Title:
A novel 12.6-kDa protein of leishmania donovani for the diagnosis of Indian visceral leishmaniasis

dc.contributor.authorDinesh Kumar
dc.contributor.authorSubodh Kumar
dc.contributor.authorJaya Chakravarty
dc.contributor.authorShyam Sundar
dc.date.accessioned2026-02-07T05:26:22Z
dc.date.issued2011
dc.description.abstractBackground: 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.identifier.doi10.1089/vbz.2011.0620
dc.identifier.issn15577759
dc.identifier.urihttps://doi.org/10.1089/vbz.2011.0620
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/22526
dc.subjectDiagnosis
dc.subjectELISA
dc.subjectMALDI-TOF
dc.subjectVisceral leishmaniasis
dc.subjectWestern blotting
dc.titleA novel 12.6-kDa protein of leishmania donovani for the diagnosis of Indian visceral leishmaniasis
dc.typePublication
dspace.entity.typeArticle

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