A Review of Avian Pathogenic Escherichia coli (APEC) in Guinea Fowls (Numida meleagris) of Southern Africa: Antimicrobial Resistance and Virulence Genomics and Control Strategies.

Authors

Nyararai Yvonne O

Department of Animal and Wildlife Sciences, Midlands State University, Gweru (Zimbabwe)

Ndau Blessing M

Department of Land and Water Management, Midlands State University, Gweru (Zimbabwe)

Muzvondiwa John V

IFAD - Horticulture Enterprise Enhancement Project (HEEP). Climate Smart Agriculture and Environmental Safeguard Specialist; Masvingo Region (Zimbabwe)

Nyoni-Phili Sizanobuhle L

Department of Animal and Wildlife Sciences, Midlands State University, Gweru (Zimbabwe)

Article Information

DOI: 10.51244/IJRSI.2026.13010152

Subject Category: Microbiology

Volume/Issue: 13/1 | Page No: 1737-1747

Publication Timeline

Submitted: 2026-01-27

Accepted: 2026-02-02

Published: 2026-02-10

Abstract

Avian Pathogenic Escherichia coli (APEC), the primary causative agent of colibacillosis, is a major and growing threat to global poultry production, leading to significant economic losses. In Southern Africa, the guinea fowl (Numida meleagris) is an economically, culturally, and nutritionally important indigenous poultry species for local communities. However, its production is constrained by infectious diseases such as colibacillosis posing a significant yet understudied challenge. This review synthesises the current, albeit limited, knowledge on APEC in Southern African guinea fowls. We detail the key virulence genes including adhesins (fimH), iron acquisition systems (iutA, fyuA), and immune evasion factors (iss) that facilitate pathogenesis. A critical concern is the convergence of these virulence genes with multidrug resistance (MDR) on mobile genetic elements. This fusion drives the emergence of dangerous, high-risk bacterial clones. Genomic studies confirm that APEC shares significant genetic overlap with human extra-intestinal pathogenic E. coli (ExPEC), such as sequence types ST95 and ST131, underscoring a substantial zoonotic threat. While conventional PCR has been instrumental in initial virulence profiling, we advocate for the widespread application of Whole-Genome Sequencing (WGS) to elucidate the unique population structure of guinea fowl APEC, precisely assess zoonotic risk, and guide interventions. Effective control requires an integrated, One Health approach encompassing stringent antibiotic stewardship, enhanced genomic surveillance, and the development of targeted strategies such as vaccines, phage therapy, and robust biosecurity measures tailored to guinea fowl farming systems. Filling these knowledge gaps is essential for safeguarding guinea fowl health, ensuring food security, and mitigating the public health crisis of antimicrobial resistance.

Keywords

Avian Pathogenic E. coli (APEC), Guinea Fowl, Virulence Genes, Antimicrobial Resistance, One Health.

Downloads

References

1. Abdallah, N., & Oluwaseun, O. A. (2025). Socio-economic and production dynamics of Guinea fowl farming in Northern Ghana: Insights into health management, challenges, and climate change impacts. Tropical Animal Health and Production, 57(181). https://doi.org/10.1007/s11250-025-04427-2 [Google Scholar] [Crossref]

2. Abdallah, N., & Oyebamiji, O. A. (2024). Guinea fowl production in Africa: Economic importance and constraints. Egyptian Veterinary Science, 18 (1), 1–5. [Google Scholar] [Crossref]

3. Abdelhamid, M. K., Hess, C., Bilic, I., Reicher, M., Tarbiat, B., Razzazi-Fazeli, E., Schmalwieser, A. W., [Google Scholar] [Crossref]

4. Hess, M., & Selberherr, E. (2024). A comprehensive study of colisepticaemia progression in layer chickens applying novel tools elucidates pathogenesis and transmission of Escherichia coli into eggs. Scientific Reports, 14, 8111. https://doi.org/10.1038/s41598-024-58794-1 [Google Scholar] [Crossref]

5. Adzitey, F., Agbolosu, A. A., & Udoka, U. J. (2019). Antibacterial Effect of Aloe Vera Gel Extract on Escherichia coli and Salmonella enterica Isolated from the Gastrointestinal Tract of Guinea Fowls. World’s Veterinary Journal, 9(3), 166–173. [Google Scholar] [Crossref]

6. Akanbi, O. B., Olorunshola, I. D., Osilojo, P., Ademola, E., Agada, G. O. A., Aiyedun, J. O., Odita, C. I., & Ola-Fadunsin, S. D. (2022). Escherichia coli Infections, and Antimicrobial Resistance In Poultry Flocks, in North Central Nigeria. MKH, 33(3), 188–207 [Google Scholar] [Crossref]

7. Alonso, C. A., Zarazaga, M., Ben Sallem, R., Jouini, A., Ben Slama, K., & Torres, C. (2017). Antibiotic resistance in Escherichia coli in husbandry animals: The African perspective. Letters in Applied Microbiology, 64(4), 318–334. https://doi.org/10.1111/lam.12724 [Google Scholar] [Crossref]

8. Barbieri, N. L., Vande Vorde, J. A., Baker, A. R., Horn, F., Li, G., Logue, C. M., & Ilcebaylik and Turkyilmaz, 2020, L. K. (2017). FNR regulates the expression of important virulence factors contributing to the pathogenicity of avian pathogenic Escherichia coli. Frontiers in Cellular and Infection Microbiology, 7, 265. https://doi.org/10.3389/fcimb.2017.00265 [Google Scholar] [Crossref]

9. Borges, C. A., Beraldo, L. G., Maluta, R. P., Cardozo, M. V., Barboza, K. B., Guastalli, E. A. L., & Ávila, F. A. (2017). Multidrug-resistant pathogenic Escherichia coli isolated from wild birds in a veterinary hospital. Avian Pathology, 46(1), 76-83. [Google Scholar] [Crossref]

10. Borzi, M. M., Cardozo, M. V., de Oliveira, E. S., Pollo, A. S., Guastalli, E. A. L., dos Santos, L. F., & de Ávila, F. A. (2018). Characterization of avian pathogenic Escherichia coli isolated from free-range [Google Scholar] [Crossref]

11. helmeted guinea fowl. Brazilian Journal of Microbiology, 49(Suppl 1), 107– [Google Scholar] [Crossref]

12. https://doi.org/10.1016/j.bjm.2018.04.011 [Google Scholar] [Crossref]

13. Doi, Y., Iovleva, A., & Bonomo, R. A. (2017). The ecology of extended-spectrum beta-lactamases [Google Scholar] [Crossref]

14. (ESBLs) in the developed world. Journal of Travel Medicine,24S44–S51. https://doi.org/10.1093/jtm/taw102 [Google Scholar] [Crossref]

15. Dozois, C. M., Dho-Moulin, M., Brée, A., Fairbrother, J. M., Desautels, C., & Curtiss, R. III. (2000). Relationship between the Tsh autotransporter and pathogenicity of avian Escherichia coli and localization and analysis of the Tsh genetic region. Infection and Immunity, 68(7), 4145–4154. https://doi.org/10.1128/IAI.68.7.4145-4154.2000 [Google Scholar] [Crossref]

16. Dube, N., & Mbanga, J. (2018). Molecular characterization and antibiotic resistance patterns of avian fecal Escherichia coli from turkeys, geese, and ducks. Veterinary World, 11(6), 859. [Google Scholar] [Crossref]

17. Dziva, F., & Stevens, M. P. (2008). Colibacillosis in poultry: Unravelling the molecular basis of virulence of avian pathogenic Escherichia coli in their natural hosts. Avian Pathology, 37(4), 355–366. [Google Scholar] [Crossref]

18. Feng, A., Akter, S., and Leigh, S. A. (2023). Genomic diversity, pathogenicity and antimicrobial resistance of Escherichia coli isolated from poultry in the southern United States. BMC Microbiology, 23, 15. [Google Scholar] [Crossref]

19. Foster-Nyarko E., Alikhan N., Ravi N., Thomson N.M., Jarju S., Kwambana- Adams B.A., Secka A., O’Grady J., Antonio M., & Pallen M.J. (2021). Genomic diversity of Escherichia coli isolates from backyard chickens and guinea fowl in the Gambia. Microbial Genomics,7:00048. https//doi.org/10.1099/mgen.0.000484 [Google Scholar] [Crossref]

20. Gao, Q., Wang, X., Xu, H., Xu, Y., Ling, J., Zhang, D., Gao, S., & Liu, X. (2012). Roles of iron acquisition systems in virulence of extraintestinal pathogenic Escherichia coli: Salmochelin and aerobactin contribute more to virulence than heme in a chicken infection model. BMC Microbiology, 12(1), 143. https://doi.org/10.1186/1471-2180-12-143 [Google Scholar] [Crossref]

21. Gil, J. D., Reidsma, P., Giller, K., Todman, L., Whitmore, A., & van Ittersum, M. (2019). Sustainable development goal 2: Improved targets and indicators for agriculture and food security. Ambio, 48(7), 685– 698. https://doi.org/10.1007/s13280-018-1101-4 [Google Scholar] [Crossref]

22. Gono, R. K., Svinurai, W., & Muzvondiwa, J. V. (2013). Constraints and opportunities to Guinea fowl production in Zimbabwe: A case study of the Midlands Province, Zimbabwe. International Journal of Science and Research, 2(3), 236–239. [Google Scholar] [Crossref]

23. Ibrahim, G. A., Salah-Eldein, A. M., Al-Zaban, M. I., El-Oksh, A. S. A., Ahmed, E. M., Farid, D. S., & Saad, E. M. (2023). Monitoring the genetic variation of some Escherichia coli strains in wild birds and cattle. Open Journal of Veterinary Research, 10(1), 1–10. [Google Scholar] [Crossref]

24. Ilcebaylik, A. and Turkyilmaz, S. (2020). Investigation of Important Virulence Genes and Antibiotic Resistance of Escherichia coli Isolated from Broiler Chickens. Israel Journal of Veterinary Medicine 75 (4), 204-214. [Google Scholar] [Crossref]

25. Janßen, T., Schwarz, C., Preikschat, P., et al. (2001). Virulence-associated genes in avian pathogenic Escherichia coli (APEC) isolated from internal organs of poultry having died from colibacillosis. International Journal of Medical Microbiology, 291, 371–378. [Google Scholar] [Crossref]

26. Jordan, T. J., & Kariyawasam, S. A. (2010). Sequence analysis and characterization of a transferable hybrid plasmid encoding multidrug resistance and enabling zoonotic potential for extra intestinal Escherichia coli. Infection and Immunity, 78(5), 1931–1942. https://doi.org/10.1128/IAI.01259-09 [Google Scholar] [Crossref]

27. Kaper, J.B., Nataro, J.P., and Mobley, H.L.T. (2004). Pathogenic Escherichia coli. Nat Rev Microbiol 2:123–40. [Google Scholar] [Crossref]

28. Karikari, B.R.F, Adomako, A.R., Prince, A., Armstrong, D. and Alhassan, H.J. (2024). The state of Guinea fowl production and challenges faced by the industry in Ghana. International Journal of Current Research, 16, (03), 27535-27542. [Google Scholar] [Crossref]

29. Kathayat, D., Lokesh, D., Ranjit, S., & Rajashekara, G. (2021). Avian Pathogenic Escherichia coli (APEC): An overview of virulence and pathogenesis factors, zoonotic potential, and control strategies. Pathogens, 10(4), 467. https://doi.org/10.3390/pathogens10040467 [Google Scholar] [Crossref]

30. Khairullah, A. R., Afnani, D. A., Riwu, K. H. P., Widodo, A., Yanestria, S. M., Moses, I. B., & Raissa, R. (2024). Avian pathogenic Escherichia coli: Epidemiology, virulence and pathogenesis, diagnosis, pathophysiology, transmission, vaccination, and control. Veterinary World, 17(12), 2747. [Google Scholar] [Crossref]

31. Kusina, N. T., Saina, H., Kusina, J. F., & Lebel, S. (2012). An insight into guinea fowl rearing practices and productivity by guinea fowl keepers in Zimbabwe. African Journal of Agricultural Research, 7(25), 3621–3625. [Google Scholar] [Crossref]

32. Landman, W. J. M., Buter, G.J., Dijkman, R., & van Eck, J. H. H. (2014). Molecular typing of avian pathogenic Escherichia coli colonies originating from outbreaks of E. coli peritonitis syndrome in chicken flocks. Avian Pathology, 43(4), 345-356. https://doi.org/10.1080/03079457.2014.935291 [Google Scholar] [Crossref]

33. Lengthang, B., Tellah, M., Nideou, D., Assadi, M., Odjigue, N., & Logtene, Y. M. (2023). Guinea fowl farming and its egg production in the Western Tandjile Department, Chad. International Journal of Poultry Science, 22(1), 24–30. [Google Scholar] [Crossref]

34. Liu, Z., Wang, K., Zhang, Y., Xia, L., Zhao, L., Guo, C., Liu, X., Qin, L., & Hao, Z. (2021). High prevalence and diversity characteristics of blaNDM, mcr, and blaESBLs harboring multidrug-resistant [Google Scholar] [Crossref]

35. Escherichia coli from chicken, pig, and cattle in China. Frontiers in Cellular and Infection Microbiology, 11, 755545. https://doi.org/10.3389/fcimb.2021.755545 [Google Scholar] [Crossref]

36. Mageiros, L., Méric, G., Bayliss, S. C., Pensar, J., Pascoe, B., Mourkas, E., & Sheppard, S. K. (2021). Genome evolution and the emergence of pathogenicity in avian Escherichia coli. Nature communications, 12(1), 765. [Google Scholar] [Crossref]

37. Malesa, R., Pierneef, R., Magwedere, K., Mafuna, T., & Matle, I. (2024). Genomic characterisation of generic Escherichia coli from food-producing animals and products of animal origin in South Africa. Frontiers in Bacteriology, 3, 1432292. https://doi.org/10.3389/fbrio.2024.1432292 [Google Scholar] [Crossref]

38. Maron, D. F., Smith, T. J. S., & Nachman, K. E. (2013). Restrictions on antimicrobial use in food animal production: An international regulatory and economic survey. Globalization and Health, 9(1), 48. https://doi.org/10.1186/1744-8603-9-48 [Google Scholar] [Crossref]

39. Mellata M. (2013). Human and avian extraintestinal pathogenic Escherichia coli: infections, zoonotic risks, and antibiotic resistance trends. Foodborne Pathogenic Diseases 10 (1),916–932. [Google Scholar] [Crossref]

40. Mosimann, S., Desiree, K., & Ebner, P. (2021). Efficacy of phage therapy in poultry: A systematic review and meta-analysis. Poultry Science, 100(12), 101477. https://doi.org/10.1016/j.psj.2021.101477 [Google Scholar] [Crossref]

41. Motola, G., Hafez, H. M., & Brüggemann-Schwarze, S. (2023). Assessment of three alternative methods for bacterial disinfection of hatching eggs in comparison with conventional approach in commercial broiler hatcheries. PloS one, 18(3), e0283699. [Google Scholar] [Crossref]

42. Oscarsson, J., Westermark, M., Löfdahl, S., Olsen, B., Palmgren, H., Mizunoe, Y., Wai, S. N., & Uhlin, B. E. (2002). Characterization of a pore-forming cytotoxin expressed by Salmonella enterica serovars typhi and paratyphi A.Infection and Immunity, 70(10), 5759–5769. https://doi.org/10.1128/IAI.70.10.5759-5769.2002 [Google Scholar] [Crossref]

43. Osman, K. M., Kappell, A. D., Elhadidy, M., ElMougy, F., El-Ghany, W. A. A., Orabi, A., Mubarak, A. S., Dawoud, T. M., Hemeg, H. A., Moussa, I. M. I., & Hessain, A. M. (2018). Poultry hatcheries as potential reservoirs for antimicrobial-resistant Escherichia coli: A risk to public health and food safety. Scientific Reports, 8, 5859. https://doi.org/10.1038/s41598-018-23962-7 [Google Scholar] [Crossref]

44. Schouler, C., Schaeffer, B., Bree, A., Mora, A., Dahbi, G., Biet, F., Oswald, E., & Moulin-Schouleur, M. (2012). Diagnostic strategy for identifying avian pathogenic Escherichia coli based on four patterns of virulence genes. Journal of Clinical Microbiology, 50(5), 1673–1678. https://doi.org/10.1128/JCM.0505711 [Google Scholar] [Crossref]

45. Soara, A. E., Talaki, E., & Tona, K. (2020). Characteristics of indigenous guinea fowl (Numida meleagris) family poultry production in northern Togo. Tropical Animal Health and Production, 52(6), 3755-3767. [Google Scholar] [Crossref]

46. Standley, C. J., Carlin, E. P., Sorrell, E. M., Barry, A. M., Bile, E., Diakite, A. S., Keita, M. S., Koivogui, L., Mane, S., Martel, L. D., & Katz, R. (2019). Assessing health systems in Guinea for prevention and control of priority zoonotic diseases: A One Health approach. One Health, 7, 100101. https://doi.org/10.1016/j.onehlt.2019.100101 [Google Scholar] [Crossref]

47. Suzuki, Y., Sato, T., Fukushima, Y., Nakajima, C., Suzuki, Y., Takahashi, S., & Yokota, S. I. (2020). Contribution of beta-lactamase and efflux pump overproduction to tazobactam-piperacillin resistance in clinical isolates of Escherichia coli. International Journal of Antimicrobial Agents, 55(3), 105919. https://doi.org/10.1016/j.ijantimicag.2020.105919 [Google Scholar] [Crossref]

48. Tcheou, P., Bedekelabou, A. P., Adjei-Mensah, B., Kpomasse, C. C., Talaki, E., & Salou, M. (2025). Antibiotic use and residue detection in guinea fowl eggs in rural Togo: An assessment of practices and risks. Veterinary and Animal Science, 28, 100110. [Google Scholar] [Crossref]

49. Tivendale, K. A., Allen, J. L., Ginns, C. A., Crabb, B. S., & Browning, G. F. (2004). Association of iss and iucA, but not tsh, with plasmid-mediated virulence of avian pathogenic Escherichia coli. Infection and Immunity, 72(11), 6554–6560. https://doi.org/10.1128/IAI.72.11.6554-6560.2004 [Google Scholar] [Crossref]

50. Tong, P., Sun, Y., Ji, X., Du, X., Guo, X., Liu, J., Zhu, L., Zhou, B., Zhou, W., Liu, G., & Li, T. (2015). Characterization of antimicrobial resistance and extended-spectrum beta-lactamase genes in Escherichia coli isolated from chickens. Foodborne Pathogens and Disease, 12(4), 345–352. https://doi.org/10.1089/fpd.2014.1874 [Google Scholar] [Crossref]

51. Van Boeckel, T. P., Brower, C., Gilbert, M., Grenfell, B. T., Levin, S. A., Robinson, T. P., Teillant, A., & Laxminarayan, R. (2015). Global trends in antimicrobial use in food animals. Proceedings of the National Academy of Sciences, 112(18), 5649–5654. https://doi.org/10.1073/pnas.1503141112 [Google Scholar] [Crossref]

52. Van den Bogaard, A. E., & Stobberingh, E. E. (2000). Epidemiology of resistance to antibiotics: Links between animals and humans. International Journal of Antimicrobial Agents, 14(4), 327–335. https://doi.org/10.1016/s0924-8579(00)00145-x [Google Scholar] [Crossref]

53. Wang, Y., Zhou, J., Li, X., Ma, L., Cao, X., Hu, W., Zhao, L., Jing, W., Lan, X., & Li, Y. (2020). Genetic diversity, antimicrobial resistance and extended-spectrum beta-lactamase type of Escherichia coli isolates from chicken, dog, pig and yak in Gansu and Qinghai Provinces, China. Journal of Global Antimicrobial Resistance, 22, 726–732. https://doi.org/10.1016/j.jgar.2020.07.005 [Google Scholar] [Crossref]

54. Wang, Z.; Lu, Q.; Mao, X.; Li, L.; Dou, J.; He, Q.; Shao, H.; Luo, Q. Prevalence of Extended-Spectrum β-Lactamase-Resistant Genes in Escherichia coli Isolates from Central China during 2016–2019. Animals 2022, 12, 3191. https://doi.org/ 10.3390/ani1222319 [Google Scholar] [Crossref]

55. Wu, C., Wang, Y., Shi, X., Wang, S., Ren, H., Shen, Z., Wang, Y., Lin, J., & Wang, S. (2018). Rapid rise of the ESBL and mcr-1 genes in Escherichia coli of chicken origin in China, 2008–2014. Emerging Microbes & Infections, 7(1), 30. https://doi.org/10.1038/s41426-018-0033-1 [Google Scholar] [Crossref]

Metrics

Views & Downloads

Similar Articles