Recombinant Protein of Immunogenic Metabolic Enzyme Epitopes of Trichomonas vaginalis are Common to Humans and Microorganisms |Biomedgrid
Journal: American Journal of Biomedical Science & Research (Vol.13, No. 6)Publication Date: 2021-08-10
Authors : JF Alderete;
Page : 630-638
Keywords : Candida Albicans; Chlamydia Trachomatis; Diagnostic; Diagnostic Targets; Enzyme Linked Immunosorbent Assay (ELISA); Epitope Chain Protein;
Abstract
The number one, non-viral sexually transmitted infection (STI) worldwide is caused by the ancient protist Trichomonas vaginalis. Recently, I reported on an ~40-kDa String-Of-Epitopes chimeric protein (AEG::SOE2) consisting of immunogenic epitopes unique to the Trichomonas vaginalis fructose-1,6bisphosphate aldolase (A), α-enolase (E), and glyceraldehyde-3-phosphate dehydrogenase (G). This report is on another construct of a 49.41-kDa AEG::SOE3 chimeric protein comprised of 8, 9 and 12 non-unique, immunogenic epitopes of A, E and G, respectively. These non-unique epitopes were detected by sera of women and men patients but not control, seronegative sera of women and men. The epitopes were found to have ≥50% to 100% sequence amino acid sequence identity with the human homolog and homologs of Candida albicans, Escherichia coli, Saccharomyces cerevisiae, Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes as well as the homologs of the STI agents Chlamydia trachomatis, Neisseria gonorrhoeae and Treponema pallidum. The AEG::SOE3 protein was not detected by mouse anti AEG::SOE2 serum and by monoclonal antibodies (MAbs) to AEG::SOE2, showing the distinctness of these two chimeric proteins.
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