Two-hundred Mexican children monitored from birth to 2 years of age in
a cohort study of diarrhea were tested for Norwalk virus (NV) and Nor
walk-related virus infection. Blood was collected quarterly and tested
by an enzyme immunoassay (EIA) using the recombinant NV (rNV) particl
es as antigen. Stool was collected weekly and tested by an EIA using h
yperimmune anti-sera from animals immunized with rNV and a reverse tra
nscription-polymerase chain reaction (RT-PCR) with primers in the RNA
polymerase region of NV. A high prevalence of serum antibody to NV (85
% at age 2 years) was found by the antibody EIA. In 54 stool specimens
selected from children who developed a high titer of serum antibody t
o rNV, none was positive for NV by the antigen EIA, but 6 yielded prod
ucts by the RT-PCR. One stool specimen (MX virus) yielded a 3.3 kb RT-
PCR product from the 3' end of the viral genome. The MX virus cDNA has
a genomic organization like other caliciviruses. Sequence comparison
showed that MX virus shares 80% nucleic acid and 91% amino acid sequen
ce identity with Snow Mountain agent (SMA), but only 62% and 60% ident
ity, respectively, with NV in the RNA polymerase region, suggesting th
at MX virus is a SMA-like virus. (C) 1995 Wiley-Liss, Inc.