Fine mapping of the antigenic epitopes of the Gc protein of Guertu virus

• Published in: PloS one Vol. 17; no. 7; p. e0271878
• Main Authors: Yusufu, Meilipaiti, Abula, Ayipairi, Jiang, Boyong, Zhumabai, Jiayinaguli, Deng, Fei, Li, Yijie, Zhang, Yujiang, Ding, Juntao, Sun, Surong
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 26.07.2022; Public Library of Science (PLoS)
• Subjects: Amino acid sequence; Amino acids; Antibodies; Antigenic determinants; Antigens; Arachnids; B cells; Biology and Life Sciences; Biosynthesis; Bunyaviruses; Cell interactions; Epitope mapping; Fever; Genetic aspects; Glycoproteins; Health risks; Homology; Immune response; Immune system; Immunoglobulin G; Immunological research; Immunology; Laboratories; Lymphocytes B; Mapping; Medical research; Medicine and Health Sciences; Methods; Nucleotide sequence; Peptide mapping; Peptides; Polyclonal antibodies; Proteins; Research and Analysis Methods; RNA polymerase; Sheep; Similarity; Structural analysis; Structure; Three dimensional analysis; Thrombocytopenia; Vaccines; Viral proteins; Viruses; China
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0271878

Guertu virus (GTV), a newly discovered member of the genus Banyangvirus in the family Phenuiviridae, poses a potential health threat to humans and animals. The viral glycoprotein (GP) binds to host cell receptors to induce a neutralizing immune response in the host. Therefore, identification of the B-cell epitopes (BCEs) in the immunodominant region of the GTV Gc protein is important for the elucidation of the virus-host cell interactions and the development of GTV epitope assays and vaccines. In this study, an improved overlapping biosynthetic peptide method and rabbit anti-GTV Gc polyclonal antibodies were used for fine mapping of the minimal motifs of linear BCEs of the GTV Gc protein. Thirteen BCE motifs were identified from eleven positive 16mer-peptides, namely EGc1 (.sup.19 KVCATTGRA.sup.27 ), EGc2 (.sup.58 KKINLKCKK.sup.66 ), EGc3 (.sup.68 SSYYVPDA.sup.75 ), EGc4 (.sup.75 ARSRCTSVRR.sup.84 ), EGc5 (.sup.79 CTSVRRCRWA.sup.88 ), EGc6 (.sup.90 DCQSGCPS.sup.97 ), EGc7 (.sup.96 PSHFTSNS.sup.103 ), EGc8 (.sup.115 AGLGFSG.sup.121 ), EGc9 (.sup.148 ENPHGVI.sup.154 ), EGc10 (.sup.179 KVFHPMS.sup.185 ), EGc11 (.sup.230 QAGMGVVG.sup.237 ), EGc12 (.sup.303 RSHDSQGKIS.sup.312 ), and EGc13 (.sup.430 DIPRFV.sup.435). Of these, 7 could be recognized by GTV IgG-positive sheep sera. Three-dimensional structural analysis revealed that all 13 BCEs were present on the surface of the Gc protein. Sequence alignment of the 13 BCEs against homologous proteins from 10 closely related strains of severe fever with thrombocytopenia syndrome virus from different geographical regions revealed that the amino acid sequences of EGc4, EGc5, EGc8, EGc11, and EGc12 were highly conserved, with 100% similarity. The remaining 8 epitopes (EGc1, EGc2, EGc3, EGc6, EGc7, EGc9, EGc10, and EGc13) showed high sequence similarity in the range of 71.43%-87.50%. These 13 BCEs of the GTV Gc protein provide a molecular foundation for future studies of the immunological properties of GTV glycoproteins and the development of GTV multi-epitope assays and vaccines.