http://repository.iitr.ac.in/handle/123456789/10814
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kumar D. | - |
dc.contributor.author | Kumar S. | - |
dc.contributor.author | Chakravarty J. | - |
dc.contributor.author | Sundar S. | - |
dc.date.accessioned | 2020-10-15T12:12:19Z | - |
dc.date.available | 2020-10-15T12:12:19Z | - |
dc.date.issued | 2011 | - |
dc.identifier.citation | Vector-Borne and Zoonotic Diseases (2011), 11(10): 1359-1364 | - |
dc.identifier.issn | 15303667 | - |
dc.identifier.other | 21923256 | - |
dc.identifier.uri | https://doi.org/10.1089/vbz.2011.0620 | - |
dc.identifier.uri | http://repository.iitr.ac.in/handle/123456789/10814 | - |
dc.description.abstract | Background: For the diagnosis of visceral leishmaniasis (VL), rK39 antigen-based rapid test is widely used. Unfortunately, up to 32% healthy individuals from endemic region test positive with this antigen. There is an urgent need to search for a more specific antigen with sensitivity similar to rK39. Methods: We identified a Leishmania donovani-specific 12.6-kDa (BHUP3) soluble promastigote antigen through sensitive western blot technique. The identified protein was partially purified from sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the antigenic response of eluted protein was determined by western blot with different groups of individual sera. The diagnostic potential was further validated by enzyme-linked immunosorbent assay using serum of 100 VL patients, 93 nonendemic healthy control individuals, 110 endemic healthy control individuals, and 110 disease control individuals. Further, it was characterized by two-dimensional gel electrophoresis followed by matrix-assisted laser desorption/ionization-time-of-flight analysis. Results: On blotting, antibody against this protein was recognized by all (9/9) VL patient's sera, but it was absent in every control group (nonendemic healthy control and endemic healthy control). Sensitivity of the enzyme-linked immunosorbent assay was 88% (89/101), whereas the specificity for endemic healthy, nonendemic healthy, and different disease groups were 96% (106/110), 100% (93/93), and 97% (107/110), respectively. The two-dimensional gel electrophoresis showed a single spot, and matrix-assisted laser desorption/ionization-time-of-flight analysis revealed that it is a 113-amino-acid-long putative uncharacterized protein of 12.6-kDa anamorsin homolog matched completely with Leishmania major (GenBank accession number: Q4QIS1). Conclusion: Despite marginally lower sensitivity of BHUP3, excellent specificity warrants its further development as a tool for diagnosis of VL. © Copyright 2011, Mary Ann Liebert, Inc. | - |
dc.language.iso | en_US | - |
dc.relation.ispartof | Vector-Borne and Zoonotic Diseases | - |
dc.subject | Diagnosis | - |
dc.subject | ELISA | - |
dc.subject | MALDI-TOF | - |
dc.subject | Visceral leishmaniasis | - |
dc.subject | Western blotting | - |
dc.title | A novel 12.6-kDa protein of leishmania donovani for the diagnosis of Indian visceral leishmaniasis | - |
dc.type | Article | - |
dc.scopusid | 57202478211 | - |
dc.scopusid | 57209548091 | - |
dc.scopusid | 16241108100 | - |
dc.scopusid | 7103328080 | - |
dc.affiliation | Kumar, D., Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India | - |
dc.affiliation | Kumar, S., Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India | - |
dc.affiliation | Chakravarty, J., Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India | - |
dc.affiliation | Sundar, S., Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India | - |
dc.description.correspondingauthor | Sundar, S.; Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India; email: drshyamsundar@hotmail.com | - |
Appears in Collections: | Journal Publications [ME] |
Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.