Spread and consequences of secondary infections in cattle affected with foot-and-mouth disease in Karbala province, Iraq

Authors

DOI:

https://doi.org/10.31210/spi2025.28.04.27

Abstract

Foot-and-mouth disease (FMD) is a highly contagious viral disease caused by aphthovirus belonging to the family of Picornaviridae. Although the primary viral infection is known to cause the typical clinical manifestations, such as fever, salivation, and the formation of vesicles around the mouth, muzzle, teats, and interdigital spaces, the breakage of these vesicles opens the entry for opportunistic microorganisms. The latter can greatly affect the disease outcome, however, neither their spread, nor the species composition diversity among cattle herds in Iraqi have not been adequately documented. Thus, the current study was aimed at isolating and identifying the secondary microbial agents that complicate the foot-and-mouth disease lesions in cattle in Karbala province, Iraq. Following the rules of asepsis, a total of one hundred smear samples were collected from the mouth cavity (n=50) and extremities (n=50) of cows that had been clinically diagnosed with FMD on the basis of the sudden appearance of the disease classical symptoms during its regional outbreak. The microbiological investigation showed a complex polymicrobial community consisting of various opportunistic pathogens that were colonizing as well as infecting the primary viral lesions. Moreover, the isolation of several pathogens from a single lesion was a common phenomenon. Among the isolated bacterial pathogens, both Gram-positive and Gram-negative forms were well represented. Trueperella pyogenes turned out to be the most predominant pathogen (18 % of total isolates). Pasteurella multocida was found to be the second (16 % of total isolates) after T. pyogenes. Notably large percentages of Staphylococcus aureus (14 %), both methicillin-sensitive and methicillin-resistant strains, as well as Escherichia coli (13 %), both commensal and pathogenic strains, were found. Other bacterial pathogens that were significant enough to be mentioned individually were Streptococcus dysgalactiae (7 %), Fusobacterium necrophorum (6 %), Pseudomonas aeruginosa (5 %). Fungal pathogens were found less frequently. They were mostly Candida sp. (5 %), as well as Cryptococcus sp. (3 %). It can be noted from these results that bacterial and fungal complications are not only incidental but also common and significant complications that occur as a result of FMD infection. These secondary infections play a vital role complicating the disease pathogenesis. Thus, this research confirmed the urgent necessity of changing the paradigm in the treatment of FMD cases, introducing integrated and holistic treatment approaches, beyond merely supportive therapy of the viral infection.

References

Jamal, S. M., & Belsham, G. J. (2013). Foot-and-mouth disease: past, present and future. Veterinary Research, 44 (1), 116. https://doi.org/10.1186/1297-9716-44-116

Knight-Jones, T. J. D., & Rushton, J. (2013). The economic impacts of foot and mouth disease – What are they, how big are they and where do they occur? Preventive Veterinary Medicine, 112 (3–4), 161–173. https://doi.org/10.1016/j.prevetmed.2013.07.013

Alexandersen, S., Zhang, Z., Donaldson, A. I., & Garland, A. J. (2003). The pathogenesis and diagnosis of foot- and-mouth disease. Journal of Comparative Pathology, 129 (1), 1–36.

Grubman, M. J., & Baxt, B. (2004). Foot-and-mouth disease. Clinical Microbiology Reviews, 17 (2), 465–493. https://doi.org/10.1128/cmr.17.2.465-493.2004

Stannard, H. J., Tulk, M. L., & Old, J. M. (2017). Dead mouse hopping: Tyzzer’s disease in spinifex hopping-mice (Notomys alexis). Veterinary Microbiology, 201, 201–207. https://doi.org/10.1016/j.vetmic.2017.01.018

André, A. C., Debande, L., & Marteyn, B. S. (2021). The selective advantage of facultative anaerobes relies on their unique ability to cope with changing oxygen levels during infection. Cellular Microbiology, 23(8), e13338. https://doi.org/10.1111/cmi.13338

Yoong, P., & Torres, V. J. (2013). The effects of Staphylococcus aureus leukotoxins on the host: cell lysis and beyond. Current Opinion in Microbiology, 16 (1), 63–69. https://doi.org/10.1016/j.mib.2013.01.012

Rzewuska, M., Kwiecień, E., Chrobak-Chmiel, D., Kizerwetter-Świda, M., Stefańska, I., & Gieryńska, M. (2019). Pathogenicity and virulence of Trueperella pyogenes: A review. International Journal of Molecular Sciences, 20 (11), 2737. https://doi.org/10.3390/ijms20112737

Yassin, A. F., Hupfer, H., Siering, C., & Schumann, P. (2011). Comparative chemotaxonomic and phylogenetic studies on the genus Arcanobacterium Collins et al. 1982 emend. Lehnen et al. 2006: proposal for Trueperella gen. nov. and emended description of the genus Arcanobacterium. International Journal of Systematic and Evolutionary Microbiology, 61 (6), 1265–1274. https://doi.org/10.1099/ijs.0.020032-0

White, B. J., & Larson, B. L. (2020). Impact of bovine respiratory disease in U.S. beef cattle. Animal Health Research Reviews, 21 (2), 132–134. https://doi.org/10.1017/s1466252320000079

Woldesenbet, A. A., Muluneh, A., Negussie, H., & Jibril, Y. (2023). Foot and mouth disease in Adama and Boset districts, East Shewa zone, Ethiopia: Seroprevalence and virus serotyping. Ethiopian Veterinary Journal, 27 (1), 143–156. https://doi.org/10.4314/evj.v27i1.7

Kurcubic, V., Djokovic, R., Vidanovic, D., Sekler, M., Matovic, K., Ilic, Z., & Stojkovic, J. (2013). Bovine respiratory disease complex (BRDC): Viral and bacterial pathogens in Serbia. Biotehnologija u Stocarstvu, 29 (1), 37–43. https://doi.org/10.2298/bah1301037k

Arzt, J., Baxt, B., Grubman, M. J., Jackson, T., Juleff, N., Rhyan, J., Rieder, E., Waters, R., & Rodriguez, L. L. (2011). The pathogenesis of foot-and-mouth disease II: viral pathways in swine, small ruminants, and wildlife; myotropism, chronic syndromes, and molecular virus-host interactions. Transboundary and Emerging Diseases, 58 (4), 305–326.

Pauli, B., Ajmera, S., & Kost, C. (2023). Determinants of synergistic cell-cell interactions in bacteria. Biological Chemistry, 404 (5), 521–534. https://doi.org/10.1515/hsz-2022-0303

Wen, X., Cheng, J., & Liu, M. (2025). Virulence factors and therapeutic methods of Trueperella pyogenes : A review. Virulence, 16 (1), 2467161. https://doi.org/10.1080/21505594.2025.2467161

Wilson, B. A., & Ho, M. (2013). Pasteurella multocida: from Zoonosis to Cellular Microbiology. Clinical Microbiology Reviews, 26 (3), 631–655. https://doi.org/10.1128/cmr.00024-13

Quinn, P. J., Markey, B. K., Leonard, F. C., FitzPatrick, E. S., Fanning, S., & Hartigan, P J. (2011). Veterinary microbiology and microbial disease (2nd ed.). John Wiley & Sons

Van Loo, I. H. M., Diederen, B. M. W., Savelkoul, P. H. M., Woudenberg, J. H. C., Roosendaal, R., van Belkum, A., Lemmens-den Toom, N., Verhulst, C., van Keulen, P. H. J., & Kluytmans, J. A. J. W. (2007). Methicillin-resistant Staphylococcus aureus in meat products, the Netherlands. Emerging Infectious Diseases, 13 (11), 1753–1755. https://doi.org/10.3201/eid1311.070358

Stenfeldt, C., Diaz-San Segundo, F., de los Santos, T., Rodriguez, L. L., & Arzt, J. (2016). The Pathogenesis of foot-and-mouth disease in pigs. Frontiers in Veterinary Science, 3, 41. https://doi.org/10.3389/fvets.2016.00041

Brito, G. I., Cerqueira, L. de A., Perecmanis, S., Borges, J. R. J., de Castro, M. B., & Câmara, A. C. L. (2025). Clinical mastitis in small ruminants referred to a veterinary teaching hospital: 23 cases. Microorganisms, 13 (7), 1512. https://doi.org/10.3390/microorganisms13071512

Seyedmousavi, S., Bosco, S. de M. G., de Hoog, S., Ebel, F., Elad, D., Gomes, R. R., Jacobsen, I. D., Jensen, H. E., Martel, A., Mignon, B., Pasmans, F., Piecková, E., Rodrigues, A. M., Singh, K., Vicente, V. A., Wibbelt, G., Wiederhold, N. P., & Guillot, J. (2018). Fungal infections in animals: a patchwork of different situations. Medical Mycology, 56(suppl 1), S165–S187. https://doi.org/10.1093/mmy/myx104

Fatima, D., & Amina, M. (2022). Treatment approaches of ovine fungal diseases using antibiotics and ethnoveterinary medicinal plants. Pakistan Journal of Zoology, 54 (4), 1917–1925. https://doi.org/10.17582/journal.pjz/20210809190836

Wong, N. S. T., Malmuthge, N., Gellatly, D., Nordi, W. M., Alexander, T. W., Ortega Polo, R., Janzen, E., Schwartzkopf-Genswein, K., & Jelinski, M. (2024). Characterization of the hoof bacterial communities in feedlot cattle affected with digital dermatitis, foot rot or both using a surface swab technique. Animal Microbiome, 6 (1), 2. https://doi.org/10.1186/s42523-023-00277-1

Li, Y., Han, D., Peng, Y., Zuo, W., Zeng, B., Xiong, D., Ai, J., & Xin, J. (2025). Application of metagenomics in the animal infectious diseases. Medycyna Weterynaryjna, 81 (04), 6990–2025. https://doi.org/10.21521/mw.6990

Downloads

Published

2025-12-26

How to Cite

Hameed, M. A. K., Al-Dawmy, F., Alqatab, A. H., Zabeel, A. K., & Ibrahim, Z. K. (2025). Spread and consequences of secondary infections in cattle affected with foot-and-mouth disease in Karbala province, Iraq. Scientific Progress & Innovations, 28(4), 172–177. https://doi.org/10.31210/spi2025.28.04.27

Most read articles by the same author(s)