Active Infection & Immunity Genetics & Molecular Biology

How do hosts control microbiome dynamics?

In plain English

AI plain-English summary

The gut’s bacterial ecosystem is constantly in flux, and a researcher is building new tools to figure out how the host’s own immune system—specifically Immunoglobulin A—steers those changes. Why this matters: The gut microbiome contains hundreds of microbial species whose populations rise and fall in complex patterns. Scientists want to engineer these communities to improve health, but the sheer complexity makes it nearly impossible to predict or control them. The host’s role in shaping these dynamics is particularly poorly understood. This project tackles that gap head-on. If successful, the research will produce a new interdisciplinary platform—combining sequencing tools, computational models, and theoretical frameworks—that can identify exactly which host-to-microbe and microbe-to-host interactions drive microbiome dynamics. This is fundamental science. There is no immediate clinical application. But a predictive understanding of how hosts control microbial ecosystems could eventually underpin therapies that stabilise or reshape the microbiome in conditions like inflammatory bowel disease, recurrent infections, or metabolic disorders—much as fundamental work on bacterial genetics and phage biology laid the groundwork for modern gene editing and antimicrobial therapies.

View original technical description
Mammalian microbiomes are dynamic ecosystems, composed of hundreds of taxa whose populations continuously rise and fall, shaped by interactions microbes have with their host and one another. Understanding the forces driving microbiome dynamics is critical if we wish to engineer them, however, the vast complexity of most microbiomes renders this a formidable challenge. I will address this challenge, developing interdisciplinary tools to understand and predict microbiome dynamics, focusing on the poorly understood role of the host in controlling microbiome dynamics. First, I will use innovative sequencing tools to quantify the impact of host immune background on the assembly and stability of the gut microbiome, then develop new computational tools to identify the specific host-to-microbe interactions causatively driving these differences. Concurrently, I will develop new computational tools to identify microbe-to-host interactions shaping host immune development. Finally, I will build a new body of theory to understand how these interactions integrate to shape overall microbiome dynamics. Throughout, I will focus on one key host adaptation: Immunoglobulin A. However, by combining targeted experimental and computational approaches with novel theory I will build an interdisciplinary platform for investigating the role of any host mechanism. Together this will transform our understanding of microbiome dynamics.

View the original record at the funder ↗

Researchers

Katharine Coyte (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Investigating the immune factors that determine commensal microbiota assembly
How does the immune system shape bacteriophage dynamics within the mammalian gut?
Drivers and consequences of host microbiome control
Causes and consequences of variation in the mammalian microbiota
The architecture and evolution of host control in a microbial symbiosis

Original classification

Career Development Award

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