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Volume 32, Number 4—April 2026
Research
Confirming ERVEBO Vaccination to Support Ebola Virus Surveillance
Figure 1

Figure 1. Antigen selection and assay optimization for study of development of multiplex assay to confirm Ebola vaccination. A) Schematic illustration of the rVSV∆G-ZEBOV-GP genome and proteins used in the assay design. Orange indicates the shared portion in GP1 and sGP. del21-nucleoprotein denotes the deletion of the N terminal 21 amino acids of VSV nucleoprotein. B–D) The effect of coupling protein concentration on detection was measured as MFI/50 beads by using mAb114 for EBOV GP1,2 (B) and EBOV sGP (C) and a serum sample from an ERVEBO vaccinee for VSV-P-N (D). Figure created using BioRender (https://www.biorender.com). Avi-tag, Avidin tag; Biot, protein biotinylation; EBOV, Ebola virus; GP, glycoprotein; His-tag, histidine tag; L, large RNA polymerase; M, matrix; mAB, monoclonal antibody; MFI, mean fluorescence intensity; N, nucleocapsid; P, phosphoprotein; P peptide, the first 60 amino acids of the VSV phosphoprotein; rVSV∆G-ZEBOV-GP, recombinant vesicular stomatitis virus where VSV glycoprotein G gene is deleted and replaced with the Ebola virus glycoprotein gene; sGP, secreted glycoprotein; VSV, vesicular stomatitis virus; VSV-P-N, vesicular stomatitis virus nucleoprotein N-terminally fused with P peptide.