Abstract

BackgroundClostridium perfringens is a Gram-positive anaerobic pathogen that causes multiple diseases in humans and animals. C. perfringens lack flagella but have type IV pili (TFP) and can glide on agar surfaces. When C. perfringens bacteria are placed on surfaces, they become elongated, flexible and have TFP on their surface, traits not seen in liquid-grown cells. In addition, the main pilin in C. perfringens TFP, PilA2, undergoes differential post-translational modification when grown in liquid or on plates. To understand the mechanisms underlying these phenotypes, bacteria were grown in three types of liquid media and on agar plates with the same medium to compare gene expression using RNA-Seq.ResultsHundreds of genes were differentially expressed, including transcriptional regulatory protein-encoding genes and genes associated with TFP functions, which were higher on plates than in liquid. Transcript levels of TFP genes reflected the proportion of each protein predicted to reside in a TFP assembly complex. To measure differences in rates of translation, the Escherichia coli reporter gene gusA gene (encoding β-glucuronidase) was inserted into the chromosome downstream of TFP promoters and in-frame with the first gene of the operon. β-glucuronidase expression was then measured in cells grown in liquid or on plates. β-glucuronidase activity was proportional to mRNA levels in liquid-grown cells, but not plate-grown cells, suggesting significant levels of post-transcriptional regulation of these TFP-associated genes occurs when cells are grown on surfaces.ConclusionsThis study reveals insights into how a non-flagellated pathogenic rod-shaped bacterium senses and responds to growth on surfaces, including inducing transcriptional regulators and activating multiple post-transcriptional regulatory mechanisms associated with TFP functions.

Highlights

  • Clostridium perfringens is a Gram-positive anaerobic pathogen that causes multiple diseases in humans and animals

  • PilA2 is the major pilin needed for adherence to mouse myoblasts We have shown in a previous report that C. perfringens strain 13 can adhere to C2C12 mouse myoblasts [10]

  • The Type IV pili (TFP) retraction ATPase PilT was shown to be necessary for efficient adherence to C2C12 cells [10]

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Summary

Introduction

Clostridium perfringens is a Gram-positive anaerobic pathogen that causes multiple diseases in humans and animals. C. perfringens lack flagella but have type IV pili (TFP) and can glide on agar surfaces. To understand the mechanisms underlying these phenotypes, bacteria were grown in three types of liquid media and on agar plates with the same medium to compare gene expression using RNA-Seq. Bacteria in liquid environments use flagella-mediated swimming to facilitate their environmental lifestyle but can switch from a planktonic lifestyle to a surface mode of existence in the form of biofilms. Mechanosensing of shear forces by TFP and the PilY1 protein led to increased levels of cyclic-diGMP and associated phenotypes such as biofilm formation [5]. A methyl-accepting chemotaxis-like protein, PilJ, interacts with the major pilin of P. aeruginosa (PilA) to regulate cAMP levels and transcriptional control of TFP and flagella genes after attachment of TFP to surfaces [6]

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