Literature DB >> 35958565

Characterization of monoclonal antibodies that specifically differentiate field isolates from vaccine strains of classical swine fever virus.

Shijiang Mi1,2, Lihua Wang3, Hongwei Li4, Fei Bao2, Rachel Madera3, Xiju Shi5, Liying Zhang6, Yingying Mao4, Renhe Yan7, Xianzhu Xia1,2, Wenjie Gong1, Jishu Shi3, Changchun Tu1,2,8.   

Abstract

Classical swine fever virus (CSFV) is a major animal pathogen threatening the global pork industry. To date, numerous anti-CSFV monoclonal antibodies (mAbs) and their recognizing epitopes have been reported. However, few mAbs were systematically characterized for the capacity to differentiate field CSFV isolates from CSF vaccine strains, and the molecular basis associated with antigenic differences between vaccines and field isolates is still largely unknown. In the present study, recombinant CSFV structural glycoproteins E2 of both virulent and vaccine strains and Erns of vaccine strain were expressed using eukaryotic cells and murine mAbs generated against E2 and Erns. After serial screening and cloning of the hybridomas, the viral spectra of mAbs were respectively determined by indirect fluorescent antibody assay (IFA) using 108 CSFVs, followed by Western blot analysis using expressed glycoproteins of all CSFV sub-genotypes including vaccine strains. The antigenic structures recognized by these mAbs were characterized by epitope mapping using truncated, chimeric, and site-directed mutated E2 and Erns proteins. We have identified two vaccine-specific, one field isolate-specific, and two universal CSFV-specific mAbs and five novel conformational epitopes with critical amino acid (aa) motifs that are associated with these five mAbs: 213EPD215, 271RXGP274, and 37LXLNDG42 on E2 and 38CKGVP42, W81, and D100/V107 on Erns. Particularly, E213 of E2 is field isolate-specific, while N40 of E2 and D100/V107 of Erns are vaccine strain-specific. Results from our study further indicate that N40D of E2 mutation in field strains was likely produced under positive selection associated with long-term mass vaccination, leading to CSFV evasion of host immune response. Taking together, this study provides new insights into the antigenic structure of CSFV E2 and Erns and the differentiating mAbs will contribute to the development of a diagnostic strategy to differentiate C-strain vaccination from natural infection (DIVA) of CSFV in terms of elimination of CSF in China.
Copyright © 2022 Mi, Wang, Li, Bao, Madera, Shi, Zhang, Mao, Yan, Xia, Gong, Shi and Tu.

Entities:  

Keywords:  CSFV; E2; Erns; characterization; differentiating mAb; epitope

Mesh:

Substances:

Year:  2022        PMID: 35958565      PMCID: PMC9361847          DOI: 10.3389/fimmu.2022.930631

Source DB:  PubMed          Journal:  Front Immunol        ISSN: 1664-3224            Impact factor:   8.786


  54 in total

1.  Epitope mapping of envelope glycoprotein E1 of hog cholera virus strain Brescia.

Authors:  P A van Rijn; H G van Gennip; E J de Meijer; R J Moormann
Journal:  J Gen Virol       Date:  1993-10       Impact factor: 3.891

2.  A second envelope glycoprotein mediates neutralization of a pestivirus, hog cholera virus.

Authors:  E Weiland; R Ahl; R Stark; F Weiland; H J Thiel
Journal:  J Virol       Date:  1992-06       Impact factor: 5.103

3.  In vitro adaptation and genome analysis of a sub-subgenotype 2.1c isolate of classical swine fever virus.

Authors:  Wenjie Gong; Zongji Lu; Li Zhang; Xiaoming Xie; Daliang Jiang; Junjie Jia; Huancheng Guo; Jishu Shi; Changchun Tu
Journal:  Virus Genes       Date:  2016-05-07       Impact factor: 2.332

4.  Epitope mapping and affinity purification of monospecific antibodies by Escherichia coli cell surface display of gene-derived random peptide libraries.

Authors:  A Christmann; A Wentzel; C Meyer; G Meyers; H Kolmar
Journal:  J Immunol Methods       Date:  2001-11-01       Impact factor: 2.303

5.  High-resolution epitope mapping for monoclonal antibodies to the structural protein Erns of classical swine fever virus using peptide array and random peptide phage display approaches.

Authors:  Min Lin; Heather McRae; Hanhong Dan; Erin Tangorra; Amanda Laverdiere; John Pasick
Journal:  J Gen Virol       Date:  2010-09-01       Impact factor: 3.891

6.  Molecular characterization of lapinized classical Swine Fever vaccine strain by full-length genome sequencing and analysis.

Authors:  Praveen K Gupta; Mohini Saini; Shyam S Dahiya; Chhabi Lal Patel; Arvind A Sonwane; D V Rai; K D Pandey
Journal:  Anim Biotechnol       Date:  2011-04       Impact factor: 2.282

Review 7.  Studying classical swine fever virus: making the best of a bad virus.

Authors:  Wei Ji; Zhen Guo; Nai-Zheng Ding; Cheng-Qiang He
Journal:  Virus Res       Date:  2014-12-12       Impact factor: 3.303

8.  Antigenic domains analysis of classical swine fever virus E2 glycoprotein by mutagenesis and conformation-dependent monoclonal antibodies.

Authors:  Chia-Yi Chang; Chin-Cheng Huang; Yu-Ju Lin; Ming-Chung Deng; Hui-Chun Chen; Chiung-Hui Tsai; Wei-Ming Chang; Fun-In Wang
Journal:  Virus Res       Date:  2010-02-02       Impact factor: 3.303

9.  Production of monoclonal antibodies against classical swine fever virus and their use for antigenic characterization of Japanese isolates.

Authors:  T Nishimori; S Yamada; M Shimizu
Journal:  J Vet Med Sci       Date:  1996-07       Impact factor: 1.267

10.  Antigenic structure of envelope glycoprotein E1 of hog cholera virus.

Authors:  P A van Rijn; G K Miedema; G Wensvoort; H G van Gennip; R J Moormann
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.