ELIGOBIOTICS® / əlɪgobiatɪks 

 (RE)PROGRAMMING
THE MICROBIOME 

Eligobiotics® – Bringing gene therapy to the microbiome 

Eligobiotics® are a first-in-class proprietary modality that enables the delivery and expression of therapeutic DNA in target bacterial populations of the microbiome. This technology allows modulation of the microbiome’s composition and function to address human disease with an unprecedented precision.

 

1/ SSAM technology

Sequence-Specific Anti-Microbials

Armed with a CRISPR system, our Eligobiotics® become highly precise antimicrobials. They kill only the harmful bacteria by creating lethal DNA breaks in target sequences of their genome, while leaving the beneficial bacteria completely intact.

Therapeutic payload: exogenous CRISPR-Cas nuclease gene and its corresponding guide RNA

MoA: Once the DNA payload is injected in the bacteria, the nuclease is expressed and its corresponding guide RNA will guide it toward bacterial genomic sequences homologous to the guide RNA. If such sequences are present, the nuclease will create targeted DNA double-strand breaks, leading to the death of the bacteria. If these sequences are absent from the bacteria, the nuclease won’t create any double-strand breaks, and the bacteria will be left intact.

 

This strategy enables the engineering of the microbiome composition with unprecedented precision, killing only the strains harboring genomic sequences targeted by the nuclease.

2/ FAME technology

Function Addition to the MicrobiomE

Our Eligobiotics® can be used to leverage microbial populations to transiently produce, display, or secrete an exogenous gene or set of genes to have a therapeutic effect on the host.

Therapeutic payload: single gene cassette/operon or multiple gene cassettes/operon(s) – up to 50kb

MoA: Once the non-replicative DNA payload is injected in the bacteria, the gene(s) will be efficiently expressed to have the desired effect on the host.

This strategy enables the engineering of the microbiome function with unprecedented modularity, either to complement the absence of a beneficial gene from the microbiome or to add a novel therapeutic function.

Foundational publications