alexa In Silico Identification of B-Cell Epitopes of Leishman
ISSN 2469-9853

Journal of Next Generation Sequencing & Applications
Open Access

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Research Article

In Silico Identification of B-Cell Epitopes of Leishmania infantum Recombinant Histone Shared with Human Sera Stably Living in Area Where Leishmania Species Does Perpetuate

Sami Lakhal1* and Malcolm S Duthie2

1Laboratory of Virology, Veterinary Research Institute of Tunisia, Rue Djebel Lakhdhar-La Rabta 1006 Tunis, Tunisia

2Infectious Disease Research Institute, Suite 400, 1616 Eastlake Ave E, Seattle, WA 98102, USA

*Corresponding Author:
Sami Lakhal
Laboratory of Virology, Veterinary Research Institute of Tunisia
Rue Djebel Lakhdhar-La Rabta 1006 Tunis, Tunisia
Tel: (+216)71564321
E-mail: [email protected]

Received date: April 24, 2017; Acceped date: June 13, 2017; Published date: June 15, 2017

Citation: Lakhal S, Duthie MS (2017) In Silico Identification of B-Cell Epitopes of Leishmania infantum Recombinant Histone Shared with Human Sera Stably Living in Area Where Leishmania Species Does Perpetuate. Next Generat Sequenc & Applic 4:146. doi:10.4172/2469-9853.1000146

Copyright: © 2017 Lakhal S, et al. This is an open-access article distributed under the terms of the creative commons attribution license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Visceral leishmaniasis (VL) can initially be misdiagnosed because its presentation is similar to many autoimmune diseases such as systemic lupus erythematosus (SLE), autoimmune hepatitis and dermatomyositis. Furthermore, serum antibodies from VL patients have been shown to strongly react against proteins that are conserved between the causative agent, L. infantum, and humans themselves. Some of these proteins, like histone, have also been described as immunogenic in several auto-immune syndromes, and the detection of antibodies against them is considered to be indicative of immune system disorders.

The potential overlap of autoimmune diseases and VL presents a situation of confounding diagnoses if cross-reactive tests are used. To explore this possibility, we screened sera from three Tunisian populations for the presence, and relative quantity, of antibodies against a panel of L. infantum antigens comprising crude extract or recombinant molecules, with special attention being given to evolutionarily conserved histones. Our data indicate that antibodies in many of the SLE at-risk individuals recognized crude soluble Leishmania antigen (SLA). This compromised the specificity of SLA-based ELISA, providing many results falsely indicating L. infantum infection. Examination of the crude Leihsmania histone (CLH) mixture, which is expected to contain nucleosomal Leishmania histones H2A, H2B and H4, as well as recombinant versions of these Leishmania histones, suggested these to be a source of the cross-reactivity. For the purposes of diagnosing VL, it is therefore important to note that the rK39 antigen was found to be more specific and not conflicting with autoimmune presentations. In silico prediction data validate and indicate that the human histones are immunologically cross-reactive with Leishmania histones.

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