A network of small RNAs regulates sporulation initiation in Clostridioides difficile.
Manuela FuchsVanessa Lamm-SchmidtTina LenčeJohannes SulzerArne BublitzJanet WackenreuterMilan GerovacTill StrowigFranziska FaberPublished in: The EMBO journal (2023)
The obligate anaerobic, enteric pathogen Clostridioides difficile persists in the intestinal tract by forming antibiotic-resistant endospores that contribute to relapsing and recurrent infections. Despite the importance of sporulation for C. difficile pathogenesis, environmental cues and molecular mechanisms that regulate sporulation initiation remain ill-defined. Here, by using RIL-seq to globally capture the Hfq-dependent RNA-RNA interactome, we discovered a network of small RNAs that bind to mRNAs encoding sporulation-related genes. We show that two of these small RNAs, SpoX and SpoY, regulate translation of the master regulator of sporulation, Spo0A, in an opposing manner, which ultimately leads to altered sporulation rates. Infection of antibiotic-treated mice with SpoX and SpoY deletion mutants revealed a global effect on gut colonization and intestinal sporulation. Our work uncovers an elaborate RNA-RNA interactome controlling the physiology and virulence of C. difficile and identifies a complex post-transcriptional layer in the regulation of spore formation in this important human pathogen.
Keyphrases
- bacillus subtilis
- clostridium difficile
- transcription factor
- multiple sclerosis
- escherichia coli
- endothelial cells
- genome wide
- single cell
- microbial community
- nucleic acid
- pseudomonas aeruginosa
- staphylococcus aureus
- cystic fibrosis
- type diabetes
- gene expression
- climate change
- heavy metals
- risk assessment
- rheumatoid arthritis
- high fat diet induced
- adipose tissue
- wild type
- oxidative stress
- dna methylation