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|Title:||Novel differential linear B‐cell epitopes to identify Zika and dengue virus infections in patients||Authors:||Siti Naqiah Amrun
Farhana Abu Bakar
Tan, Jeslin J. L.
Lim, Vanessa W. X.
Ng, Lisa F. P.
|Issue Date:||2019||Source:||Siti Naqiah Amrun., Yee, W.-X., Farhana Abu Bakar., Lee, B., Kam, Y.-W., Lum, F.-M., . . . Ng, L. F. P. (2019). Novel differential linear B‐cell epitopes to identify Zika and dengue virus infections in patients. Clinical & Translational Immunology, 8(7), e1066-. doi:10.1002/cti2.1066||Series/Report no.:||Clinical & Translational Immunology||Abstract:||Objectives: Recent Zika virus (ZIKV) outbreaks challenged existing laboratory diagnostic standards, especially for serology‐based methods. Because of the genetic and structural similarity of ZIKV with other flaviviruses, this results in cross‐reactive antibodies, which confounds serological interpretations. Methods: Plasma from Singapore ZIKV patients was screened longitudinally for antibody responses and neutralising capacities against ZIKV. Samples from healthy controls, ZIKV patients and DENV patients were further assessed using ZIKV and DENV peptides of precursor membrane (prM), envelope (E) or non‐structural 1 (NS1) viral proteins in a peptide‐based ELISA for epitope identification. Identified epitopes were re‐validated and diagnostically evaluated using sera of patients with DENV, bacteria or unknown infections from Thailand. Results: Long‐lasting ZIKV‐neutralising antibodies were elicited during ZIKV infection. Thirteen potential linear B‐cell epitopes were identified, and of these, four common flavivirus, three ZIKV‐specific and one DENV‐specific differential epitopes had more than 50% sensitivity and specificity. Notably, ZIKV‐specific peptide 26 on domain I/II of E protein (amino acid residues 271–288) presented 80% sensitivity and 85.7% specificity. Importantly, the differential epitopes also showed significance in differentiating non‐flavivirus patient samples. Conclusion: Linear B‐cell epitope candidates to differentiate between ZIKV and DENV infections were identified, providing the first step towards the design of a much‐needed serology‐based assay.||URI:||https://hdl.handle.net/10356/85705
|DOI:||http://dx.doi.org/10.1002/cti2.1066||Rights:||© 2019 The Author(s). Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology Inc. This is an open access article under the terms of theCreative Commons Attribution-NonCommercialLicense, which permits use, distribution andreproduction in any medium, provided the originalwork is properly cited and is not used for commercialpurposes||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
|Appears in Collections:||LKCMedicine Journal Articles|
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