Τhe ability of the immune system to fight off bacterial, viral and other invading agents in the gut differs between individuals. However, the biological mechanism by which this happens is not well understood, but at least part of this difference may be explained by genetic factors.
Now, scientists at EPFL's Institute of Bioengineering have published two papers in Genome Biology that make significant headway in uncovering the mechanisms by which genetics influences the ability of an organism to mount an immune reaction to an invading gut pathogen. The research was carried out by Michael Frochaux and Maroun Bou Sleiman from Bart Deplancke's research group at EPFL.
Because of obvious ethical reasons, this phenomenon is difficult to study in humans. So the scientists turned to the fruit fly Drosophila melanogaster, since it shares immany of the biological pathways involved in fighting gut infections in humans.
The scientists studied a large panel of genetically distinct fruit fly lines, which vary greatly in their ability to resist gut infection by the severe pathogen Pseudomonas entomophila. To better understand the molecular origin of this variation, the researchers isolated infected guts from each fly line and explored them using a wide array of omics approaches.
In the first paper, the researchers show that gut infection changes RNA splicing, which affects the production of messenger RNA (mRNA), a crucial molecule in the path from gene to protein. Specifically, infection seems to lengthen one end of several mRNAs.
"It is as if the organism intends to add more information in these mRNAs that could then be exploited to further finetune the overall gut immune response," says Deplancke. The change in mRNA length seems to be mediated through a protein called Lark, which binds RNA to form a complex involved in gene expression. When this complexing ability is lost, the fruit flies were less able to recover from a severe gut infection, clearly demonstrating the importance of this process in gut immunity.
The second paper reports the discovery of a number of genetic variants that alter the levels of gene expression in the gut following infection. One particular variant could be directly linked to variation in infection resistance because it modulates the expression level of a gene called Nutcracker. More resistant fly lines showed higher Nutcracker expression compared to less resistant ones.
"This study provides an intriguing example of how variation in the non-coding part of the genome could still critically affect complex traits such as height or disease susceptibility," says Deplancke. "In this case, this includes gut immunocompetence, so we need to consider the whole genome and not just its genes".
Computational Biology and Data Mining Group, Institute of Molecular Biology
The Barcelona Institute of Science and Technology
Swiss Institute of Bioinformatics
Maroun S. Bou Sleiman, Michael Frochaux, Tommaso Andreani, Dani Osman, Roderic Guigo, Bart Deplancke. Enteric infection induces Lark-mediated intron retention at the 5' end of Drosophila genes. Genome Biology DOI: 10.1186/s13059-019-1918-6
Michael V. Frochaux, Maroun Bou Sleiman, Vincent R. J. Gardeux, Riccardo Dainese, Brian Hollis, Maria Litovchenko, Virginie S. Braman, Tommaso Andreani, Dani Osman, Bart Deplancke. cis-regulatory variation modulates susceptibility to enteric infection in the Drosophila Genetic Reference Panel. Genome Biology DOI: 10.1186/s13059-019-1912-z