Epidemiology and antimicrobial resistance of dominant Salmonella serotypes in Iraqi broiler hatcheries: a comprehensive One Health analysis

Authors

DOI:

https://doi.org/10.31210/spi2026.29.02.14

Keywords:

Salmonella Enteritidis, Salmonella Kentucky, Iraq, hatchery, multidrug resistance, One Health, antimicrobial resistance

Abstract

Hatcheries are critical points for Salmonella dissemination, and the distribution of its serotypes significantly impacts public health. Despite this global threat, surveillance deficits remain regarding these foodborne pathogens within regional production environments. To address these gaps, this investigation evaluated the occurrence rates, serotype distribution, and antimicrobial resistance profiles of bacterial isolates recovered from commercial broiler production facilities. A multi-facility cross-sectional study was conducted from march to october 2023, encompassing 450 specimens stratified equally into 150 chick cecal contents, 150 eggshells, and 150 worker hand swabs. Microbiological isolation followed international horizontal protocols. Biochemical profiling and slide agglutination methods were employed for serovar identification, while phenotypic susceptibility profiles were determined utilizing the disk diffusion method under clinical laboratory criteria. The analysis detected an overall pathogen prevalence of 8.4 %, corresponding to 38 positive samples out of the 450 tested. Specific isolation rates were distributed across chick ceca at 12.0 % (18 positive samples), eggshells at 7.3 % (11 positive samples), and worker hands at 6.0 % (9 positive samples). Serological typing revealed a predominance of Salmonella Enteritidis at 34.2 % (13 isolates) and Salmonella Kentucky at 26.3 % (10 isolates), each exhibiting alarming multidrug resistance at 38.5 % (5 isolates) and 60.0 % (6 isolates), respectively. Notably, the recovered Salmonella Kentucky strains demonstrated concerning ciprofloxacin resistance at 40.0 % (4 isolates) and cefotaxime resistance at 20.0 % (2 isolates). Both dominant serotypes were consistently recovered from all three sample matrices, demonstrating active circulation within the facilities. In conclusion, commercial broiler facilities serve as reservoirs for highly resistant multidrug-resistant strains. The concurrent presence of a classic egg-associated pandemic variant and an environmentally durable, fluoroquinolone-resistant clone represents a severe threat to food safety. This scenario calls for the immediate implementation of an integrative national health framework incorporating environmental biosecurity measures, strict antimicrobial stewardship, and ongoing systematic monitoring across the production continuum.

References

1. Kirk, M. D., Pires, S. M., Black, R. E., Caipo, M., Crump, J. A., Devleesschauwer, B., Döpfer, D., Fazil, A., Fischer- Walker, C. L., Hald, T., Hall, A. J., Keddy, K. H., Lake, R. J., Lanata, C. F., Torgerson, P. R., Havelaar, A. H., & Angulo, F. J. (2015). World Health Organization estimates of the global and regional disease burden of 22 foodborne bacterial, protozoal, and viral diseases, 2010: a data synthesis. PLOS Medicine, 12(12), e1001921. https://doi.org/10.1371/journal.pmed.1001921

2. Havelaar, A. H., Kirk, M. D., Torgerson, P. R., Gibb, H. J., Hald, T., Lake, R. J., Praet, N., Bellinger, D. C., de Silva, N. R., Gargouri, N., Speybroeck, N., Cawthorne, A., Mathers, C., Stein, C., Angulo, F. J., & Devleesschauwer, B. (2015). World Health Organization global estimates and regional comparisons of the burden of foodborne disease in 2010. PLoS Medicine, 12(12), e1001923. https://doi.org/10.1371/journal.pmed.1001923

3. Issenhuth-Jeanjean, S., Roggentin, P., Mikoleit, M., Guibourdenche, M., de Pinna, E., Nair, S., Fields, P. I., & Weill, F.-X. (2014). Supplement 2008–2010 (no. 48) to the White-Kauffmann-Le Minor scheme. Research in Microbiology, 165(7), 526–530. https://doi.org/10.1016/j.resmic.2014.07.004

4. Samad, A., Hamza, M., Muazzam, A., Ahmer, A., Tariq, S., Shahid, M. J., Din, F. U., Akram, W., Kaleem, M. Z., & Ahmad, S. (2022). Overview of bacterial diseases in poultry and policies to control disease and antibiotic resistance. BULLET: Jurnal Multidisiplin Ilmu, 1(1), 1–5.

5. Almashhadany, D. A., Hassan, A. A., & Khan, I. U. H. (2025). Prevalence, serotypes, and antimicrobial resistance of Salmonella species in ready-to-eat foods in Erbil, Iraq. Microorganisms, 13(10), 2225. https://doi.org/10.3390/microorganisms13102225

6. Kanaan, M. H. G. (2023). Prevalence and antimicrobial resistance of Salmonella enterica serovars Enteritidis and Typhimurium isolated from retail chicken meat in Wasit markets, Iraq. Veterinary World, 455–463. https://doi.org/10.14202/vetworld.2023.455-463

7. Shafee, A., & Abdulwahid, M. (2024). Occurrence, antimicrobial resistance, and molecular characterization of Salmonella enterica from chicken products and human in Wasit Governorate of Iraq. Open Veterinary Journal, 14(5), 1117. https://doi.org/10.5455/ovj.2024.v14.i5.5

8. Ali, N., Abdulrahman, N., Aziz, S., & Hassan, S. (2023). Pathological and molecular investigation of paratyphoid Salmonella infection in broiler chicks in Sulaymaniyah province, Kurdistan/Iraq. Basrah Journal of Veterinary Research, 22(3), 42–56. https://doi.org/10.23975/bjvetr.2023.142197.1036

9. Gantois, I., Ducatelle, R., Pasmans, F., Haesebrouck, F., Gast, R., Humphrey, T. J., & Van Immerseel, F. (2009). Mechanisms of egg contamination by Salmonella Enteritidis. FEMS Microbiology Reviews, 33(4), 718–738. https://doi.org/10.1111/j.1574-6976.2008.00161.x

10. Şik, Z., & Akan, M. (2024). Determination of antibiotic resistance in Salmonella Typhimurium and Salmonella Kentucky serotypes of animal origin using conventional and molecular methods. Turkish Journal of Veterinary &Amp; Animal Sciences, 48(1), 72–81. https://doi.org/10.55730/1300-0128.4338

11. International Organization for Standardization. (2017). Microbiology of the food chain – Horizontal method for the detection, enumeration and serotyping of Salmonella – Part 1: Detection of Salmonella spp. (ISO Standard No. 6579-1:2017). https://www.iso.org/obp/ui/#iso:std:iso:6579:-1:ed-1:v1:en

12. Grimont, P. A. D., & Weill, F.-X. (2007). Antigenic formulae of the Salmonella serovars (9th ed.). WHO Collaborating Centre for Reference and Research on Salmonella; Institut Pasteur.

13. Cox, N. A., Bailey, J. S., Mauldin, J. M., & Blankenship, L. C. (1990). Research note: presence and impact of Salmonella contamination in commercial broiler hatcheries. Poultry Science, 69(9), 1606–1609. https://doi.org/10.3382/ps.0691606

14. Abdel-Maksoud, M., Abdel-Khalek, R., El-Gendy, A., Gamal, R. F., Abdelhady, H. M., & House, B. L. (2015). Genetic characterisation of multidrug-resistant Salmonella enterica serotypes isolated from poultry in Cairo, Egypt. African Journal of Laboratory Medicine, 4(1). https://doi.org/10.4102/ajlm.v4i1.158

15. Price, L. B., Graham, J. P., Lackey, L. G., Roess, A., Vailes, R., & Silbergeld, E. (2007). Elevated risk of carrying gentamicin-resistant Escherichia coli among U.S. poultry workers. Environmental Health Perspectives, 115(12), 1738–1742. https://doi.org/10.1289/ehp.10191

16. Whiley, H., & Ross, K. (2015). Salmonella and eggs: from production to plate. International Journal of Environmental Research and Public Health, 12(3), 2543–2556. https://doi.org/10.3390/ijerph120302543

17. Le Hello, S., Bekhit, A., Granier, S. A., Barua, H., Beutlich, J., Zając, M., Münch, S., Sintchenko, V., Bouchrif, B., Fashae, K., Pinsard, J.-L., Sontag, L., Fabre, L., Garnier, M., Guibert, V., Howard, P., Hendriksen, R. S., Christensen, J. P., Biswas, P. K., Cloeckaert, A., Rabsch, W., Wasyl, D., Doublet, B., & Weill, F.-X. (2013). The global establishment of a highly-fluoroquinolone resistant Salmonella enterica serotype Kentucky ST198 strain. Frontiers in Microbiology, 4, 395. https://doi.org/10.3389/fmicb.2013.00395

18. Borges, K., Furian, T., Souza, S., Salle, C., Moraes, H., & Nascimento, V. (2019). Antimicrobial resistance and molecular characterization of salmonella Enterica serotypes isolated from poultry sources in Brazil. Brazilian Journal of Poultry Science, 21(1). https://doi.org/10.1590/1806-9061-2018-0827

19. Ziech, R. E., Lampugnani, C., Perin, A. P., Sereno, M. J., Sfaciotte, R. A. P., Viana, C., Soares, V. M., de Almeida Nogueira Pinto, J. P., & dos Santos Bersot, L. (2016). Multidrug resistance and ESBL-producing Salmonella spp. isolated from broiler processing plants. Brazilian Journal of Microbiology, 47(1), 191–195. https://doi.org/10.1016/j.bjm.2015.11.021

20. Xiong, Z., Wang, S., Huang, Y., Gao, Y., Shen, H., Chen, Z., Bai, J., Zhan, Z., Wen, J., Liao, M., & Zhang, J. (2020). Ciprofloxacin-resistant Salmonella enterica serovar Kentucky ST198 in broiler chicken supply chain and patients, China, 2010–2016. Microorganisms, 8(1), 140. https://doi.org/10.3390/microorganisms8010140

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Published

2026-09-12

How to Cite

Ali, H. I. (2026). Epidemiology and antimicrobial resistance of dominant Salmonella serotypes in Iraqi broiler hatcheries: a comprehensive One Health analysis. Scientific Progress & Innovations, 29(2), 95–101. https://doi.org/10.31210/spi2026.29.02.14