Abstract

The intestinal ecosystem is formed by a complex, yet highly characteristic microbial community. The parameters defining whether this community permits invasion of a new bacterial species are unclear. In particular, inhibition of enteropathogen infection by the gut microbiota ( = colonization resistance) is poorly understood. To analyze the mechanisms of microbiota-mediated protection from Salmonella enterica induced enterocolitis, we used a mouse infection model and large scale high-throughput pyrosequencing. In contrast to conventional mice (CON), mice with a gut microbiota of low complexity (LCM) were highly susceptible to S. enterica induced colonization and enterocolitis. Colonization resistance was partially restored in LCM-animals by co-housing with conventional mice for 21 days (LCMcon21). 16S rRNA sequence analysis comparing LCM, LCMcon21 and CON gut microbiota revealed that gut microbiota complexity increased upon conventionalization and correlated with increased resistance to S. enterica infection. Comparative microbiota analysis of mice with varying degrees of colonization resistance allowed us to identify intestinal ecosystem characteristics associated with susceptibility to S. enterica infection. Moreover, this system enabled us to gain further insights into the general principles of gut ecosystem invasion by non-pathogenic, commensal bacteria. Mice harboring high commensal E. coli densities were more susceptible to S. enterica induced gut inflammation. Similarly, mice with high titers of Lactobacilli were more efficiently colonized by a commensal Lactobacillus reuteri RR strain after oral inoculation. Upon examination of 16S rRNA sequence data from 9 CON mice we found that closely related phylotypes generally display significantly correlated abundances (co-occurrence), more so than distantly related phylotypes. Thus, in essence, the presence of closely related species can increase the chance of invasion of newly incoming species into the gut ecosystem. We provide evidence that this principle might be of general validity for invasion of bacteria in preformed gut ecosystems. This might be of relevance for human enteropathogen infections as well as therapeutic use of probiotic commensal bacteria.

Highlights

  • The mammalian intestine hosts a microbial community of astonishing density and complexity

  • In contrast to conventional mice (CON) mice (,500 different bacterial strains in the gut), the gut microbiota of low complexity (LCM) mice includes a mixture of only 8 bacterial strains, the Altered Schaedler Flora (ASF), which are typically found in the gut of rodents [39]

  • LCM mice as model for investigating the mechanisms of colonization resistance’ (CR). It has been known for a long time, that the normal gut microbiota plays a key role in protection from infection with pathogenic bacteria

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Summary

Introduction

The mammalian intestine hosts a microbial community of astonishing density and complexity. This intricate association presumably required significant coevolution of the host and its microbiota. This coevolution has been guided by positive selection for factors that result in a state of both mutual tolerance and benefit. The adult human intestine hosts 1013 to 1014 bacteria belonging to at least 500 different species or strains [2]. It is assumed that the microbial ecosystem, once it is formed, efficiently prevents invasion by foreign species. This has been extensively studied in Author Summary

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