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Nutritional Basis for Colonization Resistance by Human Commensal Escherichia coli Strains HS and Nissle 1917 against E. coli O157:H7 in the Mouse Intestine

Overview of attention for article published in PLOS ONE, January 2013
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Title
Nutritional Basis for Colonization Resistance by Human Commensal Escherichia coli Strains HS and Nissle 1917 against E. coli O157:H7 in the Mouse Intestine
Published in
PLOS ONE, January 2013
DOI 10.1371/journal.pone.0053957
Pubmed ID
Authors

Rosalie Maltby, Mary P. Leatham-Jensen, Terri Gibson, Paul S. Cohen, Tyrrell Conway

Abstract

Escherichia coli is a single species consisting of many biotypes, some of which are commensal colonizers of mammals and others that cause disease. Humans are colonized on average with five commensal biotypes, and it is widely thought that the commensals serve as a barrier to infection by pathogens. Previous studies showed that a combination of three pre-colonized commensal E. coli strains prevents colonization of E. coli O157:H7 in a mouse model (Leatham, et al., 2010, Infect Immun 77: 2876-7886). The commensal biotypes included E. coli HS, which is known to successfully colonize humans at high doses with no adverse effects, and E. coli Nissle 1917, a human commensal strain that is used in Europe as a preventative of traveler's diarrhea. We hypothesized that commensal biotypes could exert colonization resistance by consuming nutrients needed by E. coli O157:H7 to colonize, thus preventing this first step in infection. Here we report that to colonize streptomycin-treated mice E. coli HS consumes six of the twelve sugars tested and E. coli Nissle 1917 uses a complementary yet divergent set of seven sugars to colonize, thus establishing a nutritional basis for the ability of E. coli HS and Nissle 1917 to occupy distinct niches in the mouse intestine. Together these two commensals use the five sugars previously determined to be most important for colonization of E. coli EDL933, an O157:H7 strain. As predicted, the two commensals prevented E. coli EDL933 colonization. The results support a model in which invading pathogenic E. coli must compete with the gut microbiota to obtain the nutrients needed to colonize and establish infection; accordingly, the outcome of the challenge is determined by the aggregate capacity of the native microbiota to consume the nutrients required by the pathogen.

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Geographical breakdown

Country Count As %
United States 5 2%
France 1 <1%
United Kingdom 1 <1%
Ireland 1 <1%
Japan 1 <1%
Spain 1 <1%
Unknown 303 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 75 24%
Student > Master 41 13%
Researcher 37 12%
Student > Bachelor 35 11%
Student > Doctoral Student 19 6%
Other 43 14%
Unknown 63 20%
Readers by discipline Count As %
Agricultural and Biological Sciences 74 24%
Immunology and Microbiology 55 18%
Biochemistry, Genetics and Molecular Biology 49 16%
Medicine and Dentistry 19 6%
Engineering 9 3%
Other 34 11%
Unknown 73 23%