Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens.
Nozomu ObanaKouji NakamuraNobuhiko NomuraPublished in: NPJ biofilms and microbiomes (2020)
Cells in biofilms dynamically adapt to surrounding environmental conditions, which alters biofilm architecture. The obligate anaerobic pathogen Clostridium perfringens shows different biofilm structures in different temperatures. Here we find that the temperature-regulated production of extracellular polymeric substance (EPS) is necessary for morphological changes in biofilms. We identify BsaA proteins as an EPS matrix necessary for pellicle biofilm formation at lower temperature and find that extracellularly secreted BsaA protein forms filamentous polymers. We show that sipW-bsaA operon expression is bimodal, and the EPS-producing population size is increased at a lower temperature. This heterogeneous expression of the EPS gene requires a two-component system. We find that EPS-producing cells cover EPS-nonproducing cells attaching to the bottom surface. In the deletion mutant of pilA2, encoding a type IV pilin, the EPS gene expression is ON in the whole population. This heterogeneity is further regulated by the cleavage of the pilA2 mRNA by RNase Y, causing temperature-responsive EPS expression in biofilms. As temperature is an environmental cue, C. perfringens may modulate EPS expression to induce morphological changes in biofilm structure as a strategy for adapting to interhost and external environments.
Keyphrases
- candida albicans
- biofilm formation
- pseudomonas aeruginosa
- gene expression
- staphylococcus aureus
- poor prognosis
- induced apoptosis
- cell cycle arrest
- extracellular matrix
- binding protein
- dna methylation
- escherichia coli
- cystic fibrosis
- long non coding rna
- microbial community
- transcription factor
- signaling pathway
- high resolution
- genome wide
- wastewater treatment
- mass spectrometry
- human health
- cancer therapy
- small molecule
- climate change
- cell death
- heavy metals
- pi k akt
- genome wide identification