The human intestinal microbiota contains more than 35 species of the order Bacteroidales, which collectively are the most abundant Gram negative bacteria of this microbial ecosystem. We know very little about how these intestinal bacteria interact with each other to establish health-promoting microbial communities. This application addresses antagonistic interactions mediated by Type VI secretion systems (T6SS) of the gut Bacteroidales. Until recently, T6SS were only described in Proteobacterial species. We have found that T6SS are abundant in the gut Bacteroidales and we have identified 114 T6SS loci in 205 human gut Bacteroidales genomes. We have experimentally demonstrated that two of these T6SSs mediate antagonistic interactions with other Bacteroidales species. The two aims of this proposal are designed to study the most important questions regarding these T6SSs in terms of ecosystem establishment, defense, invasion and stability.
In Aim 1, we will take a molecular approach to study the T6SSs, their range of bacterial targeting, identification of toxic effectors, the basis of theT6SS resistance observed in some strains, and regulation of T6SS firing by a transcriptional repressor of the TetR family. We will also analyze if T6SS of gut Bacteroidales target enteric pathogens, thereby contributing to the microbiota's colonization resistance function.
The second aim i s designed to utilize the mutants and molecular tools that were generated in the first aim to comprehensively study the relevance of T6SS-mediated antagonism in the mammalian gut. For this aim, we will perform experiments using a gnotobiotic mouse intestinal colonization model to determine if T6SSs facilitate the invasion of a strain into an established ecosystem, and the roles of T6SSs in thwarting colonization of competing sensitive strains. These studies will also include analyses of T6SS-mediated antagonism between naturally co- resident strains from a human gut ecosystems to determine if T6SS-mediated antagonism occurs in a naturally stable human gut microbial community. In addition, we will study the ability of T6SS to be transferred by integrative conjugative elements between strains in vitro and within the gnotobiotic mouse colon. These studies will contribute significantl to our understanding the dynamic interactions that occur between gut species and the factors that contribute to the establishment of human intestinal microbial ecosystems.
Our intestines harbor a microbial community that is essential to our health and development, yet we know very little about how the microbial members of this ecosystem interact with each other. For this project, we will study contact-dependent antagonistic interactions that occur between these bacterial members and investigate how these interactions promote the formation of stable, health-promoting communities. These studies will be informative in how to return a healthy and stable intestinal microbiota to people with imbalances of this bacterial community.
| García-Bayona, Leonor; Comstock, Laurie E (2018) Bacterial antagonism in host-associated microbial communities. Science 361: |
| Coyne, Michael J; Comstock, Laurie E (2016) A New Pillar in Pilus Assembly. Cell 165:520-1 |
| Coyne, Michael J; Roelofs, Kevin G; Comstock, Laurie E (2016) Type VI secretion systems of human gut Bacteroidales segregate into three genetic architectures, two of which are contained on mobile genetic elements. BMC Genomics 17:58 |
| Chatzidaki-Livanis, Maria; Geva-Zatorsky, Naama; Comstock, Laurie E (2016) Bacteroides fragilis type VI secretion systems use novel effector and immunity proteins to antagonize human gut Bacteroidales species. Proc Natl Acad Sci U S A 113:3627-32 |
