Article
Salmonella in Poultry: Epidemiology, Food Safety Risk, and the Growing Challenge of Antimicrobial Resistance
Salmonella remains one of the most important zoonotic pathogens associated with poultry production and public health. Although the infectious dose for salmonellosis is typically high (10⁷–10⁹ CFU/g), it can vary depending on food composition and host health status1,2. Notably, high-fat food matrices may lower the infectious dose, increasing the risk of infection even at reduced contamination levels1. This variability makes food safety risk assessment highly context-dependent in poultry-derived products.
Poultry and Foodborne Transmission
Poultry products remain the most important reservoir for human infection. Major food vehicles include meat, eggs, milk, pork, beef, and vegetables.
Serotype distribution in animals shows1:
- Salmonella Enteritidis: predominantly poultry and eggs
- Salmonella Typhimurium: broad host range (poultry, pigs, cattle)
- Salmonella Gallinarum, Salmonella Pullorum, Salmonella Heidelberg: associated with egg contamination
Routes of Egg Contamination
Egg contamination occurs through two main pathways1:
1. Horizontal transmission
- Fecal contamination of eggshell
- Contaminated litter, dust, feed, water, and environment
2. Vertical transmission
- Infection of reproductive organs
- Internal contamination of yolk, albumen, or membranes before oviposition
Both pathways are critical in hatchery and breeder management systems.
Antibiotic Use and Resistance Development
Approximately 8 million kg of antibiotics are used annually in animal farming, with nearly 70% used for non-therapeutic purposes such as growth promotion and disease prevention. In contrast, only 1.3 million kg are used in human medicine1.
This disproportionate usage contributes to:
- Selection of resistant gut microbiota
- Environmental contamination via fecal shedding
- Emergence of multidrug-resistant (MDR) Salmonella strains
Antimicrobial Resistance in Poultry-Associated Salmonella
High levels of antimicrobial resistance (AMR) are frequently reported in poultry-derived Salmonella, particularly in eggs.
Common resistance patterns include1,3,4:
- Nalidixic acid and ampicillin (high resistance)
- Tetracyclines and fluoroquinolones (variable resistance)
- Ampicillin, amoxicillin, ciprofloxacin, and colistin (complete resistance in some regions)
- Broad β-lactam resistance including amoxicillin, cefazolin, penicillin, and piperacillin
Resistance is further amplified by mobile genetic elements such as IncA/C plasmids, which carry genes conferring resistance to multiple antibiotic classes including β-lactams, aminoglycosides, tetracyclines, chloramphenicol, and sulfonamides5.
Additionally, poultry litter acts as a reservoir for horizontal transfer of resistance genes, increasing environmental dissemination risk.
Field and Public Health Implications
MDR Salmonella infections lead to:
- Longer treatment duration
- Increased hospitalization and costs
- Reduced therapeutic success
- Food safety threats across the production chain
If uncontrolled, this trend poses risks not only to human health but also to food security and environmental stability.
Conclusion
The epidemiology of Salmonella in poultry is shaped by complex interactions between host, environment, management practices, and antimicrobial use. While improvements in hygiene, biosecurity, and regulatory controls have reduced antimicrobial dependency in many regions, MDR Salmonella remains a persistent global challenge.
A sustainable control strategy must integrate:
- Strong biosecurity and hygiene systems
- Surveillance and monitoring programs
- Rational antimicrobial use
- Development of alternative, non-antibiotic technologies
Ultimately, reducing dependence on antibiotics while maintaining food safety remains the central goal for poultry production systems worldwide.
References
- Khan MA, Rahman SR. Use of phages to treat antimicrobial-resistant Salmonella infections in poultry. Veterinary Sciences. 2022 Aug 18;9(8):438. https://www.mdpi.com/2306-7381/9/8/438
- Chen HM, Wang Y, Su LH, Chiu CH. Nontyphoid Salmonella infection: microbiology, clinical features, and antimicrobial therapy. Pediatrics & Neonatology. 2013 Jun 1;54(3):147-52. https://www.sciencedirect.com/science/article/pii/S1875957213000119
- Castro-Vargas RE, Herrera-Sánchez MP, Rodríguez-Hernández R, Rondón-Barragán IS. Antibiotic resistance in Salmonella spp. isolated from poultry: A global overview. Veterinary world. 2020 Oct 3;13(10):2070. https://pmc.ncbi.nlm.nih.gov/articles/PMC7704309/pdf/Vetworld-13-2070.pdf
- Khan M. Prevalence and multidrug-resistant pattern of Salmonella from the eggs and egg-storing trays of retail markets of Bangladesh. International Journal of One Health. 2016 Jan 1. https://www.academia.edu/download/98739110/2.pdf
- Hoffmann M, Pettengill JB, Gonzalez-Escalona N, Miller J, Ayers SL, Zhao S, Allard MW, McDermott PF, Brown EW, Monday SR. Comparative sequence analysis of multidrug-resistant IncA/C plasmids from Salmonella enterica. Frontiers in microbiology. 2017 Aug 7;8:1459. https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2017.01459/pdf
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