The human gut is colonized by a diverse microbial community collectively referred to as the gut microbiota. A healthy gut microbiota provides protection against intestinal colonisation by pathogens, however disruption of the gut microbiota can weaken colonisation resistance (e.g. following exposure to antibiotics), increasing the host’s susceptibility to enteric infections. The aim of our research is to develop novel microbiome therapeutics to restore microbiota-mediated colonisation resistance and decolonise pathogens from the intestine. In our previous work we identified a bacterial metabolite (valerate) and a microbial enzyme (bile salt hydrolase) that significantly inhibits Clostridioides difficile germination and vegetative growth following faecal microbiota transplantation (FMT).
Antimicrobial resistance is a serious threat to human health, resulting in treatment failures, infection relapses, longer hospitalisations, and poor clinical outcomes. The intestine is the primary colonisation site for multidrug-resistant organisms (MDROs) and serves as a reservoir for MDROs that are responsible for invasive infections (e.g. sepsis and recurrent urinary tract infections). Studies have demonstrated that antibiotic treatment makes the host more susceptible to intestinal colonisation with carbapenem-resistant Enterobacteriaceae (CRE), vancomycin-resistant Enterococcus (VRE) and extended spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E), and FMT has been shown to successfully decolonise these pathogens from the intestine. However, the mechanism of gut microbiota-mediated colonisation resistance is unknown. The goal of our research is to determine the mechanism(s) by which gut microbiota-mediated colonisation resistance protects the host against intestinal MDRO colonisation, with the aim to develop a new microbiome therapeutic for MDRO intestinal decolonisation. We are particularly interested in gut microbiota-mediated nutrient competition and metabolite inhibition.
Our lab uses a variety of complementary approaches to study gut colonisation resistance, including artificial gut models (aka “chemostat” or “Robogut” models), batch culture experiments, and patient faecal samples. Samples are analysed using both culture-dependent and culture-independent techniques, including a variety of “omic” techniques (e.g. 16S rRNA gene sequencing, 1H-NMR spectroscopy, and mass spectrometry).
Summary of different mechanisms of gut microbiota-mediated colonisation resistance that can be used to develop new microbiome therapeutics.
Artificial gut ("chemostat") model used to study the gut microbiota.
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