# Internal Microbial War Against E.coli 0157:H7

Variations in  microbiota protect (mice) against E. coli O157:H7 infection
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Intestinal Bacteria Protect against E. coli O157:H7

DENVER – CO – May 20, 2013 – A cocktail of non-pathogenic bacteria naturally occurring in the digestive tract of healthy humans can protect against a potentially lethal E. coli infection in animal models according to research presented today at the 113th General Meeting of the American Society for Microbiology.  The research, conducted by scientists at the University of Michigan Medical School in Ann Arbor, could have important implications for the prevention or even treatment of this disease.

Enterohemorrhagic Escherichia coli (EHEC) O157:H7 is a food-borne pathogen that has been responsible for several recent outbreaks of potentially fatal disease.  Severe manifestations of this disease include both hemorrhagic colitis (HC) and hemolytic uremic syndrome (HUS), a form of acute renal disease that can result in death or permanent disability.

“EHEC is of primary concern because HUS, the most severe outcome, preferentially targets young children,” says Kathryn Eaton, a researcher on the study. “Tragically, HUS occurs late in the course of disease, often after the child has recovered from the enteric form.  Thus, children who appear to have recovered may relapse and even die.”

HUS is cause by absorption of Shigatoxins (Stx) that are produced by the bacteria in the intestine.  Stx production occurs within a few days of bacterial colonization and once it is present in the intestines it can be absorbed into the bloodstream where it may cause systemic disease and even death.   There is no specific treatment or preventative measure that prevents progression from HC to HUS.

The overall goal of research in Eaton’s laboratory is to identify potential therapies to prevent production or absorption of Stx before it can cause disease.

“In brief, the results of our study show that in a mouse model, non-pathogenic bacteria that are normal inhabitants of the human intestine can eliminate Stx from the intestinal contents and completely prevent HUS,” says Eaton.

In the study, the researchers gave EHEC to two groups of mice: one that had been been pre-colonized with a mix of bacterial species derived from normal human intestines and one that had not.  In the pre-colonized mice, Stx levels remained undetectable and all mice remained completely healthy.  In contrast, the control group had high levels of Stx and all developed kidney disease within one week of infection.

“The discovery that normal intestinal bacteria can prevent intestinal Stx accumulation and disease in an animal model may have important implications for prevention of HUS in people infected with EHEC,” says Eaton.

First, it could help explain why not everyone infected with EHEC develops HUS.  Second, and most importantly says Eaton, it identifies specific, non-pathogenic, probiotic bacteria that could be used to prevent or treat Stx-mediated diseases.

This study was funded by the National Institutes of Health (NIH).

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This research was presented as part of the 2013 General Meeting of the American Society for Microbiology held May 18-21, 2013 in Denver, Colorado.  A full press kit for the meeting, including tipsheets and additional press releases, can be found online at http://bit.ly/asm2013pk.

The American Society for Microbiology is the largest single life science society, composed of over 39,000 scientists and health professionals. ASM’s mission is to advance the microbiological sciences as a vehicle for understanding life processes and to apply and communicate this knowledge for the improvement of health and environmental and economic well-being worldwide.