Related Experiment Video
Updated: Jul 15, 2025

Live Cell Imaging of Bacillus subtilis and Streptococcus pneumoniae using Automated Time-lapse Microscopy
Published on: July 28, 2011
Diverse regulatory pathways modulate bet hedging of competence induction in epigenetically-differentiated phase
Min Jung Kwun1, Alexandru V Ion1, Marco R Oggioni2,3
1MRC Centre for Global Infectious Disease Analysis, Sir Michael Uren Hub, White City Campus, Imperial College London, London W12 0BZ, UK.
Abstract:
Despite enabling Streptococcus pneumoniae to acquire antibiotic resistance and evade vaccine-induced immunity, transformation occurs at variable rates across pneumococci. Phase variants of isolate RMV7, distinguished by altered methylation patterns driven by the translocating variable restriction-modification (tvr) locus, differed significantly in their transformation efficiencies and biofilm thicknesses. These differences were replicated when the corresponding tvr alleles were introduced into an RMV7 derivative lacking the locus. RNA-seq identified differential expression of the type 1 pilus, causing the variation in biofilm formation, and inhibition of competence induction in the less transformable variant, RMV7domi. This was partly attributable to RMV7domi's lower expression of ManLMN, which promoted competence induction through importing N-acetylglucosamine. This effect was potentiated by analogues of some proteobacterial competence regulatory machinery. Additionally, one of RMV7domi's phage-related chromosomal island was relatively active, which inhibited transformation by increasing expression of the stress response proteins ClpP and HrcA. However, HrcA increased competence induction in the other variant, with its effects depending on Ca2+ supplementation and heat shock. Hence the heterogeneity in transformation efficiency likely reflects the diverse signalling pathways by which it is affected. This regulatory complexity will modulate population-wide responses to synchronising quorum sensing signals to produce co-ordinated yet stochastic bet hedging behaviour.
Insights
Streptococcus pneumoniae transformation efficiency varies due to differing methylation patterns. This impacts antibiotic resistance and vaccine evasion, highlighting complex regulatory networks in bacterial adaptation.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Streptococcus pneumoniae transformation is crucial for acquiring antibiotic resistance and evading immunity, yet occurs at variable rates.
- Phase variants, differing in methylation patterns due to the translocating variable restriction-modification (tvr) locus, exhibit distinct transformation efficiencies and biofilm formation.
Purpose of the Study:
- To investigate the molecular mechanisms underlying variable transformation efficiency in Streptococcus pneumoniae.
- To elucidate the role of the tvr locus and associated regulatory pathways in modulating competence and biofilm formation.
Main Methods:
- Comparative analysis of phase variants using RNA-sequencing (RNA-seq).
- Genetic manipulation to introduce tvr alleles into a derivative strain.
- Assessment of transformation efficiency, biofilm thickness, and gene expression levels.
Main Results:
- Differential expression of type 1 pilus correlated with biofilm variation.
- Competence induction was inhibited in the less transformable variant (RMV7domi) due to lower ManLMN expression.
- Active phage-related chromosomal islands in RMV7domi increased stress proteins (ClpP, HrcA), inhibiting transformation, while HrcA's effect varied with conditions in the other variant.
Conclusions:
- Heterogeneity in Streptococcus pneumoniae transformation efficiency arises from complex, interconnected signaling pathways.
- Regulatory complexity influences population-level responses, contributing to bet-hedging behavior for adaptation.
More Related Videos
Related Concept Videos
Global Regulatory Systems
Gene Regulation During Sporulation
Constitutive and Regulated Gene Expression
Epigenetic Regulation
X-chromosome...
Gene Regulation in Microbial Communities: Quorum Sensing
Other Stress Responses in Bacteria

