A commercial enzyme immunoassay (EIA) for the detection of astrovirus antig
en was used to detect the virus during a 12-month survey of enteric pathoge
ns in children in outpatient (n = 238) and hospital (n = 176) settings. It
was found to have a 100% sensitivity and 98.6% specificity. Nineteen astrov
irus isolates were detected and confirmed by northern hybridization, cell c
ulture, and RT-PCR. The virus was detected mainly amongst outpatients altho
ugh a comparison of the detection rate with that in hospitalised children d
id not demonstrate a statistically significant difference (p = 0.1347). In
contrast, there was a strong association between hospitalization and rotavi
rus infection (p = 0.0371), and a strong association between infection dete
cted in outpatients and adenovirus infection (p = 0.0193). Strains of astro
virus were sequenced, genotyped and shown to be: type 1 (n = 11), type 3 (n
= 1), and type 4 (n = 7). Maximum genetic variation in type 1 isolates was
8.6% and type 3 was 7.8%. Changes did not result in amino acid substitutio
ns. (C) 2000 Elsevier Science B.V. All rights reserved.