Streptococcus pneumoniae and reactive oxygen species: an unusual approach to living with radicals

Hasan Yesilkaya1, Vahid Farshchi Andisi, Peter W Andrew

  • 1University of Leicester, Department of Infection, Immunity, and Inflammation, Maurice Shock Building, University Road, P.O. Box 138, Leicester, LE1 9HN, UK.

Trends in Microbiology
|February 19, 2013
PubMed

Insights

Streptococcus pneumoniae combats oxidative stress uniquely, lacking typical detoxifying enzymes. This study explores its distinct defense mechanisms against damaging oxygen radicals.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Pathogenesis

Background:

  • Streptococcus pneumoniae is a significant human pathogen facing constant oxidative stress from host and environment.
  • It produces hydrogen peroxide (H2O2), contributing to virulence but also self-inflicted damage.
  • Current understanding of its oxidative stress defense is incomplete, deviating from established models.

Purpose of the Study:

  • To provide an overview of how Streptococcus pneumoniae copes with oxygen radicals.
  • To highlight the unique defense strategies employed by this pathogen.
  • To compare these strategies with other pathogenic streptococci.

Main Methods:

  • Literature review and synthesis of existing research on Streptococcus pneumoniae oxidative stress response.
  • Comparative analysis of defense mechanisms across different streptococcal species.
  • Identification of knowledge gaps and future research directions.

Main Results:

  • Streptococcus pneumoniae exhibits unconventional mechanisms for managing oxidative stress.
  • It lacks canonical oxygen radical detoxifying enzymes and typical global oxidative stress regulators.
  • Its H2O2 production plays a dual role in virulence and biological challenges.

Conclusions:

  • Streptococcus pneumoniae employs a distinct strategy to survive oxidative stress, differing from common bacterial paradigms.
  • Further research is needed to fully elucidate these unique defense pathways.
  • Understanding these mechanisms could offer new insights into streptococcal pathogenesis and control.

Related Concept Videos

Radical Reactivity: Overview01:11

Radical Reactivity: Overview

Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired molecule. These three...
Oxygen Requirements and Growth Patterns01:29

Oxygen Requirements and Growth Patterns

Microorganisms exhibit diverse oxygen requirements and growth patterns driven by their metabolic strategies and environmental adaptations. Oxygen, while essential for many organisms, can also be toxic under certain conditions, shaping how microorganisms grow and survive.Oxygen Requirements of MicroorganismsMicroorganisms are classified based on their ability to use or tolerate oxygen:● Obligate aerobes like Mycobacterium tuberculosis need oxygen for energy production, as it serves as the...
Radical Reactivity: Steric Effects01:10

Radical Reactivity: Steric Effects

The presence of electron-donating, electron-withdrawing, or conjugating groups adjacent to a radical center, imparts electronic stabilization to the radicals. Examples of such electronically-stabilized radicals are triphenylmethyl, tetramethylpiperidine‐N‐oxide, and 2,2‐diphenyl‐1‐picrylhydrazyl. These radicals are remarkably stable and are known as persistent radicals. Some of the persistent radicals can even be isolated and purified.
Along with electronic factors, steric factors also account...
Radical Autoxidation01:20

Radical Autoxidation

The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
Radical Reactivity: Electrophilic Radicals01:02

Radical Reactivity: Electrophilic Radicals

Radicals adjacent to electron‐withdrawing groups are called electrophilic radicals. These radicals readily react with nucleophilic alkenes. For example, the malonate radical, in which the radical center is flanked by two electron‐withdrawing groups, reacts readily with butyl vinyl ether, which consists of an electron‐donating oxygen substituent. The reaction between electrophilic malonate radical and nucleophilic vinyl ether is favored because the radical has a low‐energy SOMO, which interacts...
Radical Reactivity: Nucleophilic Radicals01:16

Radical Reactivity: Nucleophilic Radicals

Radicals adjacent to electron-donating groups are called nucleophilic radicals. These radicals readily react with electrophilic alkenes. The SOMO–LUMO interactions are the driving force for the reaction, where the high-energy SOMO of the electron-rich, nucleophilic radicals interacts with the low-energy LUMO of the electron-deficient, electrophilic alkenes. Such SOMO–LUMO interactions are the basis of reactive radical traps, affecting the selectivity in radical reactions. For instance, consider...