Indeed, this may be important

with Mycobacterium avium subspecies paratuberculosis, a member of the often underrepresented Actinobacteria phylum [65, 66]. The absence of bifidobacteria from our dataset indicates that our clone libraries also suffer from this same bias against Actinobacteria. It is also worth noting that our analysis would not detect any viral, archaeal or eukaryotic aetiological agents. This may be important given recent evidence suggesting a role for viruses in the induction of at least some models of IBD [67]. Sequence-based microbiota ARRY-438162 chemical structure comparisons such as ours can of course only demonstrate associations and do not provide information regarding mechanism or causation. It is also difficult to differentiate between compositional changes that may play a role in disease pathogenesis and those which may simply have occurred as a result of disease. However, given the absence of a specific and recurring aetiological agent in the 4EGI-1 in vitro cumulative data across all published IBD studies, which incorporate both culture- and molecular-based methodologies, it is possible that the alterations in bacterial composition and diversity seen between healthy and IBD patients and between inflamed and non-inflamed mucosa selleck chemicals may be, to at least some extent, the result of the disturbed gut environment rather than the direct cause of disease. Indeed, there are a number of reasons why IBD is likely to result in altered conditions for bacterial growth. For

example, the gut in IBD is likely to be a less stable environment than that of healthy individuals, with more exposure to antibiotics and other drug regimes, and alterations in transit time. Microscopy studies have suggested that there is a higher penetration of bacteria and a greater bacterial load in the mucosal layer in IBD patients [47, 68] and the resulting inflammation

drives the localised release of antimicrobial compounds [69]. In addition, in UC there is a reduced mucus layer in inflamed relative to non-inflamed regions [70]. Despite proportional increases in Enterobacteriaceae and Bacteroidetes within IBD patients, if these organisms were directly responsible for disease we might expect them to be elevated at sites of inflammation and this was not shown in our analysis. Taking into account all of the above factors, the observed increases in these bacterial groups in IBD patients as a whole may therefore Methane monooxygenase simply reflect the adaptation of the individual microbiota to the IBD gut environment. Bacteroides thetaiotaomicron, for example, can adapt to inflammation in an experimental mouse model by inducing genes that metabolise host oxidative products [71] and inflammation per se has also been shown to promote the growth of Enterobacteriaceae in mouse models [72, 73]. Clearly, further similar studies are required on a far greater range of gut bacterial species so that we can better understand the response of the gut microbiota to alterations in environmental conditions.