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Non-Invasive Model of Neuropathogenic Escherichia coli Infection in the Neonatal Rat
Published on: October 29, 2014
Shiga Toxin-Producing Escherichia coli Infections in Germany †
Helge Karch1, Hans-Iko Huppertz2, Jochen Bockemühl3
1Institut für Hygiene und Mikrobiologie der Universität Würzburg, Josef-Schneider-Straße 2, D-97080 Würzburg.
Insights
Shiga toxin-producing Escherichia coli (STEC) infections in children increased from 1991 to 1994. Non-O157:H7 STEC strains are important causes of pediatric enteritis and hemolytic uremic syndrome (HUS).
Area of Science:
- Pediatric Infectious Diseases
- Microbiology
- Gastroenterology
Background:
- Shiga toxin-producing Escherichia coli (STEC) is a significant cause of pediatric enteritis and hemolytic uremic syndrome (HUS).
- The epidemiology and clinical spectrum of STEC infections in children require ongoing investigation.
Purpose of the Study:
- To assess the incidence and clinical manifestations of STEC infections in children in Germany.
- To identify the prevalence of STEC serotypes, including non-O157:H7 strains, in pediatric enteritis and HUS cases.
Main Methods:
- Prospective study of 2788 children with enteritis from 1991-1995.
- STEC detection using PCR for Shiga toxin genes (Stx1, Stx2), followed by colony blot hybridization, serotyping, and virulence gene analysis.
- STEC confirmation in 88 HUS cases by stool culture and 20 by serological analysis.
Main Results:
- STEC infection incidence rose from 0.4% in 1991 to 2.8% in 1994, stabilizing at 2.5% in 1995.
- Most STEC infections presented as painful nonbloody diarrhea; 35 patients had STEC in stools, with 25.7% being O157 strains (8.6% O157:H7, 17.1% O157:H-).
- In HUS cases, 78% of STEC strains were serogroup O157; common non-O157 serogroups included O26 and O111.
Conclusions:
- Non-O157:H7 STEC strains are prevalent in pediatric enteritis and HUS.
- Consider non-O157:H7 STEC in children with bloody diarrhea, HUS, or unexplained painful nonbloody diarrhea when standard pathogens are absent.
Abstract:
A prospective study was carried out in collaboration with two children's hospitals in Würzburg, Germany to assess the incidence and clinical manifestations of infections due to Shiga toxin-producing Escherichia coli (STEC) in children. Between 1991 and 1995, stool samples from 2788 children with enteritis were investigated for the occurrence of STEC. STEC cultures from stools were screened using PCR with primers complementary to Shiga toxin 1(Stx1) and Shiga toxin 2 (Stx2) genes. PCR-positive samples were further subjected to colony blot hybridization and probe positive colonies were serotyped and analyzed for the presence of virulence genes. There was an increase in the incidence of STEC infections from 0.4% in 1991 to 2.8% in 1994. In 1995 the number of infections remained nearly unchanged (2.5%). Infection with STEC was associated with painful nonbloody diarrhea in most patients. Among the 35 patients in this study with stools containing STEC, only 9 (25.7%) had O157 colonies of which 3 (8.6%) were O157:H7 and 6 (17.1%) were sorbitol-fermenting O157:H-. In an additional study in 1994/l995, STEC etiology in 88 patients with HUS from Germany was confirmed in our laboratories by culture of STEC from stools, and in 20 additional HUS cases by serological analysis. Of the strains from stools of HUS patients, 78% belonged to serogroup O157. The most frequently isolated non-O157 serogroups were O26 and O111. These results demonstrate that when analyzing stools of patients with bloody diarrhea, HUS, or painful nonbloody diarrhea, the occurrence of non-O157:H7 strains should be considered when classical microbiological analysis fails to yield a standard enteric pathogen, such as Campylobacter . E. coli O157:H7, Salmonella . Shigella , or Yersinia .
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