Standardization and validation of an agar gel immunodiffusion test for the diagnosis of equine infectious anemia using a recombinant p26 antigen

被引:20
作者
Alvarez, I. [1 ]
Gutierrez, G. [1 ]
Vissani, A. [1 ]
Rodriguez, S. [1 ]
Barrandeguy, M. [1 ]
Trono, K. [1 ]
机构
[1] Ctr Invest Ciencias Vet & Agron, INTA, Inst Virol, Castelar, Argentina
关键词
equine infectious anemia; p26 capsid protein; agar gel immunodiffusion; validation;
D O I
10.1016/j.vetmic.2007.01.007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We developed and validated an agar gel immunodiffusion test (AGID) test for the diagnosis of equine infectious anemia (EIA) using as antigen the p26 protein of equine infectious anemia virus (EIAV) produced in the Escherichia coli expression system. The developed rp26-AGID test showed an excellent diagnostic relative sensitivity (100%) and specificity (100%) compared to a commercial AGID assay when 1855 field serum samples were analyzed. In addition, the rp26-AGID demonstrated to be a precise assay with excellent repeatability and reproducibility. In the analytical sensitivity trial, positive sera showed nearly the same endpoint dilutions for both compared tests. No positive-reactions were observed with 35 serum samples with antibodies related to other endemic agents and also with severely hemolysed samples, demonstrating that the rp26-AGID has an excellent analytical specificity. Complete concordance with blind previous results from five proficiency test panels confirmed the capability of the assay of accurate detection of EIAV antibodies. This is the first time that a recombinant AGID assay able to identify EIAV infections has been standardized and validated in Argentina according to international guidelines. Taking into account the results obtained, the p26-AGID could be adopted as an official test method for the diagnosis and control of EIA in this country. (c) 2007 Elsevier B.V All rights reserved.
引用
收藏
页码:344 / 351
页数:8
相关论文
共 19 条
[1]  
[Anonymous], 1994, ICH HARM TRIP GUID Q
[2]  
[Anonymous], [No title captured]
[3]   DEVELOPMENT OF AN ENZYME-LINKED IMMUNOSORBENT-ASSAY FOR EQUINE INFECTIOUS-ANEMIA VIRUS DETECTION USING RECOMBINANT PR55GAG [J].
ARCHAMBAULT, D ;
WANG, ZM ;
LACAL, JC ;
GAZIT, A ;
YANIV, A ;
DAHLBERG, JE ;
TRONICK, SR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (06) :1167-1173
[4]   EQUINE LENTIVIRUS, COMPARATIVE-STUDIES ON 4 SEROLOGICAL TESTS FOR THE DIAGNOSIS OF EQUINE INFECTIOUS-ANEMIA [J].
BURKI, F ;
ROSSMANITH, W ;
ROSSMANITH, E .
VETERINARY MICROBIOLOGY, 1992, 33 (1-4) :353-360
[5]  
CHEEVERS WP, 1985, REV INFECT DIS, V7, P83
[6]   Evaluation of high functional avidity CTL to Gag epitope clusters in EIAV carrier horses [J].
Chung, CW ;
Mealey, RH ;
McGuire, TC .
VIROLOGY, 2005, 342 (02) :228-239
[7]  
COGGINS L, 1972, AM J VET RES, V33, P11
[8]  
COGGINS L, 1970, CORNELL VET, V60, P330
[9]   Maturation of the cellular and humoral immune responses to persistent infection in horses by equine infectious anemia virus is a complex and lengthy process [J].
Hammond, SA ;
Cook, SJ ;
Lichtenstein, DL ;
Issel, CJ ;
Montelaro, RC .
JOURNAL OF VIROLOGY, 1997, 71 (05) :3840-3852
[10]  
JACOBO RA, 2004, REV VET, V15, P62