Comparison of different commercial ELISAs for detection of antibodies against porcine respiratory and reproductive syndrome virus in serum

被引:29
|
作者
Sattler, Tatjana [1 ]
Wodak, Eveline [2 ]
Revilla-Fernndez, Sandra [2 ]
Schmoll, Friedrich [2 ]
机构
[1] Univ Leipzig, Large Anim Clin Internal Med, D-04103 Leipzig, Germany
[2] AGES, Inst Vet Dis Control, Tamworth, NSW 2340, Australia
来源
BMC VETERINARY RESEARCH | 2014年 / 10卷
关键词
Swine; Wild boar; Sensitivity; Specificity; Agreement; HUMORAL IMMUNE-RESPONSE; SEROLOGICAL SURVEY; WILD BOAR; PIG HERDS; PRRSV; INFECTION; PATHOGENS; VIETNAM; STRAINS; GERMANY;
D O I
10.1186/s12917-014-0300-x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: In recent years, several new ELISAs for the detection of antibodies against the porcine reproductive and respiratory disease virus (PRRSV) in pig serum have been developed. To interpret the results, specificity and sensitivity data as well as agreement to a reference ELISA must be available. In this study, three commercial ELISAs (INgezim PRRS 2.0 - ELISA II, Priocheck? PRRSV Ab porcine ? ELISA III and CIVTEST suis PRRS E/S PLUS - ELISA IV, detecting PRRSV type 1 antibodies) were compared to a standard ELISA (IDEXX PRRS X3 Ab Test - ELISA I). The serum of three pigs vaccinated with an attenuated PRRSV live vaccine (genotype 2) was tested prior to and several times after the vaccination. Furthermore, serum samples of 245 pigs of PRRSV positive herds, 309 pigs of monitored PRRSV negative herds, 256 fatteners of assumed PRRSV negative herds with unknown herd history and 92 wild boars were tested with all four ELISAs. Results: ELISAs II and III were able to detect seroconversion of vaccinated pigs with a similar reliability. According to kappa coefficient, the results showed an almost perfect agreement between ELISA I as reference and ELISA II and III (kappa > 0.8), and substantial agreement between ELISA I and ELISA IV (kappa = 0.71). Sensitivity of ELISA II, III and IV was 96.0%, 100% and 91.5%, respectively. The specificity of the ELISAs determined in samples of monitored PRRSV negative herds was 99.0%, 95.1% and 96.4%, respectively. In assumed negative farms that were not continually monitored, more positive samples were found with ELISA II to IV. The reference ELISA I had a specificity of 100% in this study. Conclusions: All tested ELISAs were able to detect a PRRSV positive herd. The specificity and sensitivity of the tested commercial ELISAs, however, differed. ELISA II had the highest specificity and ELISA III had the highest sensitivity in comparison to the reference ELISA. ELISA IV had a lower sensitivity and specificity than the other ELISAs.
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页数:6
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