Cargando…
Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library
BACKGROUND: The West Nile virus (WNV) nonstructural protein 1 (NS1) is an important antigenic protein that elicits protective antibody responses in animals and can be used for the serological diagnosis of WNV infection. Although previous work has demonstrated the vital role of WNV NS1-specific antib...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158561/ https://www.ncbi.nlm.nih.gov/pubmed/21729328 http://dx.doi.org/10.1186/1471-2180-11-160 |
_version_ | 1782210384091938816 |
---|---|
author | Sun, En-Cheng Ma, Jian-Nan Liu, Ni-Hong Yang, Tao Zhao, Jing Geng, Hong-Wei Wang, Ling-Feng Qin, Yong-Li Bu, Zhi-Gao Yang, Yin-Hui Lunt, Ross A Wang, Lin-Fa Wu, Dong-Lai |
author_facet | Sun, En-Cheng Ma, Jian-Nan Liu, Ni-Hong Yang, Tao Zhao, Jing Geng, Hong-Wei Wang, Ling-Feng Qin, Yong-Li Bu, Zhi-Gao Yang, Yin-Hui Lunt, Ross A Wang, Lin-Fa Wu, Dong-Lai |
author_sort | Sun, En-Cheng |
collection | PubMed |
description | BACKGROUND: The West Nile virus (WNV) nonstructural protein 1 (NS1) is an important antigenic protein that elicits protective antibody responses in animals and can be used for the serological diagnosis of WNV infection. Although previous work has demonstrated the vital role of WNV NS1-specific antibody responses, the specific epitopes in the NS1 have not been identified. RESULTS: The present study describes the identification of two linear B-cell epitopes in WNV NS1 through screening a phage-displayed random 12-mer peptide library with two monoclonal antibodies (mAbs) 3C7 and 4D1 that directed against the NS1. The mAbs 3C7 and 4D1 recognized phages displaying peptides with the consensus motifs LTATTEK and VVDGPETKEC, respectively. Exact sequences of both motifs were found in the NS1 ((895)LTATTEK(901 )and (925)VVDGPETKEC(934)). Further identification of the displayed B cell epitopes were conducted using a set of truncated peptides expressed as MBP fusion proteins. The data indicated that (896)TATTEK(901 )and(925)VVDGPETKEC(934 )are minimal determinants of the linear B cell epitopes recognized by the mAbs 3C7 and 4D1, respectively. Antibodies present in the serum of WNV-positive horses recognized the minimal linear epitopes in Western blot analysis, indicating that the two peptides are antigenic in horses during infection. Furthermore, we found that the epitope recognized by 3C7 is conserved only among WNV strains, whereas the epitope recognized by 4D1 is a common motif shared among WNV and other members of Japanese encephalitis virus (JEV) serocomplex. CONCLUSIONS: We identified TATTEK and VVDGPETKEC as NS1-specific linear B-cell epitopes recognized by the mAbs 3C7 and 4D1, respectively. The knowledge and reagents generated in this study may have potential applications in differential diagnosis and the development of epitope-based marker vaccines against WNV and other viruses of JEV serocomplex. |
format | Online Article Text |
id | pubmed-3158561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31585612011-08-20 Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library Sun, En-Cheng Ma, Jian-Nan Liu, Ni-Hong Yang, Tao Zhao, Jing Geng, Hong-Wei Wang, Ling-Feng Qin, Yong-Li Bu, Zhi-Gao Yang, Yin-Hui Lunt, Ross A Wang, Lin-Fa Wu, Dong-Lai BMC Microbiol Research Article BACKGROUND: The West Nile virus (WNV) nonstructural protein 1 (NS1) is an important antigenic protein that elicits protective antibody responses in animals and can be used for the serological diagnosis of WNV infection. Although previous work has demonstrated the vital role of WNV NS1-specific antibody responses, the specific epitopes in the NS1 have not been identified. RESULTS: The present study describes the identification of two linear B-cell epitopes in WNV NS1 through screening a phage-displayed random 12-mer peptide library with two monoclonal antibodies (mAbs) 3C7 and 4D1 that directed against the NS1. The mAbs 3C7 and 4D1 recognized phages displaying peptides with the consensus motifs LTATTEK and VVDGPETKEC, respectively. Exact sequences of both motifs were found in the NS1 ((895)LTATTEK(901 )and (925)VVDGPETKEC(934)). Further identification of the displayed B cell epitopes were conducted using a set of truncated peptides expressed as MBP fusion proteins. The data indicated that (896)TATTEK(901 )and(925)VVDGPETKEC(934 )are minimal determinants of the linear B cell epitopes recognized by the mAbs 3C7 and 4D1, respectively. Antibodies present in the serum of WNV-positive horses recognized the minimal linear epitopes in Western blot analysis, indicating that the two peptides are antigenic in horses during infection. Furthermore, we found that the epitope recognized by 3C7 is conserved only among WNV strains, whereas the epitope recognized by 4D1 is a common motif shared among WNV and other members of Japanese encephalitis virus (JEV) serocomplex. CONCLUSIONS: We identified TATTEK and VVDGPETKEC as NS1-specific linear B-cell epitopes recognized by the mAbs 3C7 and 4D1, respectively. The knowledge and reagents generated in this study may have potential applications in differential diagnosis and the development of epitope-based marker vaccines against WNV and other viruses of JEV serocomplex. BioMed Central 2011-07-06 /pmc/articles/PMC3158561/ /pubmed/21729328 http://dx.doi.org/10.1186/1471-2180-11-160 Text en Copyright ©2011 Sun et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sun, En-Cheng Ma, Jian-Nan Liu, Ni-Hong Yang, Tao Zhao, Jing Geng, Hong-Wei Wang, Ling-Feng Qin, Yong-Li Bu, Zhi-Gao Yang, Yin-Hui Lunt, Ross A Wang, Lin-Fa Wu, Dong-Lai Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library |
title | Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library |
title_full | Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library |
title_fullStr | Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library |
title_full_unstemmed | Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library |
title_short | Identification of two linear B-cell epitopes from West Nile virus NS1 by screening a phage-displayed random peptide library |
title_sort | identification of two linear b-cell epitopes from west nile virus ns1 by screening a phage-displayed random peptide library |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158561/ https://www.ncbi.nlm.nih.gov/pubmed/21729328 http://dx.doi.org/10.1186/1471-2180-11-160 |
work_keys_str_mv | AT sunencheng identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT majiannan identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT liunihong identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT yangtao identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT zhaojing identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT genghongwei identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT wanglingfeng identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT qinyongli identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT buzhigao identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT yangyinhui identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT luntrossa identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT wanglinfa identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary AT wudonglai identificationoftwolinearbcellepitopesfromwestnilevirusns1byscreeningaphagedisplayedrandompeptidelibrary |