Detection and Characterization of Virulence and Resistance Determinants (spa, lukS/F-PV, mecA) in Staphyllococus aureus from Mastitic Cow Milk
Abstract
Antibiotic resistance is one of the huge medical problems causes by which mastitis cuases the most economically important disease affecting dairy cattle worldwide. The current study aimed to molecular detection and characterization of selected virulence and antimicrobial resistance genes (spa, many lukS/F-PV, mecA) in Staphylococcus aureus isolates obtained from cow mastitis milk in Diyala Governorate. Hundred mastitis milk samples were collected from cows affected with clinical mastitis. Molecular positivity rate was 30.0%, total 30 positive isolates were identified from the tested 100 mastitis milk samples. Conventional PCR analysis showed that 30 (100 %), 19 (63.3 %) and 7 (23.3 %) isolates were positive for spa, mecA and lukS/F-PV respectively. The results obtained confirmed the circulation of virulence- and methicillin-resistance-genes among strains of Staphylococcus aureus isolated from bovine mastitis. Sequencing and sequence alignment of selected PCR positive amplicons at Macrogen Company showed 99% or more similarity with GenBank reference strains. By this study we can conclude that the impact of both molecular characterization and epidemiological surveillance for bovine mastitis-associated S. aureus isolates virulence gene and antibacterial susceptibility test through PCR and gene sequencing.
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References
Abd El-Razik, K. A., et al. (2025). Detection of methicillin-resistant Staphylococcus aureus in bovines with subclinical mastitis using molecular approaches. International Journal of Veterinary Science, 14, 528.
Fazal, M. A., et al. (2023). Molecular identification, antimicrobial resistance and virulence profiling of staphylococci causing subclinical mastitis. BMC Veterinary Research, 19, 109.
Getahun, D. D., et al. (2025). Virulence genes and antibiotic resistance profiling of coagulase-positive staphylococci from bovine mastitis. BMC Microbiology, 25, 226.
Ibrahim, A. A., et al. (2023). Molecular prevalence of virulence genes among Staphylococcus aureus isolated from bovine mastitis. Veterinary Medicine International, 2023, 1–8.
Khairullah, A. R., et al. (2024). Kinship analysis of mecA gene of methicillin-resistant Staphylococcus aureus isolates from dairy cattle. Veterinary World, 17, 250–258.
Klibi, A., et al. (2021). Molecular characterization of virulence genes in Staphylococcus aureus isolated from bovine mastitis. Archives of Microbiology, 203, 4121–4129.
Kumar, S., Anwer, R., Yadav, M., Sehrawat, N., Singh, M., & Kumar, V. (2021). Molecular typing and global epidemiology of Staphylococcus aureus. Current Pharmacology Reports, 7(5), 179–186.
Miyazawa, R., et al. (2022). Characterization of Staphylococcus aureus isolates from mastitic milk and bulk milk. Microorganisms, 10(11), 2117.
Mlynarczyk-Bonikowska, B., & Rudnicka, L. (2025). The pathogenicity mechanisms of Staphylococcus aureus. International Journal of Molecular Sciences, 26(24), 11803.
Moawad, A. A., et al. (2025). Genomic characterization of Staphylococcus aureus isolated from bovine mastitis. Frontiers in Microbiology, 16, 1661122.
Ramezanigardaloud, N., et al. (2025). Prevalence and diversity of Staphylococcus aureus in bulk tank milk and dairy environments. Animals, 15(14), 2153.
Sheet, O. H. (2022). Molecular detection of mecA gene in methicillin-resistant Staphylococcus aureus isolated from bovine mastitis. Iraqi Journal of Veterinary Sciences, 36(3), 751–756.
Tartor, Y. H., et al. (2024). Vancomycin-resistant Staphylococcus aureus endangers dairy cattle and public health. Journal of Advanced Veterinary and Animal Research, 11, 101–112.
Tommasoni, C., Fiore, E., Lisuzzo, A., & Gianesella, M. (2023). Mastitis in dairy cattle: on-farm diagnostics and future perspectives. Animals, 13(15), 2538.
Touaitia, R., et al. (2025). Staphylococcus aureus in bovine mastitis: A narrative review. Antibiotics, 14(8), 810.
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