ANTIBODY DETECTION IN MATCHED CHICKEN SERA AND EGG-YOLK SAMPLES BY COMMERCIAL ENZYME-LINKED-IMMUNOSORBENT-ASSAY KITS FOR NEWCASTLE-DISEASE VIRUS, INFECTIOUS-BRONCHITIS VIRUS, INFECTIOUS BURSAL DISEASE VIRUS, AND AVIAN REOVIRUS
Ld. Keck et al., ANTIBODY DETECTION IN MATCHED CHICKEN SERA AND EGG-YOLK SAMPLES BY COMMERCIAL ENZYME-LINKED-IMMUNOSORBENT-ASSAY KITS FOR NEWCASTLE-DISEASE VIRUS, INFECTIOUS-BRONCHITIS VIRUS, INFECTIOUS BURSAL DISEASE VIRUS, AND AVIAN REOVIRUS, Avian diseases, 37(3), 1993, pp. 825-828
ELISA kits have been used to detect antibody in egg yolk. The major ad
vantage eggs offer over blood samples is the ability to collect sample
s without compromising flock biosecurity. A disadvantage to using egg
yolk over sera concerns the method of preparing yolk for antibody test
ing. The technique used in this study involved a simple dilution metho
d with no mixing or extraction. To determine the adequacy of yolk samp
les to replace serum samples, a serum sample and the first six eggs we
re obtained from each of 50 commercial leghorn hens. Mean titers were
consistently larger for serum than for yolk, but the size of the diffe
rence varied with the virus. The variation of mean egg titer was compa
rable to that of the serum titer. Correlations between a hen's serum t
iter and the mean titer from hen eggs were only moderate, ranging from
0.35 to 0.85 across viruses and systems. The ability to predict the s
erum titer of a single hen by the mean titer from hen eggs may be inad
equate.