Serum antibody responses to Wolbachia surface protein in patients with human lymphatic filariasis

• Published in: Microbiology and immunology 2009-12, Vol.53 (12), p.685-693
• Main Authors: Shiny, Chandanapurath, Krushna, Nagampalli S.A., Archana, Bairavasundaram, Farzana, Begum, Narayanan, Rangarajan B.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Antibodies - blood; B-Lymphocytes - immunology; Bacterial Proteins - genetics; Bacterial Proteins - immunology; Brugia malayi; Brugia malayi - microbiology; Cloning, Molecular; DNA, Protozoan - genetics; Elephantiasis, Filarial - blood; Elephantiasis, Filarial - immunology; Elephantiasis, Filarial - microbiology; ELISA; Epitopes - analysis; Epitopes - chemistry; Epitopes - immunology; Helminth Proteins - genetics; HLA-D Antigens - immunology; Humans; Immunoglobulin E - blood; Immunoglobulin G - blood; isotype antibody; Membrane Proteins - genetics; Membrane Proteins - immunology; Polymerase Chain Reaction; T-Lymphocytes - immunology; Wolbachia - immunology; Wolbachia surface protein
• ISSN: 0385-5600; 1348-0421
• DOI: 10.1111/j.1348-0421.2009.00172.x

ABSTRACT Wolbachia surface protein (WSP), which is the most abundantly expressed protein of Wolbachia from the human filarial parasite Brugia malayi, was chosen for the present study. B‐cell epitope prediction of the WSP protein sequence indicates a high antigenicity, surface probability and hydrophilicity by DNA STAR software analysis. ProPred analysis suggests the presence of HLA class II binding regions in the WSP protein that contribute to T‐cell responses and isotype reactivity. In order to validate these findings, the gene coding for endosymbiont WSP was PCR‐amplified from the genomic DNA of the human filarial parasite Brugia malayi and cloned in T‐7 expression vector pRSET‐A. Western blot and ELISA at the total IgG level with recombiant WSP indicated a significantly elevated reactivity in CP compared to MF, EN and NEN individuals. Isotype ELISA also suggested an elevated reactivity in CP patients at the IgG1 level. In contrast, WSP‐specific IgG4 levels were found to be elevated in MF patients compared to CP and EN. Besides this, WSP‐specific IgE levels indicated an elevated reactivity in CP and MF patients compared to normals. Observations from ELISA supported the in silico predictions that indicate the presence of B‐ and T‐cell epitopes. Hence, a combinatorial approach of in silico predictions and wet‐lab studies provides interesting insights into the role of Wolbachia proteins in filarial pathogenesis.