Development of an enzyme-linked immunosorbent assay for the monitoring and surveillance of antibodies to porcine epidemic diarrhea virus based on a recombinant membrane protein

被引:33
作者
Fan, Jing-Hui [1 ]
Zuo, Yu-Zhu [1 ]
Shen, Xiao-Qiang [1 ]
Gu, Wen-Yuan [1 ]
Di, Jing-Mei [1 ]
机构
[1] Agr Univ Hebei, Coll Vet Med, Baoding 071001, Peoples R China
关键词
Porcine epidemic diarrhea virus (PEDV); M protein; ELISA; Serum antibodies; TRANSMISSIBLE GASTROENTERITIS VIRUS; MONOCLONAL-ANTIBODIES; NUCLEOCAPSID PROTEIN; IDENTIFICATION; GLYCOPROTEIN; INFECTION; ROTAVIRUS; PARTICLES; SWINE; ELISA;
D O I
10.1016/j.jviromet.2015.07.021
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The recent dramatic increase in reported cases of porcine epidemic diarrhea (PED) in pig farms is a potential threat to the global swine industry. Therefore, the accurate diagnosis, serological monitoring, and surveillance of specific antibodies in pigs resulting from porcine epidemic diarrhea virus (PEDV) infection or vaccination would be essential in helping to control the spread of PED. We developed and validated an indirect enzyme-linked immunosorbent assay (ELISA) based on the recombinant membrane (M) protein of PEDV. To detect PEDV antibodies in eight herds, 382 serum samples were collected from sows that had been immunized with a PED vaccine, and screened using the developed ELISA in parallel with a serum neutralization (SN) assay. Of the tested samples, 276 were positive for the presence of PEDV antibodies according to both assays, while 98 were negative. An excellent agreement between the ELISA and the SN assay was observed (kappa = 0.947; 95% confidence interval = 0.910-0.984; McNemar's test, P=0.727). No cross-reaction was detected for the developed ELISA with other coronaviruses or other common pig pathogens. The developed ELISA could be used for serological evaluation and indirect diagnosis of PED infection. (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:90 / 94
页数:5
相关论文
共 27 条
[1]   A Conserved Domain in the Coronavirus Membrane Protein Tail Is Important for Virus Assembly [J].
Arndt, Ariel L. ;
Larson, Blake J. ;
Hogue, Brenda G. .
JOURNAL OF VIROLOGY, 2010, 84 (21) :11418-11428
[2]   EVALUATION OF A BLOCKING ELISA USING MONOCLONAL-ANTIBODIES FOR THE DETECTION OF PORCINE EPIDEMIC DIARRHEA VIRUS AND ITS ANTIBODIES [J].
CARVAJAL, A ;
LANZA, I ;
DIEGO, R ;
RUBIO, P ;
CARMENES, P .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 1995, 7 (01) :60-64
[3]   Prevalence of porcine epidemic diarrhoea virus and transmissible gastroenteritis virus infection in Korean pigs [J].
Chae, C ;
Kim, O ;
Choi, C ;
Min, K ;
Cho, WS ;
Kim, J ;
Tai, JH .
VETERINARY RECORD, 2000, 147 (21) :606-608
[4]   VIRUS-LIKE PARTICLES ASSOCIATED WITH PORCINE EPIDEMIC DIARRHEA [J].
CHASEY, D ;
CARTWRIGHT, SF .
RESEARCH IN VETERINARY SCIENCE, 1978, 25 (02) :255-256
[5]  
Cima Greg, 2013, J Am Vet Med Assoc, V243, P30
[6]   Heterogeneity in membrane protein genes of porcine epidemic diarrhea viruses isolated in China [J].
Fan, Jing-Hui ;
Zuo, Yu-Zhu ;
Li, Jian-Hui ;
Pei, Li-Hua .
VIRUS GENES, 2012, 45 (01) :113-117
[7]   MONOCLONAL-ANTIBODIES TO THE MATRIX (E1) GLYCOPROTEIN OF MOUSE HEPATITIS-VIRUS PROTECT MICE FROM ENCEPHALITIS [J].
FLEMING, JO ;
SHUBIN, RA ;
SUSSMAN, MA ;
CASTEEL, N ;
STOHLMAN, SA .
VIROLOGY, 1989, 168 (01) :162-167
[8]   High-level prokaryotic expression of envelope exterior of membrane protein of porcine epidemic diarrhea virus [J].
Gao Shenyang ;
Zha Enhui ;
Li Baoxian ;
Qiao Xinyuan ;
Tang Lijie ;
Ge Junwei ;
Li Yijing .
VETERINARY MICROBIOLOGY, 2007, 123 (1-3) :187-193
[9]   PROPAGATION OF THE VIRUS OF PORCINE EPIDEMIC DIARRHEA IN CELL-CULTURE [J].
HOFMANN, M ;
WYLER, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (11) :2235-2239
[10]   Development and evaluation of enzyme-linked immunosorbent assay based on recombinant nucleocapsid protein for detection of porcine epidemic diarrhea (PEDV) antibodies [J].
Hou, Xi-Lin ;
Yu, Li-Yun ;
Liu, Jianzhu .
VETERINARY MICROBIOLOGY, 2007, 123 (1-3) :86-92