An Insight for the Future Development of Diagnostic Tool by Exploiting Novel Leishmania Donovani Recombinant Hypothetical Protein

Journal Title: Journal of Clinical and Diagnostic Research - Year 2018, Vol 12, Issue 11

Abstract

ABSTRACT Introduction: Assenting diagnosis of Visceral Leishmaniasis (VL) relies on the detection of Leishmania donovani (L. donovani) in splenic and bone marrow specimens obtained by invasive techniques. Thus, the development of inexpensive, non-invasive serological test encompassing high specificity, sensitivity and diagnostic efficacy is urgently needed. Aim: To assess the significance of recombinant proteins possessing B-cell epitopes in VL diagnosis. Materials and Methods: Employing immunoinformatics approach, the B-cell epitope footprint of L. donovani hypothetical proteins (derived from earlier studies) were decrypted holding good antigenic character with numerous epitopes. L. donovani hypothetical proteins XP_003860226.1 and XP_003861271.1 were first time cloned as His-tagged fusion proteins and purified as novel recombinant protein antigens, designated rLdhyb and rLdhyc respectively. Sanger sequencing method was exploited to sequence gene insert (GeneBank accession number MH479406). Results: B-cell epitopes revealed 100% conservancy with L. infantum. Immunoinformatics data revealed no significant sequence similarity with homo sapien and the causative agent of other diseases like tuberculosis, typhoid, malaria etc., resembling in symptoms to VL. Sequencing chromatogram of cloned gene Ldhyb and Ldhyc revealed 98% and 94% identity with L. donovani. ELISA revealed the absolute specificity with sensitivity of 95.4% for rLdhyb and 91% for rLdhyc. Area under curve for rLdhyb, rLdhyc and SLA were 0.99, 0.99 and 0.961, with standard error 0.002, 0.007 and 0.019 respectively. The in silico data was coherently supported by in vitro result. Conclusion: Absolute specificity, high sensitivity and diagnostic efficacy (rLdhyb: 98%; rLdhyc: 97%) advocated their excellent biomarker property. The present findings provide some basic insights for the future development of novel hypothetical proteins based non-invasive diagnostic tool for VL detection.

Authors and Affiliations

Fauzia Jamal, Manish Kumar Singh, Jagadish Hansa, Pushpanjali . , Pushkar Shivam, Sarita Kumari, Shyam Narayan, Shubhankar K Singh

Keywords

Related Articles

The Effect of Saliva Contamination on Shear Bond Strength of Two Universal Bonding Agents-An in vitro Study

ABSTRACT Introduction: Universal bonding agents are prevalent in dentistry today. The effects of both salivary contamination and subsequent decontamination protocols on these adhesives have not been studied extensively....

A Custom Made Skeletal Class II Corrector Appliance in Late Adolescent Phase

Skeletal Class II correction in deceleration phase of growth is both a challenge and dilemma with choice between extraction and myofunctional therapy. With marginal growth remaining the convenient choice is extraction fo...

Gender Variation in the Prevalence of Internet Addiction and Impact of Internet Addiction on Reaction Time and Heart Rate Variability in Medical College Students

ABSTRACT Introduction: In the present era, the internet is widely used by college students for academic, entertainment and communication purposes. College students are vulnerable to internet addiction due to various psyc...

Penile Carcinoma in Young Age Masquerading as Mondor’s Disease

Abstract A 26-year-old unmarried male presented with voiding difficulty and penile oedema, was initially diagnosed and treated for Mondor’s disease, which is a rare, benign, usually self-limiting pathology of anonymous o...

Download PDF file
  • EP ID EP524502
  • DOI 10.7860/JCDR/2018/37316.12307
  • Views 60
  • Downloads 0

How To Cite

Fauzia Jamal, Manish Kumar Singh, Jagadish Hansa, Pushpanjali . , Pushkar Shivam, Sarita Kumari, Shyam Narayan, Shubhankar K Singh (2018). An Insight for the Future Development of Diagnostic Tool by Exploiting Novel Leishmania Donovani Recombinant Hypothetical Protein. Journal of Clinical and Diagnostic Research, 12(11), 22-29. https://europub.co.uk./articles/-A-524502