Articles | Open Access |

Ecology, Pathogenesis, and One Health Implications of Pseudomonas aeruginosa and Klebsiella pneumoniae in Wild and Captive Birds: An Integrative Review of Co-Infection, Antimicrobial Resistance, and Zoonotic Risk

Tomas R. Novak , Department of Veterinary Microbiology, University of Barcelona, Spain

Abstract

The emergence and global dissemination of multidrug-resistant bacterial pathogens at the interface between wildlife, domestic animals, and humans represents one of the most critical challenges to contemporary One Health systems. Among these pathogens, Pseudomonas aeruginosa and Klebsiella pneumoniae have attracted increasing attention due to their intrinsic virulence, remarkable ecological adaptability, and escalating antimicrobial resistance profiles. While these organisms have traditionally been studied in clinical and hospital environments, a growing body of evidence indicates that wild and captive birds serve as important reservoirs, amplifiers, and dissemination vectors of both pathogens, often in co-infection contexts that exacerbate disease severity and transmission potential. The present article synthesizes and critically analyzes the available scientific evidence on P. aeruginosa and K. pneumoniae in avian hosts, drawing exclusively on the provided reference corpus.

This integrative review explores the ecological niches of both bacteria in avian populations, the pathological manifestations of mono- and co-infections, and the molecular and phenotypic mechanisms that underpin their persistence, virulence, and resistance. Empirical findings from outbreaks in ostriches, kori bustards, flamingos, goldfinches, and diverse wild and captive bird species demonstrate that these bacteria are not merely opportunistic contaminants but active drivers of disease, mortality, and population-level impacts in birds (Momotani et al., 1995; Bailey et al., 2000; Kock and Kock, 1995; Abbate et al., 2025). The review further integrates recent advances in diagnostic and molecular epidemiology, including species-specific PCR targets, multilocus sequence typing, and gene-based identification approaches, which have enabled more precise tracking of avian and environmental strains and their relationship to human and veterinary lineages (Lavenir et al., 2007; Diancourt et al., 2005; He et al., 2016).

A central focus of this work is the One Health dimension of avian-associated P. aeruginosa and K. pneumoniae. Wild birds, companion birds, and farmed avian species occupy ecological and social positions that bridge natural ecosystems, agricultural systems, and human settlements, making them powerful sentinels and vectors for antimicrobial-resistant bacteria (Abd El-Ghany, 2021; Khan et al., 2025; Abdullahi et al., 2025). By integrating data on prevalence, resistance profiles, environmental contamination, and zoonotic potential, this article demonstrates that avian-borne strains of these bacteria represent not only a veterinary problem but also a significant public health and environmental threat.

Through extensive theoretical elaboration and critical synthesis, this article provides a comprehensive, publication-ready account of how P. aeruginosa and K. pneumoniae circulate within and beyond avian populations. It identifies key knowledge gaps, methodological limitations, and research priorities, while also highlighting the urgent need for integrated surveillance, biosecurity, and antimicrobial stewardship strategies that include wildlife and companion birds as essential components of the One Health framework.

Keywords

Avian microbiology, Pseudomonas aeruginosa, Klebsiella pneumoniae, antimicrobial resistance

References

Abbate, Jessica Maria, Giulia D’Annunzio, Rosa Falleti, et al. 2025. Pathological Findings of Nestling European Goldfinches (Carduelis carduelis) Co-Infected with Klebsiella pneumoniae and Pseudomonas aeruginosa. Veterinary Sciences 12 (9): 821. https://doi.org/10.3390/vetsci12090821.

Abd El-Ghany, Wafaa A. 2021. Pseudomonas aeruginosa infection of avian origin: Zoonosis and one health implications. Veterinary World 14 (8): 2155-2159. https://doi.org/10.14202/vetworld.2021.2155-2159.

Abdullahi, Idris Nasir, Sirine Mejri, Chukwudi Cresent Okwume, et al. 2025. Global epidemiology of high priority and pandemic Pseudomonas aeruginosa in pets, livestock, wild, and aquatic animals: a systematic review and meta-analysis. Letters in Applied Microbiology 78 (3): ovaf028. https://doi.org/10.1093/lambio/ovaf028.

Bailey, T.A., C.D. Silvanose, J.N. Naldo, and J.H. Howlett. 2000. Pseudomonas aeruginosa infections in kori bustards (Ardeotis kori). Avian Pathology 29: 41-44.

Brittingham, Margaret Clark, Stanley A. Temple, and Ruth M. Duncan. 1988. A survey of the prevalence of selected bacteria in wild birds. Journal of Wildlife Diseases 24 (2): 299-307. https://doi.org/10.7589/0090-3558-24.2.299.

Diancourt, L., V. Passet, J. Verhoef, P.A.D. Grimont, and S. Brisse. 2005. Multilocus sequence typing of Klebsiella pneumoniae nosocomial isolates. Journal of Clinical Microbiology 43: 4178-4182.

Dolejska, Monika. 2020. Antibiotic-resistant bacteria in wildlife. In Antibiotic Resistance in the Environment, edited by Célia M. Manaia, Erica Donner, Ivone Vaz-Moreira, and Peiying Hong, Vol. 91. The Handbook of Environmental Chemistry. Springer International Publishing. https://doi.org/10.1007/698_2020_467.

Grilli, Guido, Maria Cristina Rapi, Laura Musa, et al. 2025. Looking for ESKAPE bacteria: Occurrence and phenotypic antimicrobial resistance profiles in wild birds from Northern and Central Italy sites. Antibiotics 14 (10): 1025. https://doi.org/10.3390/antibiotics14101025.

He, Y., X. Guo, S. Xiang, J. Li, X. Li, H. Xiang, J. He, D. Chen, and J. Chen. 2016. Comparative analyses of phenotypic methods and 16S rRNA, khe, rpoB genes sequencing for the identification of clinical isolates of Klebsiella pneumoniae. Antonie van Leeuwenhoek 109: 1029-1040.

Jiménez Gómez, P. A. 2006. Phenotypic and genotypic characterization of an outbreak of Pseudomonas aeruginosa from wild birds. In Modern Multidisciplinary Applied Microbiology. John Wiley & Sons.

Johne, R., D. Enderlein, H. Nieper, and H. Müller. 2005. Novel polyomavirus detected in the feces of a chimpanzee by nested broad-spectrum PCR. Journal of Virology 79: 3883-3887.

Khan, Bushra Nisar, Amina Tufail, Muhammad Junaid, et al. 2025. Possible role of companion birds in One Health implication of multidrug-resistant Pseudomonas aeruginosa isolated from feces of captive wild birds. Journal of Wildlife and Biodiversity 9 (1): 262-279.

Kock, N., and R. Kock. 1995. Disease epidemic in lesser flamingos (Phoeniconaias minor) in Kenya. In Proceedings of the American Association of Zoo Veterinarians, East Lansing, MI, p. 115.

Lavenir, R., D. Jocktane, F. Laurent, S. Nazaret, and B. Cournoyer. 2007. Improved reliability of Pseudomonas aeruginosa PCR detection by the use of the species-specific ecfX gene target. Journal of Microbiological Methods 70: 20-29.

Miskiewicz, Andrzej, Paweł Kowalczyk, Sanaa Mahdi Oraibi, Krystyna Cybulska, and Anna Misiewicz. 2018. Bird feathers as potential sources of pathogenic microorganisms: A new look at old diseases. Antonie van Leeuwenhoek 111: 1493-1507.

Momotani, E., M. Kiryu, M. Ohshiro, Y. Murakami, Y. Ashida, S. Watanabe, and Y. Matsubara. 1995. Granulomatous lesions caused by Pseudomonas aeruginosa in the ostrich (Struthio camelus). Journal of Comparative Pathology 112: 273-282.

Okada, F., Y. Ando, K. Honda, T. Nakayama, A. Ono, S. Tanoue, T. Maeda, and H. Mori. 2010. Acute Klebsiella pneumoniae pneumonia alone and with concurrent infection: Comparison of clinical and thin-section CT findings. British Journal of Radiology 83: 854-860.

Palazzolo, S., C. Gervasi, J.M. Abbate, E. Gjurčević, R. Falleti, M.G. Piro, G. Lanteri, C. Iaria, and F. Marino. 2024. Natural bacterial co-infection in farmed European sea bass intended for experimental research in Sicily, southern Italy: Pathological findings. Fishes 9: 360.

Rodrigues, G. C., Joana, Harisree P. Nair, Christopher O’Kane, and Caray A. Walker. 2021. Prevalence of multidrug resistance in Pseudomonas spp. isolated from wild bird feces in an urban aquatic environment. Ecology and Evolution 11 (20): 14303-14311.

Sigrist, B., J. Geers, S. Albini, D. Rubbenstroth, and N. Wolfrum. 2021. A new multiplex real-time RT-PCR for simultaneous detection and differentiation of avian bornaviruses. Viruses 13: 1358.

Sutton, D.A., D.P. Allen, C.M. Fuller, et al. 2019. Development of an avian avulavirus 1 (AAvV-1) L-gene real-time RT-PCR assay using minor groove binding probes for application as a routine diagnostic tool. Journal of Virological Methods 265: 9-14.

Todd, D., J. Weston, N.W. Ball, B.J. Borghmans, J.A. Smyth, L. Gelmini, and A. Lavazza. 2001. Nucleotide sequence-based identification of a novel circovirus of canaries. Avian Pathology 30: 321-325.

Download and View Statistics

Views: 0   |   Downloads: 0

Copyright License

Download Citations

How to Cite

Tomas R. Novak. (2026). Ecology, Pathogenesis, and One Health Implications of Pseudomonas aeruginosa and Klebsiella pneumoniae in Wild and Captive Birds: An Integrative Review of Co-Infection, Antimicrobial Resistance, and Zoonotic Risk. The American Journal of Veterinary Sciences and Wildlife Discovery, 8(2), 1–7. Retrieved from https://theamericanjournals.com/index.php/tajvswd/article/view/7353