S. Nakata et al., PREVALENCE OF HUMAN CALICIVIRUS INFECTIONS IN KENYA AS DETERMINED BY ENZYME IMMUNOASSAYS FOR 3 GENOGROUPS OF THE VIRUS, Journal of clinical microbiology (Print), 36(11), 1998, pp. 3160-3163
An epidemiological survey on human calicivirus (HuCV) infections and a
ssociated gastroenteritis in infants was conducted to clarify the prev
alence of HuCV infections in infants and adults in Kenya. Enzyme immun
o assays (EIAs) for three genogroups of HuCVs, Norwalk virus (NV), Mex
ico virus (MXV), and Sapporo virus (SV), were used to detect antigen o
r antibody. We tested 1,431 stool samples obtained from children young
er than 6 years old with acute gastroenteritis who visited outpatient
clinics in three districts in Kenya from August 1991 to July 1994. Thi
rty-two (2.2%) of these stool samples were positive for SV antigen. On
ly one (0.1%) of 1,186 samples was positive for NV antigen and none of
246 samples was positive for MXV antigen. One hundred ninety-three se
rum samples were tested for antibodies to NV and MXV, and 64 of them w
ere examined for antibody to SV. The pattern of the age-related preval
ence of serum antibody to NV was different from that of antibodies to
MXV and SV. The acquisition of serum antibodies to HuCVs in the three
genogroups appeared in early childhood, at about 1 to 2 years of age.
The prevalence of serum antibody to NV was low (about 60%) throughout
adulthood compared with a high prevalence of antibody (similar to 80 t
o 90%) to MXV and SV. These data indicate that infections with viruses
in the three genogroups of HuCVs are common in Kenya, and immunologic
al responses to NV may be different from those to MXV and SV. The EIAs
for the detection of NV and MXV antigens appear to be quite specific
for prototype NV and MXV strains, respectively, so that they can detec
t only a few strains of HuCVs related to them. Alternatively, NV and M
XV caused less severe infections that did not bring children to the ou
tpatient clinics for gastroenteritis in Kenya.