Enhancing Brucellosis diagnosis in Ovine populations: a comparative analysis of iELISA and RBPT in Thi-Qar province

Authors

  • Mokhtar H. Ramadhan Institute of Genetic Engineering and Biotechnology for Postgraduate Studies, University of Baghdad, Iraq
  • Wasan A. Garbi Institute of Genetic Engineering and Biotechnology for Postgraduate Studies, University of Baghdad, Iraq

DOI:

https://doi.org/10.5281/zenodo.10384406

Keywords:

Brucella melitensis, iELISA, Sheep, Serology, Diagnostic Techniques

Abstract

In our scholarly endeavor at Oxford University, we meticulously investigated refined methodologies for detecting anti-brucella antibodies within the serum of ovine species. This study rigorously evaluates two predominant diagnostic approaches: the Rose Bengal Plate Test (RBPT) and the indirect Enzyme-Linked Immunosorbent Assay (iELISA). The RBPT, recognized for its expeditious nature, is a slide-based agglutination test employing antigens from Brucella melitensis biovar 1, specifically the Weybridge strain number 99. In contrast, iELISA represents an indirect detection paradigm, utilizing specific antigens to accurately identify antibodies within serum samples. Both diagnostic procedures commence with the standardization of serum samples and reagents to ambient temperature. This is followed by intricate protocols encompassing antigen-antibody interactions and meticulous observation of outcomes. The RBPT is characterized by its immediate visual agglutination, typically manifesting within minutes. Conversely, the iELISA approach discerns antibodies through a sequence of enzyme-mediated reactions, culminating in observable color variations. This comprehensive study encompassed the analysis of 259 serum samples extracted from female sheep, stratified across three distinct age brackets. Within this cohort, 37 out of 259 samples (14.29%) yielded positive results through RBPT, whereas a significantly larger proportion, 222 out of 259 (85.71%), were determined to be negative. In the realm of ELISA, 67 out of 259 samples (25.87%) were positively identified, leaving 192 out of 259 (74.13%) in the negative spectrum. These samples were meticulously collected from eight disparate fields in the Thi-Qar Province, located in the southern region of Iraq. The collection period spanned from November 2022 to June 2023, encompassing animals that exhibited clinical signs of the disease or had histories of abortion. Our findings lead to a compelling conclusion: the ELISA technique demonstrates superior sensitivity and accuracy in detecting specific antibodies within physiological fluids when juxtaposed with the RBPT method. This revelation holds profound implications for the field of veterinary diagnostics, particularly in the context of brucellosis in sheep.

References

Abdoel, T., Dias, I. T., Cardoso, R., & Smits, H. L. (2008). Simple and rapid field tests for brucellosis in livestock. Veterinary Microbiology, 130(3–4), 312–319.

Al-Bayatti, S. A. (2006). BACTERIOLOGICAL & SEROLOGICAL STUDY OF BRUCELLOSIS IN BUFFALO IN BAGHDAD. The Iraqi Journal of Veterinary Medicine, 30(2), 23–30.

Al-Mossawy, F. K., Mohammed, N. S., & Al-Zubaidy, I. A. (2019). Determination of Brucella. abortus Biovars infected human in the middle and southern of iraq. Journal of Biotechnology Research Center, 13(2), 17–25.

Al-Naemi, E. (2010). STUDYING THE HISTOPATHOLOGICAL AND PHYSIOLOGICAL EFFECTS OF CRUD AND PARTIALLY PURIFIED LIPOPOLYSACCARID FROM Brucella abortus (BIO VAR6) ON LAB MICE. Iraqi Journal of Biotechnology, 9(3).

Al-Saadi, B. Q. H., & Abd, A. S. (2019). The effect of bacterial infection on male infertility. Iraqi Journal of Biotechnology, 18(3).

Aloufi, A. D., Memish, Z. A., Assiri, A. M., & McNabb, S. J. N. (2016). Trends of reported human cases of brucellosis, Kingdom of Saudi Arabia, 2004–2012. Journal of Epidemiology and Global Health, 6(1), 11–18.

Alton, G. G., Jones, L. M., Angus, R. D., & Verger, J. M. (1988). Techniques for the brucellosis laboratory. Institut National de la recherche Agronomique (INRA).

Beyene, T., & Tesega, B. (2014). Rational veterinary drug use: Its significance in public health. Journal of Veterinary Medicine and Animal Health, 6(12), 302–308.

Connelly, L. (2019). Chi-square test. Medsurg Nursing, 28(2), 127.

de Jager, W., Prakken, B. J., Bijlsma, J. W. J., Kuis, W., & Rijkers, G. T. (2005). Improved multiplex immunoassay performance in human plasma and synovial fluid following removal of interfering heterophilic antibodies. Journal of Immunological Methods, 300(1–2), 124–135.

Di Bonaventura, G., Angeletti, S., Ianni, A., Petitti, T., & Gherardi, G. (2021). Microbiological laboratory diagnosis of human brucellosis: An overview. Pathogens, 10(12), 1623.

El-Sayed, A., & Awad, W. (2018). Brucellosis: Evolution and expected comeback. International Journal of Veterinary Science and Medicine, 6, S31–S35.

Facciolà, A., Palamara, M. A. R., D’Andrea, G., Marano, F., Magliarditi, D., Puglisi, G., Picerno, I., Di Pietro, A., & Visalli, G. (2018). Brucellosis is a public health problem in southern Italy: Burden and epidemiological trend of human and animal disease. Journal of Infection and Public Health, 11(6), 861–866.

Faik, A. J. (2013). Molecular Diagnosis of Brucella species in Baghdad. Baghdad Science Journal, 10, 1.

Franc, K. A., Krecek, R. C., Haesler, B., & Arenas-Gamboa, A. M. (n.d.). Brucellosis remains a neglected disease inthe developing world: a call forinterdisciplinary action. BMC Public Health, 18(125).

Franc, K. A., Krecek, R. C., Häsler, B. N., & Arenas-Gamboa, A. M. (2018). Brucellosis remains a neglected disease in the developing world: a call for interdisciplinary action. BMC Public Health, 18(1), 1–9.

Hade, B. F. (2014). Molecular Detection to Toxoplasma gondii in Serum Sheep Samples. Iraqi Journal of Biotechnology, 13(2), 58–65.

Hamade, K. H., Jasem, K. A., & Abood, Z. H. (2010). Comparison between the efficiency of serological tests for Identification of Brucellosis. Baghdad Science Journal, 7(2).

Hill, I. D. (2005). What are the sensitivity and specificity of serologic tests for celiac disease? Do sensitivity and specificity vary in different populations? Gastroenterology, 128(4), S25–S32.

Kim, J. W., Lee, Y. J., Han, M. Y., Bae, D. H., Jung, S. C., Oh, J. S., Ha, G. W., & Cho, B. K. (2007). Evaluation of immunochromatographic assay for serodiagnosis of Brucella canis. Journal of Veterinary Medical Science, 69(11), 1103–1107.

Krueger, W. S., Lucero, N. E., Brower, A., Heil, G. L., & Gray, G. C. (2014). Evidence for unapparent Brucella canis infections among adults with occupational exposure to dogs. Zoonoses and Public Health, 61(7), 509–518.

Lopez, G., Ayala, S. M., Escobar, G. I., & Lucero, N. E. (2005). Use of Brucella canis antigen for detection of ovine serum antibodies against Brucella ovis. Veterinary Microbiology, 105(3–4), 181–187.

Merino, A. L., Santiago, R. L., Ocampo, D. A., Monroy, I. H., & Dominguez, F. G. (1991). Brucelosis: avances y perspectivas. In Brucelosis: avances y perspectivas (p. 54).

Rahawy, M. A., & AL-Timimi, I. H. (2016). Analysis of Polymorphism of Melatonin Receptor Type 1A (MTNR1A) Gene, in Iraqi Local Sheep Using PCR-RFLP Technique. Iraqi Journal of Biotechnology, 15(3).

Smits, H. L., Abdoel, T. H., Solera, J., Clavijo, E., & Diaz, R. (2003). Immunochromatographic Brucella-specific immunoglobulin M and G lateral flow assays for rapid serodiagnosis of human brucellosis. Clinical and Vaccine Immunology, 10(6), 1141–1146.

Sulaiman, K. M. (2017). Chromosomal study for Assessment of Recurrent Spontaneous Miscarriage by Fluorescence in situ Hybridization (FISH) technique in Erbil City Iraqi-Kurdistan Region. Iraqi Journal of Cancer and Medical Genetics, 10(2).

Xu, N., Wang, W., Chen, F., Li, W., & Wang, G. (2020). ELISA is superior to bacterial culture and agglutination test in the diagnosis of brucellosis in an endemic area in China. BMC Infectious Diseases, 20(1), 1–7.

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Published

2023-11-28

How to Cite

Ramadhan, M. H. ., & Garbi , W. A. . (2023). Enhancing Brucellosis diagnosis in Ovine populations: a comparative analysis of iELISA and RBPT in Thi-Qar province. Journal of Wildlife and Biodiversity, 7(Special Issue), 772–779. https://doi.org/10.5281/zenodo.10384406