EVALUATION OF A COMPUTER-ASSISTED, KINETICS-BASED ENZYME-LINKED IMMUNOSORBENT-ASSAY FOR DETECTION OF CORONAVIRUS ANTIBODIES IN CATS
EVALUATION OF A COMPUTER-ASSISTED, KINETICS-BASED ENZYME-LINKED IMMUNOSORBENT-ASSAY FOR DETECTION OF CORONAVIRUS ANTIBODIES IN CATS
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DOI:
10.1128/jcm.17.2.202-217.1983
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发表时间:
1983-01-01
影响因子:
9.4
通讯作者:
SCOTT, FW
中科院分区:
文献类型:
--
作者:
BARLOUGH, JE;JACOBSON, RH;SCOTT, FW
A computer-assisted, kinetics-based enzyme-linked immunosorbent assay (ELISA) was adapted for detection of coronavirus antibodies in feline serum. An alkaline antigen diluent (carbonate-bicarbonate buffer, pH 9.6) used in initial experiments produced diffuse, nonspecific color reactions in both viral and control antigen cuvettes which were correlated, paradoxically, with coronavirus antibody levels in test sera. These interfering reactions were minimized by use of lower-pH antigen diluents such as water and phosphate-buffered saline. Background kinetics-based ELISA reactivity directed against a noncoronaviral component of antigen tissue culture fluids could then be detected in numerous sera, particularly in samples with lower titers. Much of this reactivity was shown to be associated with bovine .gamma.-globulins in cell culture fluid. It was not serum lot or species specific; a variety of bovine serum lots and individual lots of serum from other mammalian and avian (chicken) species also reacted. Reactivity was markedly reduced when cells for antigen preparation were grown in .gamma.-globulin-free bovine serum. Generation of corrected slope values from the kinetics-based ELISA made it possible to correct for residual background reactivity in individual test sera and thus eliminate a potentially major source of false-positive reactions. These studies indicated that the control of nonspecific reactivity in feline coronavirus serology is essential to obtain useful estimates of specific antibody responses.