 128, 1–11. [Google Scholar] [CrossRef]
  33. Leinonen, I.; Williams, A.G.; Wiseman, J.; Guy, J.; Kyriazakis, I. Predicting the environmental impact of chicken systems in the UK through a life cycle assessment: Broiler production systems. Poult. Sci. 2012, 91, 8–25. [Google Scholar] [CrossRef]
  34. Leinonen, I.; Williams, A.G.; Wiseman, J.; Guy, J.; Kyriazakis, I. Comparing the environmental impact of alternative protein crops in poultry diets: The consequences of uncertainty. Agric. Syst. 2013, 121, 33–42. [Google Scholar] [CrossRef] [Green Version]
  35. Gerbens-Leenes, P.W.; Mekonnen, M.M.; Hoekstra, A.Y. The water footprint of poultry, pork and beef: A comparative study in different countries and production systems. Water Resour. Ind. 2013, 1–2, 25–36. [Google Scholar] [CrossRef] [Green Version]
  36. Magdelaine, P.; Riffard, C.; Berlier, C. Comparative survey of the organic poultry production in the European Union. In Proceedings of the XIIIth European Poultry Conference, Tours, France, 23–27 August 2010; p. 9. [Google Scholar]
  37. Sundrum, A. Possibilities and Limitations of Protein Supply in Organic Poultry and Pig Production. Report, EU Project No. SSPE-CT-2004-502397. 2005, p. 107. Available online: http://www.organic-revision.org/pub/Final_Report_EC_Revision.pdf (accessed on 25 June 2020).
  38. Donoghue, D.J. Antibiotic residues in poultry tissues and eggs: Human health concern. Poult. Sci. 2003, 82, 618–621. [Google Scholar] [CrossRef] [PubMed]
  39. Poole, T.; Sheffield, C. Use and misuse of antimicrobial drugs in poultry and livestock: Mechanisms of antimicrobial resistance. Pak. Vet. J. 2013, 33, 266–271. [Google Scholar]
  40. Roth, N.; Käsbohrer, A.; Mayrhofer, S.; Zitz, U.; Hofacre, C.; Domig, K.J. The application of antibiotics in broiler production and the resulting antibiotic resistance in Escherichia coli: A global overview. Poult. Sci. 2019, 98, 1791–1804. [Google Scholar] [CrossRef] [PubMed]
  41. Archawakulathep, A.; Kim, C.T.T.D.; Meunsene, D.; Handijatno, H.; Hassim, A.; Rovira, H.R.G.; Myint, K.S. Perspectives on antimicrobial resistance in livestock and livestock products in asean countries. Wetchasan Sattawaphaet. 2014, 44, 5–13. [Google Scholar]
  42. Van Boeckel, T.P.; Brower, C.; Gilbert, M.; Grenfell, B.T.; Levin, S.A.; Robinson, T.P.; Teillant, A.; Laxminarayan, R. Global antimicrobial use in food animals. Proc. Natl. Acad. Sci. USA 2015, 112, 5649–5654. [Google Scholar] [CrossRef] [Green Version]
  43. Agare, C.; Boamah, V.E.; Zumbi, C.N.; Osei, F.B. Anti-biotic Use in Poultry Production and Its Effects on Bacterial Resis-Tance. In Antimicrobial Resistance—A Global Threa; IntechOpen: London, UK, 2018. [Google Scholar] [CrossRef] [Green Version]
  44. Rauw, W.M.; Kanis, E.; Noordhuzen-Stassen, E.N.; Grommers, F.J. Undesirable side effects of selection for high production efficiency in farm animals: A review. Livest. Prod. Sci. 1998, 56, 15–33. [Google Scholar] [CrossRef]
  45. Coping with Climate Change—The Roles of Genetic Resources for Food and Agriculture. In Commision on Genetic Resources for Food and Agriculture. 2015, p. 110. Available online: http://www.fao.org/3/a-i3866e.pdf (accessed on 25 June 2020).
  46. Vaarst, M.; Steenfeldt, S.; Horsted, K. Sustainable development perspectives of poultry production. Worlds Poult. Sci. J. 2015, 71, 609–620. [Google Scholar] [CrossRef] [Green Version]
  47. Le Bouquin, S. Air Quality in Poultry Hatcheries. In Proceedings of the XIVth European Poultry Conference, Stavanger, Norway, 24–27 June 2014. [Google Scholar]
  48. Quandt, S.A.; Argury-Quandt, A.E.; Lawlor, E.J.; Carrillo, L.; Marín, A.J.; Grzywacz, J.G.; Arcury, T.A. 3-D Jobs and Health Disparities: The Health Implications of Latino Chicken Catchers’ Working Conditions. Am. J. Ind. Med. 2013, 56, 206–215. [Google Scholar] [CrossRef]
  49. World Livestock 2011–Livestock in Food Security; FAO: Rome, Italy, 2011; p. 115.
  50. Anonymous. Life Under Contract. 2015. Available online: https://www.farmaid.org/blog/farmer-heroes/life-under-contractpoultry-farming-in-arkansas/ (accessed on 15 July 2020).
  51. Dolberg, F. Poultry production for livelihood improvement and poverty alleviation. In Poultry in the 21st Century; FAO: Rome, Italy, 2007; p. 26. [Google Scholar]
  52. Gateway to Poultry Production and Products; FAO: Rome, Italy, 2020.
  53. Guèye, E.F. Gender issues in family poultry production systems in low-income food-deficit countries. Am. J. Altern. Agric. 2003, 18, 185–195. [Google Scholar]
  54. Thompson, P.B. Agricultural sustainability: What it is and what it is not. Int. J. Agric. Sustain. 2007, 5, 5–16. [Google Scholar] [CrossRef]
  55. Nielsen, B.L.; Thomsen, M.G.; Sorensen, P.; Young, J.F. Feed and strain effects on the use of outdoor areas by broilers. Br. Poult. Sci. 2003, 44, 161–169. [Google Scholar] [CrossRef] [PubMed]
  56. De Jong, I.C.; Enting, H.; Van Voorst, A.; Blokhuis, H.J. Do Low-Density Diets Improve Broiler Breeder Welfare During Rearing and Laying? Poult. Sci. 2005, 84, 194–203. [Google Scholar] [CrossRef] [PubMed]
  57. Van De Weerd, H.A.; Keatinge, R.; Roderick, S. A review of key health-related welfare issues in organic poultry production. World’s Poult. Sci. J. 2009, 65, 649–684. [Google Scholar] [CrossRef]
  58. Report on the Expert Consultation on Rural Poultry Development in Asia, Dhaka, Bangladesh; Technology Report 274415; FAO: Rome, Italy, 1987.
  59. Bilgili, S.F.; Hess, J.B. Placement density influences broiler carcass grade and meat yields. J. Appl. Poult. Res. 1995, 4, 384–389. [Google Scholar] [CrossRef]
  60. Kristensen, H.H.; Wathes, C.M. Ammonia and poultry welfare: A Review. World’s Poult. Sci. J. 2000, 56, 235–245. [Google Scholar] [CrossRef]
  61. Miles, D.M.; Branton, S.L.; Lott, B.D. Atmospheric ammonia is detrimental to the performance of modern commercial broilers. Poult. Sci. 2004, 83, 1650–1654. [Google Scholar] [CrossRef]
  62. Payne, J. Litter management strategies impact nutrient content. Poult. Pract. 2012, 2, 1–3. [Google Scholar]
  63. Brook, R.D.; Rajagopalan, S.; Pope, C.A.; Brook, J.R.; Bhatnagar, A.; Diez-Roux, A.V.; Holguin, F.; Hong, Y.; Luepker, R.V.; Mittleman, M.A.; et al. Particulate matter air pollution and cardiovascular disease: An update to the scientific statement from the American Heart Association. Circulation 2010, 121, 2331–2378. [Google Scholar] [CrossRef] [Green Version]
  64. Verma, K.K.; Singh, V.; Gupta, S.L.; Yadav, J.; Verma, A.K. Environmentally Controlled House-In Poultry Production. Poultry Line. 2014. Available online: https://www.researchgate.net/publication/324483130_Environmentally_Controlled_House-In_Poultry_Production (accessed on 16 October 2020).
  65. Barekatain, M.R.; Swick, R.A. Composition of more specialised pre-starter and starter diets for young broiler chickens: A review. Anim. Prod. Sci. 2016, 56, 1239–1247. [Google Scholar] [CrossRef]
  66. Hancock, A.; Hughes, J.; Watkins, S. In search of the ideal water line cleaner. Avian Adv. 2007, 9, 1–3. [Google Scholar]
  67. Jacobs, L.; Persia, M.E.; Siman-Tov, N.; McCoy, J.; Ahmad, M.; Lyman, J.; Good, L. Impact of water sanitation on broiler chicken production and welfare parameters. J. Appl. Poult. Res. 2020, 29, 258–268. [Google Scholar] [CrossRef]
  68. Cowieson, A.J.; Kluenter, A. Contribution of exogenous enzymes to potentiate the removal of antibiotic growth promoters in poultry production. Anim. Feed. Sci. Technol. 2019, 250, 81–92. [Google Scholar] [CrossRef]
  69. Cardinal, K.; Kipper, M.; Andretta, I.; Ribeiro, A.M.L. Withdrawal of antibiotic growth promoters from broiler diets: Performance indexes and economic impact. Poult. Sci. 2019, 98, 6659–6667. [Google Scholar] [CrossRef]
  70. Engster, H.M.; Marvil, D.; Stewart-Brown, B. The Effect of Withdrawing Growth Promoting Antibiotics from Broiler Chickens: A Long-Term Commercial Industry Study. J. Appl. Poult. Res. 2002, 11, 431–436. [Google Scholar] [CrossRef]
  71. Dela Cruz, P.J.D.; Dagaas, C.T.; Mangubat, K.M.M.; Angeles, A.A.; Abanto, O.D. Dietary effects of commercial probiotics on growth performance, digestibility, and intestinal morphometry of broiler chickens. Trop. Anim. Health Prod. 2019, 51, 1105–1115. [Google Scholar] [CrossRef]
  72. Ghasemi, H.A.; Kasani, N.; Taherpour, K. Effects of black cumin seed (Nigella sativa L.), a probiotic, a prebiotic and a synbiotic on growth performance, immune response and blood characteristics of male broilers. Livest. Sci. 2014, 164, 128–134. [Google Scholar] [CrossRef]
  73. Giannenas, I.; Papadopoulos, E.; Tsalie, E.; Triantafillou, E.; Henikl, S.; Teichmann, K.; Tontis, D. Assessment of dietary supplementation with probiotics on performance, intestinal morphology and microflora of chickens infected with Eimeria tenella. Vet. Parasitol. 2012, 188, 31–40. [Google Scholar] [CrossRef]
  74. Hassanein, S.M.; Soliman, N.K. Effect of probiotic (Saccharomyces cerevisiae) adding to diets on intestinal microflora and performance of hy-line layers hens. J. Am. Sci. 2010, 6, 159–169. [Google Scholar]
  75. Pan, D.; Yu, Z. Intestinal microbiome of poultry and its interaction with host and diet. Gut Microb. 2014, 5, 108–119. [Google Scholar] [CrossRef]
  76. Levkut, M.; Revajova, V.; Laukova, A.; Sevcikova, Z.; Spisakova, V.; Faixova, Z. Leukocytic Responses and Intestinal Mucin Dynamics of Broilers Protected with Enterococcus Faecium Ef55 and Challenged with Salmonella Enteritidis. Res. Vet. Sci. 2012, 93, 195–201. [Google Scholar] [CrossRef] [PubMed]
  77. Latha, S.; Vinothini, G.; John Dickson Calvin, D.; Dhanasekaran, D. In vitro probiotic profile based selection of indigenous actinobacterial probiont Streptomyces sp. Jd9 for enhanced broiler production. J. Biosci. Bioeng. 2016, 121, 124–131. [Google Scholar] [CrossRef]
  78. Zhang, Z.F.; Cho, J.H.; Kim, I.H. Effects of Bacillus subtilis Ubt-Mo2 on growth performance, relative immune Organ weight, gas concentration in excreta, and intestinal microbial shedding in broiler chickens. Livest. Sci. 2013, 155, 343–347. [Google Scholar] [CrossRef] [Green Version]
  79. Popova, T. Effect of probiotics in poultry for improving meat quality. Curr. Opin. Food Sci. 2017, 14, 72–77. [Google Scholar] [CrossRef]
  80. Liu, X.; Yan, H.; Lv, L.; Xu, Q.; Yin, C.; Zhang, K.; Wang, P.; Hu, J. Growth performance and meat quality of broiler chickens supplemented with Bacillus licheniformis in drinking water. Asian-Australas J. Anim. Sci. 2012, 25, 682–689. [Google Scholar] [CrossRef] [PubMed]
  81. Mehdi, Y.; Létourneau-Montminy, M.P.; Gaucher, M.L.; Chorfi, Y.; Suresh, G.; Rouissi, T.; Brar, S.K.; Côté, C.; Ramirez, A.A.; Godbout, S. Use of antibiotics in broiler production: Global impacts and Alternatives. Anim. Nutr. 2018, 4, 170–178. [Google Scholar] [CrossRef]
  82. Jozefiak, D.; Kaczmarek, S.; Rutkowski, A. A note on the effects of selected prebiotics on the performance and ileal microbiota of broiler chickens. J. Anim. Feed Sci. 2008, 17, 392–397. [Google Scholar] [CrossRef] [Green Version]
  83. Morales-Lopez, R.; Auclair, E.; Garcia, F.; Esteve-Garcia, E.; Brufau, J. Use of yeast cell walls; Beta-1, 3/1, 6-glucans; and mannoproteins in broiler chicken diets. Poult. Sci. 2009, 88, 601–607. [Google Scholar] [CrossRef]
  84. Zhang, A.W.; Lee, B.D.; Lee, S.K.; Lee, K.W.; An, G.H.; Song, K.B.; Lee, C.H. Effects of yeast (Saccharomyces cerevisiae) cell components on growth performance, meat quality, and ileal mucosa development of broiler chicks. Poult. Sci. 2005, 84, 1015–1021. [Google Scholar] [CrossRef]
  85. Park, S.H.; Lee, S.I.; Ricke, S.C. Microbial populations in naked neck chicken ceca raised on pasture flock fed with commercial yeast cell wall prebiotics via an illuminamiseq platform. PLoS ONE 2016, 11, 0151944. [Google Scholar] [CrossRef]
  86. Baurhoo, B.; Phillip, L.; Ruiz-Feria, C.A. Effects of purified lignin and mannan oligosaccharides on intestinal integrity and microbial populations in the ceca and litter of broiler chickens. Poult. Sci. 2007, 86, 1070–1078. [Google Scholar] [CrossRef]
  87. Baurhoo, B.; Ferket, P.R.; Zhao, X. Effects of diets containing different concentrations of manna oligosaccharide or antibiotics on growth performance, intestinal development, cecal and litter microbial populations, and carcass parameters of broilers. Poult. Sci. 2009, 88, 2262–2272. [Google Scholar] [CrossRef] [PubMed]
  88. Kum, S.; Eren, U.; Onol, A.; Sandikci, M. Effects of dietary organic acid supplementation on the intestinal mucosa in broilers. Rev. Med. Vet. 2010, 10, 463–468. [Google Scholar]
  89. Cherrington, C.A.; Hinton, M.; Mead, G.C.; Chopra, I. Organic acids: Chemistry, antibacterial activity and practical applications. Adv. Microb. Physiol. 1991, 32, 87–108. [Google Scholar]
  90. Hassan, H.M.A.; Mohamed, M.A.; Youssef, A.W.; Hassan, E.R. Effect of using organic acids to substitute antibiotic growth promoters on performance and intestinal microflora of broilers. Asian-Australas J. Anim. Sci. 2010, 23, 1348–1353. [Google Scholar] [CrossRef]
  91. Nava, G.M.; Attene-Ramos, M.S.; Gaskins, H.R.; Richards, J.D. Molecular analysis of microbial community structure in the chicken ileum following organic acid supplementation. Vet. Microbiol. 2009, 137, 345–353. [Google Scholar] [CrossRef] [PubMed]
  92. Adil, S.; Banday, T.; Bhat, G.A.; Mir, M.S.; Rehman, M. Effect of dietary supplementation of organic acids on performance, intestinal histomorphology, and serum biochemistry of broiler chicken. Vet. Med. Int. 2020, 2010, 479485. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  93. Chaveerach, P.; Keuzenkamp, D.A.; Lipman, L.J.; Van Knapen, F. Effect of organic acids in drinking water for young broilers on Campylobacter infection, volatile fatty acid production, gut microflora and histological cell changes. Poult. Sci. 2004, 83, 330–334. [Google Scholar] [CrossRef] [PubMed]
  94. Izat, A.L.; Tidwell, N.M.; Thomas, R.A.; Reiber, M.A.; Adams, M.H.; Colberg, M.; Waldroup, P.W. Effects of a buffered propionic acid in diets on the performance of broiler chickens and on microflora of the intestine and carcass. Poult. Sci. 1990, 69, 818–826. [Google Scholar] [CrossRef] [PubMed]
  95. Mohammadagheri, N.; Najafi, R.; Najafi, G. Effects of dietary supplementation of organic acids and phytase on performance and intestinal histomorphology of broilers. Vet. Res. Forum 2016, 7, 189–195. [Google Scholar]
  96. Ricke, S.C.; Dittoe, D.K.; Richardson, K.E. Formic Acid as an Antimicrobial for Poultry Production: A Review. Front. Vet. Sci. 2020, 7, 563. [Google Scholar] [CrossRef] [PubMed]
  97. Hu, Z.; Guo, Y. Effects of dietary sodium butyrate supplementation on the intestinal morphological structure, absorptive function and gut flora in chickens. Anim. Feed Sci. Technol. 2007, 132, 240–249. [Google Scholar] [CrossRef]
  98. Qaisrani, S.; Van Krimpen, M.; Kwakkel, R.; Verstegen, M.; Hendriks, W. Diet structure, butyric acid, and fermentable carbohydrates influence growth performance, gut morphology, and cecal fermentation characteristics in broilers. Poult. Sci. 2015, 94, 2152–2164. [Google Scholar] [CrossRef] [PubMed]
  99. Cowieson, A.J.; Hruby, M.; Pierson, E.E. Evolving enzyme technology: Impact on commercial poultry nutrition. Nutr. Res. Rev. 2006, 19, 90–103. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  100. Fenton, M.; Ross, P.; McAuliffe, O.; O’Mahony, J.; Coffey, A. Recombinant bacteriophage lysins as antibacterials. Bioeng. Bugs 2010, 1, 9–16. [Google Scholar] [CrossRef] [PubMed]
  101. Rios, A.C.; Moutinho, C.G.; Pinto, F.C.; Del Fiol, F.S.; Jozala, A.; Chaud, M.V. Alternatives to overcoming bacterial resistances: State-of-the-art. Microbiol. Res. 2016, 191, 51–80. [Google Scholar] [CrossRef] [PubMed]
  102. Volozhantsev, N.V.; Verevkin, V.V.; Bannov, V.A.; Krasilnikova, V.M.; Myakinina, V.P.; Zhilenkov, E.L.; Svetoch, E.A.; Stern, N.J.; Oakley, B.B.; Seal, B.S. The genome sequence and proteome of bacteriophage ΦCPV1 virulent for Clostridium perfringens. Virus Res. 2011, 155, 433–439. [Google Scholar] [CrossRef]
  103. Windisch, W.; Schedle, K.; Plitzner, C.; Kroismayr, A. Use of phytogenic products as feed additives for swine and poultry. J. Anim. Sci. 2008, 86, E140–E148. [Google Scholar] [CrossRef]
  104. Frankic, T.; Voljc, M.; Salobir, J.; Rezar, V. Use of herbs and spices and their extracts in animal nutrition. Acta Agric. Slov. 2009, 94, 95–102. [Google Scholar]
  105. Toghyani, M.; Toghyani, M.; Gheisari, A.; Ghalamkari, G.; Eghbalsaied, S. Evaluation of cinnamon and garlic as antibiotic growth promoter substitutions on performance, immune responses, serum biochemical and haematological parameters in broiler chicks. Livest. Sci. 2011, 138, 167–173. [Google Scholar] [CrossRef]
  106. Li, H.L.; Zhao, P.Y.; Lei, Y.; Hossain, M.M.; Kim, I.H. 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. Livest. Sci. 2015, 181, 1–6. [Google Scholar] [CrossRef]
  107. Mpofu, D.A.; Marume, U.; Mlambo, V.; Hugo, A. The effects of Lippia javanica dietary inclusion on growth performance, carcass characteristics and fatty acid profiles of broiler chickens. Anim. Nutr. 2016, 2, 160–167. [Google Scholar] [CrossRef] [PubMed]
  108. 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, 470–474. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  109. Khattak, F.; Ronchi, A.; Castelli, P.; Sparks, N. Effects of natural blend of essential Oil on growth performance, blood biochemistry, cecal morphology, and carcass quality of broiler chickens. Poult. Sci. 2014, 93, 132–137. [Google Scholar] [CrossRef]
  110. Peng, Q.Y.; Li, J.D.; Li, Z.; Duan, Z.Y.; Wu, Y.P. Effects of dietary supplementation with oregano essential oil on growth performance, carcass traits and jejunal morphology in broiler chickens. Anim. Feed Sci. Technol. 2016, 214, 148–153. [Google Scholar] [CrossRef]
  111. Pirgozliev, V.; Bravo, D.; Mirza, M.W.; Rose, S.P. Growth performance and endogenous losses of broilers fed wheat-based diets with and without essential oils and xylanase supplementation. Poult. Sci. 2015, 94, 1227–1232. [Google Scholar] [CrossRef]
  112. Jerzsele, A.; Szeker, K.; Csizinszky, R.; Gere, E.; Jakab, C.; Mallo, J.J.; Galfi, P. Efficacy of protected sodium butyrate, a protected blend of essential oils, their combination, and bacillus amyloliquefaciens spore suspension against artificially induced necrotic enteritis in broilers. Poult. Sci. 2012, 91, 837–843. [Google Scholar] [CrossRef]
  113. Mahmoud, U.T. Silver Nanoparticles in Poultry Production. J. Adv. Vet. Res. 2012, 2, 303–306. [Google Scholar]
  114. Gangadoo, S.; Stanley, D.; Hughes, R.J.; Moore, R.J.; Chapman, J. Nanoparticles in feed: Progress and prospects in poultry research. Trends Food Sci Technol. 2016, 58, 115–126. [Google Scholar] [CrossRef]
  115. Fuxiang, W.; Huiying, R.; Fenghua, Z.; Jinquan, S.; Jianyang, J.; Wenli, L. Effects of Nano-Selenium on the Immune Functions and Antioxidant Abilities of Broiler Chickens. Chin Agric. Sci. Bull. 2008, 2, 831–835. [Google Scholar]
  116. Hu, C.H.; Li, Y.L.; Xiong, L.; Zhang, H.; Song, J.; Xia, M.S. Comparative effects of nano elemental selenium and sodium selenite on selenium retention in broiler chickens. Anim. Feed Sci. Technol. 2012, 177, 204–210. [Google Scholar] [CrossRef]
  117. Cai, S.J.; Wu, C.X.; Gong, L.M.; Song, T.; Wu, H.; Zhang, L.Y. Effects of nano-selenium on performance, meat quality, immune function, oxidation resistance, and tissue selenium content in broilers. Poult. Sci. 2012, 91, 2532–2539. [Google Scholar] [CrossRef] [PubMed]
  118. Mohapatra, P.; Swain, R.; Mishra, S.; Behera, T.; Swain, P.; Mishra, S.; Behura, N.; Sabat, S.; Sethy, K.; Dhama, K. Effects of dietary nano-selenium on tissue selenium deposition, antioxidant status and immune functions in layer chicks. Int. J. Pharmacol. 2014, 10, 160–167. [Google Scholar] [CrossRef]
  119. Bagheri, M.; Golchin-Gelehdooni, S.; Mohamadi, M.; Tabidian, A. Comparative effects of nano, mineral and organic selenium on growth performance, immunity responses and total antioxidant activity in broiler chickens. Int. J. Biol. Pharm. Allied Sci. 2015, 4, 583–595. [Google Scholar]
  120. Selim, N.; Radwan, N.; Youssef, S.; Eldin, T.S.; Elwafa, S.A. Effect of Inclusion Inorganic, Organic or Nano Selenium Forms in Broiler Diets On: 2-Physiological, Immunological and Toxicity Statuses of Broiler Chicks. Int. J. Poult. Sci. 2015, 14, 144. [Google Scholar] [CrossRef]
  121. Mroczek-Sosnowska, N.; Lukasiewicz, M.; Wnuk, A.; Sawosz, E.; Niemiec, T.; Skot, A.; Jaworski, S.; Chwalibog, A. In ovo administration of copper nanoparticles and copper sulphate positively influences chicken performance. J. Sci. Food Agric. 2015, 96, 3058–3062. [Google Scholar] [CrossRef]
  122. Akbar, A.; Anal, A.K. Zinc Oxide nanoparticles loaded active packaging, a challenge study against Salmonellas typhymurium and Staphylococcus aureus in ready-to-eat poultry. Food Control. 2013, 38, 88–95. [Google Scholar] [CrossRef]
  123. Ravikumar, S.; Gokulakrishnan, R. The Inhibitory Effect of Metal Oxide Nanoparticles against Poultry Pathogens. Int. J. Pharm. Sci. Drug Res. 2012, 4, 157–159. [Google Scholar]
  124. Prasek, M.; Sawosz, E.; Jaworski, S.; Grodzik, M.; Ostaszewska, T.; Kamaszewski, M.; Wierzbicki, M.; Chwalibog, A. Influence of nanoparticles of platinum on chicken embryo development and brain morphology. Nanoscale Res. Lett. 2013, 8, 251. [Google Scholar] [CrossRef] [Green Version]
  125. Tang, Z.; Chen, G.; Li, L.; Wen, C.; Wang, T.; Zhou, Y. Effect of zinc-bearing zeolite clinoptilolite on growth performance, zinc accumulation, and gene expression of zinc transporters in broilers. J. Anim. Sci. 2015, 93, 620–626. [Google Scholar] [CrossRef] [Green Version]
  126. Elshuraydeh, K.N.; Al-Beitawi, N.A.; Al-Faqieh, M.A. Effect of Aqueous Nanosuspensions of Clay Minerals on Broilers’ Performance and Some Selected Antibody Titers. J. Nanotechnol. Eng. Med. 2014, 5, 011003. [Google Scholar] [CrossRef]
  127. Ghasemzadeh, A. Global Issues of Food Production. Agrotechnol 2012, 1, e102. [Google Scholar] [CrossRef] [Green Version]
  128. Roy, K.J.; Rahman, A.; Hossain, K.S.; Rahman, M.B.; Kafi, M.A. Antibacterial Investigation of Silver Nanoparticle against Staphylococcus, E. coli and Salmonella Isolated from Selected Live Bird Markets. Appl. Microbiol. 2020, 6, 170. [Google Scholar] [CrossRef]
  129. Andrew Selaledi, L.; Mohammed Hassan, Z.; Manyelo, T.G.; Mabelebele, M. The Current Status of the Alternative Use to Antibiotics in Poultry Production: An African Perspective. Antibiotics 2020, 9, 594. [Google Scholar] [CrossRef]
Figure 1. Schematic presentation of the challenges in sustainable antibiotic-free broiler production.
Figure 1. Schematic presentation of the challenges in sustainable antibiotic-free broiler production.
Biology 09 00411 g001
Figure 2. Role of gut microbial communities in the gastrointestinal tract (GIT). Green indicates the beneficial effects, and orange indicates the harmful effects of GIT bacteria. E. coli, Escherichia coli.
Figure 2. Role of gut microbial communities in the gastrointestinal tract (GIT). Green indicates the beneficial effects, and orange indicates the harmful effects of GIT bacteria. E. coli, Escherichia coli.
Biology 09 00411 g002
Table 1. General approaches for the production of antibiotic-free broilers.
Table 1. General approaches for the production of antibiotic-free broilers.
StrategySpecific Action
Apply minimum 14 day interval for new flock entry Reduce the frequency of pathogens
Treat feed to reduce bacterial pathogensMaintain bacterial CFU (colony-forming unit) to <10 after converting finely ground mash feed to capsule or <103 CFU at the farm
Process vegetable formulated feed in diet Obtain low fat and high protein and reduce the likelihood of clostridia contamination
Maintain dry litter Reduce ammonia level and stocking thickness, improve ventilation, increase the distance of shavings, etc.
Apply good sanitation program for drinking waterReduce contamination of bacteria and remove biofilm from the pipelines, regulators, and nipple drinkers
Dispose of dead birds regularlyPrevent cannibalism and minimize bacterial contamination
Use probiotic supplements for early stages of broiler feedEstablish healthy gut microorganisms and increase growth performance
Grind coarser grain to finestUpgrade the role of gizzard and digestion
Supplement with whole grain or gritsReduce the temporary loss of growth rate and feed efficiency and progress the function of gizzard and digestion
Add essential oil extracts to feedMaintain bacteria at safe levels and improve intestinal health
Reduce nonprotein nitrogen by preparing feeds based on digestible amino acidsInhibit the proliferation of bacteria
Utilize ingredients with more soluble fiberAvoid the deposit of insoluble fiber in the hindgut
Use digestible fats and starchesHelp suitable digestion, prevent non-starch polysaccharides from getting into the hindgut
Lessen the addition of ingredients like wheat, barley, and oats Minimize gut damage and subsequent enteritis
Maintain proper electrolyte balanceDecrease flushing and feed passage
Limit feed changesReduce disturbances of the gut microflora
Add exogenous enzymesExploit extraction and digestion of nutrients and minimize the viscosity of digesta
Maintain good management practicesMinimize stress
Follow good biosecurity practicesReduce the opportunity for disease
Table 2. Antibiotic alternatives and their functions and effects in broiler production. FCR, feed conversion ratio and BW, body weight.
Table 2. Antibiotic alternatives and their functions and effects in broiler production. FCR, feed conversion ratio and BW, body weight.
Antibiotic AlternativesActive IngredientsBasic FunctionsAdvantagesDisadvantagesEffects on BroilerReferences
ProbioticsBacillus subtilis, Enterococcus faecium, Lactobacillus acidophilus, Bacillus licheniformis, Bifidobacterium bifidumAppetite and digestion, stimulant, antioxidantModulation of immunity
Proliferation of beneficial bacteria
Increased nutrient absorption
No development of resistance
Stable
No antibacterial propertiesIncreased body weight and FCR
Improved absorptive surface of duodenum and ileum
Increase nutrient retention
Ghasemi et al. [72]; Giannenas et al. [73]; Levkut et al. [76]; Latha et al. [77]; Zhang et al. [78]; Popova [79]; Liu et al. [80]
PrebioticsFructo-oligosaccharides (FOS), inulin, galacto-oligosaccharides (GOS), trans-galacto-oligosaccharides (TOS)Digestion, stimulantModulation of immunity
Proliferation of beneficial bacteria
No development of resistance
Stable
No antibacterial properties
Unknown nutrient absorption
Increased growth performance
Stimulation of metabolic activity in intestine
Jozefiak et al. [82]; Morales-Lopez et al. [83]; Zhang et al. [84]; Baurhoo et al. [86]; Baurhoo et al. [87]
Organic acidsCitric acidDigestion, stimulant, increased feed efficiencyAntibacterial properties
Modulation of immunity
Increased nutrient absorption
Stable
Development of resistance is rareIncreased body weight
Improved ileal nutrient
digestibility, cell proliferation, and
epithelial and villi height
Kum et al. [88]; Hassan et al. [90]; Nava et al. [91]; Adil et al. [92]; Chaveerach et al. [93]; Izat et al. [94]; Mohammadagheri et al. [95]; Hu and Guo [97]; Qaisrani et al. [98]
Ascorbic acid
Propionic acid and sodium bentonite
Butyrate
Amino acids and enzymesPhytase, lysinsDigestion, stimulantAntibacterial properties
Modulation of immunity
Improved growth performanceCowieson et al. [99]; Fenton et al. [100]; Rios et al. [101]; Volozhantsev et al. [102]
Phytogenic feed additives PepperPiperineDigestion, stimulantModulation of immunity
Antibacterial properties
Proliferation of beneficial bacteria
Increased nutrient absorption
No development of resistance
Stable
No effect on live performanceWindisch et al. [103]; Frankic et al. [104]; Toghyani et al. [105]; Li et al. [106]; Mpofu et al. [107]; Kirubakaran et al. [108]; Khattak et al. [109]; Peng et al. [110]; Pirgozliev et al. [111]; Jerzsele et al. [112]
GarlicAllicinDigestion, stimulant, antisepticHigher body weight
GingerZingeroneGastric stimulantNo effects on performance
RosemaryCineolDigestion, stimulant, antiseptic, antioxidantImproved live weight and feed efficiency
ThymeThymolDigestion, stimulant, antiseptic, antioxidantNo significant effect on BW/FCR
MintMentholAppetite, digestion, stimulant, antisepticDecreased serum total cholesterol, triglycerides, and low-density lipoprotein concentration
Nanoparticles (NPs)Silver NPsDigestion, StimulantModulation of immunity
Antibacterial properties
Proliferation of beneficial bacteria
Increased nutrient absorption
No development of resistance
Stable
Some toxicity in broilersIncreased body weight and FCRGangadoo et al. [114]
Selenium NPsFuxiang et al. [115]; Hu et al. [116]; Cai et al. [117]; Mohapatra et al. [118]; Bagheri et al. [119]; Selim et al. [120]
Copper NPsGangadoo et al. [114]; Mroczek-Sosnowska et al. [121]
Metal NPs such as zinc oxide, zirconium dioxide, and platinumAkbar and Anal [122]; Ravikumar and Gokulakrishnan [123]; Prasek et al. [124]
Zn-bearing zeolite clinoptilolite NPsTang et al. [125]
Nanosuspensions of clay mineralsElshuraydeh [126]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Haque, M.H.; Sarker, S.; Islam, M.S.; Islam, M.A.; Karim, M.R.; Kayesh, M.E.H.; Shiddiky, M.J.A.; Anwer, M.S. Sustainable Antibiotic-Free Broiler Meat Production: Current Trends, Challenges, and Possibilities in a Developing Country Perspective. Biology 2020, 9, 411. https://doi.org/10.3390/biology9110411

AMA Style

Haque MH, Sarker S, Islam MS, Islam MA, Karim MR, Kayesh MEH, Shiddiky MJA, Anwer MS. Sustainable Antibiotic-Free Broiler Meat Production: Current Trends, Challenges, and Possibilities in a Developing Country Perspective. Biology. 2020; 9(11):411. https://doi.org/10.3390/biology9110411

Chicago/Turabian Style

Haque, Md. Hakimul, Subir Sarker, Md. Shariful Islam, Md. Aminul Islam, Md. Rezaul Karim, Mohammad Enamul Hoque Kayesh, Muhammad J. A. Shiddiky, and M. Sawkat Anwer. 2020. "Sustainable Antibiotic-Free Broiler Meat Production: Current Trends, Challenges, and Possibilities in a Developing Country Perspective" Biology 9, no. 11: 411. https://doi.org/10.3390/biology9110411

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop