Global Analysis of the Sporulation Pathway of <i>Clostridium difficile</i>

<div><p>The Gram-positive, spore-forming pathogen <i>Clostridium difficile</i> is the leading definable cause of healthcare-associated diarrhea worldwide. <i>C. difficile</i> infections are difficult to treat because of their frequent recurrence, which can cause life-threatening complications such as pseudomembranous colitis. The spores of <i>C. difficile</i> are responsible for these high rates of recurrence, since they are the major transmissive form of the organism and resistant to antibiotics and many disinfectants. Despite the importance of spores to the pathogenesis of <i>C. difficile</i>, little is known about their composition or formation. Based on studies in <i>Bacillus subtilis</i> and other <i>Clostridium</i> spp., the sigma factors σ^F, σ^E, σ^G, and σ^K are predicted to control the transcription of genes required for sporulation, although their specific functions vary depending on the organism. In order to determine the roles of σ^F, σ^E, σ^G, and σ^K in regulating <i>C. difficile</i> sporulation, we generated loss-of-function mutations in genes encoding these sporulation sigma factors and performed RNA-Sequencing to identify specific sigma factor-dependent genes. This analysis identified 224 genes whose expression was collectively activated by sporulation sigma factors: 183 were σ^F-dependent, 169 were σ^E-dependent, 34 were σ^G-dependent, and 31 were σ^K-dependent. In contrast with <i>B. subtilis</i>, <i>C. difficile</i> σ^E was dispensable for σ^G activation, σ^G was dispensable for σ^K activation, and σ^F was required for post-translationally activating σ^G. Collectively, these results provide the first genome-wide transcriptional analysis of genes induced by specific sporulation sigma factors in the Clostridia and highlight that diverse mechanisms regulate sporulation sigma factor activity in the Firmicutes.</p>