Synthetic gene-regulatory networks in the opportunistic human pathogen Streptococcus pneumoniae

Robin A Sorg1, Clement Gallay2, Laurye Van Maele3

  • 1Molecular Genetics Group, Groningen Biomolecular Sciences and Biotechnology Institute, Centre for Synthetic Biology, University of Groningen, 9747 AG, Groningen, The Netherlands.

Insights

Synthetic biology tools were developed to control gene expression in Streptococcus pneumoniae. These tools enable the study of virulence factor regulation and function in vivo, advancing our understanding of pneumococcal disease.

Area of Science:

  • Synthetic Biology
  • Microbial Pathogenesis
  • Gene Regulation

Background:

  • Streptococcus pneumoniae causes diverse infections, but studying its virulence factor expression in vitro is challenging due to the lack of natural environmental cues and immune system presence.
  • Understanding pneumococcal virulence factor control is crucial for developing effective treatments and interventions against this pathogen.

Purpose of the Study:

  • To apply synthetic biology methods for reverse-engineering gene expression control in Streptococcus pneumoniae.
  • To develop tools for identifying regulatory elements and assembling complex gene-regulatory networks.
  • To investigate the function of these synthetic networks in vivo, particularly concerning virulence factor expression.

Main Methods:

  • Developed a selection platform for identifying transcriptional regulatory elements from combinatorial libraries.
  • Engineered TetR- and LacI-regulated promoters with a four-orders-of-magnitude expression range.
  • Assembled complex regulatory networks, including AND and IMPLY gates, and single-copy genome-integrated toggle switches.

Main Results:

  • Demonstrated TetR- and LacI-regulated promoters enabling precise control over gene expression.
  • Successfully created synthetic gene-regulatory networks, including logic gates and toggle switches, leading to bimodal population distributions.
  • Rewired the capsule operon (a key virulence factor) to be externally inducible (YES gate) or conditionally expressed (IMPLY gate).
  • Validated the functionality of these synthetic networks in a murine model of influenza A virus superinfection-induced pneumonia.

Conclusions:

  • Synthetic biology provides powerful tools to engineer and study gene expression control in Streptococcus pneumoniae.
  • The developed tools allow for mimicking complex expression patterns relevant to pneumococcal virulence.
  • These findings pave the way for in vivo investigations into the role of gene expression regulation in pneumococcal pathogenicity.

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