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Published on: August 19, 2016
Insights into Streptococcus pyogenes pathogenesis from transcriptome studies
Tomas Fiedler1, Venelina Sugareva, Nadja Patenge
1Institute of Medical Microbiology, Virology & Hospital Hygiene, University Hospital Rostock, Schillingallee 70, Rostock, Germany.
Abstract:
Streptococcus pyogenes (group A Streptococcus [GAS]) is a major human pathogen, causing diseases ranging from mild superficial infections of the skin and pharyngeal mucosal membrane, up to severe systemic and invasive diseases and autoimmune sequelae. The capability of GAS to cause this wide variety of infections is due to the expression of a large set of virulence factors, their concerted transcriptional regulation, and bacterial adaptation mechanisms to various host niches, which we are now beginning to understand on a molecular level. The addition of -omics technologies for GAS pathogenesis investigation, on top of traditional molecular methods, led to fast progress in understanding GAS pathogenesis mechanisms. This article focuses on differential transcriptional analysis performed on the bacterial side as well as on the host cell side. The microarray studies discussed provide new insight into the following five topics: gene-expression patterns under infection-relevant conditions, gene-expression patterns in mutant strains compared with wild-type strains, emergence of exceptionally fit GAS clones, gene-expression patterns of eukaryotic target and immune cells in response to GAS infection, and mechanisms underlying shifts from a pharyngeal to invasive GAS lifestyle.
Insights
Streptococcus pyogenes (group A Streptococcus [GAS]) causes diverse infections due to virulence factors and adaptation. Microarray studies reveal gene expression changes in bacteria and host cells during infection, aiding understanding of GAS pathogenesis.
Area of Science:
- Microbiology
- Pathogenesis
- Genomics
Background:
- Streptococcus pyogenes (group A Streptococcus [GAS]) is a significant human pathogen responsible for a spectrum of diseases, from superficial infections to severe invasive conditions.
- GAS virulence stems from numerous factors, their coordinated regulation, and adaptive strategies within host environments.
- Understanding GAS pathogenesis is advancing with the integration of -omics technologies alongside traditional methods.
Purpose of the Study:
- To investigate differential transcriptional analysis in Streptococcus pyogenes (group A Streptococcus [GAS]) and host cells during infection.
- To explore gene-expression patterns related to infection conditions, bacterial mutants, highly fit GAS clones, host immune responses, and lifestyle transitions.
Main Methods:
- Utilized microarray studies for differential transcriptional analysis.
- Examined gene expression on both the bacterial and host cell sides.
- Compared gene expression in mutant versus wild-type GAS strains.
Main Results:
- Provided insights into gene-expression patterns under infection-relevant conditions.
- Revealed differences in gene expression between mutant and wild-type GAS strains.
- Offered new understanding of host cell responses to GAS infection and GAS adaptation mechanisms.
Conclusions:
- Differential transcriptional analysis using microarrays significantly advances the understanding of Streptococcus pyogenes (group A Streptococcus [GAS]) pathogenesis.
- Insights gained illuminate bacterial virulence, adaptation, and host-pathogen interactions, including the shift towards invasive disease.
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