Journals / Turkish Journal of Veterinary and Animal Sciences / 2015 / Cilt: 39 - Sayı: 4

Evaluation of serum enzyme activities and protein fractions in Brucella-infected cows

Pages
480–484
Publication Date
2015-08-13
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

Hence, Brucella infection has a detrimental effect on dairy cows' health and is accompanied with elevated serum ALT, AST, CK, and LDH activities and increased TP concentrations due to the increase in $\gamma$-globulin concentrations only.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The aim of this study was to evaluate potential changes in serum enzyme activities and protein fractions in Brucella-infected cows.
📊
Key Findings & Data:A total of 1100 serum samples of dairy cows were screened for Brucella infection using the Rose Bengal test (RBT).
💡
Conclusion & Impact:Hence, Brucella infection has a detrimental effect on dairy cows' health and is accompanied with elevated serum ALT, AST, CK, and LDH activities and increased TP concentrations due to the increase in $\gamma$-globulin concentrations only.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Cows · Brucella infection · serum enzymes activities

Abstract

The aim of this study was to evaluate potential changes in serum enzyme activities and protein fractions in Brucella-infected cows. A total of 1100 serum samples of dairy cows were screened for Brucella infection using the Rose Bengal test (RBT). Serum samples reacting positively to the RBT were subjected to indirect enzyme-linked immunosorbent assay for confirmation. Thirty serum samples from serologically positive cows and 30 from negative (healthy) cows were analyzed for alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatine kinase (CK), lactate dehydrogenase (LDH), alkaline phosphatase (ALP), and gamma-glutamyl transferase (GGT) activities and total protein (TP) concentrations and serum protein electrophoresis. Serum ALT, AST, CK, and LDH activities were increased in serologically positive cows and significantly higher than those measured in healthy cows. However, there were no significant differences in ALP and GGT activities. TP and $\gamma$-globulin concentrations were increased in serologically positive cows and significantly higher than those of healthy cows, but there were no significant differences in albumin or $\alpha$1-, $\alpha$2-, and ß-globulin concentrations. Hence, Brucella infection has a detrimental effect on dairy cows' health and is accompanied with elevated serum ALT, AST, CK, and LDH activities and increased TP concentrations due to the increase in $\gamma$-globulin concentrations only.

Özet

The aim of this study was to evaluate potential changes in serum enzyme activities and protein fractions in Brucella-infected cows. A total of 1100 serum samples of dairy cows were screened for Brucella infection using the Rose Bengal test (RBT). Serum samples reacting positively to the RBT were subjected to indirect enzyme-linked immunosorbent assay for confirmation. Thirty serum samples from serologically positive cows and 30 from negative (healthy) cows were analyzed for alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatine kinase (CK), lactate dehydrogenase (LDH), alkaline phosphatase (ALP), and gamma-glutamyl transferase (GGT) activities and total protein (TP) concentrations and serum protein electrophoresis. Serum ALT, AST, CK, and LDH activities were increased in serologically positive cows and significantly higher than those measured in healthy cows. However, there were no significant differences in ALP and GGT activities. TP and $\gamma$-globulin concentrations were increased in serologically positive cows and significantly higher than those of healthy cows, but there were no significant differences in albumin or $\alpha$1-, $\alpha$2-, and ß-globulin concentrations. Hence, Brucella infection has a detrimental effect on dairy cows' health and is accompanied with elevated serum ALT, AST, CK, and LDH activities and increased TP concentrations due to the increase in $\gamma$-globulin concentrations only.

🔖

Cite This Article

ELAZAB, M. F. A. (2015). Evaluation of serum enzyme activities and protein fractions in Brucella-infected cows. Turkish Journal of Veterinary and Animal Sciences, Cilt: 39 - Sayı: 4, 480–484. https://ajindex.com/articles/121432

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (11)

  1. Kakoma I, Oluoch AO, Baek BK, Rahman MS, Matsuda K. More attention warranted on Brucella abortus in animals. J Am Vet Med Assoc 2003; 222: 284. 2. Heller MC, Watson JL, Blanchard MT, Jackson KA, Stott JL, Tsolis RM. Characterization of Brucella abortus infection of bovine monocyte-derived dendritic cells. Vet Immunol Immunopathol 2012; 149: 255–261. 3. Meyer ME. Evolutionary development and taxonomy of the genus Brucella. In: Adams LG, editor. Advances in Brucellosis Research. College Station, TX, USA: Texas A&M University Press; 1990. pp. 12–35. 4. Singh G, Sharma DR, Sandhu KS, Dhand NK. Economic losses occurring due to bovine abortions in Punjab. In: 10th International Congress of Asian-Australasian Indian Association of Animal Production and World Buffalo Trust, New Delhi, India, 2002. pp. 23–27.
  2. Franco MP, Mulder M, Gilman RH, Smits HL. Human brucellosis. Lancet Infect Dis 2007; 7: 775–786.
  3. Radostits OM, Gay CC, Hinchcliff KW, Constable PD. Veterinary Medicine, A Text Book of the Diseases of Cattle, Horses, Sheep, Pigs and Goats. 10th ed. London, UK: W. B. Saunders; 2007.
  4. Gonzalez M, Andrews E, Folch H, Saez D, Cabrera A, Salgado P, Onate A. Cloning, expression and immunogenicity of the translation initiation factor 3 homologue of Brucella abortus. Immunobiology 2009; 214: 113–120.
  5. Alton GG, Jones LM, Angus RD, Verger JM. Technique for the Brucellosis Laboratory. Versailles, France: IRNA Publication; 1988.
  6. Samaha H, Mohamed TR, Khoudair RM, Ashour HM. Serodiagnosis of brucellosis in cattle and humans in Egypt. Immunobiology 2009; 214: 223–226.
  7. Carvalho Neta AV, Mol JP, Xavier MN, Paixão TA, Lage AP, Santos RL. Pathogenesis of bovine brucellosis. Vet J 2010; 184: 146–155.
  8. Poester FP, Samartino LE, Santos RL. Pathogenesis and pathobiology of brucellosis in livestock. Rev Sci Tech Off Int Epiz 2013; 32: 105–115.
  9. Nath R, Das S, Sarma S, Devi M. Comparison of blood profiles between healthy and Brucella affected cattle. Veterinary World 2014; 7: 668–670.
  10. El-Boshy M, Abbas M, El-Khoderyl H, Osman S. Cytokine response and clinicopathological findings in Brucella infected camels (Camelus dromedarius). Vet Med 2009; 54: 25–32.
  11. Hoffman WE, Solter PF. Diagnostic enzymology of domestic animals. In: Kaneko JJ Harvey JW, Bruss ML, editors. Clinical Biochemistry of Domestic Animals. 6th ed. San Diego, CA, USA: Academic Press; 2008. pp. 351–378. Bain PJ. Liver. In: Latimer KS, Mahaffey EA, Prasse KW, editors. Duncan and Prasse’s Veterinary Laboratory Medicine: Clinica