Araştırma Makalesi
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Mycobacterium avium subsp. paratuberculosis ile Enfekte Sığırlarda Oksidatif Stres Parametrelerinin İncelenmesi

Yıl 2024, Cilt: 19 Sayı: 3, 140 - 147, 29.12.2024
https://doi.org/10.17094/vetsci.1510055

Öz

Paratüberküloz sığırlarda Mycobacterium avium subsp. paratuberculosis (MAP) tarafından oluşturulan zoonotik bir hastalıktır. MAP konakçıda proinflamatuar sitokinlerin salımını artırarak reaktif oksijen türleri (ROS) oluşumuna neden olabilir. ROS artışına bağlı olarak da oksidan antioksidan denge bozulabilir ve oksidatif stres ortaya çıkabilir. Çalışmanın amacı paratüberküloz enfekte sığırlarda oksidatif stres parametrelerinin belirlenmesidir. Bu amaçla çalışmada paratüberküloz yönünden pozitif tespit edilmiş 15 adet sığır serumu ve kontrol grubu olarak 15 adet klinik açıdan sağlıklı toplam 30 adet sığır serumu kullanılmıştır. Alınan numunelerde oksidatif stres parametrelerinden total antioksidan kapasite (TAK), total oksidan kapasite (TOK), oksidatif stres indeksi (OSİ), native thiol, total thiol ve disülfid düzeyleri değerlendirilmiştir. Çalışma sonuçlarımıza göre paratüberküloz grupta TOK (21,911±11,80), OSİ (37,99±21,40), total thiol (1836,671±877,06) ve disülfid (715,420±395,32) değerleri kontrol grubundaki TOK (8,538±5,18), OSİ (10,24±7,23), total thiol (823,809±289,86) ve disülfid (197,936±131,70) değerlerine göre anlamlı düzeyde yüksek belirlenmiştir (P<,001). Paratüberküloz grubunda ki TAK (0,588±0,14) değeri ise kontrol grubunda ki TAK (0,952±0,26) değerine göre anlamlı düzeyde düşük belirlenmiştir (P<,001). Native thiol düzeyleri açısından her iki grup arasında anlamlı bir fark belirlenememiştir (P>,05). Sonuç olarak MAP enfekte sığırlarda oksidan antioksidan dengenin bozulduğu ve oksidatif stresin ortaya çıktığı belirlenmiştir. Bu nedenle hastalığın tanı ve tedavisinde oksidatif stres parametrelerinin biyobelirteç olarak kullanılabileceği kanaatine varılmıştır.

Etik Beyan

The study was conducted by the decision of the ethics committee numbered 2024/04, 19572899/031-85, taken by the "Ethics Committee Directive" of the Ministry of Agriculture and Forestry Samsun Veterinary Control Institute Animal Experiments Local Ethics Committee.

Destekleyen Kurum

The authors declared that they received no financial support for this study

Kaynakça

  • 1. Patterson C. Veterinary Medicine: A Textbook of the Diseases of Cattle, Horses, Sheep, Pigs, and Goats, 11th edition, Volumes 1 and 2. The Canadian Veterinary Journal. 2017;58(10):1116.
  • 2. Fernandez M, Benavides J, Castano P, et al. Macrophage subsets within granulomatous intestinal lesions in bovine paratuberculosis. Vet Pathol. 2017;54(1):82-93.
  • 3. Gonzalez J, Geijo MV, Garcia-Pariente C, et al. Histopathological classification of lesions associated with natural paratuberculosis infection in cattle. J Comp Pathol. 2005;133(2-3):184-196.
  • 4. Sivakumar P, Tripathi BN, Singh N, Sharma AK. Pathology of naturally occurring paratuberculosis in water buffaloes (Bubalus bubalis). Vet Pathol. 2006;43(4):455-462.
  • 5. Field NL, Mcaloon G, Gavey L, Mee JF. Mycobacterium avium subspecies paratuberculosis infection in cattle-a review in the context of seasonal pasture-based dairy herds. Ir Vet J. 2021;75(1):12.
  • 6. Rasmussen P, Barkema HW, Mason S, Beaulieu E, Hall DC. Economic losses due to Johne’s disease (paratuberculosis) in dairy cattle. J Dairy Sci. 2021;104(3):3123-3143.
  • 7. Davis WC, Kuenstner JT, Singh SV. Resolution of Crohn’s (Johne’s) disease with antibiotics: what are the next steps? Expert Rev Gastroenterol Hepatol. 2017;11(5):393-396.
  • 8. Ascençao K, Szabo C. Emerging roles of cystathionine β-synthase in various forms of cancer. Redox Biol. 2022;53:102331.
  • 9. Tozer PJ, Whelan K, Phillips RKS, Hart AL. Etiology of Perianal Crohn’s Disease: Role of genetic, microbiological, and immunological factors. Inflamm Bowel Dis. 2009;15(10):1591-1598.
  • 10. Öztürk Kalın M, Gümüşsoy KS, Hızlısoy H. The Investigation of Mycobacterium paratuberculosis by Serological and Cultural Methods in Raw Milks Retailed in Kayseri. Erciyes Üniv Vet Fak Derg. 2019;16(3):190-197.
  • 11. Kelley VA, Schorey JS. Modulation of cellular phosphatidylinositol 3-phosphate levels in primary macrophages affects heat-killed but not viable Myobacterium avium’s transport through the phagosome maturation process. Cell Microbiol. 2004;6(10):973-985.
  • 12. Fratazzi C, Arbeit RD, Carini C, et al. Macrophage apoptosis in mycobacterial infections. J Leukoc Biol. 1999;66(5):763-764.
  • 13. Fattorini L, Xiao Y, Ausiello CM, et al. Late acquisition of hyporesponsiyeness to lipopolysaccharide by Mycobacterium avium-infected human macrophages in producing tumor necrosis factor-α but not interleukin-1β and-6. J Inf Dis. 1996;173(4):1030-1034.
  • 14. Bezerra FS, Lanzetti M, Nesi RT, et al. Oxidative stress and inflammation in acute and chronic lung injuries. Antioxidants. 2023;12(3):548.
  • 15. Kryukov GV, Castellano S, Novoselov SV, et al. Characterization of mammalian selenoproteomes. Science. 2003;300(5624):1439-1443.
  • 16. Stocks CJ, Schembri MA, Sweet MJ, Kapetanovic R. For when bacterial infections persist: Toll-like receptor-inducible direct antimicrobial pathways in macrophages. J Leukoc Biol. 2018;103(1):35-51.
  • 17. Sharma P, Dubey RS. Drought induces oxidative stress and enhances the activities of antioxidant enzymes in growing rice seedlings. Plant Growth Regul. 2005;46(3):209-221.
  • 18. Manning EJB, Collins MT. Mycobacterium avium subsp. paratuberculosis: pathogen, pathogenesis and diagnosis. Rev Sci Tech. 2001;20(1):133-150.
  • 19. Kostadinovic LM, Popovic SJ, Puvaca NМ, Cabarkapa IS, Kormanjos SM, Levic JD. Influence of artemisia absinthium essential oil on antioxidative system of broilers experimentally infected with Eimeria oocysts. Vet Arh. 2016;86(2):253-264.
  • 20. Kostadinovic L, Levic J. Effects of phytoaddıtıves in poultry and pigs diseases. J Agronom Technol Eng Manag. 2018;1(1):1-7.
  • 21. Valko M, Leibfritz D, Moncol J, Cronin MTD, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol. 2007;39(1):44-84.
  • 22. Wiid I, Seaman T, Hoal EG, Benade AJS, Van Helden PD. Total antioxidant levels are low during active TB and rise with anti-tuberculosis therapy. IUBMB Life. 2004;56(2):101-106.
  • 23. Lykkesfeldt J, Svendsen O. Oxidants and antioxidants in disease: Oxidative stress in farm animals. The Vet J. 2007;173(3):502-511.
  • 24. Povoa P, Coelho L, Dal-Pizzol F, et al. How to use biomarkers of infection or sepsis at the bedside: guide to clinicians. Intensive Care Med. 2023;49(2):142-153.
  • 25. Merhan O, Bozukluhan K, Gökce G, Kocamaz D. Determination of some acute phase protein and biochemical parameter levels in cattle infected with Mycobacterium avium subsp. paratuberculosis. Bozok Vet. Sci. 2022;3(2):47-51.
  • 26. Cenesiz M, Ciftci G, Dalgin D, Kilic Y, Yarim GF, Cenesiz S. Evaluation of Oxidant and antioxidant capacity in paratuberculosis positive cattle. Pakistan J Zool. 2016;48(5):1603-1606.
  • 27. Akyuz E, Akyüz E, Kükürt A, et al. Evaluation of total sialic acid, paraoxonase activity and malondialdehyde in cows with subclinical paratuberculosis. J Hellenic Vet Med Soc. 2022;73(3):4283-4288.
  • 28. Balıkcı E, Gurdogan F. Some biochemical parameters and oxidative stress biomarkers in sheep with paratuberculosis. Med. Vet. 2015;71(11):679-682.
  • 29. El-Deeb WM, Fouda TA, El-Bahr SM. Clinico-biochemical investigation of paratuberculosis of dromedary camels in Saudi Arabia: Proinflammatory cytokines, acute phase proteins and oxidative stress biomarkers. Pak Vet J. 2014;34(4):484-488.
  • 30. Andres CMC, Perez de la Lastra JM, Juan CA, Plou FJ, Perez-Lebena E. The role of reactive species on innate immunity. Vaccines (Basel). 2022;10(10):1735.
  • 31. Emre B, Korkmaz Ö, Koyuncu I, et al. Determination of thiol/disulphide homeostasis as a new indicator of oxidative stress in dairy cows with subclinical endometritis. Vet Arh. 2021;91(2):137-148.
  • 32. Deveci MZY, Erdal H. Determination of dynamic thiol-disulfide levels in dairy cattle with foot disease. Vet Arh. 2022;92(6):657-666.
  • 33. Ertaş F, Kızıltepe Ş, Merhan O. Investigation of dynamic thiol disulfide homeostasis in young cattle with pneumonia. MAS J App Sci. 2023;8:949-954.
  • 34. Kolgelier S, Ergin M, Saltuk Demir L, et al. Impaired thiol-disulfide balance in acute brucellosis. Jpn J Infect Dis. 2017;70(3):258-262.
  • 35. Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47(18):326-332.
  • 36. Gul F, Muderris T, Yalciner G, et al. A novel method for evaluation of oxidative stress in children with OSA. Int J Pediatr Otorhinolaryngol. 2016;89:76-80.

Investigation of Oxidative Stress Parameters in Cattle Infected with Mycobacterium avium subsp. Paratuberculosis

Yıl 2024, Cilt: 19 Sayı: 3, 140 - 147, 29.12.2024
https://doi.org/10.17094/vetsci.1510055

Öz

Paratuberculosis is a zoonotic disease caused by Mycobacterium avium subsp. paratuberculosis (MAP) in cattle. MAP may cause the formation of reactive oxygen species (ROS) by increasing the release of proinflammatory cytokines in the host. Due to the increase in ROS, the oxidant-antioxidant balance may be disrupted and oxidative stress may occur. The aim of the study was to determine the oxidative stress parameters in cattle infected with paratuberculosis. For this purpose, 15 cattle sera that were positive for paratuberculosis and 15 clinically healthy 30 cattle sera were used as the control group. In the samples taken, oxidative stress parameters such as total antioxidant capacity (TAS), total oxidant capacity (TOS), oxidative stress index (OSI), native thiol, total thiol and disulphide levels were evaluated. According to our study results, TOS (21.911±11.80), OSI (37.99±21.40), total thiol (1836.671±877.06) and disulphide (715.420±395.32) values in the paratuberculosis group were significantly higher than TOS (8.538±5.18), OSI (10.24±7.23), total thiol (823.809±289.86) and disulphide (197.936±131.70) values in the control group (P<.001). The TAS (0.588±0.14) value in the paratuberculosis group was significantly lower than the TAS (0.952±0.26) value in the control group (P<.001). No significant difference was found between the two groups in terms of native thiol levels (P>.05). As a result, it was determined that the oxidant-antioxidant balance was disrupted and oxidative stress occurred in MAP infected cattle. Therefore, it was concluded that oxidative stress parameters can be used as biomarkers in the diagnosis and treatment of the disease.

Kaynakça

  • 1. Patterson C. Veterinary Medicine: A Textbook of the Diseases of Cattle, Horses, Sheep, Pigs, and Goats, 11th edition, Volumes 1 and 2. The Canadian Veterinary Journal. 2017;58(10):1116.
  • 2. Fernandez M, Benavides J, Castano P, et al. Macrophage subsets within granulomatous intestinal lesions in bovine paratuberculosis. Vet Pathol. 2017;54(1):82-93.
  • 3. Gonzalez J, Geijo MV, Garcia-Pariente C, et al. Histopathological classification of lesions associated with natural paratuberculosis infection in cattle. J Comp Pathol. 2005;133(2-3):184-196.
  • 4. Sivakumar P, Tripathi BN, Singh N, Sharma AK. Pathology of naturally occurring paratuberculosis in water buffaloes (Bubalus bubalis). Vet Pathol. 2006;43(4):455-462.
  • 5. Field NL, Mcaloon G, Gavey L, Mee JF. Mycobacterium avium subspecies paratuberculosis infection in cattle-a review in the context of seasonal pasture-based dairy herds. Ir Vet J. 2021;75(1):12.
  • 6. Rasmussen P, Barkema HW, Mason S, Beaulieu E, Hall DC. Economic losses due to Johne’s disease (paratuberculosis) in dairy cattle. J Dairy Sci. 2021;104(3):3123-3143.
  • 7. Davis WC, Kuenstner JT, Singh SV. Resolution of Crohn’s (Johne’s) disease with antibiotics: what are the next steps? Expert Rev Gastroenterol Hepatol. 2017;11(5):393-396.
  • 8. Ascençao K, Szabo C. Emerging roles of cystathionine β-synthase in various forms of cancer. Redox Biol. 2022;53:102331.
  • 9. Tozer PJ, Whelan K, Phillips RKS, Hart AL. Etiology of Perianal Crohn’s Disease: Role of genetic, microbiological, and immunological factors. Inflamm Bowel Dis. 2009;15(10):1591-1598.
  • 10. Öztürk Kalın M, Gümüşsoy KS, Hızlısoy H. The Investigation of Mycobacterium paratuberculosis by Serological and Cultural Methods in Raw Milks Retailed in Kayseri. Erciyes Üniv Vet Fak Derg. 2019;16(3):190-197.
  • 11. Kelley VA, Schorey JS. Modulation of cellular phosphatidylinositol 3-phosphate levels in primary macrophages affects heat-killed but not viable Myobacterium avium’s transport through the phagosome maturation process. Cell Microbiol. 2004;6(10):973-985.
  • 12. Fratazzi C, Arbeit RD, Carini C, et al. Macrophage apoptosis in mycobacterial infections. J Leukoc Biol. 1999;66(5):763-764.
  • 13. Fattorini L, Xiao Y, Ausiello CM, et al. Late acquisition of hyporesponsiyeness to lipopolysaccharide by Mycobacterium avium-infected human macrophages in producing tumor necrosis factor-α but not interleukin-1β and-6. J Inf Dis. 1996;173(4):1030-1034.
  • 14. Bezerra FS, Lanzetti M, Nesi RT, et al. Oxidative stress and inflammation in acute and chronic lung injuries. Antioxidants. 2023;12(3):548.
  • 15. Kryukov GV, Castellano S, Novoselov SV, et al. Characterization of mammalian selenoproteomes. Science. 2003;300(5624):1439-1443.
  • 16. Stocks CJ, Schembri MA, Sweet MJ, Kapetanovic R. For when bacterial infections persist: Toll-like receptor-inducible direct antimicrobial pathways in macrophages. J Leukoc Biol. 2018;103(1):35-51.
  • 17. Sharma P, Dubey RS. Drought induces oxidative stress and enhances the activities of antioxidant enzymes in growing rice seedlings. Plant Growth Regul. 2005;46(3):209-221.
  • 18. Manning EJB, Collins MT. Mycobacterium avium subsp. paratuberculosis: pathogen, pathogenesis and diagnosis. Rev Sci Tech. 2001;20(1):133-150.
  • 19. Kostadinovic LM, Popovic SJ, Puvaca NМ, Cabarkapa IS, Kormanjos SM, Levic JD. Influence of artemisia absinthium essential oil on antioxidative system of broilers experimentally infected with Eimeria oocysts. Vet Arh. 2016;86(2):253-264.
  • 20. Kostadinovic L, Levic J. Effects of phytoaddıtıves in poultry and pigs diseases. J Agronom Technol Eng Manag. 2018;1(1):1-7.
  • 21. Valko M, Leibfritz D, Moncol J, Cronin MTD, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol. 2007;39(1):44-84.
  • 22. Wiid I, Seaman T, Hoal EG, Benade AJS, Van Helden PD. Total antioxidant levels are low during active TB and rise with anti-tuberculosis therapy. IUBMB Life. 2004;56(2):101-106.
  • 23. Lykkesfeldt J, Svendsen O. Oxidants and antioxidants in disease: Oxidative stress in farm animals. The Vet J. 2007;173(3):502-511.
  • 24. Povoa P, Coelho L, Dal-Pizzol F, et al. How to use biomarkers of infection or sepsis at the bedside: guide to clinicians. Intensive Care Med. 2023;49(2):142-153.
  • 25. Merhan O, Bozukluhan K, Gökce G, Kocamaz D. Determination of some acute phase protein and biochemical parameter levels in cattle infected with Mycobacterium avium subsp. paratuberculosis. Bozok Vet. Sci. 2022;3(2):47-51.
  • 26. Cenesiz M, Ciftci G, Dalgin D, Kilic Y, Yarim GF, Cenesiz S. Evaluation of Oxidant and antioxidant capacity in paratuberculosis positive cattle. Pakistan J Zool. 2016;48(5):1603-1606.
  • 27. Akyuz E, Akyüz E, Kükürt A, et al. Evaluation of total sialic acid, paraoxonase activity and malondialdehyde in cows with subclinical paratuberculosis. J Hellenic Vet Med Soc. 2022;73(3):4283-4288.
  • 28. Balıkcı E, Gurdogan F. Some biochemical parameters and oxidative stress biomarkers in sheep with paratuberculosis. Med. Vet. 2015;71(11):679-682.
  • 29. El-Deeb WM, Fouda TA, El-Bahr SM. Clinico-biochemical investigation of paratuberculosis of dromedary camels in Saudi Arabia: Proinflammatory cytokines, acute phase proteins and oxidative stress biomarkers. Pak Vet J. 2014;34(4):484-488.
  • 30. Andres CMC, Perez de la Lastra JM, Juan CA, Plou FJ, Perez-Lebena E. The role of reactive species on innate immunity. Vaccines (Basel). 2022;10(10):1735.
  • 31. Emre B, Korkmaz Ö, Koyuncu I, et al. Determination of thiol/disulphide homeostasis as a new indicator of oxidative stress in dairy cows with subclinical endometritis. Vet Arh. 2021;91(2):137-148.
  • 32. Deveci MZY, Erdal H. Determination of dynamic thiol-disulfide levels in dairy cattle with foot disease. Vet Arh. 2022;92(6):657-666.
  • 33. Ertaş F, Kızıltepe Ş, Merhan O. Investigation of dynamic thiol disulfide homeostasis in young cattle with pneumonia. MAS J App Sci. 2023;8:949-954.
  • 34. Kolgelier S, Ergin M, Saltuk Demir L, et al. Impaired thiol-disulfide balance in acute brucellosis. Jpn J Infect Dis. 2017;70(3):258-262.
  • 35. Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47(18):326-332.
  • 36. Gul F, Muderris T, Yalciner G, et al. A novel method for evaluation of oxidative stress in children with OSA. Int J Pediatr Otorhinolaryngol. 2016;89:76-80.
Toplam 36 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Veteriner Biyokimya
Bölüm Araştırma Makaleleri
Yazarlar

Sena Çenesiz 0000-0002-3544-503X

Büşra Şahin 0000-0002-5245-478X

Yunus Kılıçoğlu 0000-0002-6788-9284

Volkan Yılmaz 0009-0001-1155-9518

Rahşan Koç Akpınar 0000-0003-0075-9247

Yayımlanma Tarihi 29 Aralık 2024
Gönderilme Tarihi 4 Temmuz 2024
Kabul Tarihi 4 Eylül 2024
Yayımlandığı Sayı Yıl 2024 Cilt: 19 Sayı: 3

Kaynak Göster

APA Çenesiz, S., Şahin, B., Kılıçoğlu, Y., Yılmaz, V., vd. (2024). Investigation of Oxidative Stress Parameters in Cattle Infected with Mycobacterium avium subsp. Paratuberculosis. Veterinary Sciences and Practices, 19(3), 140-147. https://doi.org/10.17094/vetsci.1510055
AMA Çenesiz S, Şahin B, Kılıçoğlu Y, Yılmaz V, Koç Akpınar R. Investigation of Oxidative Stress Parameters in Cattle Infected with Mycobacterium avium subsp. Paratuberculosis. Veterinary Sciences and Practices. Aralık 2024;19(3):140-147. doi:10.17094/vetsci.1510055
Chicago Çenesiz, Sena, Büşra Şahin, Yunus Kılıçoğlu, Volkan Yılmaz, ve Rahşan Koç Akpınar. “Investigation of Oxidative Stress Parameters in Cattle Infected With Mycobacterium Avium Subsp. Paratuberculosis”. Veterinary Sciences and Practices 19, sy. 3 (Aralık 2024): 140-47. https://doi.org/10.17094/vetsci.1510055.
EndNote Çenesiz S, Şahin B, Kılıçoğlu Y, Yılmaz V, Koç Akpınar R (01 Aralık 2024) Investigation of Oxidative Stress Parameters in Cattle Infected with Mycobacterium avium subsp. Paratuberculosis. Veterinary Sciences and Practices 19 3 140–147.
IEEE S. Çenesiz, B. Şahin, Y. Kılıçoğlu, V. Yılmaz, ve R. Koç Akpınar, “Investigation of Oxidative Stress Parameters in Cattle Infected with Mycobacterium avium subsp. Paratuberculosis”, Veterinary Sciences and Practices, c. 19, sy. 3, ss. 140–147, 2024, doi: 10.17094/vetsci.1510055.
ISNAD Çenesiz, Sena vd. “Investigation of Oxidative Stress Parameters in Cattle Infected With Mycobacterium Avium Subsp. Paratuberculosis”. Veterinary Sciences and Practices 19/3 (Aralık 2024), 140-147. https://doi.org/10.17094/vetsci.1510055.
JAMA Çenesiz S, Şahin B, Kılıçoğlu Y, Yılmaz V, Koç Akpınar R. Investigation of Oxidative Stress Parameters in Cattle Infected with Mycobacterium avium subsp. Paratuberculosis. Veterinary Sciences and Practices. 2024;19:140–147.
MLA Çenesiz, Sena vd. “Investigation of Oxidative Stress Parameters in Cattle Infected With Mycobacterium Avium Subsp. Paratuberculosis”. Veterinary Sciences and Practices, c. 19, sy. 3, 2024, ss. 140-7, doi:10.17094/vetsci.1510055.
Vancouver Çenesiz S, Şahin B, Kılıçoğlu Y, Yılmaz V, Koç Akpınar R. Investigation of Oxidative Stress Parameters in Cattle Infected with Mycobacterium avium subsp. Paratuberculosis. Veterinary Sciences and Practices. 2024;19(3):140-7.

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