Clostridium difficile Biofilm: Remodeling Metabolism and Cell Surface to Build a Sparse and Heterogeneously Aggregated Architecture

• Published in: Frontiers in microbiology 2018-09, Vol.9, p.2084-2084
• Main Authors: Poquet, Isabelle, Saujet, Laure, Canette, Alexis, Monot, Marc, Mihajlovic, Jovanna, Ghigo, Jean-Marc, Soutourina, Olga, Briandet, Romain, Martin-Verstraete, Isabelle, Dupuy, Bruno
• Format: Article
• Language: English
• Subjects: aggregates; biofilm architecture; biofilm formation; Clostridium difficile; gene expression profiling; Life Sciences; Microbiology; Microbiology and Parasitology
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2018.02084

is an opportunistic entero-pathogen causing post-antibiotic and nosocomial diarrhea upon microbiota dysbiosis. Although biofilms could contribute to colonization, little is known about their development and physiology. Strain 630Δ is able to form, in continuous-flow micro-fermentors, macro-colonies and submersed biofilms loosely adhesive to glass. According to gene expression data, in biofilm/planktonic cells, central metabolism is active and fuels fatty acid biosynthesis rather than fermentations. Consistently, succinate is consumed and butyrate production is reduced. Toxin A expression, which is coordinated to metabolism, is down-regulated, while surface proteins, like adhesins and the primary Type IV pili subunits, are over-expressed. C-di-GMP level is probably tightly controlled through the expression of both diguanylate cyclase-encoding genes, like , and phosphodiesterase-encoding genes. The coordinated expression of genes controlled by c-di-GMP and encoding the putative surface adhesin CD2831 and the major Type IV pilin PilA , suggests that c-di-GMP could be high in biofilm cells. A SinR-like regulator, CD2214, and/or CD2215, another regulator co-encoded in the same operon as CD2214, control many genes differentially expressed in biofilm, and in particular , and in a positive way. After growth in micro-titer plates and disruption, the biofilm is composed of robust aggregated structures where cells are embedded into a polymorphic material. The intact biofilm observed displays a sparse, heterogeneous and high 3D architecture made of rods and micro-aggregates. The biofilm is denser in a mutant of both and genes, but it is not affected by the inactivation of neither nor . , when over-expressed, not only increases the biofilm but also triggers its architecture to become homogeneous and highly aggregated, in a way independent of and barely dependent of . Cell micro-aggregation is shown to play a major role in biofilm formation and architecture. This thorough analysis of gene expression reprogramming and architecture remodeling in biofilm lays the foundation for a deeper understanding of this lifestyle and could lead to novel strategies to limit spread.