Type IV pili promote early biofilm formation by Clostridium difficile. Academic Article uri icon

Overview

abstract

  • Increasing morbidity and mortality from Clostridium difficile infection (CDI) present an enormous challenge to healthcare systems. Clostridium difficile express type IV pili (T4P), but their function remains unclear. Many chronic and recurrent bacterial infections result from biofilms, surface-associated bacterial communities embedded in an extracellular matrix. CDI may be biofilm mediated; T4P are important for biofilm formation in a number of organisms. We evaluate the role of T4P in C. difficile biofilm formation using RNA sequencing, mutagenesis and complementation of the gene encoding the major pilin pilA1, and microscopy. RNA sequencing demonstrates that, in comparison to other growth phenotypes, C. difficile growing in a biofilm has a distinct RNA expression profile, with significant differences in T4P gene expression. Microscopy of T4P-expressing and T4P-deficient strains suggests that T4P play an important role in early biofilm formation. A non-piliated pilA1 mutant forms an initial biofilm of significantly reduced mass and thickness in comparison to the wild type. Complementation of the pilA1 mutant strain leads to formation of a biofilm which resembles the wild-type biofilm. These findings suggest that T4P play an important role in early biofilm formation. Novel strategies for confronting biofilm infections are emerging; our data suggest that similar strategies should be investigated in CDI.

authors

  • Maldarelli, Grace
  • Piepenbrink, Kurt H
  • Scott, Alison J
  • Freiberg, Jeffrey A
  • Song, Yang
  • Achermann, Yvonne
  • Ernst, Robert K
  • Shirtliff, Mark E
  • Sundberg, Eric J
  • Donnenberg, Michael S
  • von Rosenvinge, Erik C

publication date

  • June 30, 2016

Research

keywords

  • Biofilms
  • Clostridioides difficile
  • Enterocolitis, Pseudomembranous
  • Fimbriae, Bacterial

Identity

PubMed Central ID

  • PMC5985507

Scopus Document Identifier

  • 85009728536

Digital Object Identifier (DOI)

  • 10.1093/femspd/ftw061

PubMed ID

  • 27369898

Additional Document Info

volume

  • 74

issue

  • 6