Quantitative analysis of commensal Escherichia coli populations reveals host‐specific enterotypes at the intra‐species level. Issue 4 (29th May 2015)

• Record Type: Journal Article
• Authors: Smati, Mounira; Clermont, Olivier; Bleibtreu, Alexandre; Fourreau, Frédéric; David, Anthony; Daubié, Anne‐Sophie; Hignard, Cécile; Loison, Odile; Picard, Bertrand; Denamur, Erick
• Is Part Of: MicrobiologyOpen. Volume 4:Issue 4(2015:Aug.)
• Page Start: 604
• Page End: 615
• Publication Date: 2015-05-29
• Subjects: Microbiology -- Periodicals; 579
• DOI: 10.1002/mbo3.266
• Languages: English
• ISSNs: 2045-8827

Abstract

<abstract abstract-type="main" id="mbo3266-abs-0001"> <title>Abstract</title> <p>The primary habitat of the <italic>Escherichia coli</italic> species is the gut of warm‐blooded vertebrates. The <italic>E. coli</italic> species is structured into four main phylogenetic groups A, B1, B2, and D. We estimated the relative proportions of these phylogroups in the feces of 137 wild and domesticated animals with various diets living in the Ile de France (Paris) region by real‐time PCR. We distinguished three main clusters characterized by a particular abundance of two or more phylogroups within the <italic>E. coli</italic> animal commensal populations, which we called "enterocolitypes" by analogy with the enterotypes defined in the human gut microbiota at the genus level. These enterocolitypes were characterized by a dominant (>50%) B2, B1, or A phylogroup and were associated with different host species, diets, and habitats: wild and herbivorous species (wild rabbits and deer), domesticated herbivorous species (domesticated rabbits, horses, sheep, and cows), and omnivorous species (boar, pigs, and chickens), respectively. By analyzing retrospectively the data obtained using the same approach from 98 healthy humans living in Ile de France (Smati et al. 2013, <italic>Appl. Environ. Microbiol</italic>. 79, 5005–5012), we identified a specific human enterocolitype characterized by the dominant and/or exclusive (>90%) presence of phylogroup B2. We then compared B2 strains isolated from animals and humans, and revealed that human and animal strains differ regarding O‐type and B2 subgroup. Moreover, two genes, <italic>sfa/foc</italic> and <italic>clbQ</italic>, were associated with the exclusive character of strains, observed only in humans. In conclusion, a complex network of interactions exists at several levels (genus and intra‐species) within the intestinal microbiota.</p> </abstract>