Strain-Specific Differences in the Amount of Shiga Toxin Released from Enterohemorrhagic Escherichia coli O157 following Exposure to Subinhibitory Concentrations of Antimicrobial Agents

1998 ◽  
Vol 17 (11) ◽  
pp. 761-766 ◽  
Author(s):  
K. Grif ◽  
M. P. Dierich ◽  
H. Karch ◽  
F. Allerberger
1999 ◽  
Vol 45 (9) ◽  
pp. 732-739 ◽  
Author(s):  
M Yoh ◽  
E K Frimpong ◽  
S P Voravuthikunchai ◽  
T Honda

In Japan, antimicrobial agent therapy for patients with diarrhea due to enterovirulent organisms including enterohemorrhagic Escherichia coli (EHEC) is common, and norfloxacin (NFLX), fosfomycin, and kanamycin are recommended for EHEC treatment by the Japanese Ministry of Health and Welfare. The aim of this study was to analyze the effects of antimicrobial agents which have been used or recommended for the treatment of EHEC on the production of verotoxin (VT) in vitro. Subinhibitory concentrations of quinolones, NFLX, sparofloxacin (SPFX), and grepafloxacin (GPFX) markedly stimulated the productions of VT1 and VT2. The macrolide azithromycin (AZM), erythromycin (EM), and clarithromycin (CAM) did not stimulate the production of VT at a wide range of concentrations. These in vitro results indicate that when quinolones are prescribed for a patient infected with EHEC, the concentration of antimicrobial agents used in vivo and the susceptibility of the EHEC strains against quinolones should be taken into consideration.Key words: EHEC, O157:H7, verotoxin, quinolone, macrolide.


2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Yoshitoshi Ogura ◽  
Shakhinur Islam Mondal ◽  
Md Rakibul Islam ◽  
Toshihiro Mako ◽  
Kokichi Arisawa ◽  
...  

2007 ◽  
Vol 190 (1) ◽  
pp. 438-441 ◽  
Author(s):  
Kenan C. Murphy ◽  
Jennifer M. Ritchie ◽  
Matthew K. Waldor ◽  
Anders Løbner-Olesen ◽  
M. G. Marinus

ABSTRACT Shiga toxin 2 (Stx2), one of the principal virulence factors of enterohemorrhagic Escherichia coli, is encoded by 933W, a lambda-like prophage. 933W prophage induction contributes to Stx2 production, and here, we provide evidence that Dam methyltransferase is essential for maintenance of 933W lysogeny. Our findings are consistent with the idea that the 933W prophage has a relatively low threshold for induction, which may promote Stx2 production during infection.


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