Ad. Steele et al., COMPARISON OF 2 RAPID ENZYME IMMUNOASSAYS WITH STANDARD ENZYME-IMMUNOASSAY AND LATEX AGGLUTINATION FOR THE DETECTION OF HUMAN ROTAVIRUS IN STOOLS, Journal of diarrhoeal diseases research, 12(2), 1994, pp. 117-120
We evaluated the performance of six commercially available immunoassay
s for their ability to detect rotaviruses in stool specimens. Four of
the assays were enzyme-linked immunosorbent assays (ELISA), including
two rapid enzyme immunoassays (Testpack, Abbott Laboratories, Chicago
and Pinpoint, Cambridge Biomedical, UK), and the remaining two were la
tex agglutination tests. A total of 100 specimens from children with g
astroenteritis were tested with the commercial immunoassays and compar
ed with electron microscopy (EM) and polyacrylamide gel electrophoresi
s (PAGE) as reference tests for the detection of rotavirus. Discordant
results were further evaluated by a standard blocking ELISA. The rapi
d EIAs were found to be highly sensitive (100% for the Testpack and 97
% for the Pinpoint) and more sensitive than the other immunoassays tes
ted. High specificity was also recorded with both rapid EIAs (96% and
100% for Testpack and Pinpoint, respectively). The rapid EIA tests wer
e easy to perform, required no specialized equipment, and could yield
a result in less than 15 min. The results show that each of the commer
cial assays evaluated could accurately detect rotavirus in the stools
of children with gastroenteritis, although the suitability of choice o
f assay will ultimately depend upon the requirements of the individual
laboratory.