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Updated: May 9, 2026

Live Cell Imaging of Bacillus subtilis and Streptococcus pneumoniae using Automated Time-lapse Microscopy
Published on: July 28, 2011
From models to pathogens: how much have we learned about Streptococcus pneumoniae cell division?
Orietta Massidda1, Linda Nováková, Waldemar Vollmer
1Department of Surgical Sciences, University of Cagliari, Via Porcell, 4, 09100, Cagliari, Italy.
Abstract:
Streptococcus pneumoniae is an oval-shaped Gram-positive coccus that lives in intimate association with its human host, both as a commensal and pathogen. The seriousness of pneumococcal infections and the spread of multi-drug resistant strains call for new lines of intervention. Bacterial cell division is an attractive target to develop antimicrobial drugs. This review discusses the recent advances in understanding S. pneumoniae growth and division, in comparison with the best studied rod-shaped models, Escherichia coli and Bacillus subtilis. To maintain their shape, these bacteria propagate by peripheral and septal peptidoglycan synthesis, involving proteins that assemble into distinct complexes called the elongasome and the divisome, respectively. Many of these proteins are conserved in S. pneumoniae, supporting the notion that the ovococcal shape is also achieved by rounds of elongation and division. Importantly, S. pneumoniae and close relatives with similar morphology differ in several aspects from the model rods. Overall, the data support a model in which a single large machinery, containing both the peripheral and septal peptidoglycan synthesis complexes, assembles at midcell and governs growth and division. The mechanisms generating the ovococcal or coccal shape in lactic-acid bacteria have likely evolved by gene reduction from a rod-shaped ancestor of the same group.
Insights
New research reveals that Streptococcus pneumoniae, a common pathogen, grows and divides using a conserved mechanism similar to rod-shaped bacteria. This understanding of bacterial cell division could lead to novel antimicrobial drug development.
Area of Science:
- Microbiology
- Bacterial Cell Biology
- Antimicrobial Drug Discovery
Background:
- Streptococcus pneumoniae is a significant human pathogen, causing serious infections and exhibiting multi-drug resistance.
- Bacterial cell division is a promising target for developing new antimicrobial interventions.
- Understanding the growth and division mechanisms of S. pneumoniae is crucial for therapeutic strategies.
Purpose of the Study:
- To review recent advances in understanding Streptococcus pneumoniae growth and division.
- To compare S. pneumoniae's cell division with well-studied model organisms like Escherichia coli and Bacillus subtilis.
- To elucidate the molecular machinery governing the ovococcal shape of S. pneumoniae.
Main Methods:
- Comparative analysis of peptidoglycan synthesis pathways in S. pneumoniae and model bacteria.
- Review of conserved and divergent proteins involved in bacterial elongation and division.
- Integration of data to propose a model for S. pneumoniae growth and division.
Main Results:
- Streptococcus pneumoniae utilizes peripheral and septal peptidoglycan synthesis, involving elongasome and divisome complexes, similar to rod-shaped bacteria.
- Many cell division proteins are conserved between S. pneumoniae and model rods, suggesting a shared fundamental mechanism.
- S. pneumoniae exhibits unique differences from model rods, supporting a model of a single, large midcell machinery for growth and division.
- The ovococcal shape likely evolved from a rod-shaped ancestor through gene reduction.
Conclusions:
- Streptococcus pneumoniae's growth and division are governed by a conserved, albeit potentially unified, machinery.
- The ovococcal morphology of S. pneumoniae may have evolved from rod-shaped ancestors.
- Targeting bacterial cell division in S. pneumoniae offers a viable strategy for novel antimicrobial drug development.
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