Antigen production and standardization of an in-house indirect ELISA for detection of antibodies against Anaplasma marginale

被引:1
作者
Salinas Estrella, Elizabeth [1 ]
Ortega Hernandez, Maria Guadalupe [2 ]
Flores Perez, Erika [2 ]
Montenegro Cristino, Natividad [2 ]
Preciado de la Torre, Jesus Francisco [1 ]
Cobaxin Cardenas, Mayra Elizeth [1 ]
Rodriguez, Sergio D. [1 ]
机构
[1] Ctr Nacl Invest Disciplinaria Salud Anim & Inocui, Inst Nacl Invest Forest Agricolas & Pecuarias INI, Carretera Cuernavaca Cuautla 8534,Col Progreso, Jiutepec 62574, Morelos, Mexico
[2] Serv Nacl Sanidad Inocuidad & Calidad Agroaliment, Jiutepec, Morelos, Mexico
关键词
Bovine anaplasmosis; Indirect ELISA; Serologic diagnostics; LINKED-IMMUNOSORBENT-ASSAY; INDIRECT FLUORESCENT-ANTIBODY; BABESIA-BIGEMINA; DIAGNOSIS; PROTEIN; TESTS;
D O I
10.22319/rmcp.v13i4.5976
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Serologic tests are important for the detection of specific antibodies against infectious agents. Commercial indirect ELISA are costly and usually as effective as in-house ELISAs. In the present work, it was prepared a batch of Anaplasma marginale crude antigen from infected blood, and tested it against official positive and negative serum controls and compared with an old batch of antigen. The new antigen batch showed an efficiency similar to the old batch. The sensitivity of the test was comparable between the new and old batches. Both, new and old antigen lots are being used at an excess. The new antigen lot is large enough to run thousands of tests at a more affordable price than commercial kits.
引用
收藏
页码:1079 / 1094
页数:16
相关论文
共 34 条
[1]   Development and Optimization of In-house ELISA for Detection of Human IgG Antibody to SARS-CoV-2 Full Length Spike Protein [J].
Alandijany, Thamir A. ;
El-Kafrawy, Sherif A. ;
Tolah, Ahmed M. ;
Sohrab, Sayed S. ;
Faizo, Arwa A. ;
Hassan, Ahmed M. ;
Alsubhi, Tagreed L. ;
Othman, Norah A. ;
Azhar, Esam, I .
PATHOGENS, 2020, 9 (10) :1-11
[2]  
Alexander A., 1979, Tecnica quirurgica en animales y temas de terapeutica quirurgica, V4th, P170
[3]  
AMERAULT TE, 1968, J AM VET MED ASSOC, V153, P1828
[4]   A Review of Bovine Anaplasmosis [J].
Aubry, P. ;
Geale, D. W. .
TRANSBOUNDARY AND EMERGING DISEASES, 2011, 58 (01) :1-30
[5]   A MICROPLATE ENZYME-LINKED-IMMUNOSORBENT-ASSAY FOR MEASURING ANTIBODY TO ANAPLASMA-MARGINALE IN CATTLE SERUM [J].
BARRY, DN ;
PARKER, RJ ;
DEVOS, AJ ;
DUNSTER, P ;
RODWELL, BJ .
AUSTRALIAN VETERINARY JOURNAL, 1986, 63 (03) :76-79
[6]   Improved diagnostic performance of a commercial Anaplasma antibody competitive enzyme-linked immunosorbent assay using recombinant major surface protein 5-glutathione S-transferase fusion protein as antigen [J].
Chung, Chungwon ;
Wilson, Carey ;
Bandaranayaka-Mudiyanselage, Chandima-Bandara ;
Kang, Eunah ;
Adams, D. Scott ;
Kappmeyer, Lowell S. ;
Knowles, Donald P. ;
McElwain, Terry F. ;
Evermann, James F. ;
Ueti, Massaro W. ;
Scoles, Glen A. ;
Lee, Stephen S. ;
McGuire, Travis C. .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2014, 26 (01) :61-71
[7]  
González Belkis Corona, 2014, Rev Salud Anim., V36, P73
[8]   Detection of cattle naturally infected with Anaplasma marginale in a region of endemicity by nested PCR and a competitive enzyme-linked immunosorbent assay using recombinant major surface protein 5 [J].
de Echaide, ST ;
Knowles, DP ;
McGuire, TC ;
Palmer, GH ;
Suarez, CE ;
McElwain, TF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) :777-782
[9]   MULTIPLEX POLYMERASE CHAIN-REACTION BASED ASSAY FOR THE DETECTION OF BABESIA-BIGEMINA, BABESIA-BOVIS AND ANAPLASMA-MARGINALE DNA IN BOVINE BLOOD [J].
FIGUEROA, JV ;
CHIEVES, LP ;
JOHNSON, GS ;
BUENING, GM .
VETERINARY PARASITOLOGY, 1993, 50 (1-2) :69-81
[10]   DETECTION OF BABESIA-BIGEMINA-INFECTED CARRIERS BY POLYMERASE CHAIN-REACTION AMPLIFICATION [J].
FIGUEROA, JV ;
CHIEVES, LP ;
JOHNSON, GS ;
BUENING, GM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (10) :2576-2582