We have investigated the Shiga toxin genes of Shiga toxin-producing Escheri
chia coli (STEC) strains, using polymerase chain reaction (PCR) amplifying
the full lengths of these genes. As a result, we found the Shiga toxin 2 ge
ne which was insertionally inactivated by an insertion sequence (IS). This
IS element mas identical to IS1203V which has been also found in inactivate
d Shiga toxin 2 genes, and was inverted at the same site as in the previous
paper On the other hand, both Shiga toxin 2 genes were different (98.3% id
entity). These suggested that IS1203v independently inserted into each Shig
a toxin 2 genes, and STEC strains possessing the insertionally inactivated
Shiga toxin genes are most likely to have a wide distribution. Amplificatio
n of the full length of the Shiga toxin gene is one of the effective method
s to detect the gene no matter where the IS element is included, i.e., the
insertion can be reflected in the size of amplicon.