Journals / Animal Health Production and Hygiene / 2026 / Cilt: 14 Sayı: 1

Evaluation of Oxidative Stress Parameters in Leptospira Infected Sheep

Leptospira ile Enfekte Koyunlarda Oksidatif Stres Parametrelerinin Değerlendirilmesi

Onur Taş(Samsun Veteriner Kontrol Enstitü Müdürlüğü)0000-0003-0577-4024
Semistan Kızıltepe(IGDIR UNIVERSITY, TUZLUCA VOCATIONAL SCHOOL)0000-0003-3727-8893
Büşra Şahin(ONDOKUZ MAYIS ÜNİVERSİTESİ, VETERİNER FAKÜLTESİ)0000-0002-5245-478X
Sena Çenesiz(ONDOKUZ MAYIS ÜNİVERSİTESİ, VETERİNER FAKÜLTESİ)0000-0002-3544-503X
Yunus Kılıçoğlu(Samsun Veteriner Kontrol Enstitüsü Müdürlüğü)0000-0002-6788-9284
Rahşan Koç Akpınar(Samsun Veteriner Kontrol Enstitüsü Müdürlüğü)0000-0003-0075-9247
Pages
23–30
Publication Date
2025-06-24
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

According to the results of the ELISA test performed in our study, 16 sheep serum samples were found to be positive for Leptospira interrogans ser. hardjo, while 78 samples were found to be negative.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Leptospirosis is a bacterial infection with zoonotic character which is widespread all over the world, especially in humid and temperate regions and poses a serious threat to public health.
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Key Findings & Data:In this study, 94 sheep blood sera sent to Samsun Veterinary Control Institute Directorate with suspicion of leptospirosis were firstly subjected to ELISA test for leptospirosis antibodies.
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Conclusion & Impact:According to the results of the ELISA test performed in our study, 16 sheep serum samples were found to be positive for Leptospira interrogans ser. hardjo, while 78 samples were found to be negative.
🔬Design:Araştırma Makalesi
📍Scope:78 samples
⚙️Variables:Kan serumu · Koyun · Leptospira

Abstract

Leptospirosis is a bacterial infection with zoonotic character which is widespread all over the world, especially in humid and temperate regions and poses a serious threat to public health. In this study, 94 sheep blood sera sent to Samsun Veterinary Control Institute Directorate with suspicion of leptospirosis were firstly subjected to ELISA test for leptospirosis antibodies. Total thiol, Native thiol, Disulphide, Native thiol/Total thiol, Disulphide/Native thiol, Disulphide/Total thiol, MDA levels and ADA activity were evaluated in the samples. According to the results of the ELISA test performed in our study, 16 sheep serum samples were found to be positive for Leptospira interrogans ser. hardjo, while 78 samples were found to be negative. In order to evaluate the effect of leptospirosis on oxidative stress parameters, 15 positive serum samples and 15 negative serum samples taken from healthy sheep were used as control group. According to the results of biochemical analyses; Total thiol, Native thiol, Disulphide, Native thiol/Total thiol, Disulphide/Native thiol, Disulphide/Total thiol values in the Leptospira group were not significantly different from those in the control group. However, MDA values and ADA activity in the Leptospira group were significantly higher than those in the control group. As a result, it was determined that oxidant-antioxidant balance was disturbed in sheep infected with Leptospira and oxidative stress occurred as a result. Our findings suggest that MDA and ADA activity can be used as a biomarker in the diagnosis of Leptospirosis and may give an idea about the severity of the disease.

Özet

Leptospirozis tüm dünyada özellikle de nemli ve ılıman bölgelerde yaygın olarak görülen halk sağlığını ciddi boyutta tehdit eden zoonotik karakterli bakteriyel bir enfeksiyondur. Bu çalışmada Samsun Veteriner Kontrol Enstitüsü Müdürlüğüne leptospirozis şüphesi ile gönderilen 94 adet koyun kan serumu öncelikle leptospirozis antikorları yönünden ELISA testine tabi tutuldu. Alınan numunelerde oksidatif stres parametrelerinden Total thiol, Native thiol, Disulphide, Native thiol/Total thiol, Disulphide/Native thiol, Disulphide/Total thiol, MDA düzeyleri ve ADA aktivitesi değerlendirilmiştir. Çalışmamızda yapılan ELISA testi sonuçlarına göre 16 adet koyun serum örneği Leptospira interrogans ser. hardjo yönünden pozitif olarak tespit edilirken, 78 adet örnek ise negatif olarak tespit edilmiştir. Leptospirozisin oksidatif stres parametreleri üzerindeki etkisini değerlendirmek amacıyla 15 adet pozitif serum örneği ve kontrol grubunu oluşturmak amacıyla sağlıklı koyunlardan alınan 15 adet negatif serum örneği kullanıldı. Biyokimyasal analiz sonuçlarına göre; Leptospira gruptaki Total thiol, Native thiol, Disulphide, Native thiol/Total thiol, Disulphide/Native thiol, Disulphide/Total thiol değerleri kontrol gruptaki değerler ile karşılaştırıldıklarında anlamlı düzeyde bir değişiklik bulunamamıştır. Fakat Leptospira gruptaki MDA değerleri ve ADA aktivitesi kontrol gruptaki değerlere göre anlamlı derecede yüksek bulunmuştur. Sonuç olarak Leptospira ile enfekte koyunlarda oksidan-antioksidan dengesinin bozulduğu ve bunun sonucunda oksidatif stressin meydana geldiği belirlendi. Bulgularımız MDA ve ADA aktivitesinin leptospirozis tanısında bir biyobelirteç olarak kullanılabileceğini ve hastalığın şiddeti hakkında fikir verebileceğini düşündürmektedir.

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Cite This Article

Taş, O., Kızıltepe, S., Şahin, B., Çenesiz, S., Kılıçoğlu, Y., Akpınar, R. K. (2025). Evaluation of Oxidative Stress Parameters in Leptospira Infected Sheep. Animal Health Production and Hygiene, Cilt: 14 Sayı: 1, 23–30. https://doi.org/10.53913/aduveterinary.1636302

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References (51)

  1. Adler, B., De La Peña Moctezuma, A. (2009). Leptospira and leptospirosis. Veterinary Microbiology, 140(3–4), 287–296. https://doi.org/10.1016/j.vetmic.2009.03.012
  2. Antoniolli, A., Guis, H., Picardeau, M., Goarant, C., & Flamand, C. (2024). One Health field approach applied to Leptospirosis: a Systematic review and meta-analysis across humans, animals and the environment. Open Forum Infectious Diseases, 12(1), ofae757. https://doi.org/10.1093/ofid/ofae757
  3. Arent, Z., Frizzell, C., Gilmore, C., Mackie, D., & Ellis, W.A. (2013). Isolation of Leptospires from genital tract of sheep. Veterinary Record, 173(23), 582. https://doi.org/10.1136/vr.101969
  4. Arent, Z., Gilmore, C., Brem, S., & Ellis, W.A. (2015). Molecular studies on European equine isolates of Leptospira interrogans serovars Bratislava and Muenchen. Infection Genetics and Evolution, 34, 26–31. https://doi.org/10.1016/j.meegid.2015.07.009
  5. Arent, Z., Frizzell, C., Gilmore, C., Allen, A., & Ellis, W. (2016). Leptospira interrogans serovars Bratislava and Muenchen animal infections: Implications for epidemiology and control. Veterinary Microbiology, 190, 19–26. https://doi.org/10.1016/j.vetmic.2016.05.004
  6. Arent, Z.J., Gilmore, C., Ayanz, J.M. S., Neyra, L.Q., & García-Peña, F.J. (2017a). Molecular epidemiology of Leptospira serogroup pomona infections among wild and domestic animals in Spain. EcoHealth, 14(1), 48–57. https://doi.org/10.1007/s10393-017-1210-8
  7. Arent, Z., Gilmore, C., Barlow, A.M., Smith, L., & Ellis, W.A. (2017b). Leptospira interrogans serogroup Pomona infections in the UK: is there a real threat for farm animals? Veterinary Record, 180(17), 424. https://doi.org/10.1136/vr.103891
  8. Atakiş̇ i̇, E., Kirmizigül, A. H., Atakiş̇, O., Sari, E. K., Öğün, M., Maraşli, Ş., Çelebi,̇ Ö. (2014). Leptospirozlu sığırlarda plazma nitrik oksit (NO) ve tümör nekrozis faktör-α (TNF-α) düzeyleri ile adenozin deaminaz (ADA), gama glutamil transferaz (GGT) aktiviteleri ve perifer kan lökositlerinde alfa naftil asetat esteraz (ANAE) yöntemiyle lenfosit oranlarının belirlenmesi. Kafkas Universitesi Veteriner Fakultesi Dergisi, 20(3), 451-455. https://doi.org/10.9775/kvfd.2013.10427
  9. Bertelloni, F., Cilia, G., Turchi, B., Pinzauti, P., Cerri, D., & Fratini, F. (2019). Epidemiology of leptospirosis in North-Central Italy: Fifteen years of serological data (2002–2016). Comparative Immunology Microbiology and Infectious Diseases, 65, 14–22. https://doi.org/10.1016/j.cimid.2019.04.001
  10. Blasdell, K.R., Morand, S., Perera, D., & Firth, C. (2019). Association of rodent-borne Leptospira spp. with urban environments in Malaysian Borneo. PLoS Neglected Tropical Diseases, 13(2), e0007141. https://doi.org/10.1371/journal.pntd.0007141
  11. Busch, C. J., & Binder, C. J. (2016). Malondialdehyde epitopes as mediators of sterile inflammation. Biochimica Et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 1862(4), 398–406. https://doi.org/10.1016/j.bbalip.2016.06.016
  12. Celi, P. (2011). Biomarkers of oxidative stress in ruminant medicine. Immunopharmacology and Immunotoxicolology, 33(2), 233-40. https://doi.org/10.3109/08923973.2010.514917
  13. Chakraborty, A., Miyahara, S., Villanueva, S.Y., Saito, M., Gloriani, N.G., & Yoshida, S. (2011). A novel combination of selective agents for isolation of Leptospira species. Microbiology and Immunology, 55(7), 494–501. https://doi.org/10.1111/j.1348-0421.2011.00347.x
  14. Cordero, O.J., Salgado, F.J., Fernández-Alonso, C.M., Herrera, C., Lluis, C., Franco, R., Nogueira, M. (2001). Cytokines regulate membrane adenosine deaminase on human activated lymphocytes. Journal of Leukocyte Biology, 70(6), 920-30. https://doi.org/10.1189/jlb.70.6.920
  15. Costa, F., Hagan, J.E., Calcagno, J., Kane, M., Torgerson, P., Martinez- Silveira, M.S., Stein, C., Abela-Ridder, B., & Ko, A.I. (2015). Global morbidity and mortality of Leptospirosis: A Systematic Review. PLoS Neglected Tropical Diseases, 17, 9(9), e0003898. https://doi.org/10.1371/journal.pntd.0003898
  16. Daniel, W.W. (1999). Biostatistics: A Foundation for Analysis in the Health Sciences. 7th edn. New York: John Wiley & Sons
  17. Del Rio, D., Stewart, A.J., & Pellegrini, N. (2005). A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutrition Metabolism and Cardiovascular Diseases, 15(4), 316–328. https://doi.org/10.1016/j.numecd.2005.05.003
  18. Ellis, W.A., Montgomery, J., & Cassells, J.A. (1985). Dihydrostreptomycin treatment of bovine carriers of Leptospira interrogans serovar hardjo. Research in Veterinary Science, 39(3):292-5
  19. Ellis, W.A. (1994). Leptospirosis as a cause of reproductive failure. Veterinary Clinics of North America Food Animal Practice, 10(3), 463–478. https://doi.org/10.1016/s0749-0720(15)30532-6
  20. Ellis, W.A. (2014). Animal leptospirosis. Current Topics in Microbiology and Immunology, 99–137. https://doi.org/10.1007/978-3-662-45059-8_6
  21. Erdogan, H.M., Karapehlivan, M., Citil, M., Atakisi, O., Uzlu, E., & Unver, A. (2008). Serum sialic acid and oxidative stress parameters changes in cattle with leptospirosis. Veterinary Research Communications, 32(4), 333–339. https://doi.org/10.1007/s11259-008-9036-z
  22. Erel, O., & Neselioglu, S. (2014). A novel and automated assay for thiol/ disulphide homeostasis. Clinical Biochemistry, 47(18), 326-32. https://doi.org/10.1016/j.clinbiochem.2014.09.026
  23. Esterbauer, H., Eckl, P., & Ortner, A. (1990). Possible mutagens derived from lipids and lipid precursors. Mutation Research/ Reviews in Genetic Toxicology, 238(3), 223–233. https://doi.org/10.1016/0165-1110(90)90014-3
  24. Franco, R., Casadó, V., Ciruela, F., Saura, C., Mallol, J., Canela, E. I., & Lluis, C. (1997). Cell surface adenosine deaminase: Much more than an ectoenzyme. Progress in Neurobiology, 52(4), 283–294. https://doi.org/10.1016/s0301-0082(97)00013-0
  25. Gazioğlu, A., Güvenç, M. (2015). Oxidative stress and some biochemical parameters in calves with leptospirosis. Firat University Veterinary Journal of Health Sciences, 29 (1), 45-048
  26. Giusti, G. (1974). Adenosine deaminase. In Elsevier eBooks (pp. 1092–1099). https://doi.org/10.1016/b978-0-12-091302-2.50108-0
  27. Guglielmini, J., Bourhy, P., Schiettekatte, O., Zinini, F., Brisse, S., Picardeau, M. (2019). Genus-wide Leptospira core genome multilocus sequence typing for strain taxonomy and global surveillance. PLoS Neglected Tropical Disease, 13(4), e0007374. https://doi.org/10.1371/journal.pntd.0007374
  28. Haake, D.A., & Levett, P.N. (2015). Leptospirosis in humans. Current Topics in Microbiology and Immunology, 65–97. https://doi.org/10.1007/978-3-662-45059-8_5
  29. Harran, E., Hilan, C., Djelouadji, Z., & Ayral, F. (2022). Epidemiology of Leptospirosis: The first literature review of the neglected disease in the Middle East. Tropical Medicine and Infectious Disease, 7(10), 260. https://doi.org/10.3390/tropicalmed7100260
  30. Hornsby, R. L., Alt, D. P., & Nally, J. E. (2020). Isolation and propagation of leptospires at 37°C directly from the mammalian host. Scientific Reports, 10(1), 9620. https://doi.org/10.1038/s41598-020-66526-4
  31. Kim, Y.G., Jeon, D.Y., & Yang, M.K. (1997). Superoxide dismutase activity and lipid peroxidation in the liver of Guinea Pig infected with Leptospira interrogans. Free Radical Research, 26(1), 1–6. https://doi.org/10.3109/10715769709097779
  32. Levett, P.N. (2014). Systematics of Leptospiraceae. Current Topics in Microbiology and Immunology, 11–20. https://doi.org/10.1007/978-3-662-45059-8_2
  33. Lilenbaum, W., Varges, R., Ristow, P., Cortez, A., Souza, S., Richtzenhain, L., & Vasconcellos, S. (2009). Identification of Leptospira spp. Carriers among seroreactive goats and sheep by polymerase chain reaction. Research in Veterinary Science, 87(1), 16–19. https://doi.org/10.1016/j.rvsc.2008.12.014
  34. List of Prokaryotic names with Standing in Nomenclature (LPSN). Leptospira species. https://lpsn.dsmz.de/search?word=leptospira (accessed 10 December 2024).
  35. Lykkesfeldt, J., & Svendsen, O. (2007). Oxidants and antioxidants in disease: Oxidative stress in farm animals. The Veterinary Journal, 173(3), 502–511. https://doi.org/10.1016/j.tvjl.2006.06.005
  36. Marnett, L.J. (1999). Lipid peroxidation—DNA damage by malondialdehyde. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 424:(1–2), 83–95. https://doi.org/10.1016/s0027-5107(99)00010-x
  37. Merendino, R.A., Salvo F., Saija A., Di Pasquale G., Tomaino A., Minciullo P.L., Fraccica G., & Gangemi, S. (2003). Malondialdehyde in benign prostate hypertrophy: a useful marker? Mediators of Inflammation, 12, 127–128. https://doi.org/10.1080/0962935031000097745
  38. Nally, J. E., Ahmed, A. A., Putz, E.J., Palmquist, D.E., & Goris, M.G.A. (2020). Comparison of Real-Time PCR, Bacteriologic Culture and Fluorescent Antibody Test for the Detection of leptospira borgpetersenii in Urine of Naturally Infected Cattle. Veterinary Sciences, 7(2), 66. https://doi.org/10.3390/vetsci7020066
  39. Niroomandi, E., Maleki, S., Abdollahpour, G., Zakian, A., & Ahmadvand, H. (2022). The effect of natural infection with different Leptospira interrogansserovars on oxidative stress biomarkers and acutephase responses in horses and cattle. Veterinary Clinical Pathology, 51(1), 84–92. https://doi.org/10.1111/vcp.13042
  40. Philip, N., Affendy, N.B., Masri, S.N., Yuhana, M.Y., Than, L.T.L., Sekawi, Z., & Neela, V.K. (2020). Combined PCR and MAT improves the early diagnosis of the biphasic illness leptospirosis. PLoS One, 15(9), e0239069. https://doi.org/10.1371/journal.pone.0239069
  41. Picardeau, M. (2017). Virulence of the zoonotic agent of leptospirosis: still terra incognita? Nature Reviews Microbiology, 15(5), 297–307. https://doi.org/10.1038/nrmicro.2017.5
  42. Reller, M.E., Wunder, E.A., Jr., Miles, J.J., Flom, J.E., Mayorga, O., Woods, C.W., Ko, A.I., Dumler, J.S., & Matute, A.J. (2014). Unsuspected leptospirosis is a cause of acute febrile illness in Nicaragua. PLoS Neglected Tropical Disease, 8(7), e2941. https://doi.org/10.1371/journal.pntd.0002941
  43. Stocker, R., Hunt, N.H., Buffinton, G.D., Weidemann, M.J., Lewis- Hughes, P.H., & Clark, I. A. (1985). Oxidative stress and protective mechanisms in erythrocytes in relation to Plasmodium vinckei load. Proceedings of the National Academy of Sciences, 82(2), 548–551. https://doi.org/10.1073/pnas.82.2.548
  44. Sohm, C., Steiner, J., Jöbstl, J., Wittek, T., Firth, C., Steinparzer, R., & Desvars-Larrive, A. (2023). A systematic review on leptospirosis in cattle: A European perspective. One Health, 17, 100608. https://doi.org/10.1016/j.onehlt.2023.100608
  45. Tonin, A.A., Pimentel, V.C., Da Silva, A.S., De Azevedo, M.I., Souza, V.C., Wolkmer, P., & Lopes, S.T. (2011). Adenosine deaminase activity in serum, erythrocytes and lymphocytes of rats infected with Leptospira icterohaemorrhagiae. Research in Veterinary Science, 92(2), 197–201. https://doi.org/10.1016/j.rvsc.2011.01.013
  46. Valko, M., Leibfritz, D., Moncol, J., Cronin, M. T., Mazur, M., & Telser, J. (2006). Free radicals and antioxidants in normal physiological functions and human disease. The International Journal of Biochemistry & Cell Biology, 39(1), 44–84. https://doi.org/10.1016/j.biocel.2006.07.001
  47. Valyi-Nagy, T., & Dermody, T.S. (2005). Role of oxidative damage in the pathogenesis of viral infections of the nervous system. Histology and Histopathology, 20(3), 957–967. https://doi.org/10.14670/hh-20.957
  48. Vincent, A.T., Schiettekatte, O., Goarant, C., Neela, V.K., Bernet, E., Thibeaux, R., & Picardeau, M. (2019). Revisiting the taxonomy and evolution of pathogenicity of the genus Leptospira through the prism of genomics. PLoS Neglected Tropical Diseases, 13(5), e0007270. https://doi.org/10.1371/journal.pntd.0007270
  49. Voitkun, V., & Zhitkovich, A. (1999). Analysis of DNA–protein crosslinking activity of malondialdehyde in vitro. Mutation Research/ Fundamental and Molecular Mechanisms of Mutagenesis, 424(1–2), 97–106. https://doi.org/10.1016/s0027-5107(99)00011-1
  50. Yoshioka, T., Kawada, K., Shimada, T., & Mori, M. (1979). Lipid peroxidation in maternal and cord blood and protective mechanism against activated-oxygen toxicity in the blood. American Journal of Obstetrics and Gynecology, 135(3), 372–376. https://doi.org/10.1016/0002-9378(79)90708-7
  51. Atakiş̇ i̇, E., Kirmizigül, A. H., Atakiş̇, O., Sari, E. K., Öğün, M., Maraşli, Ş., Çelebi,̇ Ö. (2014). Leptospirozlu sığırlarda plazma nitrik oksit (NO) ve tümör nekrozis faktör-α (TNF-α) düzeyleri ile adenozin deaminaz (ADA), gama glutamil transferaz (GGT) aktiviteleri ve perifer kan lökositlerinde alfa naftil asetat esteraz (ANAE) yöntemiyle lenfosit oranlarının belirlenmesi. Kafkas Universitesi Veteriner Fakultesi Dergisi, 20(3), 451-455. https://doi.org/10.9775/kvfd.2013.10427