J. Noel et al., IDENTIFICATION OF ADENOVIRUSES IN FECES FROM PATIENTS WITH DIARRHEA AT THE HOSPITALS-FOR-SICK-CHILDREN, LONDON, 1989-1992, Journal of medical virology, 43(1), 1994, pp. 84-90
Faecal samples from 137 patients that had been shown to contain adenov
iruses by electron microscopy were identified in a series of enzyme im
munoassays (EIA) using a single monoclonal antibody (Mab) to adenoviru
s 40 and four different Mabs to adenovirus 41. Adenoviruses were parti
ally characterised by restriction enzyme analysis (REA) of DNA extract
s using Smal. Samples were also run in a commercial EIA (Adenovirus ID
EIA; Dako, Ltd.) which detects group antigen. The majority (84%) of ad
enoviruses were subgenus F: adenovirus type 41, 87 (64%) and adenoviru
s type 40, 28 (20.4%). Subgenus A viruses were identified in ten, (7%)
patients, eight were type 31, and two type 12. The adeno IDEIA test w
as sensitive and specific, detecting 127 of 131 positives and giving n
o false-positive results with other enteric viruses. Use of monoclonal
-based EIAs showed significant differences depending on which adeno 41
Mab was used, although the restriction patterns obtained using Smal a
ppeared to be identical for 66 of 69 samples that produced recognisabl
e bands. The Mab that performed best, M 4.3.1, was raised against stra
ins obtained from children in England and detected 83 of 84 (99%) of t
he adenovirus 41 samples tested. In contrast Mab JH/41 raised against
the prototype strain of adenovirus 41 (Tak) detected only of 69 of 87
(79%). (C) 1994 Wiley-Liss, Inc.