Next Article in Journal
Effects of Road Dust Particle Size on Mineralogy, Chemical Bulk Content, Pollution and Health Risk Analyses
Previous Article in Journal
Social Processes of Young Adults’ Recovery and Identity Formation during Life-Disruptive Mental Distress—A Meta-Ethnography
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Practical Preventive Considerations for Reducing the Public Health Burden of Poultry-Related Salmonellosis

by
Rabin Raut
1,2,
Pramir Maharjan
1,* and
Aliyar Cyrus Fouladkhah
2,3,*
1
Cooperative Extension Program, Tennessee State University, Nashville, TN 37209, USA
2
Public Health Microbiology Laboratory, Tennessee State University, Nashville, TN 37209, USA
3
Public Health Microbiology FoundationSM, Nashville, TN 37209, USA
*
Authors to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2023, 20(17), 6654; https://doi.org/10.3390/ijerph20176654
Submission received: 25 April 2023 / Revised: 20 August 2023 / Accepted: 23 August 2023 / Published: 25 August 2023

Abstract

:
With poultry products as one of the leading reservoirs for the pathogen, in a typical year in the United States, it is estimated that over one million individuals contract non-typhoidal Salmonella infections. Foodborne outbreaks associated with Salmonella infections in poultry, thus, continue to remain a significant risk to public health. Moreover, the further emergence of antimicrobial resistance among various serovars of Salmonella is an additional public health concern. Feeding-based strategies (such as use of prebiotics, probiotics, and/or phytobiotics as well as essential oils), non-feeding-based strategies (such as use of bacteriophages, vaccinations, and in ovo strategies), omics tools and surveillance for identifying antibiotic-resistance genes, post-harvest application of antimicrobials, and biosecurity measures at poultry facilities are practical interventions that could reduce the public health burden of salmonellosis and antibiotic resistance associated with poultry products. With the escalating consumption of poultry products around the globe, the fate, prevalence, and transmission of Salmonella in agricultural settings and various poultry-processing facilities are major public health challenges demanding integrated control measures throughout the food chain. Implementation of practical preventive measures discussed in the current study could appreciably reduce the public health burden of foodborne salmonellosis associated with poultry products.

1. Introduction

The Salmonella serovars have a complex and evolving nomenclature and since their discovery over 100 years ago, they continue to be a major global, national, and regional public health challenge [1,2,3]. In a typical year, more than one million individuals are estimated to contract non-typhoidal Salmonella infections in the United States [4]. Similarly, around 27 million global cases of salmonellosis are estimated to be associated with typhoidal Salmonella serovars [5]. Various typhoidal and non-typhoidal Salmonella serovars are capable of forming complex biofilms on biotic and abiotic surfaces, further complicating the challenges associated with the control of this prevalent and opportunistic pathogen [6,7,8]. Under the landscape of a changing climate, the public health challenges associated with Salmonella serovars, and with antibiotic resistance are expected to be further augmented in the future [9,10]. Poultry-processing facilities and poultry products are among the main reservoirs of both typhoidal and non-typhoidal serovars of Salmonella.
Poultry contributes significantly to meat and egg production around the globe. According to the global livestock environmental assessment (GLEAM) conducted by the Food and Agriculture Organization (FAO), the production of eggs in 2016 was estimated at 73 million tons, while the production of chicken meat was estimated at 100 million tons. These statistics are expected to increase in the coming years because of the increases in global population, higher incomes, and rapid urbanization [11,12,13]. The increasing consumption of meat, mainly chicken and turkey, is due to the lower cost incurred in production [14]. Poultry, as a major source of animal protein, is typically considered superior to plant-based protein in providing micronutrients such as vitamin A, vitamin B, iron, zinc, and calcium in addition to all essential amino acids [11]. Moreover, it has no major restrictions for consumption in communities holding different religious beliefs [11,15].
In the last seventy years, not a single poultry-producing area of the world has been free of foodborne bacteria [16]. Meat and eggs can be contaminated and re-contaminated with different species of bacteria. Salmonella serovars, Campylobacter jejuni, Campylobacter coli, and Clostridium perfringens are more frequently detected as the major pathogens of meat and eggs [17]. Besides these, Staphylococcus aureus, Listeria monocytogenes, and pathogenic serogroups of Escherichia coli are abundant in various value-added poultry products [16,17]. Among the plethora of bacteria associated with poultry, Salmonella serovars have been the most important pathogen of public health concern in poultry meat [18,19].
Despite the robust control and preventive approaches applied against Salmonella, foodborne outbreaks associated with Salmonella are still a serious concern [20,21]. The age and genetics of the birds, the stress induced by overstocking, the extent of pathogen exposure, and the virulence of the specific strain contribute to the colonization of Salmonella in broilers [22,23]. Salmonella can infect broilers immediately after hatching and for the first few days by vertical or horizontal transmissions in hatcheries during activities such as feeding, handling, and transportation [24,25]. Moreover, ingestion of contaminated litter, and changes in crop pH and intestinal microbiota predispose the birds to higher susceptibility [26,27].
Salmonella is a Gram-negative bacterium that primarily inhabits the gastrointestinal tract of many warm-blooded animals. It is a facultative anaerobe, meaning it can survive with or without oxygen, and it does not form spores [28]. Most Salmonella serovars possess peritrichous flagella, allowing them to exhibit motility and move in various directions. However, there are notable exemptions including Salmonella Pullorum and Salmonella Gallinarum which are typically considered to be non-motile but are highly pathogenic to poultry [29]. As a non-fastidious bacterium, Salmonella can colonize and replicate even under adverse environmental conditions on various biotic and abiotic surfaces. It is capable of multiplication at water activity levels as low as 0.94 and can withstand a pH range of 3.7 to 9.5 [30]. The prevalence of Salmonella is common in dairy products, meat products, and fresh produce contaminated with poultry-industry by-products [31]. The different forms of salmonellosis in humans are typhoid, paratyphoid, and non-typhoid Salmonella infections [4,32,33].
Poultry products are linked to 29% of Salmonella infections [34,35,36,37]. Salmonellosis in poultry is recognized as a zoonotic disease with economic and public health implications on a global scale [20,38,39,40]. Poultry meat and various value-added poultry products are considered as two of the main reservoirs of various Salmonella serovars with Salmonella Enteritidis and Salmonella Typhimurium being among the most epidemiologically significant serovars associated with poultry-related outbreaks.
Some specific serovars of Salmonella can exhibit a high degree of antimicrobial resistance, and thus they have drawn the attention of stakeholders and policymakers. The spread of S. enterica serovar Typhimurium DT104, as an example, along with other multi-drug-resistant strains are partly responsible for the spread of antibiotic-resistant Salmonella in the poultry food chain [41]. Additionally, some new strains of S. Kentucky continue to illustrate resistance toward carbapenems and fluoroquinolones, and may bring life-threatening diseases in humans. These emerging and re-emerging Salmonella serovars with antibiotic-resistance characteristics highlight the public health importance of infectious diseases associated with poultry products [42]. The rampant use of antimicrobials in both animal production and the treatment of human and animal diseases could be a contributing factor in Salmonella serovars’ resistance to one or more antibiotics [43]. And poultry is more prone to continuous use of antibiotics as it alters the gut microbiota which may have negative effects on overall health and thus the optimal production of meat or eggs. As such, antibiotic-free (ABF) strategies promote alternative methods for disease prevention, improved animal health, and the production of safer poultry products, thus contributing to the overall sustainability and health of the poultry industry. Different alternatives, like herbal plants, organic acids, prebiotics, and probiotics, are available for the purpose of growth promotion. Better on-farm management strategies such as the availability of clean water, and robust biosecurity measures can aid in reducing the public health burden of Salmonella [44]. In the ABF approach, feeding-based and non-feeding-based interventions are in existence to control the Salmonella burden in poultry flocks. Strategies involving the modification of poultry feed (such as use of prebiotics, probiotics, synbiotics, postbiotics, and phytobiotics) involve using substances and/or microorganisms that are consumed to promote healthy gut microbiota. On the other hand, non-feeding-based strategies, such as vaccinations, application of bacteriophages, and in ovo interventions are methods that do not involve direct consumption and aim to modulate the gut microbiota or target specific pathogens [28]. The purpose of the current study was to examine the fate, prevalence, and transmission of Salmonella in poultry-processing facilities and discuss practical interventions to reduce the public health burden of poultry-related Salmonellosis (Figure 1).

2. Identification of Salmonella Serovars

Although Salmonella has a complex nomenclature, the bacterium genus consists of only two species—S. enterica and S. bongri. While the latter is not typically associated with human health complications, the subspecies of S. enterica are enterica, arizonae salamae, indica, diarizonae, and houtenae which could be pathogenic to humans. Isolates from these species and subspecies are frequently classified according to their antigenic characteristics and over 2600 serovars are reported to exist [45]. The division of Salmonella serovars is done as per the O (somatic), H (flagellar), and Vi (antigen) combinations. The O antigens are present on the surface of the outer membrane, the H antigens are found in the flagella, and the Vi antigens overlie the O antigens [46]. Identification based on this method is used to serotype more than 2600 serovars currently in existence [47]. With the rapid rise of serovars, identification was simplified to three types of Salmonella, namely, non-typhoidal Salmonella, Salmonella typhi, and Salmonella paratyphi [48]. Non-typhoidal Salmonella infections cause dehydration, elevated body temperature, episodes of vomiting, and discomfort in the abdominal region in humans, typically 6–72 h after exposure [49]. Patients suffering from typhoidal salmonellosis typically have symptoms such as headache, body aches, fever, constipation, or diarrhea [48]. The infective doses of different Salmonella serotypes can vary depending on the type of food involved and the susceptibility of the patient. In the case of fat-rich foods, such as certain dairy products, the bacterium has been found to exhibit enhanced survival. As a result, even a relatively small number of the bacterial cells, usually fewer than 100 cells, could be sufficient to cause illness if ingested [50]. Therefore, implementing a higher standard of detection in various products including ready-to-eat (RTE) foods would be critical to safeguard the public health [51].

3. Colonization of Salmonella Serovars in Poultry Flocks

When litter is contaminated with a high dose of Salmonella serovars, the bacterium could understandably colonize in the intestine of poultry and, due to genetic similarity of the birds, the bacterium could subsequently spread rapidly in the flock [52]. Then, it competes with other microflora occupying its niche that supply nutrients for its multiplication, and invades the host’s immune system [53]. Salmonella is well-equipped with virulent factors, prophages, and plasmids (mobile genetic elements) that enable it to cause infections in the host’s gut [54,55]. Salmonella pathogenic island 1 (SPI-1), a genetic cluster, is responsible for invading the enterocyte by generating a type III secretion system, a mechanism used by the bacterium to secrete effector proteins into the cells of the host. Similarly, other SPIs (such as SPIs 2 to 4), enable survival of the bacterium in biotic environments and subsequently lead to the release of secondary metabolites during infections in gastrointestinal areas. The bacterium then needs other pathogenic islands to adapt to other specific environments and hosts [56,57]. In the 20th century, outbreaks associated with Salmonella Gallinarum were worrisome on commercial farms globally [58]. Following that period, public health was threatened by the emergence of S. Typhimurium and S. Enteritidis in poultry flocks and food items such as chicken and turkey meat and eggs [59,60,61]. During the 1990s, S. Enteritidis outnumbered other serovars in poultry environments, and foodborne illness associated with it was noticed in many countries [62]. In recent years, Salmonella serovars like Heidelberg, Minnesota, Montevideo, Tennessee, and Kentucky continued to rise within poultry food chains and food products at a global scale [8,63,64]. The use of phages as an alternative to antibiotics has other co-benefits as well. As an example, phages, due to their specificity to pathogens, typically do not interfere with the commensal microflora of poultry [65] and could be used in combination with prebiotic and/or probiotic additives.

4. Salmonella in the Poultry Production System at the Preharvest Level

Poultry can acquire Salmonella infections from different sources such as contaminated feed, breeder flocks, hatcheries, farm environments, contaminated litter, and feed withdrawal.

4.1. Feed

Various Salmonella serovars are able to survive in a wide range of environmental conditions and, additionally, can survive low-moisture conditions for extended periods of time, making this pathogen an important pathogen of concern in animal feed. Application of thermal processing of the feed could eliminate the pathogen but Salmonella could be re-introduced to the feed in poultry-processing facilities [66].
Feed, as a potential source of Salmonella, can compromise the bird’s performance if contaminated with pathogens of poultry health concern. The infected birds that consume contaminated feed excrete Salmonella into the farm environment. Non-uniform distribution of microorganisms in the feed could complicate the proper detection of Salmonella in poultry feed. Additionally, sub-lethally injured but viable Salmonella might not be detected properly using traditional laboratory analysis [37]. Raw feed ingredients can be contaminated by Salmonella at several stages of manufacturing. The multiplication of microorganisms at the feed plant is affected by moisture, the composition of the feed, and the thermal processing intensity applied during preparation.

4.2. Parent Stock and Hatchery

Broiler breeders require vaccination to control the vertical transmission of Salmonella serovars to the hatching progeny and minimize their distribution in the processing plant [67]. A study of vaccinated breeders showed a significantly lower Salmonella load in the ceca (38%) and reproductive tracts (14.22%) than in non-vaccinated breeders (64.2% and 51.7%). Consequently, the progeny of vaccinated breeders also exhibited a lower population of Salmonella (18.1%) when compared to non-vaccinated breeders (33.5%) [68]. Infection of a hatching chick at the hatchery is through vertical and/or horizontal transmission. Vertical transmission is due to the laying of eggs by contaminated poultry [69,70]. In horizontal transmission, newly hatched chicks are exposed to Salmonella through the hatching of contaminated eggs. Furthermore, exposure to contaminants at the farm, could contaminate the outer surface of the eggshell and could penetrate into the egg [71]. Epidemiological studies further indicate that horizontal transmission is an important aspect due to the genetic similarities of the birds and the prevalence of various Salmonella serovars in poultry production facilities [72].

4.3. Litter

Litter offers comfort to broiler chickens as a source of bedding material [73]. Good litter management contributes to poultry welfare, disease prevention, and more efficiency in production. Litter is a significant source of dust [74] and thus could be a source for Salmonella survival and multiplication. Dust-related transmission is mainly remediated by controlling the moisture content of the litter [75]. Various studies have identified the relationship between strains detected in litter and broiler carcass contamination. Thus, the Salmonella prevalence in the litter at the rearing facilities can disseminate to poultry carcasses during processing [76].

4.4. Feed Withdrawal

Before transferring broilers to the processing mill, withdrawing feed for 8 to 12 h is a common practice in some facilities. However, feed withdrawal has been found to be a cause of the increased presence of Salmonella in the ceca and poultry products [77]. In search of food under feed-deprived environments, birds may be exposed to contaminated litter and this may lead to contamination of the ceca and poultry products. Some studies have shown the association of Salmonella prevalence in poultry products with a drop in lactic acid production. Feed withdrawal increases pH in the crop as a result of a drop in Lactobacillus fermentation [73].

5. Contribution of Poultry as a Reservoir of Antimicrobial Resistance

Poultry products are one of the leading contributing factors to Salmonella infections in humans [78]. Additionally, the excessive therapeutic and sub-therapeutic application of various antibiotics in the poultry food chain in various regions of the world is a potential contributing factor to the prevalence of antimicrobial-resistant bacteria in the food chain [79]. The increasing resistance of different Salmonella isolates to various antibiotics that are intended to treat invasive infections is a matter of great concern for public health [5]. As the efficacy of traditional antibiotics such as ampicillin, chloramphenicol, and trimethoprim–sulfamethoxazole has reduced in recent years, fluoroquinolones and broad-spectrum cephalosporins have been the drugs of choice to treat salmonellosis [80,81]. The link between human infections and non-typhoidal Salmonella and poultry products has been well understood [78,82]. Modern intensive poultry production in many regions of the world utilizes antibiotics, both for growth (sub-therapeutic) and treatment (therapeutic) purposes. Zoonotic disease can be transmitted to humans through three different routes: (i) direct contact between humans and animals; (ii) consumption of contaminated food; and (iii) exposure to a contaminated environment [83]. Eggs and meat can be contaminated with water and feed containing antibiotic-resistant bacteria (ARB) harboring antibiotic-resistant genes (ARGs). This makes the food chain one of the significant routes of ARB transmission [84]. For instance, the excessive use of enrofloxacin in poultry farming, in the 1990s is potentially responsible for the reduced susceptibility of S. Typhimurium DT104 to ciprofloxacin isolated from poultry food and subsequently from human isolates. The connection between the use of nitrofurans in poultry-producing regions and the persistence of S. Enteritidis in poultry has been similarly established. This correlation has led to an increased risk of human salmonellosis in Portugal, as an example, due to the transmission of antibiotic-resistant Salmonella through the food chain [85]. Another observational study of poultry producers in Canada also points to the potential linkage between the poultry industry and the prevalence of ceftiofur-resistant S. Heidelberg, a significant serotype of Salmonella in poultry production. The prevalence of S. Heidelberg was reduced due to the voluntary withdrawal of ceftiofur from both human infection treatments and retail poultry, however, resistance levels again rose after the reintroduction of antibiotic use [86].
A review of recent observational studies indicates that poultry and poultry products are an important reservoir for antibiotic-resistant bacteria in food chains, with a high tendency for dissemination to humans [87]. In addition to Salmonella serovars, Gram-positive bacteria are considered as a main reservoir for class 1 antibiotic resistance integrons in poultry production facilities as well [88]. In harmony with the overall recommended approach of the current study, other studies also emphasize the critical importance of prevention as well as incorporating a holistic “one health” approach for reducing the public health burden of antibiotic-resistant microorganisms associated with poultry products and production [89].

6. Control and Prevention of Salmonella

Controlling Salmonella in poultry productions and poultry meat, and thus preventing its entry into the food chain requires multiple interventions. As discussed earlier, the threat of ARB increases by administering antibiotics in the poultry industry for prophylactic and therapeutic purposes. Thus, non-antibiotic alternatives in poultry production have gained increasing attention in recent years. These alternatives are feeding-based interventions, such as probiotics, prebiotics, phytobiotics, and postbiotics. In addition to the feeding-based approach, non-feeding-based alternatives focused on using bacteriophages, vaccines, and in ovo strategies are also common practical interventions in the poultry industry to minimize the Salmonella burden [28]. More recently, whole genome sequencing (WGS), an application of genomics, has been used in the diagnosis, epidemiological studies, and surveillance of Salmonella [90].

6.1. Feeding-Based Strategies

6.1.1. Prebiotics

Probiotics are types of food ingredients that have a positive impact on the host’s health by selectively promoting the multiplication and activity of specific bacteria in the colon. This definition emphasizes the non-digestible nature of prebiotics and their ability to improve the overall well-being of the host through the modulation of beneficial gut bacteria. [91]. Improvement in broiler growth is achieved through the increased production of amylase within the intestinal tract of chickens [92] and the minimization of Salmonella colonization during hen molting [93]. Some studies have indicated the potential of prebiotics to combat Salmonella by providing binding sites for bacteria to be excreted out of the digestive tract [94]. Some studies have reported a drop in Salmonella numbers by supplementing prebiotics, which increases the short-chain fatty acid (SCFA) concentrations [95]. Prebiotics like trehalose and Aspergillus meal prevent horizontal transmission of Salmonella by minimizing its colonization in caeca. The positive impact of prebiotics is due to their potential in modulating the gut microbiota, making toll-like receptors that are important mediators of inflammation-related pathways in the gastrointestinal area [96].

6.1.2. Probiotics

Probiotics are live and direct-fed microorganisms that provide health benefits to the host by modulating the immune system, if administered in adequate amounts [97]. Administration of probiotics to chicks soon after the hatch is thought to reduce infective pathogens due to ‘competitive exclusion’ [98]. The core concept of competitive exclusion is the competition of bacteria for space and nutrients and pathogenic microorganisms could be flushed out of the digestive tract via this mechanism. Several reports have documented the potential of probiotics to mitigate Salmonella infections [99]. Probiotics for poultry are mainly the various species of bacteria such as Bifidobacterium, Lactobacillus, and Bacillus.

6.1.3. Phytobiotics

Phytobiotics are compounds of plant origin such as herbs, spices, and extracted oils that have shown promising effects on poultry production by increasing feed intake, stimulating the release of endogenous enzymes, and exerting antibacterial properties [100]. Moreover, they improve nutrient absorption by adjusting the fluidity and permeability of the cell membranes [101]. In the poultry industry, they are commonly obtained from alfalfa, bergamot, peppermint, black chili, cumin, clove, garlic, cinnamon, and oregano [28]. A drop in the S. Enteritidis population was observed in the liver/spleen and ceca of the broilers upon the inclusion of 5 ppm capsaicin [102].

6.1.4. Essential Oils

Essential oils could be another practical feed additive to further combat Salmonella. Cinnamon, clove, oregano, and red thyme essential oils were shown to be efficacious for controlling the prevalence of the pathogen in poultry feed [103]. Utilization of clove, peppermint, litsea, lemongrass, and cinnamon essential oils were additionally investigated as an efficacious feed additive in the poultry industry [104]. Most recently, oregano, thyme, and grapefruit essential oils were studied as alternatives to antibiotics in poultry feed [105].

6.2. Non-Feeding Strategies

6.2.1. Bacteriophages

Bacteriophages, also called phages, are known as predators of bacteria specific to the host and are considered as the alternative to antibiotics in animal therapy, prophylaxis, and minimizing bacterial population in animal-based food products [106]. Since they are typically host-specific, their therapeutic use is generally considered natural, non-toxic, and feasible, thus targeting the specific bacteria and protecting the rest of the microbiota [107]. Another advantage of phages over antibiotics is preventing allergies in the host as the immune system typically can tolerate phages more favorably [28]. Moreover, phages have the potential to combat antibiotic-resistant strains [108]. Some trials have shown the successful application of phages for mitigating foodborne pathogens such as Salmonella [109].

6.2.2. Vaccines

Vaccines continue to be one of the most significant health-management strategies for boosting immunity in the poultry flock. Vaccination reduces shedding of Salmonella by poultry and could reduce vertical and horizontal transmission of the pathogen in the poultry chain [110]. In addition to these beneficial effects, vaccines are also the most efficacious and cost-effective tools to prevent diseases in birds [111]. The manufacturing of poultry vaccines is typically conducted using Typhimurium and/or Enteritidis serovars of Salmonella [112]. Different types of vaccines are available in the market, including live-attenuated, inactivated, and subunit vaccines, providing a range of options for disease prevention in poultry [113]. The production type, biosecurity status of the poultry premises, specific trend of the disease, level of maternal-derived antibodies, vaccine availability, administration methods, and vaccination cost are among the factors that play a crucial role in the application of this preventive measure. Typically, Salmonella-killed vaccines for poultry are preferred compared to the other vaccines due to the adverse effects that Salmonella-live vaccines could exert. The secondary mutations in live vaccines can cause reversion to virulence which could affect the overall health of flocks and thus should be carefully considered [114]. Both observational and randomized studies associated with the use of vaccines are very abundant in the literature and could be the subject of a review and systematic analysis in future studies.

6.2.3. In Ovo Strategies

In ovo technology incorporates the administration of a small number of materials into the bird’s embryo, a new approach that delivers bioactive substances before hatching. Numerous studies have shown the benefits of in ovo strategies, at an early stage of development and involving feed additives, in avoiding metabolic disorders, compromised immunity, and pathogen load [115]. In addition to these, nutrients injected through the in ovo route enhance absorption, enzyme expression, and faster maturation of the digestive system and muscle tissues [116]. These beneficial effects directly and/or indirectly aid in the control of Salmonella infection. In a vaccination experiment, Salmonella flagellin was delivered to 18-day-old embryonated eggs in broilers. The study found elevation of inflammation-related chIL-6 and chIL-8 cytokine transcript levels 24 h after vaccination and elevated titers of FliC-specific antibodies 21 days after hatching [117]. In another experiment, increased resistance of chicks to S. Typhimurium was observed in broilers when the probiotic was injected into the air cells after 18 days of incubation [118].

6.3. Omics Tool for Identifying Antibiotic-Resistance Genes

The use of omics tools (studying the genome of organisms), such as whole genome sequencing (WGS) technology in agricultural production has led to advances in identifying genes associated with antibiotic-resistant bacteria. For instance, next-generation sequencing (NGS) technology has been applied to study over 30,000 genomes of S. Enteritidis from 98 countries over a span of 71 years to predict and understand the global dissemination of this pathogen [119]. Certain genes (such as TLR4), natural resistance-associated macrophage protein, and the QTL SAL1 in the genomic regions are central to controlling Salmonella infection in chickens [120].

6.4. Treatment of Salmonella in Poultry-Processing Facilities (Post-Harvest)

The journey of poultry from the farm to the consumer is a crucial aspect of the poultry industry. Any kind of contamination in poultry meat at this stage is correlated with negative impacts on public health. The duration for which these products can be stored before typical consumption ranges from 4 to 10 days, depending on the nature of processing after slaughter [121]. Salmonella is reported in higher proportion in fresh poultry products in comparison to other meat [122]. Thus, it is imperative that processors employ stringent measures to prevent Salmonella infection. In recent years, the reduction of pathogen contamination during processing has been achieved through post-chill decontamination tanks coupled with other preventive measures throughout the supply chain [123]. Antimicrobial strategies have been in implementation to minimize foodborne pathogens such as Salmonella and Campylobacter and to meet microbiological performance standards [124]. The potency of antimicrobials is influenced by the organic load present in the chilled water during immersion chilling [125]. Chemical applications such as chlorine, peracetic acid (PAA), and hydrogen peroxide are also effective in inhibiting microbial proliferation and prolonging the shelf-life of the product [126].
Chlorine has long been applied in processing facilities in the United States due to its cost-effectiveness and potential for eliminating a broad range of carcass microorganisms as well as microorganisms present in processing water and within processing plants [127]. However various studies have revealed the discouraging effects of chlorine including its negative impacts on meat quality, its sensitivity to pH changes, and its diminished effectiveness with time due to the presence of organic matter in the processing tank [128]. Peracetic acid is another organic compound commonly used to disinfect poultry equipment. However, attention should be paid to using peracetic acid in maximum concentrations, as it can corrode the equipment and bring health hazards to workers [129]. Sodium bisulfate may be a good substitute for peracetic acid against Salmonella in poultry facilities due to its less corrosive nature [130,131]. Other organic acids like lactic acid, citric acid, and acetic acid are also popular in meat-processing plants. While assessing the effectiveness of these organic acids on S. Typhimurium contaminated chicken meat, the reduction in CFU/g was observed to be 66%, 55%, and 51% for lactic acid (1% solution), acetic acid (1%), and citric acid (1%), respectively [132]. Additives and processing aids should be used after careful compliance with regulatory requirements to ensure efficacy of the treatments and safety of the workers and consumers.

6.5. Biosecurity at the Poultry Farm

Poultry production is compromised if there is no effective adoption of management and physical measures intended to mitigate the introduction and dissemination of infections or infestations in poultry premises and facilities [133]. The physical barriers used in robust biosecurity programs include fences, mesh wire, use of footbaths, and disinfection of farm equipment in and around poultry production facilities [134]. Biosecurity practices could be the most efficacious and inexpensive preventive measures, aimed at managing the risks posed by diseases to the economy, environment, and human health [135]. Overall, biosecurity measures are associated with isolation, traffic control, and sanitation practices [136]. Isolation addresses keeping the birds confined within a controlled environment. Traffic control looks at controlling the flow of traffic on a farm to mitigate cross-contamination and horizontal transmission of infectious diseases. The objective of sanitation is to clean and disinfect equipment and materials that enter or remain on the farms and it includes the personal hygiene of farm staff [137]. In addition to these biosecurity measures, sanitation of eggs, incubators, and the hatchery could substantially reduce the prevalence of microbial pathogens associated with poultry production. It is noteworthy that biosecurity measures not only minimize the risk of poultry-related infectious diseases but, as well, they are important from a regulatory perspective. Regulatory agencies such as United States Department of Agriculture’s Animal and Plant Health Inspection Services (USDA APHIS) or those regulations articulated for poultry farmers in the European Union are examples of reputable and efficacious policies and regulations if implemented properly. The Preventive Control for Animal Food regulation of the U.S. Food Safety Modernization Act could be another great resource for ensuring the safety of poultry products [138].

7. Conclusions

In a typical year, over one million American individuals and around 27 million people around the globe are estimated to contract non-typhoidal and typhoidal Salmonella infections, respectively. Considering that infectious diseases associated with Salmonellae and antibiotic resistance are expected to be augmented under the landscape of climate change, and considering that poultry-processing facilities and poultry products are one of the main reservoirs of Salmonella serovars, implementation of practical preventive measures is of great importance for reducing the public health burden of this pathogen. Feeding-based strategies (including use of prebiotics, probiotics, phytobiotics, and/or essential oils), non-feeding-based strategies (such as application of bacteriophages, vaccinations, and in ovo interventions), omics tools and surveillance for identifying antibiotic-resistance genes, post-harvest application of antimicrobials, and enhanced biosecurity at the poultry facilities are practical interventions that could reduce the public health burden of salmonellosis and antibiotic resistance associated with poultry products.

Author Contributions

R.R. co-wrote the first version of the paper; P.M. contributed to co-editing the manuscript; and A.C.F. co-wrote, co-edited, and revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

Financial support provided, in part, by the Public Health Microbiology FoundationSM in Nashville, Tennessee, and USDA National Institute of Food and Agriculture (2023-70020-40768) are sincerely appreciated by the study authors. This publication is additionally supported by a publication scholarship of a graduate course of the Public Health Microbiology Laboratory of Tennessee State University (AGSC 5540 Food Policies and Regulations; Fall 2022).

Conflicts of Interest

The authors have no conflict of interest to declare. It is important to emphasize that the funding agencies of this study had no role in the design, data collection, analyses, or interpretation and writing associated with this project. Thus, the views expressed in this publication do not necessarily reflect the views of the funding agencies.

References

  1. Asefaw, S.; Aras, S.; Kabir, M.N.; Wadood, S.; Chowdhury, S.; Fouladkhah, A.C. Public Health Importance of Preventive Measures for Salmonella Tennessee and Salmonella Typhimurium Strain LT2 Biofilms. Microbiol. Res. 2023, 14, 714–726. [Google Scholar]
  2. Kumar, A.; Allison, A.; Henry, M.; Scales, A.; Fouladkhah, A.C. Development of salmonellosis as affected by bioactive food compounds. Microorganisms 2019, 7, 364. [Google Scholar] [PubMed]
  3. Abd El-Ghany, W.A. Salmonellosis: A food borne zoonotic and public health disease in Egypt. J. Infect. Dev. Ctries 2020, 14, 674–678. [Google Scholar] [PubMed]
  4. Scallan, E.; Hoekstra, R.M.; Angulo, F.J.; Tauxe, R.V.; Widdowson, M.A.; Roy, S.L.; Jones, J.L.; Griffin, P.M. Foodborne illness acquired in the United States—Major pathogens. Emerg. Infect. Dis. 2011, 17, 7. [Google Scholar]
  5. Crump, J.A.; Luby, S.P.; Mintz, E.D. The global burden of typhoid fever. Bull. World Health Organ. 2004, 82, 346–353. [Google Scholar] [PubMed]
  6. Fouladkhah, A.; Geornaras, I.; Sofos, J.N. Biofilm formation of O157 and Non-O157 Shiga toxin-producing Escherichia coli and multidrug-resistant and susceptible Salmonella Typhimurium and Newport and their inactivation by sanitizers. J. Food Sci. 2013, 78, M880–M886. [Google Scholar]
  7. Allison, A.; Fouladkhah, A.C. Sensitivity of planktonic cells and biofilm of wild-type and pressure-stressed Cronobacter sakazakii and Salmonella enterica serovars to sodium hypochlorite. Food Prot. Trends 2021, 41, 195–203. [Google Scholar]
  8. Chowdhury, A.; Aras, S.; Kabir, N.; Wadood, S.; Allison, A.; Chowdhury, S.; Fouladkhah, A.C. Susceptibility of pathogenic nontyphoidal Salmonella serovars and avirulent Salmonella LT2 to elevated hydrostatic pressure and citricidalTM. J. Tenn. Acad. Sci. 2021, 96, 49–54. [Google Scholar]
  9. Fouladkhah, A.C.; Thompson, B.; Camp, J.S. Safety of food and water supplies in the landscape of changing climate. Microorganisms 2019, 7, 469. [Google Scholar]
  10. Fouladkhah, A.C.; Thompson, B.; Camp, J.S. The threat of antibiotic resistance in changing climate. Microorganisms 2020, 8, 748. [Google Scholar]
  11. Mottet, A.; Tempio, G. Global poultry production: Current state and future outlook and challenges. World’s Poult. Sci. J. 2017, 73, 245–256. [Google Scholar]
  12. Magdelaine, P.; Spiess, M.P.; Valceschini, E. Poultry meat consumption trends in Europe. Worlds Poult. Sci. J. 2008, 64, 53–64. [Google Scholar]
  13. Alexandratos, N.; Bruinsma, J. World Agriculture towards 2030/2050: The 2012 Revision. 2012. Available online: https://www.fao.org/3/ap106e/ap106e.pdf (accessed on 2 October 2022).
  14. Organisation for Economic Co-Operation and Development. Meat Consumption. 2022. Available online: https://data.oecd.org/agroutput/meat-consumption.htm (accessed on 8 November 2022).
  15. Farrell, D. The role of poultry in human nutrition. In Poultry Development Review; Food and Agriculture Organization: Rome, Italy, 2013; pp. 2–9. [Google Scholar]
  16. Gomes, B.C.; Franco, B.D.G.D.M.; De Martinis, E.C.P. Microbiological food safety issues in Brazil: Bacterial pathogens. Foodborne Pathog. Dis. 2013, 10, 197–205. [Google Scholar]
  17. Abebe, E.; Gugsa, G.; Ahmed, M. Review on major food-borne zoonotic bacterial pathogens. J. Trop. Med. 2020, 2020, 4674235. [Google Scholar]
  18. Ravel, A.; Greig, J.; Tinga, C.; Todd, E.; Campbell, G.; Cassidy, M.; Marshall, B.; Pollari, F. Exploring historical Canadian foodborne outbreak data sets for human illness attribution. J. Food Prot. 2009, 72, 1963–1976. [Google Scholar]
  19. Guo, C.; Hoekstra, R.M.; Schroeder, C.M.; Pires, S.M.; Ong, K.L.; Hartnett, E.; Naugle, A.; Harman, J.; Bennett, P.; Cieslak, P.; et al. Application of Bayesian techniques to model the burden of human salmonellosis attributable to U.S. food commodities at the point of processing: Adaptation of a Danish model. Foodborne Pathog. Dis. 2011, 8, 509–516. [Google Scholar]
  20. Antunes, P.; Mourão, J.; Campos, J.; Peixe, L. Salmonellosis: The role of poultry meat. Clin. Microbiol. Infect. 2016, 22, 110–121. [Google Scholar]
  21. Williams, M.S.; Ebel, E.D.; Golden, N.J.; Schlosser, W.D. Temporal patterns in the occurrence of Salmonella in raw meat and poultry products and their relationship to human illnesses in the United States. Food Control. 2014, 35, 267–273. [Google Scholar]
  22. Lee, M.D.; Newell, D.G. Campylobacter in poultry: Filling an ecological niche. Avian Dis. 2006, 50, 1–9. [Google Scholar]
  23. Cox, N.A.; Berrang, M.E.; Cason, J.A. Salmonella penetration of egg shells and proliferation in broiler hatching eggs—A review. Poult. Sci. 2000, 79, 1571–1574. [Google Scholar]
  24. Lahellec, C.; Colin, P. Relationship between serotypes of Salmonellae from hatcheries and rearing farms and those from processed poultry carcases. Br. Poult. Sci. 1985, 26, 179–186. [Google Scholar] [CrossRef]
  25. Opitz, H.M.; El-Begearmi, M.; Flegg, P.; Beane, D. Effectiveness of five feed additives in chicks infected with Salmonella enteritidis phage type 13a. J. Appl. Poult. Res. 1993, 2, 147–153. [Google Scholar] [CrossRef]
  26. Ramirez, G.A.; Sarlin, L.L.; Caldwell, D.J.; Yezak Jr, C.R.; Hume, M.E.; Corrier, D.E.; Deloach, J.R.; Hargis, B.M. Effect of feed withdrawal on the incidence of Salmonella in the crops and ceca of market age broiler chickens. Poult. Sci. 1997, 76, 654–656. [Google Scholar] [CrossRef]
  27. Dunkley, K.D.; McReynolds, J.L.; Hume, M.E.; Dunkley, C.S.; Callaway, T.R.; Kubena, L.F.; Nisbet, D.J.; Ricke, S.C. Molting in Salmonella Enteritidis-challenged laying hens fed alfalfa crumbles: II. Fermentation and microbial ecology response. Poult. Sci. 2007, 86, 2101–2109. [Google Scholar] [PubMed]
  28. Ruvalcaba-Gómez, J.M.; Villagrán, Z.; Valdez-Alarcón, J.J.; Martínez-Núñez, M.; Gomez-Godínez, L.J.; Ruesga-Gutiérrez, E.; Anaya-Esparza, L.M.; Arteaga-Garibay, R.I.; Villarruel-López, A. Non-Antibiotics Strategies to Control Salmonella Infection in Poultry. J. Anim. 2022, 12, 102. [Google Scholar] [CrossRef]
  29. Bhunia, A.K. Salmonella Enterica. In Foodborne Microbial Pathogens; Springer: New York, NY, USA, 2008; pp. 201–216. [Google Scholar]
  30. Pui, C.F.; Wong, W.C.; Chai, L.C.; Tunung, R.; Jeyaletchumi, P.; Hidayah, N.; Ubong, A.; Farinazleen, M.G.; Cheah, Y.K.; Son, R. Salmonella: A foodborne pathogen. Int. Food Res. J. 2011, 18, 465–473. [Google Scholar]
  31. Mouttotou, N.; Ahmad, S.; Kamran, Z.; Koutoulis, K.C. Prevalence, Risks and Antibiotic Resistance of Salmonella in Poultry Production Chain. In Current Topics in Salmonella and Salmonellosis; Mares, M., Ed.; InTechOpen: London, UK, 2017; p. 67438. [Google Scholar]
  32. World Health Organization. Salmonella (Non-Typhoidal). Available online: https://www.who.int/news-room/fact-sheets/detail/salmonella-(non-typhoidal) (accessed on 20 August 2023).
  33. Flint, J.A.; Van Duynhoven, Y.T.; Angulo, F.J.; DeLong, S.M.; Braun, P.; Kirk, M.; Scallan, E.; Fitzgerald, M.; Adak, G.K.; Sockett, P.; et al. Estimating the burden of acute gastroenteritis, foodborne disease, and pathogens commonly transmitted by food: An international review. Clin. Infect. Dis. 2005, 41, 698–704. [Google Scholar] [CrossRef]
  34. FDA. Human Health Impact of Fluoroquinolone Resistant Campylobacter Associated with the Consumption of Chicken. 2000. Available online: https://www.fda.gov/media/76429/download (accessed on 20 August 2023).
  35. U.S. Department of Agriculture, Food Safety and Inspection Service. Modernization of Poultry Slaughter Inspection. Available online: https://www.fsis.usda.gov/inspection/inspection-programs/inspection-poultry-products/modernization-poultry-slaughter (accessed on 20 August 2023).
  36. Braden, C.R. Salmonella enterica serotype Enteritidis and eggs: A national epidemic in the United States. Clin. Infect. Dis. 2006, 43, 512–517. [Google Scholar] [CrossRef]
  37. Painter, J.A.; Hoekstra, R.M.; Ayers, T.; Tauxe, R.V.; Braden, C.R.; Angulo, F.J.; Griffin, P.M. Attribution of foodborne illnesses, hospitalizations, and deaths to food commodities by using outbreak data, United States, 1998–2008. Emerg. Infect. Dis. 2013, 19, 407. [Google Scholar] [CrossRef] [PubMed]
  38. Gast, R.K. Serotype-specific and serotype-independent strategies for preharvest control of food-borne Salmonella in poultry. Avian Dis. 2007, 51, 817–828. [Google Scholar] [CrossRef]
  39. Ferrari, R.G.; Rosario, D.K.; Cunha-Neto, A.; Mano, S.B.; Figueiredo, E.E.; Conte-Junior, C.A. Worldwide epidemiology of Salmonella serovars in animal-based foods: A meta-analysis. Appl. Environ. Microbiol. 2019, 85, e00591-19. [Google Scholar] [CrossRef] [PubMed]
  40. Popa, G.L.; Papa, M.I. Salmonella spp. Infection—A continuous threat worldwide. Germs 2021, 11, 88. [Google Scholar] [CrossRef] [PubMed]
  41. Threlfall, E.J.; Frost, J.A.; Ward, L.R.; Rowe, B. Increasing spectrum of resistance in multiresistant Salmonella typhimurium. Lancet 1996, 347, 1053–1054. [Google Scholar] [CrossRef]
  42. Le Hello, S.; Harrois, D.; Bouchrif, B.; Sontag, L.; Elhani, D.; Guibert, V.; Zerouli, K.; Weill, F.X. Highly drug-resistant Salmonella enterica serotype Kentucky ST198-X1: A microbiological study. Lancet Infect. Dis. 2013, 13, 672–679. [Google Scholar] [CrossRef]
  43. Swartz, M.N. Human diseases caused by foodborne pathogens of animal origin. Clin. Infect. Dis. 2002, 34, S111–S122. [Google Scholar] [CrossRef] [PubMed]
  44. Haque, M.H.; Sarker, S.; Islam, M.S.; Islam, M.A.; Karim, M.R.; Kayesh, M.E.H.; Shiddiky, M.J.A.; Answer, M.S. Sustainable Antibiotic-Free Broiler Meat Production: Current Trends, Challenges, and Possibilities in a Developing Country Perspective. Biology 2020, 9, 411. [Google Scholar] [CrossRef]
  45. Issenhuth-Jeanjean, S.; Roggentin, P.; Mikoleit, M.; Guibourdenche, M.; De Pinna, E.; Nair, S.; Fields, P.I.; Weill, F.X. Supplement 2008–2010 (no. 48) to the white–Kauffmann–Le minor scheme. Res. Microbiol. 2014, 165, 526–530. [Google Scholar] [CrossRef]
  46. Alikhan, N.F.; Zhou, Z.; Sergeant, M.J.; Achtman, M. A genomic overview of the population structure of Salmonella. PLoS Genet. 2018, 14, e1007261. [Google Scholar] [CrossRef]
  47. Mkangara, M.; Mwakapuja, R.; Chilongola, J.; Ndakidemi, P.; Mbega, E.; Chacha, M. Mechanisms for Salmonella infection and potential management options in chicken. J. Anim. Plant Sci. 2020, 30, 259–279. [Google Scholar]
  48. Forsythe, S.J. The Microbiology of Safe Food; Wiley-Blackwell: Hoboken, NJ, USA, 2020. [Google Scholar]
  49. Kurtz, J.R.; Goggins, J.A.; McLachlan, J.B. Salmonella infection: Interplay between the bacteria and host immune system. Immunol. Lett. 2017, 190, 42–50. [Google Scholar] [CrossRef] [PubMed]
  50. The U.S. Food and Drug Administration. Bad Bug Book: Handbook of Foodborne Pathogenic Microorganisms and Natural Toxins; CreateSpace Independent Publishing Platform: Scotts Valley, CA, USA, 2017. Available online: https://www.fda.gov/food/foodborne-pathogens/bad-bug-book-second-edition (accessed on 20 August 2023).
  51. ISO 6579-1:2017; Microbiology of Food and Feeding Stuffs—Horizontal Method for the Detection of Salmonella spp. in the Food Production Chain. ISO: Geneve, Switzerland, 2017.
  52. Dunkley, K.D.; Callaway, T.R.; Chalova, V.I.; McReynolds, J.L.; Hume, M.E.; Dunkley, C.S.; Kubena, L.F.; Nisbet, D.J.; Ricke, S.C. Foodborne Salmonella ecology in the avian gastrointestinal tract. Anaerobe 2009, 15, 26–35. [Google Scholar] [CrossRef] [PubMed]
  53. Tanner, J.R.; Kingsley, R.A. Evolution of Salmonella within Hosts. Trends Microbiol. 2018, 26, 986–998. [Google Scholar] [CrossRef]
  54. Mebrhatu, M.T.; Cenens, W.; Aertsen, A. An overview of the domestication and impact of the Salmonella mobilome. Crit. Rev. Microbiol. 2014, 40, 63–75. [Google Scholar] [CrossRef]
  55. Staes, I.; Passaris, I.; Cambré, A.; Aertsen, A. Population heterogeneity tactics as driving force in Salmonella virulence and survival. Food Res. Int. 2019, 125, 108560. [Google Scholar] [CrossRef] [PubMed]
  56. Cheng, R.A.; Eade, C.R.; Wiedmann, M. Embracing Diversity: Differences in Virulence Mechanisms, Disease Severity, and Host Adaptations Contribute to the Success of Nontyphoidal Salmonella as a Foodborne Pathogen. Front. Microbiol. 2019, 10, 1368. [Google Scholar] [CrossRef]
  57. Marcus, S.L.; Brumell, J.H.; Pfeifer, C.G.; Finlay, B.B. Salmonella pathogenicity islands: Big virulence in small packages. Microbes Infect. 2000, 2, 145–156. [Google Scholar] [CrossRef]
  58. Shivaprasad, H.L.; Barrow, P.A. Pullorum disease and fowl typhoid. In Diseases of Poultry, 12th ed.; Blackwell Publishing Professional: Ames, IA, USA, 2008; pp. 620–634. [Google Scholar]
  59. Oakley, B.B.; Lillehoj, H.S.; Kogut, M.H.; Kim, W.K.; Maurer, J.J.; Pedroso, A.; Lee, M.D.; Collett, S.R.; Johnson, T.J.; Cox, N.A. The chicken gastrointestinal microbiome. FEMS Microbiol. Lett. 2014, 360, 100–112. [Google Scholar] [CrossRef]
  60. Tavechio, A.T.; Fernandes, S.A.; Neves, B.C.; Dias, A.M.G.; Irino, K. Changing patterns of Salmonella serovars: Increase of Salmonella enteritidis in São Paulo, Brazil. Rev. Inst. Med. Trop. 1996, 38, 315–322. [Google Scholar] [CrossRef] [PubMed]
  61. Bäumler, A.J.; Hargis, B.M.; Tsolis, R.M. Tracing the origins of Salmonella outbreaks. Science 2000, 287, 50–52. [Google Scholar] [CrossRef]
  62. Silva, E.N.D.; Duarte, A. Salmonella Enteritidis em aves: Retrospectiva no Brasil. Braz. J. Poult. Sci. 2002, 4, 85–100. [Google Scholar] [CrossRef]
  63. Foley, S.L.; Lynne, A.M.; Nayak, R. Salmonella challenges: Prevalence in swine and poultry and potential pathogenicity of such isolates. J. Anim. Sci. 2008, 86, E149–E162. [Google Scholar] [CrossRef] [PubMed]
  64. Voss-Rech, D.; Vaz, C.S.; Alves, L.; Coldebella, A.; Leao, J.A.; Rodrigues, D.P.; Back, A. A temporal study of Salmonella enterica serotypes from broiler farms in Brazil. Poult. Sci. 2015, 94, 433–441. [Google Scholar] [CrossRef]
  65. Wernicki, A.; Nowaczek, A.; Urban-Chmiel, R. Bacteriophage therapy to combat bacterial infections in poultry. Virology J. 2017, 14, 179. [Google Scholar] [CrossRef]
  66. Jones, F.T. A review of practical Salmonella control measures in animal feed. J. Appl. Poult. Res. 2011, 20, 102–113. [Google Scholar] [CrossRef]
  67. Jones, F.T.; Axtell, R.C.; Rives, D.V.; Scheideler, S.E.; Tarver, F.R., Jr.; Walker, R.L.; Wineland, M.J. A survey of Salmonella contamination in modern broiler production. J. Food Prot. 1991, 54, 502–507. [Google Scholar] [CrossRef]
  68. Dórea, F.C.; Cole, D.J.; Hofacre, C.; Zamperini, K.; Mathis, D.; Doyle, M.P.; Lee, M.D.; Maurer, J.J. Effect of Salmonella vaccination of breeder chickens on contamination of broiler chicken carcasses in integrated poultry operations. Appl. Environ. Microbiol. 2010, 76, 7820–7825. [Google Scholar] [CrossRef]
  69. Timoney, J.F. Egg transmission after infection of hens with Salmonella enteritidis phage type 4. Vet. Rec. 1989, 125, 600–601. [Google Scholar] [PubMed]
  70. Shivaprasad, H.L.; Timoney, J.F.; Morales, S.; Lucio, B.; Baker, R.C. Pathogenesis of Salmonella enteritidis infection in laying chickens. I. Studies on egg transmission, clinical signs, fecal shedding, and serologic responses. Avian Dis. 1990, 34, 548–557. [Google Scholar] [CrossRef] [PubMed]
  71. Rizk, S.S.; Ayres, J.C.; Kraft, A.A. Effect of holding condition on the development of salmonellae in artificially inoculated hens’ eggs. Poult. Sci. 1966, 45, 825–829. [Google Scholar] [CrossRef]
  72. Heyndrickx, M.; Vandekerchove, D.; Herman, L.; Rollier, I.; Grijspeerdt, K.; De Zutter, L. Routes for Salmonella contamination of poultry meat: Epidemiological study from hatchery to slaughterhouse. Epidemiol. Infect. 2022, 129, 253–265. [Google Scholar] [CrossRef]
  73. Alali, W.Q.; Hofacre, C.L. Preharvest Food Safety in Broiler Chicken Production. Microbiol. Spectr. 2016, 4, 69–86. [Google Scholar] [CrossRef]
  74. David, B.; Mejdell, C.; Michel, V.; Lund, V.; Moe, R.O. Air Quality in Alternative Housing Systems may have an Impact on Laying Hen Welfare: Part II—Ammonia. J. Anim. 2015, 5, 886–896. [Google Scholar] [CrossRef] [PubMed]
  75. Pal, A.; Bailey, M.A.; Talorico, A.A.; Krehling, J.T.; Macklin, K.S.; Price, S.B.; Buhr, R.J.; Bourassa, D.V. Impact of poultry litter Salmonella levels and moisture on transfer of Salmonella through associated in vitro generated dust. Poult. Sci. 2021, 100, 101236. [Google Scholar] [CrossRef]
  76. Bhatia, T.R.S.; McNabb, G.D. Dissemination of Salmonella in broiler-chicken operations. Avian Dis. 1980, 24, 616–624. [Google Scholar] [CrossRef] [PubMed]
  77. Corrier, D.E.; Byrd, J.A.; Hargis, B.M.; Hume, M.E.; Bailey, R.H.; Stanker, L.H. Survival of Salmonella in the crop contents of market-age broilers during feed withdrawal. Avian Dis. 1999, 43, 453–460. [Google Scholar] [CrossRef]
  78. European Centre for Disease Prevention and Control; European Food Safety Authority. European Medicines Agency and European Commission’s Scientific Committee on Emerging and Newly Identified Health Risks 2009. EFSA J. 2009, 7, 1372. [Google Scholar]
  79. Threlfall, E.J. Antimicrobial drug resistance in Salmonella: Problems and perspectives in food- and water-borne infections. FEMS Microbiol. Rev. 2002, 26, 141–148. [Google Scholar] [CrossRef] [PubMed]
  80. Parry, C.M.; Threlfall, E.J. Antimicrobial resistance in typhoidal and nontyphoidal salmonellae. Curr. Opin. Infect. Dis. 2008, 21, 531–538. [Google Scholar] [CrossRef]
  81. Chen, H.M.; Wang, Y.; Su, L.H.; Chiu, C.H. Nontyphoid Salmonella infection: Microbiology, clinical features, and antimicrobial therapy. Pediatr. Neonato. 2013, 54, 147–152. [Google Scholar] [CrossRef]
  82. Aarestrup, F.M. The livestock reservoir for antimicrobial resistance: A personal view on changing patterns of risks, effects of interventions and the way forward. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2015, 370, 20140085. [Google Scholar] [CrossRef]
  83. O’Neill, J. Antimicrobials in Agriculture and the Environment: Reducing Unnecessary Use and Waste. 2015. Available online: https://amr-review.org/Publications.html (accessed on 20 August 2023).
  84. Roberts, M.C. Antibiotics and Resistance in the Environment. In Antimicrobial Resistance in the 21st Century; Springer: Cham, Switzerlands, 2018; pp. 383–407. [Google Scholar]
  85. Antunes, P.; Machado, J.; Peixe, L. Illegal use of nitrofurans in food animals: Contribution to human salmonellosis? Clin. Microbiol. Infect. 2006, 12, 1047–1049. [Google Scholar] [CrossRef] [PubMed]
  86. Dutil, L.; Irwin, R.; Finley, R.; Ng, L.K.; Avery, B.; Boerlin, P.; Bourgault, A.M.; Cole, L.; Daignault, D.; Desruisseau, A.; et al. Ceftiofur resistance in Salmonella enterica serovar Heidelberg from chicken meat and humans, Canada. Emerg. Infect. Dis. 2010, 16, 48. [Google Scholar] [CrossRef]
  87. Moulana, Z.; Asgharpour, F. Prevalence and Antimicrobial Resistance of Salmonella enterica Serovar Infantis Isolates from Poultry: A review. Poult. Sci. J. 2022, 10, 13–26. [Google Scholar]
  88. Nandi, S.; Maurer, J.J.; Hofacre, C.; Summers, A.O. Gram-positive bacteria are a major reservoir of Class 1 antibiotic resistance integrons in poultry litter. Proc. Natl. Acad. Sci. USA 2004, 101, 7118–7122. [Google Scholar] [CrossRef]
  89. Yang, Y.; Ashworth, A.J.; Willett, C.; Cook, K.; Upadhyay, A.; Owens, P.R.; Ricke, S.C.; DeBruyn, J.M.; Moore Jr, P.A. Review of antibiotic resistance, ecology, dissemination, and mitigation in US broiler poultry systems. Front. Microbiol. 2019, 10, 2639. [Google Scholar] [CrossRef] [PubMed]
  90. Didelot, X.; Fraser, C.; Gardy, J.; Colijn, C. Genomic Infectious Disease Epidemiology in Partially Sampled and Ongoing Outbreaks. Mol. Biol. Evol. 2017, 34, 997–1007. [Google Scholar] [CrossRef]
  91. Butel, M.J.; Waligora-Dupriet, A.J.; Wydau-Dematteis, S. The developing gut microbiota and its consequences for health. Dev. Orig. Health Dis. 2018, 9, 590–597. [Google Scholar] [CrossRef]
  92. Xu, Z.R.; Hu, C.H.; Xia, M.S.; Zhan, X.A.; Wang, M.Q. Effects of dietary fructooligosaccharide on digestive enzyme activities, intestinal microflora and morphology of male broilers. Poult. Sci. 2003, 82, 1030–1036. [Google Scholar] [CrossRef]
  93. Donalson, L.M.; McReynolds, J.L.; Kim, W.K.; Chalova, V.I.; Woodward, C.L.; Kubena, L.F.; Nisbet, D.J.; Ricke, S.C. The influence of a fructooligosaccharide prebiotic combined with alfalfa molt diets on the gastrointestinal tract fermentation, Salmonella enteritidis infection, and intestinal shedding in laying hens. Poult. Sci. 2008, 87, 1253–1262. [Google Scholar] [CrossRef] [PubMed]
  94. Charalampopoulos, D.; Rastall, R.A. (Eds.) Prebiotics and Probiotics Science and Technology; Springer Science & Business Media LLC: Berlin/Heidelberg, Germany, 2009. [Google Scholar]
  95. Durant, J.A.; Corrier, D.E.; Ricke, S.C. Short-chain volatile fatty acids modulate the expression of the hilA and invF genes of Salmonella typhimurium. J. Food Prot. 2000, 63, 573–578. [Google Scholar] [CrossRef]
  96. El-Shall, N.A.; Awad, A.M.; El-Hack, M.E.A.; Naiel, M.A.; Othman, S.I.; Allam, A.A.; Sedeik, M.E. The simultaneous administration of a probiotic or prebiotic with live Salmonella vaccine improves growth performance and reduces fecal shedding of the bacterium in Salmonella-challenged broilers. J. Anim. 2019, 10, 70. [Google Scholar] [CrossRef] [PubMed]
  97. Borchers, A.T.; Selmi, C.; Meyers, F.J.; Keen, C.L.; Gershwin, M.E. Probiotics and immunity. J. Gastroenterol. 2009, 44, 26–46. [Google Scholar] [CrossRef]
  98. Tellez, G.; Pixley, C.; Wolfenden, R.E.; Layton, S.L.; Hargis, B.M. Probiotics/direct fed microbials for Salmonella control in poultry. Food Res. Int. 2012, 45, 628–633. [Google Scholar] [CrossRef]
  99. Higgins, J.P.; Andreatti Filho, R.L.; Higgins, S.E.; Wolfenden, A.D.; Téllez, G.; Hargis, B.M. Evaluation of Salmonella-lytic properties of bacteriophages isolated from commercial broiler houses. Avian Dis. 2008, 52, 139–142. [Google Scholar] [CrossRef] [PubMed]
  100. Gheisar, M.M.; Hosseindoust, A.; Kim, I.H. Evaluating the effect of microencapsulated blends of organic acids and essential oils in broiler chickens diet. J. Appl. Poult. Res. 2015, 24, 511–519. [Google Scholar] [CrossRef]
  101. Amad, A.A.; Männer, K.; Wendler, K.R.; Neumann, K.; Zentek, J. Effects of a phytogenic feed additive on growth performance and ileal nutrient digestibility in broiler chickens. Poult. Sci. 2011, 90, 2811–2816. [Google Scholar] [CrossRef]
  102. Orndorff, B.W.; Novak, C.L.; Pierson, F.W.; Caldwell, D.J.; McElroy, A.P. Comparison of prophylactic or therapeutic dietary administration of capsaicin for reduction of Salmonella in broiler chickens. Avian Dis. 2005, 49, 527–533. [Google Scholar] [CrossRef]
  103. Solarte, A.L.; Astorga, R.J.; Aguiar, F.; Galán-Relaño, Á.; Maldonado, A.; Huerta, B. Combination of antimicrobials and essential oils as an alternative for the control of Salmonella enterica multiresistant strains related to foodborne disease. Foodborne Pathog. Dis. 2017, 14, 558–563. [Google Scholar] [CrossRef]
  104. Ebani, V.V.; Nardoni, S.; Bertelloni, F.; Tosi, G.; Massi, P.; Pistelli, L.; Mancianti, F. In vitro antimicrobial activity of essential oils against Salmonella enterica serotypes Enteritidis and Typhimurium strains isolated from poultry. Molecules 2019, 24, 900. [Google Scholar] [CrossRef]
  105. Rochín-Medina, J.J.; Mendoza-López, I.A.; Castro-del Campo, N.; Bastidas-Bastidas, P.J.; Ramírez, K. Activity of plant essential oils against clinically and environmentally isolated Salmonella enterica serotypes: In vitro assays and molecular docking. Lett. Appl. Microbiol. 2023, 76, ovad045. [Google Scholar] [CrossRef] [PubMed]
  106. Abedon, S.T.; Loc-Carrillo, C. Pros and cons of phage therapy. Bacteriophage 2011, 1, 111–114. [Google Scholar]
  107. Żbikowska, K.; Michalczuk, M.; Dolka, B. The use of bacteriophages in the poultry industry. Animals 2023, 10, 872. [Google Scholar] [CrossRef] [PubMed]
  108. Nilsson, A.S. Phage therapy—Constraints and possibilities. Ups. J. Med. Sci. 2014, 119, 192–198. [Google Scholar] [CrossRef] [PubMed]
  109. Wong, C.L.; Sieo, C.C.; Tan, W.S.; Abdullah, N.; Hair-Bejo, M.; Abu, J.; Ho, Y.W. Evaluation of a lytic bacteriophage, Φ st1, for biocontrol of Salmonella enterica serovar Typhimurium in chickens. Int. J. Food Microbiol. 2014, 172, 92–101. [Google Scholar] [CrossRef]
  110. Centre for Disease Control and Prevention. Whole Genome Sequencing. 2016. Available online: https://www.cdc.gov/pulsenet/pathogens/wgs.html (accessed on 5 November 2022).
  111. Acevedo-Villanueva, K.Y.; Akerele, G.O.; Al Hakeem, W.G.; Renu, S.; Shanmugasundaram, R.; Selvaraj, R.K. A Novel Approach against Salmonella: A Review of Polymeric Nanoparticle Vaccines for Broilers and Layers. Vaccines 2021, 9, 1041. [Google Scholar] [CrossRef]
  112. Renu, S.; Han, Y.; Dhakal, S.; Lakshmanappa, Y.S.; Ghimire, S.; Feliciano-Ruiz, N.; Senapati, S.; Narasimhan, B.; Selvaraj, R.; Renukaradhya, G.J. Chitosan-adjuvanted Salmonella subunit nanoparticle vaccine for poultry delivered through drinking water and feed. Carbohydr. Polym. 2020, 243, 116434. [Google Scholar] [CrossRef] [PubMed]
  113. Rabie, N.S.; Amin Girh, Z.M.S. Bacterial vaccines in poultry. Bull. Natl. Res. Cent. 2020, 44, 15. [Google Scholar] [CrossRef]
  114. Jia, S.; McWhorter, A.R.; Andrews, D.M.; Underwood, G.J.; Chousalkar, K.K. Challenges in Vaccinating Layer Hens against Salmonella Typhimurium. Vaccines 2020, 8, 696. [Google Scholar] [CrossRef]
  115. Shehata, A.M.; Paswan, V.K.; Attia, Y.A.; Abdel-Moneim, A.M.E.; Abougabal, M.S.; Sharaf, M.; Elmazoudy, R.; Alghafari, W.T.; Osman, M.A.; Farag, M.R.; et al. Managing gut microbiota through in ovo nutrition influences early-life programming in broiler chickens. J. Anim. 2021, 11, 3491. [Google Scholar] [CrossRef]
  116. Alagawany, M.; Elnesr, S.S.; Farag, M.R.; Abd El-Hack, M.E.; Barkat, R.A.; Gabr, A.A.; Foda, M.A.; Noreldin, A.E.; Khafaga, A.F.; El-Sabrout, K.; et al. Potential role of important nutraceuticals in poultry performance and health—A comprehensive review. Res. Vet. Sci. 2021, 137, 9–29. [Google Scholar] [CrossRef]
  117. Vaezirad, M.M.; Koene, M.G.; Wagenaar, J.A.; Van Putten, J.P.M. Chicken immune response following in ovo delivery of bacterial flagellin. Vaccine 2018, 36, 2139–2146. [Google Scholar] [CrossRef]
  118. Cox, C.M.; Dalloul, R.A. Immunomodulatory role of probiotics in poultry and potential in ovo application. Benef. Microbes 2015, 6, 45–52. [Google Scholar] [CrossRef]
  119. Li, S.; He, Y.; Mann, D.A.; Deng, X. Global spread of Salmonella Enteritidis via centralized sourcing and international trade of poultry breeding stocks. Nat. Commun. 2021, 12, 5109. [Google Scholar] [CrossRef]
  120. Calenge, F.; Lecerf, F.; Demars, J.; Feve, K.; Vignoles, F.; Pitel, F.; Vignal, A.; Velge, P.; Sellier, N.; Beaumont, C. QTL for resistance to Salmonella carrier state confirmed in both experimental and commercial chicken lines. Anim. Genet. 2009, 40, 590–597. [Google Scholar] [CrossRef]
  121. Patsias, A.; Chouliara, I.; Badeka, A.; Savvaidis, I.N.; Kontominas, M.G. Shelf-life of a chilled precooked chicken product stored in air and under modified atmospheres: Microbiological, chemical, sensory attributes. Food Microbiol. 2006, 23, 423–429. [Google Scholar] [CrossRef]
  122. Geornaras, I.; de Jesus, A.E.; von Holy, A. Bacterial populations associated with the dirty area of a South African poultry abattoir. J. Food Prot. 1998, 61, 700–703. [Google Scholar] [CrossRef] [PubMed]
  123. Russell, S.M. Salmonella reduction calls for multi-hurdle approach. WATT Poult. USA. 2010, 15487544. [Google Scholar]
  124. Scott, B.R.; Yang, X.; Geornaras, I.; Delmore, R.J.; Woerner, D.R.; Reagan, J.O.; Morgan, J.B.; Belk, K.E. Antimicrobial Efficacy of a Sulfuric Acid and Sodium Sulfate Blend, Peroxyacetic Acid, and Cetylpyridinium chloride against Salmonella on Inoculated Chicken Wings. J. Food Prot. 2015, 78, 1967–1972. [Google Scholar] [CrossRef]
  125. Smith, J.; Corkran, S.; McKee, S.R.; Bilgili, S.F.; Singh, M. Evaluation of post-chill applications of antimicrobials against Campylobacter jejuni on poultry carcasses. J. Appl. Poult. Res. 2015, 24, 451–456. [Google Scholar] [CrossRef]
  126. Bolton, D.J.; Meredith, H.; Walsh, D.; McDowell, D.A. The effect of chemical treatments in laboratory and broiler plant studies on the microbial status and shelf-life of poultry. Food Control. 2014, 36, 230–237. [Google Scholar] [CrossRef]
  127. Hinton, A.; Northcutt, J.K., Jr.; Smith, D.P.; Musgrove, M.T.; Ingram, K.D. Spoilage microflora of broiler carcasses washed with electrolyzed oxidizing or chlorinated water using an inside-outside bird washer. Poult. Sci. 2007, 86, 123–127. [Google Scholar] [CrossRef]
  128. Wideman, N.; Bailey, M.; Bilgili, S.F.; Thippareddi, H.; Wang, L.; Bratcher, C.; Sanchez-Plata, M.; Singh, M. Evaluating best practices for Campylobacter and Salmonella reduction in poultry processing plants. Poult. Sci. 2016, 95, 306–315. [Google Scholar] [CrossRef] [PubMed]
  129. Kim, Y.Y.; Kil, D.Y.; Oh, H.K.; Han, I.K. Acidifier as an alternative material to antibiotics in animal feed. Asian-Australas. J. Anim. Sci. 2005, 18, 1048–1060. [Google Scholar] [CrossRef]
  130. Dittoe, D.K.; Ricke, S.C.; Kiess, A.S. Organic acids and potential for modifying the avian gastrointestinal tract and reducing pathogens and disease. Front. Vet. Sci. 2018, 5, 216. [Google Scholar] [CrossRef]
  131. Ryan, D.; Ojha, U.K.; Jaiswal, S.; Padhi, C.; Suar, M. The small RNA DsrA influences the acid tolerance response and virulence of Salmonella enterica serovar Typhimurium. Front. Microbiol. 2016, 7, 599. [Google Scholar] [CrossRef]
  132. Madushanka, D.N.N.; Jayaweera, T.S.P.; Jayasinghe, J.M.C.S.; Yasawathie, D.G.; Ruwandeepika, H.A.D. Decontaminating effect of organic acids and natural compounds on broiler chicken meat contaminated with Salmonella typhimurium. Asian Food Sci. J. 2018, 3, 1–9. [Google Scholar] [CrossRef]
  133. Eltholth, M.M.; Mohamed, R.A.; Elgohary, F.A.; Abo Elfadl, E.A. Assessment of biosecurity practices in broiler chicken farms in Gharbia Governorate, Egypt. Alex. J. Vet. Sci. 2016, 49, 68. [Google Scholar] [CrossRef]
  134. Aiyedun, J.O.; Oludairo, O.O.; Olorunsola, I.D.; Daodu, O.B.; Furo, N.A. Effectiveness of biosecurity measures in some selected farms in Kwara state, Nigeria. J. Res. For. Wildl. Environ. 2018, 10, 17–23. [Google Scholar]
  135. Conan, A.; Goutard, F.L.; Sorn, S.; Vong, S. Biosecurity measures for backyard poultry in developing countries: A systematic review. BMC Vet. Res. 2012, 8, 240. [Google Scholar] [CrossRef]
  136. Kouam, M.K.; Jacouba, M.; Nsangou, I.N.; Teguia, A. Assessment of biosecurity level in small-scale broiler farms in the Western highlands of Cameroon (Central Africa). Trop. Anim. Health Prod. 2018, 50, 1529–1538. [Google Scholar] [CrossRef]
  137. Wijesinghe, W.M.J.B.; De Silva, P.G.J.C.; Gunaratne, S.P. Evaluation of biosecurity status in commercial broiler farms in Sri Lanka. Int. J. Sci. Res. Publ. 2017, 7, 114–119. [Google Scholar]
  138. Fouladkhah, A. The Need for evidence-based outreach in the current food safety regulatory landscape. J. Ext. 2017, 55, 20. [Google Scholar] [CrossRef]
Figure 1. Practical considerations for reducing the public health burden of foodborne salmonellosis associated with poultry products.
Figure 1. Practical considerations for reducing the public health burden of foodborne salmonellosis associated with poultry products.
Ijerph 20 06654 g001
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Raut, R.; Maharjan, P.; Fouladkhah, A.C. Practical Preventive Considerations for Reducing the Public Health Burden of Poultry-Related Salmonellosis. Int. J. Environ. Res. Public Health 2023, 20, 6654. https://doi.org/10.3390/ijerph20176654

AMA Style

Raut R, Maharjan P, Fouladkhah AC. Practical Preventive Considerations for Reducing the Public Health Burden of Poultry-Related Salmonellosis. International Journal of Environmental Research and Public Health. 2023; 20(17):6654. https://doi.org/10.3390/ijerph20176654

Chicago/Turabian Style

Raut, Rabin, Pramir Maharjan, and Aliyar Cyrus Fouladkhah. 2023. "Practical Preventive Considerations for Reducing the Public Health Burden of Poultry-Related Salmonellosis" International Journal of Environmental Research and Public Health 20, no. 17: 6654. https://doi.org/10.3390/ijerph20176654

APA Style

Raut, R., Maharjan, P., & Fouladkhah, A. C. (2023). Practical Preventive Considerations for Reducing the Public Health Burden of Poultry-Related Salmonellosis. International Journal of Environmental Research and Public Health, 20(17), 6654. https://doi.org/10.3390/ijerph20176654

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