Published In
Indian Journal of Animal Research
Article Metrics

0
Views
0
Citations
Reviewed By
In this Article
APC
APC cover the cost of turning a manuscript into a published manuscript through peer-review process, editorial work as well as the cost of hosting, distributing, indexing and promoting the manuscript.
Publish With US
Submit your manuscript through user friendly platform and acquire the maximum impact for your research by publishing with ARCC Journals.
Become a Reviewer/Member
Join our esteemed reviewers panel and become an editorial board member with international experts in the domain of numerous specializations.
Open Access
Filling the gap between research and communication ARCC provide Open Access of all journals which empower research community in all the ways which is accessible to all.
Products and Services
We provide prime quality of services to assist you select right product of your requirement.
Support and Policies
Finest policies are designed to ensure world class support to our authors, members and readers. Our efficient team provides best possible support for you.
Follow us
volume 43 issue 2 (june 2009) : 111-113
A COMPARATIVE STUDY BETWEEN MICROSCOPIC AGGLUTINATION TEST AND DIFFERENT PROTEIN ANTIGENS BASED ENZVME-LINKED IMMUNOSORBENT' ASSAY FOR THE DETECTION OF LEPTOSPIROSIS IN BOVINE
1Division of Bacteriology and Mycology
Indian Veterinary Research Institute, Izatnagar-243 122, India.
Cite article:- Sankar Surya, Harshan M. Hiron, Chaudhary Pallab, Srivastava K. S. (2025). A COMPARATIVE STUDY BETWEEN MICROSCOPIC AGGLUTINATION TEST AND DIFFERENT PROTEIN ANTIGENS BASED ENZVME-LINKED IMMUNOSORBENT' ASSAY FOR THE DETECTION OF LEPTOSPIROSIS IN BOVINE. Indian Journal of Animal Research. 43(2): 111-113. doi: .
ABSTRACT
The present study compared the efficacy of Microscopic Agglutination Test (MAT) with UpL32
and UpL41 recombinant antigen based Enzyme-linked immunosorbent assay (ELISA) for the
diagnosis of bovine leptospirosis. The UpL32 and 41 genes were amplified using specific primers
and the polymerase chain reaction products (peR) were cloned. The gene inserts from positive
recombinant clones were inserted into expression vector and transformed in Escherichia coli DH5il
cells. The recombinant UpL32 and 41 proteins were expressed, purified and standardized. The
optimum antigen concentration of 100ng of each anti..;en was used for the screening of serum
samples from cattle suspected of leptospirosis. It was found that recombinant antigen ELISA detected
more positive cases of illness than MAT. Between the two recombinant antigens ELISA, UpL32 ELISA
was able to detect more positives.
and UpL41 recombinant antigen based Enzyme-linked immunosorbent assay (ELISA) for the
diagnosis of bovine leptospirosis. The UpL32 and 41 genes were amplified using specific primers
and the polymerase chain reaction products (peR) were cloned. The gene inserts from positive
recombinant clones were inserted into expression vector and transformed in Escherichia coli DH5il
cells. The recombinant UpL32 and 41 proteins were expressed, purified and standardized. The
optimum antigen concentration of 100ng of each anti..;en was used for the screening of serum
samples from cattle suspected of leptospirosis. It was found that recombinant antigen ELISA detected
more positive cases of illness than MAT. Between the two recombinant antigens ELISA, UpL32 ELISA
was able to detect more positives.
REFERENCES
- Biolin, C.A, et al. (1989). Am. J. Vet. Res., 50: 1001-1003.
- Cousins, D.V., et al. (1985). Vet. Microbiol., 10: 439-450.
- Engvall, E. and Perlmann, P. (1971). Immuno Chern., 8: 871-874.
- Faine S. (1982). Guidelines for the Control of Leptospirosis. 67. WHO Offset Publication, Geneva, 172pp.
- flannery, B., et a/. (2001). J. Clin. Microbiol., 39(9): 3303-3310.
- Maria Rosa, Q.B., et al. (2005). Vet. Microbiol., 109: 89-94.
- Mariya, R., etal. (2006). Compo Immunol. Microbiol. Infect. Dis., 29(5-6): 269-77.
- Pappas, M.G., et a/. (1985). Am. J. Trop. Med. Hyg., 34: 346-354.
- Thierman, AB. and Gareit, L.A (1983). Am. J .Vet. Res., 44: 883-887.
- Thrusfield, M. (1995). Veterinary Epidemiology, 2nded. The Blackwell Science Publications, U. K.
- Viajyachari, P., et al. (2001). Indian J. Med. Res., 114: 99-106.
- Wright, P.w., et al. (1993). Rev. Sci. Tech. Off. Int. Epiz., 12: 435-450.
Disclaimer :
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Copyright :
This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
In this Article
APC
APC cover the cost of turning a manuscript into a published manuscript through peer-review process, editorial work as well as the cost of hosting, distributing, indexing and promoting the manuscript.
Publish With US
Submit your manuscript through user friendly platform and acquire the maximum impact for your research by publishing with ARCC Journals.
Become a Reviewer/Member
Join our esteemed reviewers panel and become an editorial board member with international experts in the domain of numerous specializations.
Open Access
Filling the gap between research and communication ARCC provide Open Access of all journals which empower research community in all the ways which is accessible to all.
Products and Services
We provide prime quality of services to assist you select right product of your requirement.
Support and Policies
Finest policies are designed to ensure world class support to our authors, members and readers. Our efficient team provides best possible support for you.
Follow us
Published In
Indian Journal of Animal Research