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The National Institute of Infectious Diseases (NIID) is a research institute attached to the Ministry of Health, Labour and Welfare for conducting (i) fundamental and applied research on infectious diseases and (ii) national test for lot release and development of antibiotics and vaccines. This site will be to close two notable important news of infectious diseases in Japan. It will also present many comprehensive informations of latest researches being done on all depertments including Infectious Disease Surveillance Center.

Jpn. J. Infect. Dis., 65 (4), 322-325, 2012

To see a printable version of the article in the Adobe file format, click this [PDF] link.

Kimiko Kawano1, Hidetoshi Ono2, Osamu Iwashita3, Mai Kurogi3, Takeshi Haga4, Ken Maeda5, and Yoshitaka Goto4*

1Miyazaki Prefectural Institute for Public Health and Environment, Miyazaki 889-2155; 2Hyuga Meat Inspection Center, Miyazaki 883-0021; 3Tsuno Meat Inspection Center, Miyazaki 889-1201; 4Department of Microbiology, University of Miyazaki, Miyazaki 889-2192; and 5Department of Microbiology, Yamaguchi University, Yamaguchi 753-8515, Japan

(Received November 15, 2011. Accepted May 7, 2012)


*Corresponding author: Mailing address: Department of Microbiology, University of Miyazaki, Gakuen Kibanadai Nishi 1-1, Miyazaki, Miyazaki 889-2192, Japan. Tel & Fax: +81-985-58-7275, E-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.


SUMMARY: To determine the expression level of Shiga toxin (Stx) 2-related toxins (Stx2 and Stx2c) produced by each of 33 Stx-producing Escherichia coli (STEC) O157 strains, stx2 and stx2c mRNAs (stx2-related mRNA) were measured using real-time PCR with primers that recognize sequences common to stx2 and stx2c. The amount of Stx2 and Stx2c protein was measured using a reversed passive latex agglutination (RPLA) kit. Expression of stx2-related mRNA was significantly higher in STEC O157 strains carrying the stx2 gene (i.e., stx2, stx1/stx2, or stx2/stx2c) than in most strains that carried the stx2c gene but not the stx2 gene (i.e., stx2c or stx1/stx2c). RPLA might not measure the precise amount of each toxin variant; nevertheless, stx2-inclusive strains had 40-fold higher mean toxin titers than did strains that carried the stx2c gene but not the stx2 gene, with the exception of 1 stx2c strain. Interestingly, 1 stx2c strain that was isolated from a patient with severe hemorrhagic diarrhea had the highest stx2-related mRNA expression and the highest toxin titer of all 33 STEC O157 strains. Taken together, these findings indicated that measurement of stx2-related mRNA expression could reflect differences in production levels of toxins among STEC strains.

Copyright 1998 National Institute of Infectious Diseases, Japan