Molecular and Phylogenetic Identification of Some Virulence Genes of Klebsiella Spp. Isolated from Ear Infection in dogs.

Authors

  • Mas Aamer University of Baghdad

DOI:

https://doi.org/10.36320/ajb/v18.i2.23787

Keywords:

Klebsiella spp., Molecular identification, 16S rRNA, Virulence genes, Phylogenetic analysis.

Abstract

Klebsiella species such as (Klebsiellapneumoniae, Klebsiella aerogenes), opportunistic pathogens belong to the family Enterobacteriaceae are gram-negative bacteria, especially in immunocompromised dogs. A total of No. 50 ear swab samples of dogs, samples were cultured on MacConkeyagar, Blood agar, and Chromogenic agar to isolate Klebsiella spp. followed using Molecular method to confirm the bacterial identity, by PCR amplification 16S rRNA gene, phylogentic analysis and detection of some virulence gene (blaCTX-M, magA, and mrkA), and susceptibility test. Bacteriological analysis revealed that Klebsiella spp. was accounting for a 14% in dogs (85.71%K. pneumoniae, Klebsiella aerogenes 14.28%), they were detected in dogs isolates blaCTX-M 1(14.3%), magA3(42.9%) and mrkA1(14.3%). Sequencing and Phylogenetic analysis confirmed that the majority of isolates belonged to Klebsiella Spp. ( K. pneumoniae,Klebsiella aerogenes), Phylogenetic analysis revealed high identity (99–100%) with reference strains deposited in GenBank (ID: PV490247.1, ID: PV490248.1, ID: PV490249.1, ID: PV490250.1,  ID: PV490251.1, ID: PV490252.1, ID: PV490253.1). Klebsiella spp. isolates showed complete resistance (100%) to Amoxicillin/Clavulanic acid and Imipenem, with high resistance to both Amikacin and Cefotaxime (71.4%), while showing complete sensitivity to Levofloxacin, Co-trimoxazole, and Chloramphenicol. In feline isolates, complete resistance (100%) was recorded to Co-trimoxazole, Amoxicillin/Clavulanic acid, and Imipenem, in addition to high resistance to Amikacin(66.6%), while all isolates showed complete sensitivity to Levofloxacin, Chloramphenicol, Trimethoprim, and Cefotaxime. Most of these results were highly significant (P ≤ 0.01).

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References

Gotthelf, L. N. (2004). Otitis media and interna in dogs and cats. Veterinary Clinics of North America, 34(2), 469–487.

Harvey, R. G., Harari, J., & Delauche, A. J. (2001). Ear diseases of the dog and cat.

Hafidh, R. R., & Alsodani, M. H. (2025). Assessment of biofilm formation and hypermucoviscosity in Klebsiella oxytoca from clinical and community sources. Journal of the Faculty of Medicine Baghdad, 67, 66–77.

Paczosa, M. K., & Mecsas, J. (2016). Klebsiella pneumoniae: Going on the offense with a strong defense. Microbiology and Molecular Biology Reviews, 80, 629–661.

Mihu, M. L., Nadăş, G. C., Bouari, C. M., Fiț, N. I., & Răpuntean, S. (2026). Klebsiella pneumoniae infections in dogs: A One Health review of antimicrobial resistance, virulence factors, zoonotic risk, and emerging alternatives. Microorganisms, 14(1), 149.

Bachman, M. A., Breen, P., Deornellas, V., Mu, Q., Zhao, L., Wu, W., Cavalcoli, J. D., & Mobley, H. L. (2015). Genome-wide identification of Klebsiella pneumoniae fitness genes during lung infection. mBio, 6(3), e00775.

Martin, R. M., Cao, J., Brisse, S., Passet, V., Wu, W., Zhao, L., Malani, P. N., Rao, K., & Bachman, M. A. (2016). Molecular epidemiology of colonizing and infecting isolates of Klebsiella pneumoniae. mSphere, 1(5), e00261–16.

Mirzaie, A., & Ranjbar, R. (2021). Antibiotic resistance, virulence-associated genes analysis and molecular typing of Klebsiella pneumoniae strains recovered from clinical samples. AMB Express, 11, 122.

Wyres, K. L., & Holt, K. E. (2018). Klebsiella pneumoniae as a key trafficker of drug resistance genes from environmental to clinically important bacteria. Current Opinion in Microbiology, 45, 131–139.

MacFaddin, J. F. (2000). Biochemical tests for identification of medical bacteria. Lippincott Williams & Wilkins.

Rawy, D. K., El-Mokhtar, M. A., Sameeh, et al. (2020). Isolation, characterization and identification of Klebsiella pneumoniae from Assiut University Hospital and sewage water. Assiut University Journal of Multidisciplinary Scientific Research, 49, 60–76.

AL-Nassry, B. S. (2011). Isolation and identification of bacterial isolates from ear infection and their sensitivity to usual antibiotics in humans and dogs. Iraqi Journal of Veterinary Medicine, 35, 159–166.

Ibrahim, Z. I., & Alwaan, M. J. (2008). Experimental infection of Klebsiella pneumoniae in urinary tract of rats and guinea pigs. Iraqi Journal of Veterinary Medicine, 32, 68–79.

Doğan, M., & Uğraklı, S. (2023). Phenotypic and genotypic identification of carbapenem-resistant Klebsiella pneumoniae and determination of antibiotic susceptibility. Selçuk Medical Journal, 39, 75–83.

Abdel-Rhman, S. H. (2020). Characterization of β-lactam resistance in Klebsiella pneumoniae associated with ready-to-eat processed meat in Egypt. PLOS ONE, 15, e0238747.

Alhassan, U. M. A., & Abdul-Kareem, I. Q. (2025). Molecular identification of virulence and antimicrobial resistance genes of Klebsiella pneumoniae isolated from patients. Journal of Medicinal and Pharmaceutical Chemistry Research, 7, 733–744.

Kot, B., Witeska, M., Szweda, P., et al. (2025). Antibiotic resistance, virulence genes, and molecular diversity of clinical Klebsiella pneumoniae isolates from patients in Poland. Pathogens, 14, 648.

Salman, S. B., & Al-Mathkhury, H. J. F. (2023). Molecular detection of Klebsiella pneumoniae serotype K2 isolated clinically. Iraqi Journal of Science, 57, 89–103.

Hayyawi, S. M. (2012). Comparison of microbial isolates from external ear canal of sheep and their susceptibility to antibiotics. Iraqi Journal of Veterinary Medicine, 36, 41–48.

Piperaki, E. T., et al. (2017). Klebsiella pneumoniae: Epidemiology and antimicrobial resistance. Journal of Global Antimicrobial Resistance, 12, 47–54.

Abd Kadhum, A. (2024). Antibiotic resistance patterns of bacteria isolated from otitis patients. Central Asian Journal of Medical and Natural Science, 5.

Alwan, A. H., & Abass, S. M. (2017). Effects of UV light on mrkA and mrkD genes in local isolates of Klebsiella pneumoniae. Al-Mustansiriyah Journal of Science, 27.

Jasim, J. S., & Hussein, A. R. (2025). Detection of class 1 integron among Klebsiella pneumoniae clinical isolates in Baghdad hospitals. Journal of the Faculty of Medicine Baghdad, 67, 384–394.

Kim, H., et al. (2024). Prevalence of bacterial pathogens in canine otitis externa: A systematic review and meta-analysis.

O’Neill, D. G., Volk, A. V., Soares, T., Church, D. B., Brodbelt, D. C., & Pegram, C. (2021). Frequency and predisposing factors for canine otitis externa in the UK. Canine Medicine and Genetics, 8, 7.

Hassan, M., et al. (2023). Otitis externa in dogs: Distribution and antimicrobial susceptibility patterns of Staphylococcus spp. Macedonian Veterinary Review, 46(1), 43–50.

Hillier, A., Lloyd, D. H., Weese, J. S., Blondeau, J. M., Boothe, D., Breitschwerdt, E., Guardabassi, L., Papich, M. G., Rankin, S. C., Turnidge, J. D., & Sykes, J. E. (2012). Guidelines for diagnosis and antimicrobial therapy of canine

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Published

2026-08-01

How to Cite

Aamer, M. (2026). Molecular and Phylogenetic Identification of Some Virulence Genes of Klebsiella Spp. Isolated from Ear Infection in dogs. Al-Kufa University Journal for Biology, 18(2). https://doi.org/10.36320/ajb/v18.i2.23787

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